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    <title>Recent uclastat_oapdeposits items</title>
    <link>https://escholarship.org/uc/uclastat_oapdeposits/rss</link>
    <description>Recent eScholarship items from Open Access Policy Deposits</description>
    <pubDate>Sat, 13 Jun 2026 04:32:32 +0000</pubDate>
    <item>
      <title>Safe inference outside of randomized trials: Application of the stability-controlled quasi-experiment to the effects of three COVID-19 therapies</title>
      <link>https://escholarship.org/uc/item/3805286t</link>
      <description>When estimating the effects of medical therapies from their use outside of randomized trials, researchers often rely on assumptions that are difficult to justify and typically impossible to verify. The resulting estimates may thus be far from their intended causal targets, potentially making a harmful treatment appear beneficial or vice versa. We review the stability-controlled quasi-experiment (SCQE), a method suited to settings where a treatment's prevalence changes sharply over a short period, and apply it to assess the effects of remdesivir, hydroxychloroquine, and dexamethasone on COVID-19 mortality. Rather than requiring debate about the absence (or limited strength) of unobserved confounding, about "parallel trends'', or other well-known strategies, the SCQE asks users to reason about a "baseline trend'' assumption. In this setting, this asks"How much could COVID-19 mortality have changed over a short period, absent the treatment change in question?'' Any plausible range...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3805286t</guid>
      <pubDate>Wed, 3 Jun 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Wulf, David Ami</name>
      </author>
      <author>
        <name>Hazlett, Chad</name>
        <uri>https://orcid.org/0000-0003-1819-1928</uri>
      </author>
      <author>
        <name>Hill, Brian L</name>
      </author>
      <author>
        <name>Chiang, Jeffrey N</name>
      </author>
      <author>
        <name>Goodman-Meza, David</name>
      </author>
      <author>
        <name>Pasanuic, Bogdan</name>
      </author>
      <author>
        <name>Arah, Onyebuchi A</name>
        <uri>https://orcid.org/0000-0002-9067-1697</uri>
      </author>
      <author>
        <name>Erlandson, Kristine M</name>
      </author>
      <author>
        <name>Montague, Brian T</name>
      </author>
    </item>
    <item>
      <title>SnakeAltPromoter Facilitates Differential Alternative Promoter Analysis.</title>
      <link>https://escholarship.org/uc/item/2gt2908g</link>
      <description>&lt;b&gt;Background:&lt;/b&gt; Alternative promoter usage contributes to isoform diversity and gene regulation in mammals but remains difficult to study at scale. Cap Analysis of Gene Expression precisely maps transcription start sites, but its cost limits large-scale application. Alternatively, ProActiv, Salmon, and DEXSeq can be utilized with widely available RNA sequencing (RNA-seq) data to infer promoter activity. However, there is currently no framework available to automate the generation of reproducible results for these methods. &lt;b&gt;Results:&lt;/b&gt; SnakeAltPromoter, a scalable end-to-end Snakemake workflow, has been developed to automate alternative promoter analysis from raw RNA-seq data. The workflow performs quality control, alignment, and promoter quantification using 3 complementary RNA-seq analysis methods (junction-based, transcript-based, and first-exon-based), followed by promoter classification and differential activity or usage analysis. SnakeAltPromoter supports both command-line...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2gt2908g</guid>
      <pubDate>Mon, 27 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Tan, Jiang</name>
      </author>
      <author>
        <name>Wu, Yuqing</name>
      </author>
      <author>
        <name>Barve, Ruteja</name>
      </author>
      <author>
        <name>Lalmansingh, Jared</name>
      </author>
      <author>
        <name>Li, Fuhai</name>
      </author>
      <author>
        <name>Payne, Philip</name>
      </author>
      <author>
        <name>Kong, Nahyun</name>
      </author>
      <author>
        <name>Jin, Sheng</name>
      </author>
      <author>
        <name>Shan, Yuqi</name>
      </author>
      <author>
        <name>Zhou, Ruiwen</name>
      </author>
      <author>
        <name>Ge, Xinzhou</name>
      </author>
      <author>
        <name>Li, Jingyi Jessica</name>
      </author>
      <author>
        <name>Head, Richard</name>
      </author>
      <author>
        <name>Sun, Yidan</name>
      </author>
    </item>
    <item>
      <title>Assessing spatial disparities: a Bayesian linear regression approach</title>
      <link>https://escholarship.org/uc/item/2px762ds</link>
      <description>Epidemiological investigations of regionally aggregated spatial data often involve detecting spatial health disparities among neighboring regions on a map of disease mortality or incidence rates. Analyzing such data introduces spatial dependence among health outcomes and seeks to report statistically significant spatial disparities by delineating boundaries that separate neighboring regions with disparate health outcomes. However, there are statistical challenges to appropriately define what constitutes a spatial disparity and to construct robust probabilistic inferences for spatial disparities. We enrich the familiar Bayesian linear regression framework to introduce spatial autoregression and offer model-based detection of spatial disparities. We derive exploitable analytical tractability that considerably accelerates computation. Simulation experiments conducted on a county map of the entire United States demonstrate the effectiveness of our method, and we apply our method to...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2px762ds</guid>
      <pubDate>Thu, 23 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Wu, Kyle</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Toward spatio-temporal models to support national-scale forest carbon monitoring and reporting</title>
      <link>https://escholarship.org/uc/item/9f38z5mc</link>
      <description>National forest inventory (NFI) programs provide vital information on forest parameters’ status, trend, and change. Most NFI designs and estimation methods are tailored to estimate status over large areas but are not well suited to estimate trend and change, especially over small spatial areas and/or over short time periods (e.g. annual estimates). Fine-scale space-time indexed estimates are critical to a variety of environmental, ecological, and economic monitoring efforts. In the United States, for example, NFI data are used to estimate forest carbon status, trend, and change to support national, state, and local user group needs. Increasingly, these users seek finer spatial and temporal scale estimates to evaluate existing land use policies and management practices, and inform future activities. Here we propose a spatio-temporal Bayesian small area estimation modeling framework that delivers statistically valid estimates with complete uncertainty quantification for status,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9f38z5mc</guid>
      <pubDate>Wed, 22 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Shannon, Elliot S</name>
      </author>
      <author>
        <name>Finley, Andrew O</name>
      </author>
      <author>
        <name>Domke, Grant M</name>
      </author>
      <author>
        <name>May, Paul B</name>
      </author>
      <author>
        <name>Andersen, Hans-Erik</name>
      </author>
      <author>
        <name>Gaines, George C</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Nonstationary Spatial Process Models with Spatially Varying Covariance Kernels</title>
      <link>https://escholarship.org/uc/item/5455t7kv</link>
      <description>Building spatial process models that capture nonstationary behavior while delivering computationally efficient inference is challenging. Nonstationary spatially varying kernels (see, e.g., Paciorek, 2003) offer flexibility and richness, but computation is impeded by high-dimensional parameter spaces resulting from spatially varying process parameters. Matters are exacerbated if the number of locations recording measurements is massive. With limited theoretical tractability, obviating computational bottlenecks requires synergy between model construction and algorithm development. We build a class of scalable nonstationary spatial process models using spatially varying covariance kernels. We implement a Bayesian modeling framework using Hybrid Monte Carlo with nested interweaving. We conduct experiments on synthetic data sets to explore model selection and parameter identifiability, and assess inferential improvements accrued from nonstationary modeling. We illustrate strengths...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5455t7kv</guid>
      <pubDate>Wed, 22 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Coube-Sisqueille, Sébastien</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Liquet, Benoît</name>
      </author>
    </item>
    <item>
      <title>Bayesian Inference for Spatially‐Temporally Misaligned Data Using Predictive Stacking</title>
      <link>https://escholarship.org/uc/item/1ph8n2x4</link>
      <description>ABSTRACT Air pollution remains a major environmental risk factor that is often associated with adverse health outcomes. However, quantifying and evaluating its effects on human health is challenging due to the complex nature of exposure data. Recent technological advances have led to the collection of various indicators of air pollution at increasingly high spatial‐temporal resolutions (e.g., daily averages of pollutant levels at spatial locations referenced by latitude‐longitude). However, health outcomes are typically aggregated over several spatial‐temporal coordinates (e.g., annual prevalence for a county) to comply with survey regulations. This article develops a Bayesian hierarchical model to analyze such spatially‐temporally misaligned exposure and health outcome data. We develop Bayesian predictive stacking for spatially and temporally misaligned data to optimally combine inference from multiple predictive spatial‐temporal models. Stacking allows us to avoid iterative...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1ph8n2x4</guid>
      <pubDate>Wed, 22 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Pan, Soumyakanti</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Multivariate Spatial Process Models</title>
      <link>https://escholarship.org/uc/item/9s65f7gx</link>
      <description>Multivariate Spatial Process Models</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9s65f7gx</guid>
      <pubDate>Mon, 13 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Gelfand, Alan E</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Bayesian Nonstationary and Nonparametric Covariance Estimation for Large Spatial Data</title>
      <link>https://escholarship.org/uc/item/3283h08x</link>
      <description>In spatial statistics, it is often assumed that the spatial field of interest is stationary and its covariance has a simple parametric form, but these assumptions are not appropriate in many applications. Given replicate observations of a Gaussian spatial field, we propose nonstationary and nonparametric Bayesian inference on the spatial dependence. Instead of estimating the quadratic (in the number of spatial locations) entries of the covariance matrix, the idea is to infer a near-linear number of nonzero entries in a sparse Cholesky factor of the precision matrix. Our prior assumptions are motivated by recent results on the exponential decay of the entries of this Cholesky factor for Matérn-type covariances under a specific ordering scheme. Our methods are highly scalable and parallelizable. We conduct numerical comparisons and apply our methodology to climate-model output, enabling statistical emulation of an expensive physical model.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3283h08x</guid>
      <pubDate>Mon, 13 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Kidd, Brian</name>
      </author>
      <author>
        <name>Katzfuss, Matthias</name>
      </author>
    </item>
    <item>
      <title>Spatial Gradients and Wombling</title>
      <link>https://escholarship.org/uc/item/0328s58h</link>
      <description>Spatial Gradients and Wombling</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0328s58h</guid>
      <pubDate>Mon, 13 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>CellScope: high-performance cell atlas workflow with tree-structured representation</title>
      <link>https://escholarship.org/uc/item/5qn8k5m8</link>
      <description>Single-cell sequencing enables comprehensive profiling of individual cells, revealing cellular heterogeneity and function with unprecedented resolution. However, current analysis frameworks lack the ability to simultaneously explore and visualize cellular hierarchies at multiple biological levels. To address these limitations, we present CellScope, a promising framework for constructing high-resolution cell atlases at multiple clustering levels. CellScope employs a two-stage manifold fitting process for gene selection and noise reduction, followed by agglomerative clustering, and integrates UMAP visualization with hierarchical clustering to intuitively represent cellular relationships simultaneously at multiple levels—such as cell lineage, cell type, and cell subtype levels. Compared to established pipelines such as Seurat and Scanpy, CellScope comprehensively improves clustering performance, visualization clarity, computational efficiency, and algorithm interpretability, while...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5qn8k5m8</guid>
      <pubDate>Thu, 2 Apr 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Li, Bingjie</name>
      </author>
      <author>
        <name>Lin, Runyu</name>
      </author>
      <author>
        <name>Ni, Tianhao</name>
      </author>
      <author>
        <name>Yan, Guanao</name>
      </author>
      <author>
        <name>Burns, Mannix</name>
      </author>
      <author>
        <name>Li, Jingyi Jessica</name>
        <uri>https://orcid.org/0000-0002-9288-5648</uri>
      </author>
      <author>
        <name>Yao, Zhigang</name>
      </author>
    </item>
    <item>
      <title>Causal Machine Learning: A Deductive–Inductive Framework for Sociological Research</title>
      <link>https://escholarship.org/uc/item/66f206ff</link>
      <description>Causal explanation is central to sociological research, shaping both theoretical development and empirical inquiry. This paper argues that causal machine learning—which integrates deductive identification strategies with inductive estimation techniques—offers an analytical approach for modeling complex, nonlinear social processes within the potential outcomes framework. We argue that causal machine learning operates through an iterative feedback loop: Theoretical assumptions guide flexible estimation, which inductively uncovers complex heterogeneities and nonlinearities, and these discoveries subsequently refine and expand sociological knowledge. Drawing on a&amp;nbsp;systematic review of recent sociological research (2014–2024), we highlight how causal machine learning is advancing work in three key areas: causal effect heterogeneity, causal mediation analysis, and time-varying causal inference. These developments expand the methodological tool kit available to sociologists and strengthen...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/66f206ff</guid>
      <pubDate>Wed, 11 Mar 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Jeon, Nanum</name>
      </author>
      <author>
        <name>Brand, Jennie E</name>
      </author>
    </item>
    <item>
      <title>Fairness-Aware Kidney Exchange and Kidney Paired Donation</title>
      <link>https://escholarship.org/uc/item/03g771qt</link>
      <description>The kidney paired donation (KPD) program provides an innovative solution to overcome incompatibility challenges in kidney transplants by matching incompatible donor-patient pairs and facilitating kidney exchanges. To address unequal access to transplant opportunities, there are two widely used fairness criteria: group fairness and individual fairness. However, these criteria do not consider protected patient features, which refer to characteristics legally or ethically recognized as needing protection from discrimination, such as race and gender. Motivated by the calibration principle in machine learning, we introduce a new fairness criterion: the matching outcome should be conditionally independent of the protected feature, given the sensitization level. We integrate this fairness criterion as a constraint within the KPD optimization framework and propose a computationally efficient solution using linearization strategies and column-generation methods. Theoretically, we analyze...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/03g771qt</guid>
      <pubDate>Wed, 11 Feb 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Mingrui, Zhang</name>
      </author>
      <author>
        <name>Xiaowu, Dai</name>
      </author>
      <author>
        <name>Lexin, Li</name>
      </author>
    </item>
    <item>
      <title>Online Auction Design Using Distribution-Free Uncertainty Quantification with Applications to E-Commerce</title>
      <link>https://escholarship.org/uc/item/9xg083mf</link>
      <description>Online auction is a cornerstone of e-commerce, and a key challenge is designing incentive-compatible mechanisms that maximize expected revenue. Existing approaches often assume known bidder value distributions and fixed sets of bidders and items, but these assumptions rarely hold in real-world settings where bidder values are unknown, and the number of future participants is uncertain. In this article, we introduce the Conformal Online Auction Design (COAD), a novel mechanism that maximizes revenue by quantifying uncertainty in bidder values without relying on known distributions. COAD incorporates both bidder and item features, using historical data to design an incentive-compatible mechanism for online auctions. Unlike traditional methods, COAD leverages distribution-free uncertainty quantification techniques and integrates machine learning methods, such as random forests, kernel methods, and deep neural networks, to predict bidder values while ensuring revenue guarantees. Moreover,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9xg083mf</guid>
      <pubDate>Wed, 14 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Han, Jiale</name>
      </author>
      <author>
        <name>Dai, Xiaowu</name>
      </author>
    </item>
    <item>
      <title>Nonparametric estimation via partial derivatives</title>
      <link>https://escholarship.org/uc/item/4jw0w6kv</link>
      <description>Traditional nonparametric estimation methods often lead to a slow convergence rate in large dimensions and require unrealistically large dataset sizes for reliable conclusions. We develop an approach based on partial derivatives, either observed or estimated, to effectively estimate the function at near-parametric convergence rates. This novel approach and computational algorithm could lead to methods useful to practitioners in many areas of science and engineering. Our theoretical results reveal behaviour universal to this class of nonparametric estimation problems. We explore a general setting involving tensor product spaces and build upon the smoothing spline analysis of variance framework. For &lt;i&gt;d&lt;/i&gt;-dimensional models under full interaction, the optimal rates with gradient information on &lt;i&gt;p&lt;/i&gt; covariates are identical to those for the  -interaction models without gradients and, therefore, the models are immune to the &lt;i&gt;curse of interaction&lt;/i&gt;. For additive models,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4jw0w6kv</guid>
      <pubDate>Wed, 14 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Dai, Xiaowu</name>
      </author>
    </item>
    <item>
      <title>Gridding and Parameter Expansion for Scalable Latent Gaussian Models of Spatial Multivariate Data.</title>
      <link>https://escholarship.org/uc/item/9h9878br</link>
      <description>Scalable spatial GPs for massive datasets can be built via sparse Directed Acyclic Graphs (DAGs) where a small number of directed edges is sufficient to flexibly characterize spatial dependence. The DAG can be used to devise fast algorithms for posterior sampling of the latent process, but these may exhibit pathological behavior in estimating covariance parameters. In this article, we introduce gridding and parameter expansion methods to improve the practical performance of MCMC algorithms in terms of effective sample size per unit time (ESS/s). Gridding is a model-based strategy that reduces the number of expensive operations necessary during MCMC on irregularly spaced data. Parameter expansion reduces dependence in posterior samples in spatial regression for high resolution data. These two strategies lead to computational gains in the big data settings on which we focus. We consider popular constructions of univariate spatial processes based on Matérn covariance functions and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9h9878br</guid>
