BioSciences
Parent: Lawrence Berkeley National Laboratory
eScholarship stats: Breakdown by Item for May through August, 2026
| Item | Title | Total requests | Download | View-only | %Dnld |
|---|---|---|---|---|---|
| 1h3515gn | BBMap: A Fast, Accurate, Splice-Aware Aligner | 1,345 | 250 | 1,095 | 18.6% |
| 57f5059w | Dynamic root exudate chemistry and microbial substrate preferences drive patterns in rhizosphere microbial community assembly | 1,291 | 702 | 589 | 54.4% |
| 28w1d3zs | A Korarchael Genome Reveals Insights into the Evolution of the Archaea | 1,174 | 30 | 1,144 | 2.6% |
| 4j8893w1 | Targeted Apoptosis of Senescent Cells Restores Tissue Homeostasis in Response to Chemotoxicity and Aging | 1,078 | 84 | 994 | 7.8% |
| 3gz3w9v7 | Accurate prediction of protein structures and interactions using a three-track neural network | 919 | 770 | 149 | 83.8% |
| 60s4z9wm | Tumour exosome integrins determine organotropic metastasis | 798 | 344 | 454 | 43.1% |
| 6rg9n14p | A unified catalog of 204,938 reference genomes from the human gut microbiome | 757 | 326 | 431 | 43.1% |
| 6xs6568m | Slot Blot Assay for Detection of R Loops | 753 | 612 | 141 | 81.3% |
| 7vn8q02v | Persistence and plasticity in bacterial gene regulation | 716 | 480 | 236 | 67.0% |
| 5fw223fd | Microbial secondary metabolites: advancements to accelerate discovery towards application | 711 | 384 | 327 | 54.0% |
| 5n75t404 | Pre-metastatic niches: organ-specific homes for metastases | 706 | 214 | 492 | 30.3% |
| 9d4221mc | De novo DNA synthesis using polymerase-nucleotide conjugates | 686 | 277 | 409 | 40.4% |
| 2n42n48w | The Impact of Electric Fields on Processes at Electrode Interfaces | 678 | 502 | 176 | 74.0% |
| 96n6w63s | Identification of mobile genetic elements with geNomad | 663 | 492 | 171 | 74.2% |
| 9315g04c | The Artificial Intelligence Ontology: LLM-Assisted Construction of AI Concept Hierarchies | 652 | 214 | 438 | 32.8% |
| 9pm0x5mh | Machine learning for metabolic engineering: A review | 648 | 353 | 295 | 54.5% |
| 4z5380qs | Gaussian processes for autonomous data acquisition at large-scale synchrotron and neutron facilities | 630 | 485 | 145 | 77.0% |
| 12v5v27c | A call for caution in the biological interpretation of viral auxiliary metabolic genes | 626 | 274 | 352 | 43.8% |
| 69z6h6mx | Feed Your Friends: Do Plant Exudates Shape the Root Microbiome? | 622 | 467 | 155 | 75.1% |
| 38f0c7zv | Labr3:Ce scintillators for gamma ray spectroscopy | 604 | 102 | 502 | 16.9% |
| 9v80x6j2 | Reduction of microbial diversity in grassland soil is driven by long-term climate warming | 603 | 429 | 174 | 71.1% |
| 7956s6h6 | The Human Phenotype Ontology in 2024: phenotypes around the world | 597 | 239 | 358 | 40.0% |
| 0xk6c2hf | Structures of a phycobilisome in light-harvesting and photoprotected states | 596 | 443 | 153 | 74.3% |
| 4zh090xt | Uncovering Earth’s virome | 592 | 386 | 206 | 65.2% |
| 6x297461 | A global metagenomic map of urban microbiomes and antimicrobial resistance | 592 | 411 | 181 | 69.4% |
| 2mq4z3j6 | Complete biosynthesis of QS-21 in engineered yeast | 589 | 358 | 231 | 60.8% |
| 5wk090j4 | A genomic perspective on fungal diversity and evolution | 575 | 268 | 307 | 46.6% |
| 7s7342wx | Evaluation of bacterial hosts for conversion of lignin-derived p-coumaric acid to 4-vinylphenol | 573 | 60 | 513 | 10.5% |
| 8sr171mx | Synthetic Scientific Image Generation with VAE, GAN, and Diffusion Model Architectures | 564 | 222 | 342 | 39.4% |
| 3k8311t2 | Mapping genome-wide transcription-factor binding sites using DAP-seq | 547 | 121 | 426 | 22.1% |
| 8pw2x188 | Ancient gene linkages support ctenophores as sister to other animals | 539 | 216 | 323 | 40.1% |
| 7007x1s9 | Visualizing and accessing correlated SAXS data sets with Similarity Maps and Simple Scattering web resources | 509 | 425 | 84 | 83.5% |
| 0cf9v4c4 | Increased enhancer–promoter interactions during developmental enhancer activation in mammals | 501 | 221 | 280 | 44.1% |
| 61w6w086 | Introduction to Computational Metagenomics | 500 | 307 | 193 | 61.4% |
| 0126f84t | Structure, function and diversity of the healthy human microbiome | 481 | 60 | 421 | 12.5% |
| 3799153s | 33 Unresolved Questions in Nanoscience and Nanotechnology | 481 | 142 | 339 | 29.5% |
| 5rg2z05p | Large-scale genetic characterization of the model sulfate-reducing bacterium, Desulfovibrio vulgaris Hildenborough | 475 | 163 | 312 | 34.3% |
| 1gq1w12k | Mitochondrial Dysfunction Induces Senescence with a Distinct Secretory Phenotype | 471 | 120 | 351 | 25.5% |
| 2zw971kg | Metabolic engineering strategies for sesquiterpene production in microorganism | 469 | 172 | 297 | 36.7% |
| 44v0c3r5 | Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution | 468 | 123 | 345 | 26.3% |
| 53j5t3m7 | Phage therapy: From biological mechanisms to future directions | 461 | 325 | 136 | 70.5% |
| 9bk272nb | Evolution-guided tolerance engineering of Pseudomonas putida KT2440 for production of the aviation fuel precursor isoprenol | 460 | 418 | 42 | 90.9% |
| 77f5s184 | The flavonoid procyanidin C1 has senotherapeutic activity and increases lifespan in mice | 457 | 161 | 296 | 35.2% |
| 06z731jw | A conserved PLPLRT/SD motif of STING mediates the recruitment and activation of TBK1 | 455 | 215 | 240 | 47.3% |
| 3qf33012 | Binary vector copy number engineering improves Agrobacterium-mediated transformation | 453 | 296 | 157 | 65.3% |
| 1xt5762k | Improving photosynthesis and crop productivity by accelerating recovery from photoprotection | 446 | 231 | 215 | 51.8% |
| 5ns091ht | Atacama Large Aperture Submillimeter Telescope (AtLAST) science: Resolving the hot and ionized Universe through the Sunyaev-Zeldovich effect | 446 | 303 | 143 | 67.9% |
| 8rk2x6pj | A chromosome-based draft sequence of the hexaploid bread wheat (Triticum aestivum) genome | 442 | 159 | 283 | 36.0% |
| 0636v49k | Unlocking the magic in mycelium: Using synthetic biology to optimize filamentous fungi for biomanufacturing and sustainability | 437 | 274 | 163 | 62.7% |
| 2hg7004n | Systematic assessment of long-read RNA-seq methods for transcript identification and quantification | 437 | 349 | 88 | 79.9% |
Note: Due to the evolving nature of web traffic, the data presented here should be considered approximate and subject to revision. Learn more.