Navigating through natural environments requires localizing objects along three distinct spatial axes. Information about position along the horizontal and vertical axes is available from an object's position on the retina, while position along the depth axis must be inferred based on second-order cues such as the disparity between the images cast on the two retinae. Past work has revealed that object position in two-dimensional (2D) retinotopic space is robustly represented in visual cortex and can be robustly predicted using a multivariate encoding model, in which an explicit axis is modeled for each spatial dimension. However, no study to date has used an encoding model to estimate a representation of stimulus position in depth. Here, we recorded BOLD fMRI while human subjects viewed a stereoscopic random-dot sphere at various positions along the depth (z) and the horizontal (x) axes, and the stimuli were presented across a wider range of disparities (out to ∼40 arcmin) compared to previous neuroimaging studies. In addition to performing decoding analyses for comparison to previous work, we built encoding models for depth position and for horizontal position, allowing us to directly compare encoding between these dimensions. Our results validate this method of recovering depth representations from retinotopic cortex. Furthermore, we find convergent evidence that depth is encoded most strongly in dorsal area V3A.

Increasingly, users of health and biomedical libraries need assistance with challenges they face in working with their own and others' data. Librarians have a unique opportunity to provide valuable support and assistance in data science and open science but may need to add to their expertise and skill set to have the most impact. This article describes the rationale for and development of the Medical Library Association Data Services Competency, which outlines a set of five key skills for data services and provides a course of study for gaining these skills.

A wealth of viral data sits untapped in publicly available metagenomic data sets when it might be extracted to create a usable index for the virological research community. We hypothesized that work of this complexity and scale could be done in a hackathon setting. Ten teams comprised of over 40 participants from six countries, assembled to create a crowd-sourced set of analysis and processing pipelines for a complex biological data set in a three-day event on the San Diego State University campus starting 9 January 2019. Prior to the hackathon, 141,676 metagenomic data sets from the National Center for Biotechnology Information (NCBI) Sequence Read Archive (SRA) were pre-assembled into contiguous assemblies (contigs) by NCBI staff. During the hackathon, a subset consisting of 2953 SRA data sets (approximately 55 million contigs) was selected, which were further filtered for a minimal length of 1 kb. This resulted in 4.2 million (Mio) contigs, which were aligned using BLAST against all known virus genomes, phylogenetically clustered and assigned metadata. Out of the 4.2 Mio contigs, 360,000 contigs were labeled with domains and an additional subset containing 4400 contigs was screened for virus or virus-like genes. The work yielded valuable insights into both SRA data and the cloud infrastructure required to support such efforts, revealing analysis bottlenecks and possible workarounds thereof. Mainly: (i) Conservative assemblies of SRA data improves initial analysis steps; (ii) existing bioinformatic software with weak multithreading/multicore support can be elevated by wrapper scripts to use all cores within a computing node; (iii) redesigning existing bioinformatic algorithms for a cloud infrastructure to facilitate its use for a wider audience; and (iv) a cloud infrastructure allows a diverse group of researchers to collaborate effectively. The scientific findings will be extended during a follow-up event. Here, we present the applied workflows, initial results, and lessons learned from the hackathon.