      <pubDate>Fri, 9 Jan 2026 00:00:00 +0000</pubDate>
      <author>
        <name>Peruzzi, Michele</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Dunson, David B</name>
      </author>
      <author>
        <name>Finley, Andrew O</name>
      </author>
    </item>
    <item>
      <title>Quantifying microbial interactions based on compositional data using an iterative approach for solving generalized Lotka-Volterra equations.</title>
      <link>https://escholarship.org/uc/item/32f0w92z</link>
      <description>Understanding microbial interactions is fundamental for exploring population dynamics, particularly in microbial communities where interactions affect stability and host health. Generalized Lotka-Volterra (gLV) models have been widely used to investigate system dynamics but depend on absolute abundance data, which are often unavailable in microbiome studies. To address this limitation, we introduce an iterative Lotka-Volterra (iLV) model, a novel framework tailored for compositional data that leverages relative abundances and iterative refinements for parameter estimation. The iLV model features two key innovations: an adaptation of the gLV framework to compositional constraints and an iterative optimization strategy combining linear approximations with nonlinear refinements to enhance parameter estimation accuracy. Using simulations and real-world datasets, we demonstrate that iLV surpasses existing methodologies, such as the compositional LV (cLV) and the generalized LV (gLV)...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/32f0w92z</guid>
      <pubDate>Wed, 19 Nov 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Huang, Yue</name>
      </author>
      <author>
        <name>Tang, Tianqi</name>
      </author>
      <author>
        <name>Dai, Xiaowu</name>
      </author>
      <author>
        <name>Sun, Fengzhu</name>
      </author>
    </item>
    <item>
      <title>Bayesian Geostatistics Using Predictive Stacking</title>
      <link>https://escholarship.org/uc/item/0hf5z4t4</link>
      <description>We develop Bayesian predictive stacking for geostatistical models, where the primary inferential objective is to provide inference on the latent spatial random field and conduct spatial predictions at arbitrary locations. We exploit analytically tractable posterior distributions for regression coefficients of predictors and the realizations of the spatial process conditional upon process parameters. We subsequently combine such inference by stacking these models across the range of values of the hyper-parameters. We devise stacking of means and posterior densities in a manner that is computationally efficient without resorting to iterative algorithms such as Markov chain Monte Carlo (MCMC) and can exploit the benefits of parallel computations. We offer novel theoretical insights into the resulting inference within an infill asymptotic paradigm and through empirical results showing that stacked inference is comparable to full sampling-based Bayesian inference at a significantly...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0hf5z4t4</guid>
      <pubDate>Mon, 13 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Lu</name>
      </author>
      <author>
        <name>Tang, Wenpin</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Dynamic Bayesian Learning for Spatiotemp oral Mechanistic Models</title>
      <link>https://escholarship.org/uc/item/07f7p3q3</link>
      <description>Dynamic Bayesian Learning for Spatiotemp oral Mechanistic Models</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/07f7p3q3</guid>
      <pubDate>Mon, 13 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Chen, Xiang</name>
      </author>
      <author>
        <name>Frankenburg, Ian</name>
      </author>
      <author>
        <name>Zhou, Daniel</name>
      </author>
    </item>
    <item>
      <title>Beware of counter-intuitive levels of false discoveries in datasets with strong intra-correlations</title>
      <link>https://escholarship.org/uc/item/58n6n0k9</link>
      <description>The false discovery rate (FDR) controlling method by Benjamini and Hochberg (BH) is a popular choice in the omics fields. Here, we demonstrate that in datasets with a large degree of dependencies between features, FDR correction methods like BH can sometimes counter-intuitively report very high numbers of false positives, potentially misleading researchers. We call the attention of researchers to use suited multiple testing strategies and approaches like synthetic null data (negative control) to identify and minimize caveats related to false discoveries, as in the cases where false findings do occur, they may be numerous.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/58n6n0k9</guid>
      <pubDate>Fri, 10 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kanduri, Chakravarthi</name>
      </author>
      <author>
        <name>Mamica, Maria</name>
      </author>
      <author>
        <name>Olstad, Emilie Willoch</name>
      </author>
      <author>
        <name>Zucknick, Manuela</name>
      </author>
      <author>
        <name>Li, Jingyi Jessica</name>
        <uri>https://orcid.org/0000-0002-9288-5648</uri>
      </author>
      <author>
        <name>Sandve, Geir Kjetil</name>
      </author>
    </item>
    <item>
      <title>Spatial transcriptomics iterative hierarchical clustering (stIHC): A novel method for identifying spatial gene co‐expression modules</title>
      <link>https://escholarship.org/uc/item/55r7d8v2</link>
      <description>Abstract Recent advancements in spatial transcriptomics (ST) technologies allow researchers to simultaneously measure RNA expression levels for hundreds to thousands of genes while preserving spatial information within tissues, providing critical insights into spatial gene expression patterns, tissue organization, and gene functionality. However, existing methods for clustering spatially variable genes (SVGs) into co‐expression modules often fail to detect rare or unique spatial expression patterns. To address this, we present spatial transcriptomics iterative hierarchical clustering (stIHC), a novel method for clustering SVGs into co‐expression modules, representing groups of genes with shared spatial expression patterns. Through three simulations and applications to ST datasets from technologies such as 10x Visium, 10x Xenium, and Spatial Transcriptomics, stIHC outperforms clustering approaches used by popular SVG detection methods, including SPARK, SPARK‐X, MERINGUE, and SpatialDE....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/55r7d8v2</guid>
      <pubDate>Thu, 9 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Higgins, Catherine</name>
      </author>
      <author>
        <name>Li, Jingyi Jessica</name>
        <uri>https://orcid.org/0000-0002-9288-5648</uri>
      </author>
      <author>
        <name>Carey, Michelle</name>
      </author>
    </item>
    <item>
      <title>Systematic benchmarking of computational methods to identify spatially variable genes</title>
      <link>https://escholarship.org/uc/item/16x872z6</link>
      <description>BackgroundSpatially resolved transcriptomics offers unprecedented insight by enabling the profiling of gene expression within the intact spatial context of cells, effectively adding a new and essential dimension to data interpretation. To efficiently detect spatial structure of interest, an essential step in analyzing such data involves identifying spatially variable genes (SVGs). Despite researchers having developed several computational methods to accomplish this task, the lack of a comprehensive benchmark evaluating their performance remains a considerable gap in the field.ResultsHere, we systematically evaluate 14 methods using 96 spatial datasets and 6 metrics. We compare the methods regarding gene ranking and classification based on real spatial variation, statistical calibration, and computation scalability and investigate the impact of identified SVGs on downstream applications such as spatial domain detection. Finally, we explore the applicability of the methods to spatial...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/16x872z6</guid>
      <pubDate>Thu, 9 Oct 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Li, Zhijian</name>
      </author>
      <author>
        <name>M.Patel, Zain</name>
      </author>
      <author>
        <name>Song, Dongyuan</name>
      </author>
      <author>
        <name>Yasa, Sai Nirmayi</name>
      </author>
      <author>
        <name>Cannoodt, Robrecht</name>
      </author>
      <author>
        <name>Yan, Guanao</name>
      </author>
      <author>
        <name>Li, Jingyi Jessica</name>
        <uri>https://orcid.org/0000-0002-9288-5648</uri>
      </author>
      <author>
        <name>Pinello, Luca</name>
      </author>
    </item>
    <item>
      <title>Leveraging national forest inventory data to estimate forest carbon density status and trends for small areas</title>
      <link>https://escholarship.org/uc/item/6xg4h80q</link>
      <description>Leveraging national forest inventory data to estimate forest carbon density status and trends for small areas</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6xg4h80q</guid>
      <pubDate>Wed, 24 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Shannon, Elliot S</name>
      </author>
      <author>
        <name>Finley, Andrew O</name>
      </author>
      <author>
        <name>May, Paul B</name>
      </author>
      <author>
        <name>Domke, Grant M</name>
      </author>
      <author>
        <name>Andersen, Hans-Erik</name>
      </author>
      <author>
        <name>Gaines, George C</name>
      </author>
      <author>
        <name>Nothdurft, Arne</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Bayesian Data Sketching for Varying Coefficient Regression Models.</title>
      <link>https://escholarship.org/uc/item/3nh2v07d</link>
      <description>Varying coefficient models are popular for estimating nonlinear regression functions in functional data models. Their Bayesian variants have received limited attention in large data applications, primarily due to prohibitively slow posterior computations using Markov chain Monte Carlo (MCMC) algorithms. We introduce Bayesian data sketching for varying coefficient models to obviate computational challenges presented by large sample sizes. To address the challenges of analyzing large data, we compress the functional response vector and predictor matrix by a random linear transformation to achieve dimension reduction and conduct inference on the compressed data. Our approach distinguishes itself from several existing methods for analyzing large functional data in that it requires neither the development of new models or algorithms, nor any specialized computational hardware while delivering fully model-based Bayesian inference. Well-established methods and algorithms for varying...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3nh2v07d</guid>
      <pubDate>Wed, 24 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Guhaniyogi, Rajarshi</name>
      </author>
      <author>
        <name>Baracaldo, Laura</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Statistical modelling of networked evolutionary public goods games</title>
      <link>https://escholarship.org/uc/item/0k23w5jh</link>
      <description>Abstract: 

               Repeated small dynamic networks are integral to studies in evolutionary game theory, where networked public goods games offer novel insights into human behaviours. Building on these findings, it is necessary to develop a statistical model that effectively captures dependencies across multiple small dynamic networks. While separable temporal exponential-family random graph models (STERGMs) have demonstrated success in modelling a large single dynamic network, their application to multiple small dynamic networks with less than 10 actors, remains unexplored. In this study, we extend the STERGM framework to accommodate multiple small dynamic networks, offering an approach to analysing such systems. Taking advantage of the small network sizes, our proposed approach improves accuracy in statistical inference through direct computation, unlike conventional approaches that rely on Markov Chain Monte Carlo methods. We demonstrate the validity of this framework...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0k23w5jh</guid>
      <pubDate>Mon, 15 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Ando, Hiroyasu</name>
      </author>
      <author>
        <name>Nishi, Akihiro</name>
        <uri>https://orcid.org/0000-0003-1629-5985</uri>
      </author>
      <author>
        <name>Handcock, Mark S</name>
        <uri>https://orcid.org/0000-0002-9985-2785</uri>
      </author>
    </item>
    <item>
      <title>Simultaneous Optimal Target Season Estimation and Local Climate Reconstruction Using Tree Rings</title>
      <link>https://escholarship.org/uc/item/9sm483fh</link>
      <description>Abstract: 
Tree rings provide a natural archive of past environmental variability and are a valuable resource for paleoclimate reconstructions of the Common Era. However, tree rings typically only provide climate information during a portion of the year and uncertainty in the seasonality of climate influence on the proxy formation adds to the challenge of separating climatic signal from non‐climatic noise. We propose a Bayesian hierarchical model for the simultaneous estimation of a target reconstruction season and reconstruction of local climate. We estimate the target reconstruction season through the introduction of latent monthly weights, whose priors can be adjusted to reflect expert knowledge. Model behavior is explored using pseudoproxy experiments and applications to tree‐ring chronologies with known seasonal biases. Our proposed model provides meaningful information about the true growth‐determining season of the proxy and leads to improved uncertainty quantification...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9sm483fh</guid>
      <pubDate>Thu, 11 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hwangbo, Nathan</name>
      </author>
      <author>
        <name>McKinnon, Karen A</name>
        <uri>https://orcid.org/0000-0003-3314-8442</uri>
      </author>
      <author>
        <name>Anchukaitis, Kevin J</name>
      </author>
    </item>
    <item>
      <title>Two Perspectives on Amplified Warming over Tropical Land Examined in CMIP6 Models</title>
      <link>https://escholarship.org/uc/item/3xb8q8s3</link>
      <description>Abstract: 

Climate change projections show amplified warming associated with dry conditions over tropical land. We compare two perspectives explaining this amplified warming: one based on tropical atmospheric dynamics and the other focusing on soil moisture and surface fluxes. We first compare the full spatiotemporal distribution of changes in key variables in the two perspectives under a quadrupling of CO2 using daily output from the CMIP6 simulations. Both perspectives center around the partitioning of the total energy/energy flux into the temperature and humidity components. We examine the contribution of this temperature/humidity partitioning in the base climate and its change under warming to rising temperatures by deriving a diagnostic linearized perturbation model that relates the magnitude of warming to 1) changes in the total energy/energy flux, 2) the base-climate temperature/humidity partitioning, and 3) changes in the partitioning under warming. We show that the spatiotemporal...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3xb8q8s3</guid>
      <pubDate>Thu, 11 Sep 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Duan, Suqin Q</name>
      </author>
      <author>
        <name>McKinnon, Karen A</name>
        <uri>https://orcid.org/0000-0003-3314-8442</uri>
      </author>
      <author>
        <name>Simpson, Isla R</name>
      </author>
    </item>
    <item>
      <title>: The Accidental Equalizer: How Luck Determines Pay After College</title>
      <link>https://escholarship.org/uc/item/5nd992bf</link>
      <description>: The Accidental Equalizer: How Luck Determines Pay After College</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5nd992bf</guid>
      <pubDate>Wed, 16 Jul 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Brand, Jennie E</name>
      </author>
    </item>
    <item>
      <title>Gender and racial diversity socialization in science</title>
      <link>https://escholarship.org/uc/item/07d4c30w</link>
      <description>Scientific collaboration networks are a form of unequally distributed social capital that shapes both researcher job placement and long-term research productivity and prominence. However, the role of collaboration networks in shaping the gender and racial diversity of the scientific workforce remains unclear. Here we propose a computational null model to investigate the degree to which early-career scientific collaborators with representationally diverse cohorts of scholars are associated with forming or participating in more diverse research groups as established researchers. When testing this hypothesis using two large-scale, longitudinal datasets on scientific collaborations, we find that the gender and racial diversity in a researcher’s early-career collaboration environment is strongly associated with the diversity of their collaborators in their established period. This diversity-association effect is particularly prominent for men. Coupled with gender and racial homophily...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/07d4c30w</guid>
      <pubDate>Wed, 21 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Li, Weihua</name>
      </author>
      <author>
        <name>Zheng, Hongwei</name>
      </author>
      <author>
        <name>Brand, Jennie E</name>
      </author>
      <author>
        <name>Clauset, Aaron</name>
      </author>
    </item>
    <item>
      <title>The Farm Animal Genotype–Tissue Expression (FarmGTEx) Project</title>
      <link>https://escholarship.org/uc/item/7qw8m94p</link>
      <description>Genetic mutation and drift, coupled with natural and human-mediated selection and migration, have produced a wide variety of genotypes and phenotypes in farmed animals. We here introduce the Farm Animal Genotype–Tissue Expression (FarmGTEx) Project, which aims to elucidate the genetic determinants of gene expression across 16 terrestrial and aquatic domestic species under diverse biological and environmental contexts. For each species, we aim to collect multiomics data, particularly genomics and transcriptomics, from 50 tissues of 1,000 healthy adults and 200 additional animals representing a specific context. This Perspective provides an overview of the priorities of FarmGTEx and advocates for coordinated strategies of data analysis and resource-sharing initiatives. FarmGTEx aims to serve as a platform for investigating context-specific regulatory effects, which will deepen our understanding of molecular mechanisms underlying complex phenotypes. The knowledge and insights provided...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7qw8m94p</guid>
      <pubDate>Sun, 11 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Fang, Lingzhao</name>
      </author>
      <author>
        <name>Teng, Jinyan</name>
      </author>
      <author>
        <name>Lin, Qing</name>
      </author>
      <author>
        <name>Bai, Zhonghao</name>
      </author>
      <author>
        <name>Liu, Shuli</name>
      </author>
      <author>
        <name>Guan, Dailu</name>
      </author>
      <author>
        <name>Li, Bingjie</name>
      </author>
      <author>
        <name>Gao, Yahui</name>
      </author>
      <author>
        <name>Hou, Yali</name>
      </author>
      <author>
        <name>Gong, Mian</name>
      </author>
      <author>
        <name>Pan, Zhangyuan</name>
      </author>
      <author>
        <name>Yu, Ying</name>
      </author>
      <author>
        <name>Clark, Emily L</name>
      </author>
      <author>
        <name>Smith, Jacqueline</name>
      </author>
      <author>
        <name>Rawlik, Konrad</name>
      </author>
      <author>
        <name>Xiang, Ruidong</name>
      </author>
      <author>
        <name>Chamberlain, Amanda J</name>
      </author>
      <author>
        <name>Goddard, Michael E</name>
      </author>
      <author>
        <name>Littlejohn, Mathew</name>
      </author>
      <author>
        <name>Larson, Greger</name>
      </author>
      <author>
        <name>MacHugh, David E</name>
      </author>
      <author>
        <name>O’Grady, John F</name>
      </author>
      <author>
        <name>Sørensen, Peter</name>
      </author>
      <author>
        <name>Sahana, Goutam</name>
      </author>
      <author>
        <name>Lund, Mogens Sandø</name>
      </author>
      <author>
        <name>Jiang, Zhihua</name>
      </author>
      <author>
        <name>Pan, Xiangchun</name>
      </author>
      <author>
        <name>Gong, Wentao</name>
      </author>
      <author>
        <name>Zhang, Haihan</name>
      </author>
      <author>
        <name>He, Xi</name>
      </author>
      <author>
        <name>Zhang, Yuebo</name>
      </author>
      <author>
        <name>Gao, Ning</name>
      </author>
      <author>
        <name>He, Jun</name>
      </author>
      <author>
        <name>Yi, Guoqiang</name>
      </author>
      <author>
        <name>Liu, Yuwen</name>
      </author>
      <author>
        <name>Tang, Zhonglin</name>
      </author>
      <author>
        <name>Zhao, Pengju</name>
      </author>
      <author>
        <name>Zhou, Yang</name>
      </author>
      <author>
        <name>Fu, Liangliang</name>
      </author>
      <author>
        <name>Wang, Xiao</name>
      </author>
      <author>
        <name>Hao, Dan</name>
      </author>
      <author>
        <name>Liu, Lei</name>
      </author>
      <author>
        <name>Chen, Siqian</name>
      </author>
      <author>
        <name>Young, Robert S</name>
      </author>
      <author>
        <name>Shen, Xia</name>
      </author>
      <author>
        <name>Xia, Charley</name>
      </author>
      <author>
        <name>Cheng, Hao</name>
      </author>
      <author>
        <name>Ma, Li</name>
      </author>
      <author>
        <name>Cole, John B</name>
      </author>
      <author>
        <name>Baldwin, Ransom L</name>
      </author>
      <author>
        <name>Li, Cong-jun</name>
      </author>
      <author>
        <name>Van Tassell, Curtis P</name>
      </author>
      <author>
        <name>Rosen, Benjamin D</name>
      </author>
      <author>
        <name>Bhowmik, Nayan</name>
      </author>
      <author>
        <name>Lunney, Joan</name>
      </author>
      <author>
        <name>Liu, Wansheng</name>
      </author>
      <author>
        <name>Guan, Leluo</name>
      </author>
      <author>
        <name>Zhao, Xin</name>
      </author>
      <author>
        <name>Ibeagha-Awemu, Eveline M</name>
      </author>
      <author>
        <name>Luo, Yonglun</name>
      </author>
      <author>
        <name>Lin, Lin</name>
      </author>
      <author>
        <name>Canela-Xandri, Oriol</name>
      </author>
      <author>
        <name>Derks, Martijn FL</name>
      </author>
      <author>
        <name>Crooijmans, Richard PMA</name>
      </author>
      <author>
        <name>Gòdia, Marta</name>
      </author>
      <author>
        <name>Madsen, Ole</name>
      </author>
      <author>
        <name>Groenen, Martien AM</name>
      </author>
      <author>
        <name>Koltes, James E</name>
      </author>
      <author>
        <name>Tuggle, Christopher K</name>
      </author>
      <author>
        <name>McCarthy, Fiona M</name>
      </author>
      <author>
        <name>Rocha, Dominique</name>
      </author>
      <author>
        <name>Giuffra, Elisabetta</name>
      </author>
      <author>
        <name>Amills, Marcel</name>
      </author>
      <author>
        <name>Clop, Alex</name>
      </author>
      <author>
        <name>Ballester, Maria</name>
      </author>
      <author>
        <name>Tosser-Klopp, Gwenola</name>
      </author>
      <author>
        <name>Li, Jing</name>
      </author>
      <author>
        <name>Fang, Chao</name>
      </author>
      <author>
        <name>Fang, Ming</name>
      </author>
      <author>
        <name>Wang, Qishan</name>
      </author>
      <author>
        <name>Hou, Zhuocheng</name>
      </author>
      <author>
        <name>Wang, Qin</name>
      </author>
      <author>
        <name>Zhao, Fuping</name>
      </author>
      <author>
        <name>Jiang, Lin</name>
      </author>
      <author>
        <name>Zhao, Guiping</name>
      </author>
      <author>
        <name>Zhou, Zhengkui</name>
      </author>
      <author>
        <name>Zhou, Rong</name>
      </author>
      <author>
        <name>Liu, Hehe</name>
      </author>
      <author>
        <name>Deng, Juan</name>
      </author>
      <author>
        <name>Jin, Long</name>
      </author>
      <author>
        <name>Li, Mingzhou</name>
      </author>
      <author>
        <name>Mo, Delin</name>
      </author>
      <author>
        <name>Liu, Xiaohong</name>
      </author>
      <author>
        <name>Chen, Yaosheng</name>
      </author>
      <author>
        <name>Yuan, Xiaolong</name>
      </author>
      <author>
        <name>Li, Jiaqi</name>
      </author>
      <author>
        <name>Zhao, Shuhong</name>
      </author>
      <author>
        <name>Zhang, Yi</name>
      </author>
      <author>
        <name>Ding, Xiangdong</name>
      </author>
      <author>
        <name>Sun, Dongxiao</name>
      </author>
    </item>
    <item>
      <title>scDEED: a statistical method for detecting dubious 2D single-cell embeddings and optimizing t-SNE and UMAP hyperparameters</title>
      <link>https://escholarship.org/uc/item/3nv767g4</link>
      <description>Two-dimensional (2D) embedding methods are crucial for single-cell data visualization. Popular methods such as t-SNE and UMAP are commonly used for visualizing cell clusters; however, it is well known that t-SNE and UMAP's 2D embedding might not reliably inform the similarities among cell clusters. Motivated by this challenge, we developed a statistical method, scDEED, for detecting dubious cell embeddings output by any 2D-embedding method. By calculating a reliability score for every cell embedding, scDEED identifies the cell embeddings with low reliability scores as dubious and those with high reliability scores as trustworthy. Moreover, by minimizing the number of dubious cell embeddings, scDEED provides intuitive guidance for optimizing the hyperparameters of an embedding method. Applied to multiple scRNA-seq datasets, scDEED demonstrates its effectiveness for detecting dubious cell embeddings and optimizing the hyperparameters of t-SNE and UMAP.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3nv767g4</guid>
      <pubDate>Sun, 11 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Xia, Lucy</name>
      </author>
      <author>
        <name>Lee, Christy</name>
      </author>
      <author>
        <name>Li, Jingyi Jessica</name>
        <uri>https://orcid.org/0000-0002-9288-5648</uri>
      </author>
    </item>
    <item>
      <title>Comment on “Data Fission: Splitting a Single Data Point” Data Fission for Unsupervised Learning: A Discussion on Post-Clustering Inference and the Challenges of Debiasing</title>
      <link>https://escholarship.org/uc/item/2fc64719</link>
      <description>Comment on “Data Fission: Splitting a Single Data Point” Data Fission for Unsupervised Learning: A Discussion on Post-Clustering Inference and the Challenges of Debiasing</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2fc64719</guid>
      <pubDate>Sun, 11 May 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Wang, Changhu</name>
      </author>
      <author>
        <name>Ge, Xinzhou</name>
      </author>
      <author>
        <name>Song, Dongyuan</name>
      </author>
      <author>
        <name>Li, Jingyi Jessica</name>
        <uri>https://orcid.org/0000-0002-9288-5648</uri>
      </author>
    </item>
    <item>
      <title>Developmental isoform diversity in the human neocortex informs neuropsychiatric risk mechanisms</title>
      <link>https://escholarship.org/uc/item/2253m06c</link>
      <description>RNA splicing is highly prevalent in the brain and has strong links to neuropsychiatric disorders; yet, the role of cell type-specific splicing and transcript-isoform diversity during human brain development has not been systematically investigated. In this work, we leveraged single-molecule long-read sequencing to deeply profile the full-length transcriptome of the germinal zone and cortical plate regions of the developing human neocortex at tissue and single-cell resolution. We identified 214,516 distinct isoforms, of which 72.6% were novel (not previously annotated in Gencode version 33), and uncovered a substantial contribution of transcript-isoform diversity-regulated by RNA binding proteins-in defining cellular identity in the developing neocortex. We leveraged this comprehensive isoform-centric gene annotation to reprioritize thousands of rare de novo risk variants and elucidate genetic risk mechanisms for neuropsychiatric disorders.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2253m06c</guid>
      <pubDate>Sat, 12 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Patowary, Ashok</name>
        <uri>https://orcid.org/0000-0001-7507-3907</uri>
      </author>
      <author>
        <name>Zhang, Pan</name>
      </author>
      <author>
        <name>Jops, Connor</name>
      </author>
      <author>
        <name>Vuong, Celine K</name>
      </author>
      <author>
        <name>Ge, Xinzhou</name>
      </author>
      <author>
        <name>Hou, Kangcheng</name>
      </author>
      <author>
        <name>Kim, Minsoo</name>
      </author>
      <author>
        <name>Gong, Naihua</name>
      </author>
      <author>
        <name>Margolis, Michael</name>
      </author>
      <author>
        <name>Vo, Daniel</name>
      </author>
      <author>
        <name>Wang, Xusheng</name>
      </author>
      <author>
        <name>Liu, Chunyu</name>
      </author>
      <author>
        <name>Pasaniuc, Bogdan</name>
        <uri>https://orcid.org/0000-0002-0227-2056</uri>
      </author>
      <author>
        <name>Li, Jingyi Jessica</name>
        <uri>https://orcid.org/0000-0002-9288-5648</uri>
      </author>
      <author>
        <name>Gandal, Michael J</name>
      </author>
      <author>
        <name>de la Torre-Ubieta, Luis</name>
        <uri>https://orcid.org/0000-0001-8059-6243</uri>
      </author>
    </item>
    <item>
      <title>Methods for the Analysis of 26 Million VOC Area Measurements during the Deepwater Horizon Oil Spill Clean-up</title>
      <link>https://escholarship.org/uc/item/8hs7k1c5</link>
      <description>The NIEHS GuLF STUDY is an epidemiologic study of the health of workers who participated in the 2010 Deepwater Horizon oil spill response and clean-up effort. Even with a large database of approximately 28 000 personal samples that were analyzed for total hydrocarbons (THCs) and other oil-related chemicals, resulting in nearly 160 000 full-shift personal measurements, there were still exposure scenarios where the number of measurements was too limited to rigorously assess exposures. Also available were over 26 million volatile organic compounds (VOCs) area air measurements of approximately 1-min duration, collected from direct-reading instruments on 38 large vessels generally located near the leaking well. This paper presents a strategy for converting the VOC database into hourly average air concentrations by vessel as the first step of a larger process designed to use these data to supplement full-shift THC personal exposure measurements. We applied a Bayesian method to account...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8hs7k1c5</guid>
      <pubDate>Fri, 11 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Groth, Caroline P</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
      <author>
        <name>Blair, Aaron</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Stenzel, Mark R</name>
      </author>
    </item>
    <item>
      <title>Exposure Assessment Techniques Applied to the Highly Censored Deepwater Horizon Gulf Oil Spill Personal Measurements</title>
      <link>https://escholarship.org/uc/item/5q93m8k4</link>
      <description>The GuLF Long-term Follow-up Study (GuLF STUDY) is investigating potential adverse health effects of workers involved in the Deepwater Horizon (DWH) oil spill response and cleanup (OSRC). Over 93% of the 160 000 personal air measurements taken on OSRC workers were below the limit of detection (LOD), as reported by the analytic labs. At this high level of censoring, our ability to develop exposure estimates was limited. The primary objective here was to reduce the number of measurements below the labs' reported LODs to reflect the analytic methods' true LODs, thereby facilitating the use of a relatively unbiased and precise Bayesian method to develop exposure estimates for study exposure groups (EGs). The estimates informed a job-exposure matrix to characterize exposure of study participants. A second objective was to develop descriptive statistics for relevant EGs that did not meet the Bayesian criteria of sample size ≥5 and censoring ≤80% to achieve the aforementioned level of...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5q93m8k4</guid>
      <pubDate>Fri, 11 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Stenzel, Mark R</name>
      </author>
      <author>
        <name>Groth, Caroline P</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
    </item>
    <item>
      <title>Fixed-Domain Asymptotics Under Vecchia's Approximation of Spatial Process Likelihoods.</title>
      <link>https://escholarship.org/uc/item/47p289r3</link>
      <description>Statistical modeling for massive spatial data sets has generated a substantial literature on scalable spatial processes based upon Vecchia's approximation. Vecchia's approximation for Gaussian process models enables fast evaluation of the likelihood by restricting dependencies at a location to its neighbors. We establish inferential properties of microergodic spatial covariance parameters within the paradigm of fixed-domain asymptotics when they are estimated using Vecchia's approximation. The conditions required to formally establish these properties are explored, theoretically and empirically, and the effectiveness of Vecchia's approximation is further corroborated from the standpoint of fixed-domain asymptotics.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/47p289r3</guid>
      <pubDate>Fri, 11 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zhang, Lu</name>
      </author>
      <author>
        <name>Tang, Wenpin</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Linear Relationships Between Total Hydrocarbons and Benzene, Toluene, Ethylbenzene, Xylene, and n-Hexane during the Deepwater Horizon Response and Clean-up</title>
      <link>https://escholarship.org/uc/item/37n9r3qt</link>
      <description>OBJECTIVES: Our objectives were to (i) determine correlations between measurements of THC and of BTEX-H, (ii) apply these linear relationships to predict BTEX-H from measured THC, (iii) use these correlations as informative priors in Bayesian analyses to estimate exposures.
METHODS: We used a Bayesian left-censored bivariate framework for all 3 objectives. First, we modeled the relationships (i.e. correlations) between THC and each BTEX-H chemical for various overarching groups of measurements using linear regression to determine if correlations derived from linear relationships differed by various exposure determinants. We then used the same linear regression relationships to predict (or impute) BTEX-H measurements from THC when only THC measurements were available. Finally, we used the same linear relationships as priors for the final exposure models that used real and predicted data to develop exposure estimate statistics for each individual exposure group.
RESULTS: Correlations...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/37n9r3qt</guid>
      <pubDate>Fri, 11 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Groth, Caroline P</name>
      </author>
      <author>
        <name>Huynh, Tran B</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
      <author>
        <name>Quick, Harrison</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
      <author>
        <name>Blair, Aaron</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Stenzel, Mark R</name>
      </author>
    </item>
    <item>
      <title>Estimates of Inhalation Exposures to Oil-Related Components on the Supporting Vessels During the Deepwater Horizon Oil Spill</title>
      <link>https://escholarship.org/uc/item/2qz312wt</link>
      <description>The Deepwater Horizon oil spill response and clean-up (OSRC) involved over 9000 large and small vessels deployed in waters of the Gulf of Mexico across four states (Alabama, Florida, Louisiana, and Mississippi). For the GuLF STUDY, we developed exposure estimates of oil-related components for many work groups to capture a wide range of OSRC operations on these vessels, such as supporting the four rig vessels charged with stopping the spill at the wellhead; skimming oil; in situ burning of oil; absorbing and containing oil by boom; and environmental monitoring. Work groups were developed by: (i) vessel activity; (ii) location (area of the Gulf or state); and (iii) time period. Using Bayesian methods, we computed exposure estimates for these groups for: total hydrocarbons measured as total petroleum hydrocarbons (THC), benzene, toluene, ethylbenzene, xylene, and n-hexane (BTEX-H). Estimates of the arithmetic means for THC ranged from 0.10 ppm [95% credible interval (CI) 0.04, 0.38...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2qz312wt</guid>
      <pubDate>Fri, 11 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Huynh, Tran B</name>
      </author>
      <author>
        <name>Groth, Caroline P</name>
      </author>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Stenzel, Mark</name>
      </author>
      <author>
        <name>Blair, Aaron</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
    </item>
    <item>
      <title>Exposure Group Development in Support of the NIEHS GuLF Study</title>
      <link>https://escholarship.org/uc/item/2fz6w3pz</link>
      <description>In the GuLF Study, a study investigating possible adverse health effects associated with work on the oil spill response and clean-up (OSRC) following the Deepwater Horizon disaster in the Gulf of Mexico, we used a job-exposure matrix (JEM) approach to estimate exposures. The JEM linked interview responses of study participants to measurement data through exposure groups (EGs). Here we describe a systematic process used to develop transparent and precise EGs that allowed characterization of exposure levels among the large number of OSRC activities performed across the Gulf of Mexico over time and space. EGs were identified by exposure determinants available to us in our measurement database, from a substantial body of other spill-related information, and from responses provided by study participants in a detailed interview. These determinants included: job/activity/task, vessel and type of vessel, weathering of the released oil, area of the Gulf of Mexico, Gulf coast state, and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2fz6w3pz</guid>
      <pubDate>Fri, 11 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Stenzel, Mark R</name>
      </author>
      <author>
        <name>Groth, Caroline P</name>
      </author>
      <author>
        <name>Huynh, Tran B</name>
      </author>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Blair, Aaron</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
    </item>
    <item>
      <title>spNNGP R Package for Nearest Neighbor Gaussian Process Models</title>
      <link>https://escholarship.org/uc/item/9vm1x6vp</link>
      <description>spNNGP R Package for Nearest Neighbor Gaussian Process Models</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9vm1x6vp</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Finley, Andrew O</name>
      </author>
      <author>
        <name>Datta, Abhirup</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Bayesian Multi-Group Gaussian Process Models for Heterogeneous Group-Structured Data.</title>
      <link>https://escholarship.org/uc/item/9p86p9d3</link>
      <description>Gaussian processes are pervasive in functional data analysis, machine learning, and spatial statistics for modeling complex dependencies. Scientific data are often heterogeneous in their inputs and contain multiple known discrete groups of samples; thus, it is desirable to leverage the similarity among groups while accounting for heterogeneity across groups. We propose multi-group Gaussian processes (MGGPs) defined over  , where  is a finite set representing the group label, by developing general classes of valid (positive definite) covariance functions on such domains. MGGPs are able to accurately recover relationships between the groups and efficiently share strength across samples from all groups during inference, while capturing distinct group-specific behaviors in the conditional posterior distributions. We demonstrate inference in MGGPs through simulation experiments, and we apply our proposed MGGP regression framework to gene expression data to illustrate the behavior and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9p86p9d3</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Li, Didong</name>
      </author>
      <author>
        <name>Jones, Andrew</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Engelhardt, Barbara</name>
      </author>
    </item>
    <item>
      <title>Fine Particulate Matter and Lung Function among Burning-Exposed Deepwater Horizon Oil Spill Workers</title>
      <link>https://escholarship.org/uc/item/9d97h3hm</link>
      <description>BACKGROUND: During the 2010 &lt;i&gt;Deepwater Horizon&lt;/i&gt; (&lt;i&gt;DWH&lt;/i&gt;) disaster, controlled burning was conducted to remove oil from the water. Workers near combustion sites were potentially exposed to increased fine particulate matter [with aerodynamic diameter  ()] levels. Exposure to  has been linked to decreased lung function, but to our knowledge, no study has examined exposure encountered in an oil spill cleanup.
OBJECTIVE: We investigated the association between estimated  only from burning/flaring of oil/gas and lung function measured 1-3 y after the &lt;i&gt;DWH&lt;/i&gt; disaster.
METHODS: We included workers who participated in response and cleanup activities on the water during the &lt;i&gt;DWH&lt;/i&gt; disaster and had lung function measured at a subsequent home visit ().  concentrations were estimated using a Gaussian plume dispersion model and linked to work histories via a job-exposure matrix. We evaluated forced expiratory volume in 1 s (FEV1; milliliters), forced vital capacity (FVC; milliliters),...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/9d97h3hm</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Chen, Dazhe</name>
      </author>
      <author>
        <name>Lawrence, Kaitlyn G</name>
      </author>
      <author>
        <name>Pratt, Gregory C</name>
      </author>
      <author>
        <name>Stenzel, Mark R</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
      <author>
        <name>Groth, Caroline P</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Christenbury, Kate</name>
      </author>
      <author>
        <name>Curry, Matthew D</name>
      </author>
      <author>
        <name>Jackson, W Braxton</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Blair, Aaron</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
    </item>
    <item>
      <title>The GuLF STUDY: A Prospective Study of Persons Involved in the Deepwater Horizon Oil Spill Response and Clean-Up</title>
      <link>https://escholarship.org/uc/item/96k681bp</link>
      <description>BACKGROUND: The 2010 &lt;i&gt;Deepwater Horizon&lt;/i&gt; disaster led to the largest ever marine oil spill. Individuals who worked on the spill were exposed to toxicants and stressors that could lead to adverse effects.
OBJECTIVES: The GuLF STUDY was designed to investigate relationships between oil spill exposures and multiple potential physical and mental health effects.
METHODS: Participants were recruited by telephone from lists of individuals who worked on the oil spill response and clean-up or received safety training. Enrollment interviews between 2011 and 2013 collected information about spill-related activities, demographics, lifestyle, and health. Exposure measurements taken during the oil spill were used with questionnaire responses to characterize oil exposures of participants. Participants from Gulf states completed a home visit in which biological and environmental samples, anthropometric and clinical measurements, and additional health and lifestyle information were collected....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/96k681bp</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Miller, Aubrey K</name>
      </author>
      <author>
        <name>Blair, Aaron</name>
      </author>
      <author>
        <name>Curry, Matthew D</name>
      </author>
      <author>
        <name>Jackson, W Braxton</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
      <author>
        <name>Stenzel, Mark R</name>
      </author>
      <author>
        <name>Birnbaum, Linda S</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
      <author>
        <name>Team, for the GuLF STUDY Research</name>
      </author>
    </item>
    <item>
      <title>Estimates of Occupational Inhalation Exposures to Six Oil-Related Compounds on the Four Rig Vessels Responding to the Deepwater Horizon Oil Spill</title>
      <link>https://escholarship.org/uc/item/94w1933v</link>
      <description>BACKGROUND: The 2010 Deepwater Horizon (DWH) oil spill involved thousands of workers and volunteers to mitigate the oil release and clean-up after the spill. Health concerns for these participants led to the initiation of a prospective epidemiological study (GuLF STUDY) to investigate potential adverse health outcomes associated with the oil spill response and clean-up (OSRC). Characterizing the chemical exposures of the OSRC workers was an essential component of the study. Workers on the four oil rig vessels mitigating the spill and located within a 1852 m (1 nautical mile) radius of the damaged wellhead [the Discoverer Enterprise (Enterprise), the Development Driller II (DDII), the Development Driller III (DDIII), and the HelixQ4000] had some of the greatest potential for chemical exposures.
OBJECTIVES: The aim of this paper is to characterize potential personal chemical exposures via the inhalation route for workers on those four rig vessels. Specifically, we presented our...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/94w1933v</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Huynh, Tran B</name>
      </author>
      <author>
        <name>Groth, Caroline P</name>
      </author>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Stenzel, Mark</name>
      </author>
      <author>
        <name>Quick, Harrison</name>
      </author>
      <author>
        <name>Blair, Aaron</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
    </item>
    <item>
      <title>Exposure to volatile hydrocarbons and neurologic function among oil spill workers up to 6 years after the Deepwater Horizon disaster</title>
      <link>https://escholarship.org/uc/item/8v75h432</link>
      <description>BACKGROUND: During the 2010 Deepwater Horizon (DWH) disaster, oil spill response and cleanup (OSRC) workers were exposed to toxic volatile components of crude oil. Few studies have examined exposure to individual volatile hydrocarbon chemicals below occupational exposure limits in relation to neurologic function among OSRC workers.
OBJECTIVES: To investigate the association of several spill-related chemicals (benzene, toluene, ethylbenzene, xylene, n-hexane, i.e., BTEX-H) and total petroleum hydrocarbons (THC) with neurologic function among DWH spill workers enrolled in the Gulf Long-term Follow-up Study.
METHODS: Cumulative exposure to THC and BTEX-H across the oil spill cleanup period were estimated using a job-exposure matrix that linked air measurement data to detailed self-reported DWH OSRC work histories. We ascertained quantitative neurologic function data via a comprehensive test battery at a clinical examination that occurred 4-6 years after the DWH disaster. We used...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8v75h432</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Chen, Dazhe</name>
      </author>
      <author>
        <name>Werder, Emily J</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
      <author>
        <name>Stenzel, Mark R</name>
      </author>
      <author>
        <name>Gerr, Fredric E</name>
      </author>
      <author>
        <name>Lawrence, Kaitlyn G</name>
      </author>
      <author>
        <name>Groth, Caroline P</name>
      </author>
      <author>
        <name>Huynh, Tran B</name>
      </author>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Jackson Ii, W Braxton</name>
      </author>
      <author>
        <name>Christenbury, Kate</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
    </item>
    <item>
      <title>Bayesian State Space Modeling of Physical Processes in Industrial Hygiene</title>
      <link>https://escholarship.org/uc/item/8n7895tp</link>
      <description>Exposure assessment models are deterministic models derived from physical-chemical laws. In real workplace settings, chemical concentration measurements can be noisy and indirectly measured. In addition, inference on important parameters such as generation and ventilation rates are usually of interest since they are difficult to obtain. In this article, we outline a flexible Bayesian framework for parameter inference and exposure prediction. In particular, we devise Bayesian state space models by discretizing the differential equation models and incorporating information from observed measurements and expert prior knowledge. At each time point, a new measurement is available that contains some noise, so using the physical model and the available measurements, we try to obtain a more accurate state estimate, which can be called filtering. We consider Monte Carlo sampling methods for parameter estimation and inference under nonlinear and non-Gaussian assumptions. The performance...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8n7895tp</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Abdalla, Nada</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Arnold, Susan</name>
      </author>
    </item>
    <item>
      <title>bayesassurance: An R Package for Calculating Sample Size and Bayesian Assurance</title>
      <link>https://escholarship.org/uc/item/7wt436gr</link>
      <description>bayesassurance: An R Package for Calculating Sample Size and Bayesian Assurance</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7wt436gr</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Pan, Jane</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Assessing Exposures from the Deepwater Horizon Oil Spill Response and Clean-up</title>
      <link>https://escholarship.org/uc/item/7vq389qj</link>
      <description>The GuLF Study is investigating adverse health effects from work on the response and clean-up after the Deepwater Horizon explosion and oil release. An essential and necessary component of that study was the exposure assessment. Bayesian statistical methods and over 135 000 measurements of total hydrocarbons (THC), benzene, ethylbenzene, toluene, xylene, and n-hexane (BTEX-H) were used to estimate inhalation exposures to these chemicals for &amp;gt;3400 exposure groups (EGs) formed from three exposure determinants: job/activity/task, location, and time period. Recognized deterministic models were used to estimate airborne exposures to particulate matter sized 2.5 µm or less (PM2.5) and dispersant aerosols and vapors. Dermal exposures were estimated for these same oil-related substances using a model modified especially for this study from a previously published model. Exposures to oil mist were assessed using professional judgment. Estimated daily THC arithmetic means (AMs) were in...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7vq389qj</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Stewart, Patricia</name>
      </author>
      <author>
        <name>Groth, Caroline P</name>
      </author>
      <author>
        <name>Huynh, Tran B</name>
      </author>
      <author>
        <name>Ng, Melanie Gorman</name>
      </author>
      <author>
        <name>Pratt, Gregory C</name>
      </author>
      <author>
        <name>Arnold, Susan F</name>
      </author>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Cherrie, John W</name>
      </author>
      <author>
        <name>Christenbury, Kate</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Blair, Aaron</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
      <author>
        <name>Stenzel, Mark R</name>
      </author>
    </item>
    <item>
      <title>Scalable Predictions for Spatial Probit Linear Mixed Models Using Nearest Neighbor Gaussian Processes</title>
      <link>https://escholarship.org/uc/item/7vb7h60j</link>
      <description>Spatial probit generalized linear mixed models (spGLMM) with a linear fixed effect and a spatial random effect, endowed with a Gaussian Process prior, are widely used for analysis of binary spatial data. However, the canonical Bayesian implementation of this hierarchical mixed model can involve protracted Markov Chain Monte Carlo sampling. Alternate approaches have been proposed that circumvent this by directly representing the marginal likelihood from spGLMM in terms of multivariate normal cummulative distribution functions (cdf). We present a direct and fast rendition of this latter approach for predictions from a spatial probit linear mixed model. We show that the covariance matrix of the cdf characterizing the marginal cdf of binary spatial data from spGLMM is amenable to approximation using Nearest Neighbor Gaussian Processes (NNGP). This facilitates a scalable prediction algorithm for spGLMM using NNGP that only involves sparse or small matrix computations and can be deployed...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7vb7h60j</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Saha, Arkajyoti</name>
      </author>
      <author>
        <name>Datta, Abhirup</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Bayesian Modeling and Analysis of Geostatistical Data</title>
      <link>https://escholarship.org/uc/item/7qz8z1vc</link>
      <description>The most prevalent spatial data setting is, arguably, that of so-called geostatistical data, data that arise as random variables observed at fixed spatial locations. Collection of such data in space and in time has grown enormously in the past two decades. With it has grown a substantial array of methods to analyze such data. Here, we attempt a review of a fully model-based perspective for such data analysis, the approach of hierarchical modeling fitted within a Bayesian framework. The benefit, as with hierarchical Bayesian modeling in general, is full and exact inference, with proper assessment of uncertainty. Geostatistical modeling includes univariate and multivariate data collection at sites, continuous and categorical data at sites, static and dynamic data at sites, and datasets over very large numbers of sites and long periods of time. Within the hierarchical modeling framework, we offer a review of the current state of the art in these settings.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7qz8z1vc</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Gelfand, Alan E</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Dynamic spatial regression models for space‐varying forest stand tables</title>
      <link>https://escholarship.org/uc/item/7qq523j6</link>
      <description>Many forest management planning decisions are based on information about the number of trees by species and diameter per unit area. This information is commonly summarized in astand table, where a stand is defined as a group of forest trees of sufficiently uniform species composition, age, condition, or productivity to be considered a homogeneous unit for planning purposes. Typically, information used to construct stand tables is gleaned from observed subsets of the forest selected using a probability‐based sampling design. Such sampling campaigns are expensive, and hence, only a small number of sample units are typically observed. This data paucity means that stand tables can only be estimated for relatively large areal units. Contemporary forest management planning and spatially explicit ecosystem models require stand table input at higher spatial resolution than can be affordably provided using traditional approaches. We propose a dynamic multivariate Poisson spatial regression...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7qq523j6</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Finley, Andrew O</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Weiskittel, Aaron R</name>
      </author>
      <author>
        <name>Babcock, Chad</name>
      </author>
      <author>
        <name>Cook, Bruce D</name>
      </author>
    </item>
    <item>
      <title>Bayesian Models for Detecting Difference Boundaries in Areal Data.</title>
      <link>https://escholarship.org/uc/item/7pr5t3cv</link>
      <description>With increasing accessibility to Geographical Information Systems (GIS) software, researchers and administrators in public health routinely encounter &lt;i&gt;areal&lt;/i&gt; data compiled as &lt;i&gt;aggregates&lt;/i&gt; over areal regions, such as counts or rates across counties in a state. Spatial models for areal data attempt to deliver smoothed maps by accounting for high variability in certain regions. Subsequently, inferential interest is focused upon formally identifying the "diffrence edges" or " difference boundaries" on the map, which delineate adjacent regions with vastly disparate outcomes, perhaps caused by latent risk factors. We propose nonparametric Bayesian models for areal data that can formally identify boundaries between disparate neighbors. After elucidating these models and their estimation methods, we conduct simulation experiments to assess their effectiveness and subsequently analyze Pneumonia and Influenza hospitalization maps from the SEER-Medicare program in Minnesota, where...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7pr5t3cv</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Li, Pei</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Hanson, Timothy A</name>
      </author>
      <author>
        <name>McBean, Alexander M</name>
      </author>
    </item>
    <item>
      <title>Elemental composition of fine and coarse particles across the greater Los Angeles area: Spatial variation and contributing sources</title>
      <link>https://escholarship.org/uc/item/7n7144xs</link>
      <description>The inorganic components of particulate matter (PM), especially transition metals, have been shown to contribute to PM toxicity. In this study, the spatial distribution of PM elements and their potential sources in the Greater Los Angeles area were studied. The mass concentration and detailed elemental composition of fine (PM&lt;sub&gt;2.5&lt;/sub&gt;) and coarse (PM&lt;sub&gt;2.5-10&lt;/sub&gt;) particles were assessed at 46 locations, including urban traffic, urban community, urban background, and desert locations. Crustal enrichment factors (EFs), roadside enrichments (REs), and bivariate correlation analysis revealed that Ba, Cr, Cu, Mo, Pd, Sb, Zn, and Zr were associated with traffic emissions in both PM&lt;sub&gt;2.5&lt;/sub&gt; and PM&lt;sub&gt;2.5-10&lt;/sub&gt;, while Fe, Li, Mn, and Ti were affected by traffic emissions mostly in PM&lt;sub&gt;2.5&lt;/sub&gt;. The concentrations of Ba, Cu, Mo, Sb, Zr (brake wear tracers), Pd (tailpipe tracer), and Zn (associated with tire wear) were higher at urban traffic sites than urban background...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7n7144xs</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Oroumiyeh, Farzan</name>
      </author>
      <author>
        <name>Jerrett, Michael</name>
      </author>
      <author>
        <name>Del Rosario, Irish</name>
      </author>
      <author>
        <name>Lipsitt, Jonah</name>
      </author>
      <author>
        <name>Liu, Jonathan</name>
      </author>
      <author>
        <name>Paulson, Suzanne E</name>
        <uri>https://orcid.org/0000-0003-0855-7615</uri>
      </author>
      <author>
        <name>Ritz, Beate</name>
      </author>
      <author>
        <name>Schauer, James J</name>
      </author>
      <author>
        <name>Shafer, Martin M</name>
      </author>
      <author>
        <name>Shen, Jiaqi</name>
      </author>
      <author>
        <name>Weichenthal, Scott</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Zhu, Yifang</name>
        <uri>https://orcid.org/0000-0002-0591-3322</uri>
      </author>
    </item>
    <item>
      <title>Graph-constrained analysis for multivariate functional data</title>
      <link>https://escholarship.org/uc/item/7jq9g523</link>
      <description>The manuscript considers multivariate functional data analysis with a known graphical model among the functional variables representing their conditional relationships (e.g., brain region-level fMRI data with a prespecified connectivity graph among brain regions). Functional Gaussian graphical models (GGM) used for analyzing multivariate functional data customarily estimate an unknown graphical model, and cannot preserve knowledge of a given graph. We propose a method for multivariate functional analysis that exactly conforms to a given inter-variable graph. We first show the equivalence between partially separable functional GGM and graphical Gaussian processes (GP), proposed recently for constructing optimal multivariate covariance functions that retain a given graphical model. The theoretical connection helps to design a new algorithm that leverages Dempster's covariance selection for obtaining the maximum likelihood estimate of the covariance function for multivariate functional...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7jq9g523</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Dey, Debangan</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Lindquist, Martin A</name>
      </author>
      <author>
        <name>Datta, Abhirup</name>
      </author>
    </item>
    <item>
      <title>Volatile Hydrocarbon Exposures and Incident Coronary Heart Disease Events: Up to Ten Years of Follow-up among Deepwater Horizon Oil Spill Workers</title>
      <link>https://escholarship.org/uc/item/78s76888</link>
      <description>BACKGROUND: During the 2010 &lt;i&gt;Deepwater Horizon&lt;/i&gt; (&lt;i&gt;DWH&lt;/i&gt;) disaster, response and cleanup workers were potentially exposed to toxic volatile components of crude oil. However, to our knowledge, no study has examined exposure to individual oil spill-related chemicals in relation to cardiovascular outcomes among oil spill workers.
OBJECTIVES: Our aim was to investigate the association of several spill-related chemicals [benzene, toluene, ethylbenzene, xylene, &lt;i&gt;n&lt;/i&gt;-hexane (BTEX-H)] and total hydrocarbons (THC) with incident coronary heart disease (CHD) events among workers enrolled in a prospective cohort.
METHODS: Cumulative exposures to THC and BTEX-H across the cleanup period were estimated via a job-exposure matrix that linked air measurement data with self-reported &lt;i&gt;DWH&lt;/i&gt; spill work histories. We ascertained CHD events following each worker's last day of cleanup work as the first self-reported physician-diagnosed myocardial infarction (MI) or a fatal CHD event....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/78s76888</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Chen, Dazhe</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
      <author>
        <name>Keil, Alexander P</name>
      </author>
      <author>
        <name>Heiss, Gerardo</name>
      </author>
      <author>
        <name>Whitsel, Eric A</name>
      </author>
      <author>
        <name>Edwards, Jessie K</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
      <author>
        <name>Stenzel, Mark R</name>
      </author>
      <author>
        <name>Groth, Caroline P</name>
      </author>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Huynh, Tran B</name>
      </author>
      <author>
        <name>Jackson, W Braxton</name>
      </author>
      <author>
        <name>Blair, Aaron</name>
      </author>
      <author>
        <name>Lawrence, Kaitlyn G</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
    </item>
    <item>
      <title>Joint hierarchical models for sparsely sampled high-dimensional LiDAR and forest variables</title>
      <link>https://escholarship.org/uc/item/76z6d3zv</link>
      <description>Recent advancements in remote sensing technology, specifically Light
Detection and Ranging (LiDAR) sensors, provide the data needed to quantify
forest characteristics at a fine spatial resolution over large geographic
domains. From an inferential standpoint, there is interest in prediction and
interpolation of the often sparsely sampled and spatially misaligned LiDAR
signals and forest variables. We propose a fully process-based Bayesian
hierarchical model for above ground biomass (AGB) and LiDAR signals. The
process-based framework offers richness in inferential capabilities, e.g.,
inference on the entire underlying processes instead of estimates only at
pre-specified points. Key challenges we obviate include misalignment between
the AGB observations and LiDAR signals and the high-dimensionality in the model
emerging from LiDAR signals in conjunction with the large number of spatial
locations. We offer simulation experiments to evaluate our proposed models and
also apply them...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/76z6d3zv</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Finley, Andrew O</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Zhou, Yuzhen</name>
      </author>
      <author>
        <name>Cook, Bruce D</name>
      </author>
      <author>
        <name>Babcock, Chad</name>
      </author>
    </item>
    <item>
      <title>Spatial Factor Models for High-Dimensional and Large Spatial Data: An Application in Forest Variable Mapping.</title>
      <link>https://escholarship.org/uc/item/7388m5df</link>
      <description>Gathering information about forest variables is an expensive and arduous activity. As such, directly collecting the data required to produce high-resolution maps over large spatial domains is infeasible. Next generation collection initiatives of remotely sensed Light Detection and Ranging (LiDAR) data are specifically aimed at producing complete-coverage maps over large spatial domains. Given that LiDAR data and forest characteristics are often strongly correlated, it is possible to make use of the former to model, predict, and map forest variables over regions of interest. This entails dealing with the high-dimensional (~10&lt;sup&gt;2&lt;/sup&gt;) spatially dependent LiDAR outcomes over a large number of locations (~10&lt;sup&gt;5&lt;/sup&gt;-10&lt;sup&gt;6&lt;/sup&gt;). With this in mind, we develop the Spatial Factor Nearest Neighbor Gaussian Process (SF-NNGP) model, and embed it in a two-stage approach that connects the spatial structure found in LiDAR signals with forest variables. We provide a simulation...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7388m5df</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Taylor-Rodriguez, Daniel</name>
      </author>
      <author>
        <name>Finley, Andrew O</name>
      </author>
      <author>
        <name>Datta, Abhirup</name>
      </author>
      <author>
        <name>Babcock, Chad</name>
      </author>
      <author>
        <name>Andersen, Hans-Erik</name>
      </author>
      <author>
        <name>Cook, Bruce D</name>
      </author>
      <author>
        <name>Morton, Douglas C</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Association between spill-related exposure to fine particulate matter and peripheral motor and sensory nerve function among oil spill response and cleanup workers following the Deepwater Horizon oil spill</title>
      <link>https://escholarship.org/uc/item/6wq055ds</link>
      <description>BackgroundBurning/flaring of oil/gas during the Deepwater Horizon oil spill response and cleanup (OSRC) generated high concentrations of fine particulate matter (PM2.5). Personnel working on the water during these activities may have inhaled combustion products. Neurologic effects of PM2.5 have been reported previously but few studies have examined lasting effects following disaster exposures. The association of brief, high exposures and adverse effects on sensory and motor nerve function in the years following exposure have not been examined for OSRC workers.ObjectivesWe assessed the relationship between exposure to burning/flaring-related PM2.5 and measures of sensory and motor nerve function among OSRC workers.MethodsPM2.5 concentrations were estimated from Gaussian plume dispersion models and linked to self-reported work histories. Quantitative measures of sensory and motor nerve function were obtained 4–6 years after the disaster during a clinical exam restricted to those...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6wq055ds</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Norris, Christina L</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
      <author>
        <name>Pratt, Gregory C</name>
      </author>
      <author>
        <name>Stenzel, Mark R</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
      <author>
        <name>Jackson, W Braxton</name>
      </author>
      <author>
        <name>Gerr, Fredric E</name>
      </author>
      <author>
        <name>Groth, Caroline</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Lawrence, Kaitlyn G</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Werder, Emily J</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
    </item>
    <item>
      <title>Spatial Difference Boundary Detection for Multiple Outcomes Using Bayesian Disease Mapping</title>
      <link>https://escholarship.org/uc/item/6fh8g6pz</link>
      <description>Regional aggregates of health outcomes over delineated administrative units (e.g., states, counties, and zip codes), or areal units, are widely used by epidemiologists to map mortality or incidence rates and capture geographic variation. To capture health disparities over regions, we seek "difference boundaries" that separate neighboring regions with significantly different spatial effects. Matters are more challenging with multiple outcomes over each unit, where we capture dependence among diseases as well as across the areal units. Here, we address multivariate difference boundary detection for correlated diseases. We formulate the problem in terms of Bayesian pairwise multiple comparisons and seek the posterior probabilities of neighboring spatial effects being different. To achieve this, we endow the spatial random effects with a discrete probability law using a class of multivariate areally referenced Dirichlet process models that accommodate spatial and interdisease dependence....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6fh8g6pz</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Gao, Leiwen</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Ritz, Beate</name>
      </author>
    </item>
    <item>
      <title>A Comparison of the β-Substitution Method and a Bayesian Method for Analyzing Left-Censored Data</title>
      <link>https://escholarship.org/uc/item/6b5495q7</link>
      <description>Classical statistical methods for analyzing exposure data with values below the detection limits are well described in the occupational hygiene literature, but an evaluation of a Bayesian approach for handling such data is currently lacking. Here, we first describe a Bayesian framework for analyzing censored data. We then present the results of a simulation study conducted to compare the β-substitution method with a Bayesian method for exposure datasets drawn from lognormal distributions and mixed lognormal distributions with varying sample sizes, geometric standard deviations (GSDs), and censoring for single and multiple limits of detection. For each set of factors, estimates for the arithmetic mean (AM), geometric mean, GSD, and the 95th percentile (X0.95) of the exposure distribution were obtained. We evaluated the performance of each method using relative bias, the root mean squared error (rMSE), and coverage (the proportion of the computed 95% uncertainty intervals containing...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6b5495q7</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Huynh, Tran</name>
      </author>
      <author>
        <name>Quick, Harrison</name>
      </author>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Stenzel, Mark</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Blair, Aaron</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
    </item>
    <item>
      <title>Predicting tree biomass growth in the temperate–boreal ecotone: Is tree size, age, competition, or climate response most important?</title>
      <link>https://escholarship.org/uc/item/6314k964</link>
      <description>As global temperatures rise, variation in annual climate is also changing, with unknown consequences for forest biomes. Growing forests have the ability to capture atmospheric CO2 and thereby slow rising CO2 concentrations. Forests' ongoing ability to sequester C depends on how tree communities respond to changes in climate variation. Much of what we know about tree and forest response to climate variation comes from tree-ring records. Yet typical tree-ring datasets and models do not capture the diversity of climate responses that exist within and among trees and species. We address this issue using a model that estimates individual tree response to climate variables while accounting for variation in individuals' size, age, competitive status, and spatially structured latent covariates. Our model allows for inference about variance within and among species. We quantify how variables influence aboveground biomass growth of individual trees from a representative sample of 15 northern...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6314k964</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Foster, Jane R</name>
      </author>
      <author>
        <name>Finley, Andrew O</name>
      </author>
      <author>
        <name>D'Amato, Anthony W</name>
      </author>
      <author>
        <name>Bradford, John B</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>spBayes for Large Univariate and Multivariate Point-Referenced Spatio-Temporal Data Models</title>
      <link>https://escholarship.org/uc/item/5w96w3qd</link>
      <description>spBayes for Large Univariate and Multivariate Point-Referenced Spatio-Temporal Data Models</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5w96w3qd</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Finley, Andrew O</name>
      </author>
      <author>
        <name>Bsnerjee, Sudipto</name>
      </author>
      <author>
        <name>Gelfand, Alan E</name>
      </author>
    </item>
    <item>
      <title>Comparison of Methods for Analyzing Left-Censored Occupational Exposure Data</title>
      <link>https://escholarship.org/uc/item/5v58j5f3</link>
      <description>The National Institute for Environmental Health Sciences (NIEHS) is conducting an epidemiologic study (GuLF STUDY) to investigate the health of the workers and volunteers who participated from April to December of 2010 in the response and cleanup of the oil release after the Deepwater Horizon explosion in the Gulf of Mexico. The exposure assessment component of the study involves analyzing thousands of personal monitoring measurements that were collected during this effort. A substantial portion of these data has values reported by the analytic laboratories to be below the limits of detection (LOD). A simulation study was conducted to evaluate three established methods for analyzing data with censored observations to estimate the arithmetic mean (AM), geometric mean (GM), geometric standard deviation (GSD), and the 95th percentile (X0.95) of the exposure distribution: the maximum likelihood (ML) estimation, the β-substitution, and the Kaplan-Meier (K-M) methods. Each method was...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5v58j5f3</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Huynh, Tran</name>
      </author>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Monteiro, Joao</name>
      </author>
      <author>
        <name>Stenzel, Mark</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Blair, Aaron</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
    </item>
    <item>
      <title>On nearest‐neighbor Gaussian process models for massive spatial data</title>
      <link>https://escholarship.org/uc/item/5qm7b5js</link>
      <description>Gaussian Process (GP) models provide a very flexible nonparametric approach to modeling location-and-time indexed datasets. However, the storage and computational requirements for GP models are infeasible for large spatial datasets. Nearest Neighbor Gaussian Processes (Datta A, Banerjee S, Finley AO, Gelfand AE. Hierarchical nearest-neighbor gaussian process models for large geostatistical datasets. &lt;i&gt;J Am Stat Assoc&lt;/i&gt; 2016., JASA) provide a scalable alternative by using local information from few nearest neighbors. Scalability is achieved by using the neighbor sets in a conditional specification of the model. We show how this is equivalent to sparse modeling of Cholesky factors of large covariance matrices. We also discuss a general approach to construct scalable Gaussian Processes using sparse local kriging. We present a multivariate data analysis which demonstrates how the nearest neighbor approach yields inference indistinguishable from the full rank GP despite being several...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5qm7b5js</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Datta, Abhirup</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Finley, Andrew O</name>
      </author>
      <author>
        <name>Gelfand, Alan E</name>
      </author>
    </item>
    <item>
      <title>Development of a total hydrocarbon ordinal job-exposure matrix for workers responding to the Deepwater Horizon disaster: The GuLF STUDY</title>
      <link>https://escholarship.org/uc/item/53g1c6d9</link>
      <description>The GuLF STUDY is a cohort study investigating the health of workers who responded to the Deepwater Horizon oil spill in the Gulf of Mexico in 2010. The objective of this effort was to develop an ordinal job-exposure matrix (JEM) of airborne total hydrocarbons (THC), dispersants, and particulates to estimate study participants’ exposures. Information was collected on participants’ spill-related tasks. A JEM of exposure groups (EGs) was developed from tasks and THC air measurements taken during and after the spill using relevant exposure determinants. THC arithmetic means were developed for the EGs, assigned ordinal values, and linked to the participants using determinants from the questionnaire. Different approaches were taken for combining exposures across EGs. EGs for dispersants and particulates were based on questionnaire responses. Considerable differences in THC exposure levels were found among EGs. Based on the maximum THC level participants experienced across any job held,...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/53g1c6d9</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
      <author>
        <name>Stenzel, Mark R</name>
      </author>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Huynh, Tran B</name>
      </author>
      <author>
        <name>Groth, Caroline P</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Blair, Aaron</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
    </item>
    <item>
      <title>Modeling Multivariate Spatial Dependencies Using Graphical Models.</title>
      <link>https://escholarship.org/uc/item/4qs5q89j</link>
      <description>Graphical models have witnessed significant growth and usage in spatial data science for modeling data referenced over a massive number of spatial-temporal coordinates. Much of this literature has focused on a single or relatively few spatially dependent outcomes. Recent attention has focused upon addressing modeling and inference for substantially large number of outcomes. While spatial factor models and multivariate basis expansions occupy a prominent place in this domain, this article elucidates a recent approach, graphical Gaussian Processes, that exploits the notion of conditional independence among a very large number of spatial processes to build scalable graphical models for fully model-based Bayesian analysis of multivariate spatial data.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4qs5q89j</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Dey, Debangan</name>
      </author>
      <author>
        <name>Datta, Abhirup</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Modeled Air Pollution from In Situ Burning and Flaring of Oil and Gas Released Following the Deepwater Horizon Disaster</title>
      <link>https://escholarship.org/uc/item/3h36j9kb</link>
      <description>The GuLF STUDY, initiated by the National Institute of Environmental Health Sciences, is investigating the health effects among workers involved in the oil spill response and clean-up (OSRC) after the Deepwater Horizon (DWH) explosion in April 2010 in the Gulf of Mexico. Clean-up included in situ burning of oil on the water surface and flaring of gas and oil captured near the seabed and brought to the surface. We estimated emissions of PM2.5 and related pollutants resulting from these activities, as well as from engines of vessels working on the OSRC. PM2.5 emissions ranged from 30 to 1.33e6 kg per day and were generally uniform over time for the flares but highly episodic for the in situ burns. Hourly emissions from each source on every burn/flare day were used as inputs to the AERMOD model to develop average and maximum concentrations for 1-, 12-, and 24-h time periods. The highest predicted 24-h average concentrations sometimes exceeded 5000 µg m-3 in the first 500 m downwind...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3h36j9kb</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Pratt, Gregory C</name>
      </author>
      <author>
        <name>Stenzel, Mark R</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Groth, Caroline P</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Arnold, Susan F</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
    </item>
    <item>
      <title>Association of Deepwater Horizon Oil Spill Response and Cleanup Work With Risk of Developing Hypertension</title>
      <link>https://escholarship.org/uc/item/39m1k1g3</link>
      <description>Importance: Exposure to hydrocarbons, fine particulate matter (PM2.5), and other chemicals from the April 20, 2010, Deepwater Horizon disaster may be associated with increased blood pressure and newly detected hypertension among oil spill response and cleanup workers.
Objective: To determine whether participation in cleanup activities following the disaster was associated with increased risk of developing hypertension.
Design, Setting, and Participants: This cohort study was conducted via telephone interviews and in-person home exams. Participants were 6846 adults who had worked on the oil spill cleanup (workers) and 1505 others who had completed required safety training but did not do cleanup work (nonworkers). Eligible participants did not have diagnosed hypertension at the time of the oil spill. Statistical analyses were performed from June 2018 to December 2021.
Exposures: Engagement in cleanup activities following the Deepwater Horizon oil spill disaster, job classes, quintiles...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/39m1k1g3</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Jackson, W Braxton</name>
      </author>
      <author>
        <name>Curry, Matthew D</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
      <author>
        <name>McGrath, John A</name>
      </author>
      <author>
        <name>Stenzel, Mark</name>
      </author>
      <author>
        <name>Huynh, Tran B</name>
      </author>
      <author>
        <name>Groth, Caroline P</name>
      </author>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Pratt, Gregory C</name>
      </author>
      <author>
        <name>Miller, Aubrey K</name>
      </author>
      <author>
        <name>Zhang, Xian</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
    </item>
    <item>
      <title>Inference for Gaussian Processes with Matern Covariogram on Compact Riemannian Manifolds</title>
      <link>https://escholarship.org/uc/item/3962t4w8</link>
      <description>Inference for Gaussian Processes with Matern Covariogram on Compact Riemannian Manifolds</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3962t4w8</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Li, Didong</name>
      </author>
      <author>
        <name>Tang, Wenpin</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Efficient Algorithms for Bayesian Nearest Neighbor Gaussian Processes</title>
      <link>https://escholarship.org/uc/item/2gv8z2vt</link>
      <description>We consider alternate formulations of recently proposed hierarchical Nearest Neighbor Gaussian Process (NNGP) models (Datta et al., 2016a) for improved convergence, faster computing time, and more robust and reproducible Bayesian inference. Algorithms are defined that improve CPU memory management and exploit existing high-performance numerical linear algebra libraries. Computational and inferential benefits are assessed for alternate NNGP specifications using simulated datasets and remotely sensed light detection and ranging (LiDAR) data collected over the US Forest Service Tanana Inventory Unit (TIU) in a remote portion of Interior Alaska. The resulting data product is the first statistically robust map of forest canopy for the TIU.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2gv8z2vt</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Finley, Andrew O</name>
      </author>
      <author>
        <name>Datta, Abhirup</name>
      </author>
      <author>
        <name>Cook, Bruce D</name>
      </author>
      <author>
        <name>Morton, Douglas C</name>
      </author>
      <author>
        <name>Andersen, Hans E</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Estimates of Inhalation Exposures among Land Workers during the Deepwater Horizon Oil Spill Clean-up Operations</title>
      <link>https://escholarship.org/uc/item/2gp1x97b</link>
      <description>Following the Deepwater Horizon oil spill disaster, thousands of workers and volunteers cleaned the shoreline across four coastal states of the Gulf of Mexico. For the GuLF STUDY, we developed quantitative estimates of oil-related chemical exposures [total petroleum hydrocarbons (THC), benzene, toluene, ethylbenzene, xylene, and n-hexane (BTEX-H)] from personal measurements on workers performing various spill clean-up operations on land. These operations included decontamination of vessels, equipment, booms, and personnel; handling of oily booms; hazardous waste management; beach, marsh, and jetty clean-up; aerial missions; wildlife rescue and rehabilitation; and administrative support activities. Exposure estimates were developed for unique groups of workers by (i) activity, (ii) state, and (iii) time period. Estimates of the arithmetic means (AMs) for THC ranged from 0.04 to 3.67 ppm. BTEX-H estimates were substantially lower than THC (in the parts per billion range). Both THC...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2gp1x97b</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Huynh, Tran B</name>
      </author>
      <author>
        <name>Groth, Caroline P</name>
      </author>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Stenzel, Mark</name>
      </author>
      <author>
        <name>Blair, Aaron</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
    </item>
    <item>
      <title>Associations between airborne crude oil chemicals and symptom-based asthma</title>
      <link>https://escholarship.org/uc/item/17w8x9r9</link>
      <description>RATIONALE: The 2010 Deepwater Horizon (DWH) oil spill response and cleanup (OSRC) workers were exposed to airborne total hydrocarbons (THC), benzene, toluene, ethylbenzene, o-, m-, and p-xylenes and n-hexane (BTEX-H) from crude oil and PM&lt;sub&gt;2&lt;/sub&gt;&lt;sub&gt;.5&lt;/sub&gt; from burning/flaring oil and natural gas. Little is known about asthma risk among oil spill cleanup workers.
OBJECTIVES: We assessed the relationship between asthma and several oil spill-related exposures including job classes, THC, individual BTEX-H chemicals, the BTEX-H mixture, and PM&lt;sub&gt;2.5&lt;/sub&gt; using data from the Gulf Long-Term Follow-up (GuLF) Study, a prospective cohort of 24,937 cleanup workers and 7,671 nonworkers following the DWH disaster.
METHODS: Our analysis largely focused on the 19,018 workers without asthma before the spill who had complete exposure, outcome, and covariate information. We defined incident asthma 1-3&amp;nbsp;years following exposure using both self-reported wheeze and self-reported physician...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/17w8x9r9</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Lawrence, Kaitlyn G</name>
      </author>
      <author>
        <name>Niehoff, Nicole M</name>
      </author>
      <author>
        <name>Keil, Alexander P</name>
      </author>
      <author>
        <name>Jackson, W Braxton</name>
      </author>
      <author>
        <name>Christenbury, Kate</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
      <author>
        <name>Stenzel, Mark R</name>
      </author>
      <author>
        <name>Huynh, Tran B</name>
      </author>
      <author>
        <name>Groth, Caroline P</name>
      </author>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Pratt, Gregory C</name>
      </author>
      <author>
        <name>Curry, Matthew D</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
    </item>
    <item>
      <title>Towards a Multidimensional Approach to Bayesian Disease Mapping</title>
      <link>https://escholarship.org/uc/item/0mb40557</link>
      <description>Multivariate disease mapping enriches traditional disease mapping studies by analysing several diseases jointly. This yields improved estimates of the geographical distribution of risk from the diseases by enabling borrowing of information across diseases. Beyond multivariate smoothing for several diseases, several other variables, such as sex, age group, race, time period, and so on, could also be jointly considered to derive multivariate estimates. The resulting multivariate structures should induce an appropriate covariance model for the data. In this paper, we introduce a formal framework for the analysis of multivariate data arising from the combination of more than two variables (geographical units and at least two more variables), what we have called Multidimensional Disease Mapping. We develop a theoretical framework containing both separable and non-separable dependence structures and illustrate its performance on the study of real mortality data in Comunitat Valenciana...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0mb40557</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Martinez-Beneito, Miguel A</name>
      </author>
      <author>
        <name>Botella-Rocamora, Paloma</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>A unifying modeling framework for highly multivariate disease mapping</title>
      <link>https://escholarship.org/uc/item/0cv3d5bc</link>
      <description>Multivariate disease mapping refers to the joint mapping of multiple diseases from regionally aggregated data and continues to be the subject of considerable attention for biostatisticians and spatial epidemiologists. The key issue is to map multiple diseases accounting for any correlations among themselves. Recently, Martinez-Beneito (2013) provided a unifying framework for multivariate disease mapping. While attractive in that it colligates a variety of existing statistical models for mapping multiple diseases, this and other existing approaches are computationally burdensome and preclude the multivariate analysis of moderate to large numbers of diseases. Here, we propose an alternative reformulation that accrues substantial computational benefits enabling the joint mapping of tens of diseases. Furthermore, the approach subsumes almost all existing classes of multivariate disease mapping models and offers substantial insight into the properties of statistical disease mapping models.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0cv3d5bc</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Botella‐Rocamora, P</name>
      </author>
      <author>
        <name>Martinez‐Beneito, MA</name>
      </author>
      <author>
        <name>Banerjee, S</name>
      </author>
    </item>
    <item>
      <title>Scalable inference for space‐time Gaussian Cox processes</title>
      <link>https://escholarship.org/uc/item/0cv290sg</link>
      <description>The log‐Gaussian Cox process is a flexible and popular stochastic process for modeling point patterns exhibiting spatial and space‐time dependence. Model fitting requires approximation of stochastic integrals which is implemented through discretization over the domain of interest. With fine scale discretization, inference based on Markov chain Monte Carlo is computationally burdensome because of the cost of matrix decompositions and storage, such as the Cholesky, for high dimensional covariance matrices associated with latent Gaussian variables. This article addresses these computational bottlenecks by combining two recent developments: (i) a data augmentation strategy that has been proposed for space‐time Gaussian Cox processes that is based on exact Bayesian inference and does not require fine grid approximations for infinite dimensional integrals, and (ii) a recently developed family of sparsity‐inducing Gaussian processes, called nearest‐neighbor Gaussian processes, to avoid...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0cv290sg</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Shirota, Shinichiro</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>Using Real-Time Area VOC Measurements to Estimate Total Hydrocarbons Exposures to Workers Involved in the Deepwater Horizon Oil Spill</title>
      <link>https://escholarship.org/uc/item/0b53f59g</link>
      <description>Even though the Deepwater Horizon oil spill response and clean-up (OSRC) had one of the largest exposure monitoring efforts of any oil spill, a number of exposure groups did not have sufficient personal data available or there were gaps in days measured to adequately characterize exposures for the GuLF STUDY, an epidemiologic study investigating the health of the OSRC workers. Area measurements were available from real-time air monitoring instruments and used to supplement the personal exposure measurements.
OBJECTIVES: The objective was to present a method that used real-time volatile organic compounds (VOCs) area measurements transformed to daily total hydrocarbons (THC) time-weighted averages (TWAs) to supplement THC personal full-shift measurements collected using passive charcoal badges. A second objective was to develop exposure statistics using these data for workers on vessels piloting remotely operated vehicle (ROV) vessels and other marine vessels (MVs) not at the job...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0b53f59g</guid>
      <pubDate>Wed, 9 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Ramachandran, Gurumurthy</name>
      </author>
      <author>
        <name>Groth, Caroline P</name>
      </author>
      <author>
        <name>Huynh, Tran B</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Stewart, Patricia A</name>
      </author>
      <author>
        <name>Engel, Lawrence S</name>
      </author>
      <author>
        <name>Kwok, Richard K</name>
      </author>
      <author>
        <name>Sandler, Dale P</name>
      </author>
      <author>
        <name>Stenzel, Mark</name>
      </author>
    </item>
    <item>
      <title>Threat perceptions, loyalties and attitudes towards peace: The effects of civilian victimization among Syrian refugees in Turkey</title>
      <link>https://escholarship.org/uc/item/4jr0f02m</link>
      <description>For refugees who have fled civil conflict, do experiences of victimization by one armed group push them to support the opposing armed groups? Or, does victimization cause refugees to revoke their support for all armed groups, whatever side they are on, and call instead for peace? This paper studies the effect of civilian victimization on threat perceptions, loyalties, and attitudes toward peace in the context of Syrian refugees in Turkey, many of whom faced regime-caused violence prior to their departure. Our research strategy leverages variation in home destruction caused by barrel bombs to examine the effect of violence on refugees' views. We find that refugees who lose their home to barrel bombs withdraw support from armed actors and are more supportive of ending the war and finding peace. Suggestive evidence shows that while victims do not disengage from issues in Syria, they do show less optimism about an opposition victory.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/4jr0f02m</guid>
      <pubDate>Mon, 7 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Fabbe, Kristin</name>
      </author>
      <author>
        <name>Hazlett, Chad</name>
        <uri>https://orcid.org/0000-0003-1819-1928</uri>
      </author>
      <author>
        <name>Sinmazdemir, Tolga</name>
      </author>
    </item>
    <item>
      <title>Decoding heterogeneous single-cell perturbation responses</title>
      <link>https://escholarship.org/uc/item/80d1k93n</link>
      <description>Understanding how cells respond differently to perturbation is crucial in cell biology, but existing methods often fail to accurately quantify and interpret heterogeneous single-cell responses. Here we introduce the perturbation-response score (PS), a method to quantify diverse perturbation responses at a single-cell level. Applied to single-cell perturbation datasets such as Perturb-seq, PS outperforms existing methods in quantifying partial gene perturbations. PS further enables single-cell dosage analysis without needing to titrate perturbations, and identifies ‘buffered’ and ‘sensitive’ response patterns of essential genes, depending on whether their moderate perturbations lead to strong downstream effects. PS reveals differential cellular responses on perturbing key genes in contexts such as T cell stimulation, latent HIV-1 expression and pancreatic differentiation. Notably, we identified a previously unknown role for the coiled-coil domain containing 6 (CCDC6) in regulating...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/80d1k93n</guid>
      <pubDate>Wed, 2 Apr 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Song, Bicna</name>
      </author>
      <author>
        <name>Liu, Dingyu</name>
      </author>
      <author>
        <name>Dai, Weiwei</name>
      </author>
      <author>
        <name>McMyn, Natalie F</name>
      </author>
      <author>
        <name>Wang, Qingyang</name>
      </author>
      <author>
        <name>Yang, Dapeng</name>
      </author>
      <author>
        <name>Krejci, Adam</name>
      </author>
      <author>
        <name>Vasilyev, Anatoly</name>
      </author>
      <author>
        <name>Untermoser, Nicole</name>
      </author>
      <author>
        <name>Loregger, Anke</name>
      </author>
      <author>
        <name>Song, Dongyuan</name>
      </author>
      <author>
        <name>Williams, Breanna</name>
      </author>
      <author>
        <name>Rosen, Bess</name>
      </author>
      <author>
        <name>Cheng, Xiaolong</name>
      </author>
      <author>
        <name>Chao, Lumen</name>
      </author>
      <author>
        <name>Kale, Hanuman T</name>
      </author>
      <author>
        <name>Zhang, Hao</name>
      </author>
      <author>
        <name>Diao, Yarui</name>
      </author>
      <author>
        <name>Bürckstümmer, Tilmann</name>
      </author>
      <author>
        <name>Siliciano, Janet D</name>
      </author>
      <author>
        <name>Li, Jingyi Jessica</name>
        <uri>https://orcid.org/0000-0002-9288-5648</uri>
      </author>
      <author>
        <name>Siliciano, Robert F</name>
      </author>
      <author>
        <name>Huangfu, Danwei</name>
      </author>
      <author>
        <name>Li, Wei</name>
        <uri>https://orcid.org/0000-0001-9931-5990</uri>
      </author>
    </item>
    <item>
      <title>A genome-wide spectrum of tandem repeat expansions in 338,963 humans</title>
      <link>https://escholarship.org/uc/item/8xp669gb</link>
      <description>Graphical Abstract (original)&lt;p&gt;

&lt;/p&gt;</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/8xp669gb</guid>
      <pubDate>Wed, 12 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Cui, Ya</name>
      </author>
      <author>
        <name>Ye, Wenbin</name>
        <uri>https://orcid.org/0000-0002-7811-2710</uri>
      </author>
      <author>
        <name>Li, Jason Sheng</name>
      </author>
      <author>
        <name>Li, Jingyi Jessica</name>
        <uri>https://orcid.org/0000-0002-9288-5648</uri>
      </author>
      <author>
        <name>Vilain, Eric</name>
        <uri>https://orcid.org/0000-0003-1216-7134</uri>
      </author>
      <author>
        <name>Sallam, Tamer</name>
      </author>
      <author>
        <name>Li, Wei</name>
      </author>
    </item>
    <item>
      <title>A twenty-first century structural change in Antarctica’s sea ice system</title>
      <link>https://escholarship.org/uc/item/75g2d5z5</link>
      <description>Abstract: 

          From 1979 to 2016, total Antarctic sea ice extent experienced a positive trend with record winter maxima in 2012 and 2014. Record summer minima followed within the period 2017-2024, raising the possibility that the Antarctic sea ice system might be changing state. Here we use a Bayesian reconstruction of Antarctic sea ice extent which extends the record back to 1899, to show that the sequence of extreme minima in summer Antarctic sea ice extent is unlikely to have happened in the 20th century. We show that they represent a structural change in the sea ice system, manifest by increased persistence in the sea ice extent anomalies and a strongly reduced tendency to return to the mean state. Further, our analysis suggests that we may no longer rely on the past, long-term, behavior of the sea ice system to predict its future state. Extreme conditions may characterize the future state of Antarctic sea ice.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/75g2d5z5</guid>
      <pubDate>Wed, 12 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Raphael, Marilyn N</name>
      </author>
      <author>
        <name>Maierhofer, Thomas J</name>
      </author>
      <author>
        <name>Fogt, Ryan L</name>
      </author>
      <author>
        <name>Hobbs, William R</name>
      </author>
      <author>
        <name>Handcock, Mark S</name>
        <uri>https://orcid.org/0000-0002-9985-2785</uri>
      </author>
    </item>
    <item>
      <title>Enhancing spatially-disaggregated simulations with large language models</title>
      <link>https://escholarship.org/uc/item/6jm237hj</link>
      <description>Enhancing spatially-disaggregated simulations with large language models</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6jm237hj</guid>
      <pubDate>Wed, 12 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Zaslavsky, Ilya</name>
      </author>
      <author>
        <name>Lei, Jiaxi</name>
      </author>
      <author>
        <name>Graham, Rishi</name>
      </author>
      <author>
        <name>Handcock, Mark S</name>
        <uri>https://orcid.org/0000-0002-9985-2785</uri>
      </author>
      <author>
        <name>Aronoff-Spencer, Eliah</name>
      </author>
    </item>
    <item>
      <title>Semisynthetic simulation for microbiome data analysis</title>
      <link>https://escholarship.org/uc/item/2cp2j6t8</link>
      <description>High-throughput sequencing data lie at the heart of modern microbiome research. Effective analysis of these data requires careful preprocessing, modeling, and interpretation to detect subtle signals and avoid spurious associations. In this review, we discuss how simulation can serve as a sandbox to test candidate approaches, creating a setting that mimics real data while providing ground truth. This is particularly valuable for power analysis, methods benchmarking, and reliability analysis. We explain the probability, multivariate analysis, and regression concepts behind modern simulators and how different implementations make trade-offs between generality, faithfulness, and controllability. Recognizing that all simulators only approximate reality, we review methods to evaluate how accurately they reflect key properties. We also present case studies demonstrating the value of simulation in differential abundance testing, dimensionality reduction, network analysis, and data integration....</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2cp2j6t8</guid>
      <pubDate>Wed, 12 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sankaran, Kris</name>
      </author>
      <author>
        <name>Kodikara, Saritha</name>
      </author>
      <author>
        <name>Li, Jingyi Jessica</name>
        <uri>https://orcid.org/0000-0002-9288-5648</uri>
      </author>
      <author>
        <name>Cao, Kim-Anh Lê</name>
      </author>
    </item>
    <item>
      <title>20th Century Antarctic sea ice extent anomaly reconstruction by sector</title>
      <link>https://escholarship.org/uc/item/1s07p9gp</link>
      <description>This repository contains the resonstructions of the monthly Antarctic sea ice extent anomaly in total and by sector (‘Total’, ‘King Haakon VII’, ‘Ross Sea’, ‘East Antarctica’, ‘Weddell Sea’, ‘Bellingshausen Amundsen Sea’) for the 20th Century. We provide an ensemble of 2500 reconstructions.

The methodology used to create these reconstructions is in the paper: ‘A Bayesian Model for 20th Century Antarctic Sea Ice Extent Reconstruction’

by Thomas J. Maierhofer, Marilyn N. Raphael, Ryan L. Fogt, and Mark S. Handcock. It appears in Earth and Space Science, 11, 10 (2024).

For each sector we provide one CSV file. The rows in these data sets correspond the reconstructed month, e.g. reconstructions for January 1950 are found in row ’t1950_1’ and the columns correspond to the 2500 reconstructions. The numbers of the reconstructions correspond to one another across sectors, such that the 1st ‘Total’ reconstruction is the sum of the 1st reconstruction in all sectors.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1s07p9gp</guid>
      <pubDate>Wed, 12 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Raphael, Marilyn</name>
      </author>
      <author>
        <name>Maierhofer, Thomas</name>
      </author>
      <author>
        <name>Fogt, Ryan</name>
      </author>
      <author>
        <name>Hobbs, Will</name>
      </author>
      <author>
        <name>Handcock, Mark</name>
        <uri>https://orcid.org/0000-0002-9985-2785</uri>
      </author>
    </item>
    <item>
      <title>A Twenty-First Century Structural Change in Antarctica’s Sea Ice System: Data and Code Repository</title>
      <link>https://escholarship.org/uc/item/0vf2k4nk</link>
      <description>This repository contains the R source code and derived data products to reproduce analyses in the paper:

‘A Twenty-First Century Structural Change in Antarctica’s Sea ice System’

by Marilyn N. Raphael, Thomas J. Maierhofer, Ryan L. Fogt, William R. Hobbs, and Mark S. Handcock. It appears in Nature-Communications Earth &amp;amp; Environment, 6, 131 (2025), under DOI: 10.1038/s43247-025-02107-5.

There is also a detailed support site on GitHub: https://github.com/RaphaelLab/StructuralChangeInAntarcticSeaIceSystem</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0vf2k4nk</guid>
      <pubDate>Wed, 12 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Raphael, Marilyn N</name>
      </author>
      <author>
        <name>Maierhofer, Thomas J</name>
      </author>
      <author>
        <name>Fogt, Ryan</name>
      </author>
      <author>
        <name>Handcock, Mark S</name>
        <uri>https://orcid.org/0000-0002-9985-2785</uri>
      </author>
      <author>
        <name>Hobbs, William R</name>
      </author>
    </item>
    <item>
      <title>Better individual-level risk models can improve the targeting and life-saving potential of early-mortality interventions</title>
      <link>https://escholarship.org/uc/item/6cp7t6wt</link>
      <description>Infant mortality remains high and uneven in much of sub-Saharan Africa. Even low-cost, highly effective therapies can only save lives in proportion to how successfully they can be targeted to those children who, absent the treatment, would have died. This places great value on maximizing the accuracy of any targeting or means-testing algorithm. Yet, the interventions that countries deploy in hopes of reducing mortality are often targeted based on simple models of wealth or income or a few additional variables. Examining 22 countries in sub-Saharan Africa, we illustrate the use of flexible (machine learning) risk models employing up to 25 generally available pre-birth variables from the Demographic and Health Surveys. Using these models, we construct risk scores such that the 10 percent of the population at highest risk account for 15-30 percent of infant mortality, depending on the country. Successful targeting in these models turned on several variables other than wealth, while...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6cp7t6wt</guid>
      <pubDate>Fri, 7 Mar 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Hazlett, Chad</name>
        <uri>https://orcid.org/0000-0003-1819-1928</uri>
      </author>
      <author>
        <name>Ramos, Antonio P</name>
      </author>
      <author>
        <name>Smith, Stephen</name>
      </author>
    </item>
    <item>
      <title>Categorization of 34 computational methods to detect spatially variable genes from spatially resolved transcriptomics data</title>
      <link>https://escholarship.org/uc/item/90h565s1</link>
      <description>In the analysis of spatially resolved transcriptomics data, detecting spatially variable genes (SVGs) is crucial. Numerous computational methods exist, but varying SVG definitions and methodologies lead to incomparable results. We review 34 state-of-the-art methods, classifying SVGs into three categories: overall, cell-type-specific, and spatial-domain-marker SVGs. Our review explains the intuitions underlying these methods, summarizes their applications, and categorizes the hypothesis tests they use in the trade-off between generality and specificity for SVG detection. We discuss challenges in SVG detection and propose future directions for improvement. Our review offers insights for method developers and users, advocating for category-specific benchmarking.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/90h565s1</guid>
      <pubDate>Wed, 12 Feb 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Yan, Guanao</name>
      </author>
      <author>
        <name>Hua, Shuo Harper</name>
      </author>
      <author>
        <name>Li, Jingyi Jessica</name>
        <uri>https://orcid.org/0000-0002-9288-5648</uri>
      </author>
    </item>
    <item>
      <title>Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay</title>
      <link>https://escholarship.org/uc/item/0d28p32x</link>
      <description>SMARCC2 (BAF170) is one of the invariable core subunits of the ATP-dependent chromatin remodeling BAF (BRG1-associated factor) complex and plays a crucial role in embryogenesis and corticogenesis. Pathogenic variants in genes encoding other components of the BAF complex have been associated with intellectual disability syndromes. Despite its significant biological role, variants in SMARCC2 have not been directly associated with human disease previously. Using whole-exome sequencing and a web-based gene-matching program, we identified 15 individuals with variable degrees of neurodevelopmental delay and growth retardation harboring one of 13 heterozygous variants in SMARCC2, most of them novel and proven de novo. The clinical presentation overlaps with intellectual disability syndromes associated with other BAF subunits, such as Coffin-Siris and Nicolaides-Baraitser syndromes and includes prominent speech impairment, hypotonia, feeding difficulties, behavioral abnormalities, and...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0d28p32x</guid>
      <pubDate>Thu, 30 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Machol, Keren</name>
      </author>
      <author>
        <name>Rousseau, Justine</name>
      </author>
      <author>
        <name>Ehresmann, Sophie</name>
      </author>
      <author>
        <name>Garcia, Thomas</name>
      </author>
      <author>
        <name>Nguyen, Thi Tuyet Mai</name>
      </author>
      <author>
        <name>Spillmann, Rebecca C</name>
      </author>
      <author>
        <name>Sullivan, Jennifer A</name>
      </author>
      <author>
        <name>Shashi, Vandana</name>
      </author>
      <author>
        <name>Jiang, Yong-hui</name>
      </author>
      <author>
        <name>Stong, Nicholas</name>
      </author>
      <author>
        <name>Fiala, Elise</name>
      </author>
      <author>
        <name>Willing, Marcia</name>
      </author>
      <author>
        <name>Pfundt, Rolph</name>
      </author>
      <author>
        <name>Kleefstra, Tjitske</name>
      </author>
      <author>
        <name>Cho, Megan T</name>
      </author>
      <author>
        <name>McLaughlin, Heather</name>
      </author>
      <author>
        <name>Piera, Monica Rosello</name>
      </author>
      <author>
        <name>Orellana, Carmen</name>
      </author>
      <author>
        <name>Martínez, Francisco</name>
      </author>
      <author>
        <name>Caro-Llopis, Alfonso</name>
      </author>
      <author>
        <name>Monfort, Sandra</name>
      </author>
      <author>
        <name>Roscioli, Tony</name>
      </author>
      <author>
        <name>Nixon, Cheng Yee</name>
      </author>
      <author>
        <name>Buckley, Michael F</name>
      </author>
      <author>
        <name>Turner, Anne</name>
      </author>
      <author>
        <name>Jones, Wendy D</name>
      </author>
      <author>
        <name>van Hasselt, Peter M</name>
      </author>
      <author>
        <name>Hofstede, Floris C</name>
      </author>
      <author>
        <name>van Gassen, Koen LI</name>
      </author>
      <author>
        <name>Brooks, Alice S</name>
      </author>
      <author>
        <name>van Slegtenhorst, Marjon A</name>
      </author>
      <author>
        <name>Lachlan, Katherine</name>
      </author>
      <author>
        <name>Sebastian, Jessica</name>
      </author>
      <author>
        <name>Madan-Khetarpal, Suneeta</name>
      </author>
      <author>
        <name>Sonal, Desai</name>
      </author>
      <author>
        <name>Sakkubai, Naidu</name>
      </author>
      <author>
        <name>Thevenon, Julien</name>
      </author>
      <author>
        <name>Faivre, Laurence</name>
      </author>
      <author>
        <name>Maurel, Alice</name>
      </author>
      <author>
        <name>Petrovski, Slavé</name>
      </author>
      <author>
        <name>Krantz, Ian D</name>
      </author>
      <author>
        <name>Tarpinian, Jennifer M</name>
      </author>
      <author>
        <name>Rosenfeld, Jill A</name>
      </author>
      <author>
        <name>Lee, Brendan H</name>
      </author>
      <author>
        <name>Network, Undiagnosed Diseases</name>
      </author>
      <author>
        <name>Adams, David R</name>
      </author>
      <author>
        <name>Alejandro, Mercedes E</name>
      </author>
      <author>
        <name>Allard, Patrick</name>
        <uri>https://orcid.org/0000-0001-7765-1547</uri>
      </author>
      <author>
        <name>Azamian, Mahshid S</name>
      </author>
      <author>
        <name>Bacino, Carlos A</name>
      </author>
      <author>
        <name>Balasubramanyam, Ashok</name>
      </author>
      <author>
        <name>Barseghyan, Hayk</name>
      </author>
      <author>
        <name>Batzli, Gabriel F</name>
      </author>
      <author>
        <name>Beggs, Alan H</name>
      </author>
      <author>
        <name>Behnam, Babak</name>
      </author>
      <author>
        <name>Bican, Anna</name>
      </author>
      <author>
        <name>Bick, David P</name>
      </author>
      <author>
        <name>Birch, Camille L</name>
      </author>
      <author>
        <name>Bonner, Devon</name>
      </author>
      <author>
        <name>Boone, Braden E</name>
      </author>
      <author>
        <name>Bostwick, Bret L</name>
      </author>
      <author>
        <name>Briere, Lauren C</name>
      </author>
      <author>
        <name>Brown, Donna M</name>
      </author>
      <author>
        <name>Brush, Matthew</name>
      </author>
      <author>
        <name>Burke, Elizabeth A</name>
      </author>
      <author>
        <name>Burrage, Lindsay C</name>
      </author>
      <author>
        <name>Chen, Shan</name>
      </author>
      <author>
        <name>Clark, Gary D</name>
      </author>
      <author>
        <name>Coakley, Terra R</name>
      </author>
      <author>
        <name>Cogan, Joy D</name>
      </author>
      <author>
        <name>Cooper, Cynthia M</name>
      </author>
      <author>
        <name>Cope, Heidi</name>
      </author>
      <author>
        <name>Craigen, William J</name>
      </author>
      <author>
        <name>D’Souza, Precilla</name>
      </author>
      <author>
        <name>Davids, Mariska</name>
      </author>
      <author>
        <name>Dayal, Jyoti G</name>
      </author>
      <author>
        <name>Dell’Angelica, Esteban C</name>
      </author>
      <author>
        <name>Dhar, Shweta U</name>
      </author>
      <author>
        <name>Dillon, Ani</name>
      </author>
      <author>
        <name>Dipple, Katrina M</name>
      </author>
      <author>
        <name>Donnell-Fink, Laurel A</name>
      </author>
      <author>
        <name>Dorrani, Naghmeh</name>
      </author>
      <author>
        <name>Dorset, Daniel C</name>
      </author>
      <author>
        <name>Douine, Emilie D</name>
      </author>
      <author>
        <name>Draper, David D</name>
      </author>
      <author>
        <name>Eckstein, David J</name>
      </author>
      <author>
        <name>Emrick, Lisa T</name>
      </author>
      <author>
        <name>Eng, Christine M</name>
      </author>
      <author>
        <name>Eskin, Ascia</name>
      </author>
      <author>
        <name>Esteves, Cecilia</name>
      </author>
      <author>
        <name>Estwick, Tyra</name>
      </author>
      <author>
        <name>Ferreira, Carlos</name>
      </author>
      <author>
        <name>Fogel, Brent L</name>
      </author>
      <author>
        <name>Friedman, Noah D</name>
      </author>
      <author>
        <name>Gahl, William A</name>
      </author>
      <author>
        <name>Glanton, Emily</name>
      </author>
      <author>
        <name>Godfrey, Rena A</name>
      </author>
      <author>
        <name>Goldstein, David B</name>
      </author>
      <author>
        <name>Gould, Sarah E</name>
      </author>
      <author>
        <name>Gourdine, Jean-Philippe F</name>
      </author>
    </item>
    <item>
      <title>A Hybrid EM Algorithm for Linear Two-Way Interactions With Missing Data</title>
      <link>https://escholarship.org/uc/item/5vv5d5s0</link>
      <description>We study an Expectation-Maximization (EM) algorithm for estimating product-term regression models with missing data. The study of such problems in the frequentist tradition has thus far been restricted to an EM algorithm method using full numerical integration. However, under most missing data patterns, we show that this problem can be solved analytically, and numerical approximations are only needed under specific conditions. Thus we propose a hybrid EM algorithm, which uses analytic solutions when available and approximate solutions only when needed. The theoretical framework of our algorithm is described herein, along with three empirical experiments using both simulated and real data. We demonstrate that our algorithm provides greater estimation accuracy, exhibits robustness to distributional violations, and confers higher power to detect interaction effects. We conclude with a discussion of extensions and topics of further research.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/5vv5d5s0</guid>
      <pubDate>Wed, 29 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Kim, Dale S</name>
      </author>
    </item>
    <item>
      <title>Systematic evaluation of methylation-based cell type deconvolution methods for plasma cell-free DNA</title>
      <link>https://escholarship.org/uc/item/3xn518nr</link>
      <description>BackgroundPlasma cell-free DNA (cfDNA) is derived from cellular death in various tissues. Investigating the tissue origin of cfDNA through cell type deconvolution, we can detect changes in tissue homeostasis that occur during disease progression or in response to treatment. Consequently, cfDNA has emerged as a valuable noninvasive biomarker for disease detection and treatment monitoring. Although there are many methylation-based methods for cfDNA cell type deconvolution, a comprehensive and systematic evaluation of these methods has yet to be conducted.ResultsIn this study, we benchmark five methods: MethAtlas, cfNOMe toolkit, CelFiE, CelFEER, and UXM. Utilizing deep whole-genome bisulfite sequencing data from 35 human cell types, we generate in silico cfDNA samples with ground truth cell type proportions to assess the deconvolution performance of the five methods under multiple scenarios. Our findings indicate that multiple factors, including reference marker selection, sequencing...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3xn518nr</guid>
      <pubDate>Mon, 6 Jan 2025 00:00:00 +0000</pubDate>
      <author>
        <name>Sun, Tongyue</name>
      </author>
      <author>
        <name>Yuan, Jinqi</name>
      </author>
      <author>
        <name>Zhu, Yacheng</name>
      </author>
      <author>
        <name>Li, Jingqi</name>
      </author>
      <author>
        <name>Yang, Shen</name>
      </author>
      <author>
        <name>Zhou, Junpeng</name>
      </author>
      <author>
        <name>Ge, Xinzhou</name>
      </author>
      <author>
        <name>Qu, Susu</name>
      </author>
      <author>
        <name>Li, Wei</name>
        <uri>https://orcid.org/0000-0001-9931-5990</uri>
      </author>
      <author>
        <name>Li, Jingyi Jessica</name>
        <uri>https://orcid.org/0000-0002-9288-5648</uri>
      </author>
      <author>
        <name>Li, Yumei</name>
      </author>
    </item>
    <item>
      <title>Integrated molecular and functional characterization of the intrinsic apoptotic machinery identifies therapeutic vulnerabilities in glioma</title>
      <link>https://escholarship.org/uc/item/2s86f706</link>
      <description>Genomic profiling often fails to predict therapeutic outcomes in cancer. This failure is, in part, due to a myriad of genetic alterations and the plasticity of cancer signaling networks. Functional profiling, which ascertains signaling dynamics, is an alternative method to anticipate drug responses. It is unclear whether integrating genomic and functional features of solid tumours can provide unique insight into therapeutic vulnerabilities. We perform combined molecular and functional characterization, via BH3 profiling of the intrinsic apoptotic machinery, in glioma patient samples and derivative models. We identify that standard-of-care therapy rapidly rewires apoptotic signaling in a genotype-specific manner, revealing targetable apoptotic vulnerabilities in gliomas containing specific molecular features (e.g., TP53 WT). However, integration of BH3 profiling reveals high mitochondrial priming is also required to induce glioma apoptosis. Accordingly, a machine-learning approach...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/2s86f706</guid>
      <pubDate>Mon, 9 Dec 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Fernandez, Elizabeth G</name>
      </author>
      <author>
        <name>Mai, Wilson X</name>
      </author>
      <author>
        <name>Song, Kai</name>
      </author>
      <author>
        <name>Bayley, Nicholas A</name>
      </author>
      <author>
        <name>Kim, Jiyoon</name>
      </author>
      <author>
        <name>Zhu, Henan</name>
      </author>
      <author>
        <name>Pioso, Marissa</name>
      </author>
      <author>
        <name>Young, Pauline</name>
      </author>
      <author>
        <name>Andrasz, Cassidy L</name>
      </author>
      <author>
        <name>Cadet, Dimitri</name>
      </author>
      <author>
        <name>Liau, Linda M</name>
        <uri>https://orcid.org/0000-0002-4053-0052</uri>
      </author>
      <author>
        <name>Li, Gang</name>
      </author>
      <author>
        <name>Yong, William H</name>
        <uri>https://orcid.org/0000-0002-0879-0209</uri>
      </author>
      <author>
        <name>Rodriguez, Fausto J</name>
      </author>
      <author>
        <name>Dixon, Scott J</name>
      </author>
      <author>
        <name>Souers, Andrew J</name>
      </author>
      <author>
        <name>Li, Jingyi Jessica</name>
        <uri>https://orcid.org/0000-0002-9288-5648</uri>
      </author>
      <author>
        <name>Graeber, Thomas G</name>
        <uri>https://orcid.org/0000-0001-8574-9181</uri>
      </author>
      <author>
        <name>Cloughesy, Timothy F</name>
      </author>
      <author>
        <name>Nathanson, David A</name>
      </author>
    </item>
    <item>
      <title>Response to "Neglecting normalization impact in semi-synthetic RNA-seq data simulation generates artificial false positives" and "Winsorization greatly reduces false positives by popular differential expression methods when analyzing human population samples"</title>
      <link>https://escholarship.org/uc/item/63v8k539</link>
      <description>Two correspondences raised concerns or comments about our analyses regarding exaggerated false positives found by differential expression&amp;nbsp;(DE) methods. Here, we discuss the points they raise and explain why we agree or disagree with these points.&amp;nbsp;We add new analysis to confirm that the Wilcoxon rank-sum test remains the most robust method compared to the other five DE methods (DESeq2, edgeR, limma-voom, dearseq, and NOISeq) in two-condition DE analyses after considering normalization and winsorization, the data preprocessing steps discussed in the two correspondences.</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/63v8k539</guid>
      <pubDate>Sat, 16 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Ge, Xinzhou</name>
      </author>
      <author>
        <name>Li, Yumei</name>
      </author>
      <author>
        <name>Li, Wei</name>
        <uri>https://orcid.org/0000-0001-9931-5990</uri>
      </author>
      <author>
        <name>Li, Jingyi Jessica</name>
        <uri>https://orcid.org/0000-0002-9288-5648</uri>
      </author>
    </item>
    <item>
      <title>Spatial Data Analysis</title>
      <link>https://escholarship.org/uc/item/1k45h15z</link>
      <description>With increasing accessibility to geographic information systems (GIS) software, statisticians and data analysts routinely encounter scientific data sets with geocoded locations. This has generated considerable interest in statistical modeling for location-referenced spatial data. In public health, spatial data routinely arise as aggregates over regions, such as counts or rates over counties, census tracts, or some other administrative delineation. Such data are often referred to as areal data. This review article provides a brief overview of statistical models that account for spatial dependence in areal data. It does so in the context of two applications: disease mapping and spatial survival analysis. Disease maps are used to highlight geographic areas with high and low prevalence, incidence, or mortality rates of a specific disease and the variability of such rates over a spatial domain. They can also be used to detect hot spots or spatial clusters that may arise owing to common...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1k45h15z</guid>
      <pubDate>Mon, 11 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
    </item>
    <item>
      <title>The pace of change of summertime temperature extremes</title>
      <link>https://escholarship.org/uc/item/1f50w896</link>
      <description>Summer temperature extremes can have large impacts on humans and the biosphere, and an increase in heat extremes is one of the most visible symptoms of climate change. Multiple mechanisms have been proposed that would predict faster warming of heat extremes than typical summer days, but it is unclear whether this is occurring. Here, we show that, in both observations and historical climate model simulations, the hottest summer days have warmed at the same pace as the median globally, in each hemisphere, and in the tropics from 1959 to 2023. In contrast, the coldest summer days have warmed more slowly than the median in the global average, a signal that is not simulated in any of 262 simulations across 28 CMIP6 models. The observed stretching of the cold tail indicates that observed summertime temperatures have become more variable despite the lack of hot day amplification. The interannual variability and trend in the warming of both hot and cold extremes compared to the median...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/1f50w896</guid>
      <pubDate>Sat, 9 Nov 2024 00:00:00 +0000</pubDate>
      <author>
        <name>McKinnon, Karen A</name>
        <uri>https://orcid.org/0000-0003-3314-8442</uri>
      </author>
      <author>
        <name>Simpson, Isla R</name>
      </author>
      <author>
        <name>Williams, A Park</name>
        <uri>https://orcid.org/0000-0001-8176-8166</uri>
      </author>
    </item>
    <item>
      <title>Spatiotemporal multilevel joint modeling of longitudinal and survival outcomes in end-stage kidney disease</title>
      <link>https://escholarship.org/uc/item/62n4b02n</link>
      <description>Individuals with end-stage kidney disease (ESKD) on dialysis experience high mortality and excessive burden of hospitalizations over time relative to comparable Medicare patient cohorts without kidney failure. A key interest in this population is to understand the time-dynamic effects of multilevel risk factors that contribute to the correlated outcomes of longitudinal hospitalization and mortality. For this we utilize multilevel data from the United States Renal Data System (USRDS), a national database that includes nearly all patients with ESKD, where repeated measurements/hospitalizations over time are nested in patients and patients are nested within (health service) regions across the contiguous U.S. We develop a novel spatiotemporal multilevel joint model (STM-JM) that accounts for the aforementioned hierarchical structure of the data while considering the spatiotemporal variations in both outcomes across regions. The proposed STM-JM includes time-varying effects of multilevel...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/62n4b02n</guid>
      <pubDate>Thu, 24 Oct 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Kürüm, Esra</name>
      </author>
      <author>
        <name>Nguyen, Danh V</name>
      </author>
      <author>
        <name>Qian, Qi</name>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Rhee, Connie M</name>
        <uri>https://orcid.org/0000-0002-9703-6469</uri>
      </author>
      <author>
        <name>Şentürk, Damla</name>
      </author>
    </item>
    <item>
      <title>A Bayesian Model for 20th Century Antarctic Sea Ice Extent Reconstruction</title>
      <link>https://escholarship.org/uc/item/6fv058mc</link>
      <description>Abstract: 
Antarctic sea ice, a key component in the complex Antarctic climate system, is an important driver and indicator of the global climate. In the relatively short satellite‐observed period from 1979 to 2022 the sea ice extent has continuously increased (contrasting a major decrease in Arctic sea ice) up to a dramatic decrease between 2014 and 2017. Recent years have seen record sea ice lows in February 2022–February 2023. We use a statistical ensemble reconstruction of Antarctic sea ice to put the observed changes into the historical context of the entire 20th century. We propose a seasonal Vector Auto‐Regressive Moving Average (VARMA) model fit in a Bayesian framework using regularized horseshoe priors on the regression coefficients to create a stochastic ensemble reconstruction of monthly Antarctic Sea ice extent from 1900 to 1979. This novel model produces a set of 2,500 plausible sea ice extent reconstructions for the sea ice by sector that incorporate the autocorrelation...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/6fv058mc</guid>
      <pubDate>Wed, 23 Oct 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Maierhofer, TJ</name>
      </author>
      <author>
        <name>Raphael, MN</name>
      </author>
      <author>
        <name>Fogt, RL</name>
      </author>
      <author>
        <name>Handcock, MS</name>
        <uri>https://orcid.org/0000-0002-9985-2785</uri>
      </author>
    </item>
    <item>
      <title>kpop: a kernel balancing approach for reducing specification assumptions in survey weighting</title>
      <link>https://escholarship.org/uc/item/53b358cd</link>
      <description>With the precipitous decline in response rates, researchers and pollsters have been left with highly nonrepresentative samples, relying on constructed weights to make these samples representative of the desired target population. Though practitioners employ valuable expert knowledge to choose what variables  must be adjusted for, they rarely defend particular functional forms relating these variables to the response process or the outcome. Unfortunately, commonly used calibration weights-which make the weighted mean of  in the sample equal that of the population-only ensure correct adjustment when the portion of the outcome and the response process left unexplained by linear functions of  are independent. To alleviate this functional form dependency, we describe kernel balancing for population weighting (&lt;i&gt;kpop&lt;/i&gt;). This approach replaces the design matrix  with a kernel matrix,  encoding high-order information about  . Weights are then found to make the weighted average row...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/53b358cd</guid>
      <pubDate>Fri, 13 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Hartman, Erin</name>
        <uri>https://orcid.org/0000-0003-4824-5405</uri>
      </author>
      <author>
        <name>Hazlett, Chad</name>
        <uri>https://orcid.org/0000-0003-1819-1928</uri>
      </author>
      <author>
        <name>Sterbenz, Ciara</name>
      </author>
    </item>
    <item>
      <title>Multivariate spatiotemporal functional principal component analysis for modeling hospitalization and mortality rates in the dialysis population</title>
      <link>https://escholarship.org/uc/item/41s024r1</link>
      <description>Dialysis patients experience frequent hospitalizations and a higher mortality rate compared to other Medicare populations, in whom hospitalizations are a major contributor to morbidity, mortality, and healthcare costs. Patients also typically remain on dialysis for the duration of their lives or until kidney transplantation. Hence, there is growing interest in studying the spatiotemporal trends in the correlated outcomes of hospitalization and mortality among dialysis patients as a function of time starting from transition to dialysis across the United States Utilizing national data from the United States Renal Data System (USRDS), we propose a novel multivariate spatiotemporal functional principal component analysis model to study the joint spatiotemporal patterns of hospitalization and mortality rates among dialysis patients. The proposal is based on a multivariate Karhunen-Loéve expansion that describes leading directions of variation across time and induces spatial correlations...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/41s024r1</guid>
      <pubDate>Wed, 4 Sep 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Qian, Qi</name>
      </author>
      <author>
        <name>Nguyen, Danh V</name>
      </author>
      <author>
        <name>Telesca, Donatello</name>
      </author>
      <author>
        <name>Kurum, Esra</name>
        <uri>https://orcid.org/0000-0003-1767-1671</uri>
      </author>
      <author>
        <name>Rhee, Connie M</name>
        <uri>https://orcid.org/0000-0002-9703-6469</uri>
      </author>
      <author>
        <name>Banerjee, Sudipto</name>
      </author>
      <author>
        <name>Li, Yihao</name>
      </author>
      <author>
        <name>Senturk, Damla</name>
      </author>
    </item>
    <item>
      <title>Association between wildfires and coccidioidomycosis incidence in California, 2000–2018: a synthetic control analysis</title>
      <link>https://escholarship.org/uc/item/7md8g1zd</link>
      <description>The frequency and severity of wildfires in the Western United States have increased over recent decades, motivating hypotheses that wildfires contribute to the incidence of coccidioidomycosis, an emerging fungal disease in the Western United States with sharp increases in incidence observed since 2000. While coccidioidomycosis outbreaks have occurred among wildland firefighters clearing brush, it remains unknown whether fires are associated with an increased incidence among the general population.
Methods: We identified 19 wildfires occurring within California's highly endemic San Joaquin Valley between 2003 and 2015. Using geolocated surveillance records, we applied a synthetic control approach to estimate the effect of each wildfire on the incidence of coccidioidomycosis among residents that lived within a hexagonal buffer of 20 km radii surrounding the fire.
Results: We did not detect excess cases due to wildfires in the 12 months (pooled estimated percent change in cases:...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/7md8g1zd</guid>
      <pubDate>Thu, 29 Aug 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Phillips, Sophie</name>
        <uri>https://orcid.org/0000-0002-8084-4929</uri>
      </author>
      <author>
        <name>Jones, Isabel</name>
      </author>
      <author>
        <name>Sondermyer-Cooksey, Gail</name>
      </author>
      <author>
        <name>Yu, Alexander T</name>
      </author>
      <author>
        <name>Heaney, Alexandra K</name>
      </author>
      <author>
        <name>Zhou, Bo</name>
      </author>
      <author>
        <name>Bhattachan, Abinash</name>
      </author>
      <author>
        <name>Weaver, Amanda K</name>
      </author>
      <author>
        <name>Campo, Simon K</name>
      </author>
      <author>
        <name>Mgbara, Whitney</name>
      </author>
      <author>
        <name>Wagner, Robert</name>
      </author>
      <author>
        <name>Taylor, John</name>
      </author>
      <author>
        <name>Lettenmaier, Dennis</name>
      </author>
      <author>
        <name>Okin, Gregory S</name>
      </author>
      <author>
        <name>Jain, Seema</name>
      </author>
      <author>
        <name>Vugia, Duc</name>
      </author>
      <author>
        <name>Remais, Justin V</name>
        <uri>https://orcid.org/0000-0002-0223-4615</uri>
      </author>
      <author>
        <name>Head, Jennifer R</name>
      </author>
    </item>
    <item>
      <title>Disparate Effects of Disruptive Events on Children</title>
      <link>https://escholarship.org/uc/item/399870ks</link>
      <description>Disruptive events such as economic recessions, natural disasters, job loss, and divorce are highly prevalent among American families. These events can have a long-lasting impact when experienced during childhood, potentially altering academic achievement, socioemotional well-being, health and development, and later life socioeconomic status. Much research has considered the overall impact of disruptive events on children's lives, but the consequences of disruption also vary across groups. The same event may have profound negative consequences for some groups, minor or no impact for others, and even be a generative or positive turning point for other groups. This issue focuses on the disparate consequences of disruptive events on children. We consider theoretical approaches accounting for effect heterogeneity and methodological challenges in identifying unequal impacts. We also review an emerging multidisciplinary literature accounting for variation in the impact of disruption...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/399870ks</guid>
      <pubDate>Wed, 31 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Torche, Florencia</name>
      </author>
      <author>
        <name>Fletcher, Jason</name>
      </author>
      <author>
        <name>Brand, Jennie E</name>
      </author>
    </item>
    <item>
      <title>The legacy of Robert D. Mare</title>
      <link>https://escholarship.org/uc/item/0cc6255n</link>
      <description>The legacy of Robert D. Mare</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/0cc6255n</guid>
      <pubDate>Wed, 17 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Brand, Jennie E</name>
      </author>
      <author>
        <name>Xie, Yu</name>
      </author>
    </item>
    <item>
      <title>Observed humidity trends in dry regions contradict climate models</title>
      <link>https://escholarship.org/uc/item/3mr095df</link>
      <description>Arid and semi-arid regions of the world are particularly vulnerable to greenhouse gas-driven hydroclimate change. Climate models are our primary tool for projecting the future hydroclimate that society in these regions must adapt to, but here, we present a concerning discrepancy between observed and model-based historical hydroclimate trends. Over the arid/semi-arid regions of the world, the predominant signal in all model simulations is an increase in atmospheric water vapor, on average, over the last four decades, in association with the increased water vapor-holding capacity of a warmer atmosphere. In observations, this increase in atmospheric water vapor has not happened, suggesting that the availability of moisture to satisfy the increased atmospheric demand is lower in reality than in models in arid/semi-arid regions. This discrepancy is most clear in locations that are arid/semi-arid year round, but it is also apparent in more humid regions during the most arid months of...</description>
      <guid isPermaLink="true">https://escholarship.org/uc/item/3mr095df</guid>
      <pubDate>Mon, 8 Jul 2024 00:00:00 +0000</pubDate>
      <author>
        <name>Simpson, Isla R</name>
      </author>
      <author>
        <name>McKinnon, Karen A</name>
        <uri>https://orcid.org/0000-0003-3314-8442</uri>
      </author>
      <author>
        <name>Kennedy, Daniel</name>
      </author>
      <author>
        <name>Lawrence, David M</name>
      </author>
      <author>
        <name>Lehner, Flavio</name>
      </author>
      <author>
        <name>Seager, Richard</name>
      </author>
    </item>
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