Experiments
Searchable full-text extractions: founding hypothesis, core claims, experimental setups, key results and statistics — pulled out of each paper as structure. Search a cell line, an assay or an entity (e.g. HUH7) and find every paper that worked with it. This corpus stands on its own: most entries carry no reproduction assessment (yet).
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Predicting preferential DNA vector insertion sites: implications for functional genomics and gene therapy.
PMID 18047689 · PMC2106846 · Genome biology · 2007 · 8 claims · 6 setups
Vector insertion site preferences differ substantially between viral vectors and transposons, affecting both oncogenic risk in gene therapy and utility for functional genomics
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An AI-Enabled Single-Cell Transcriptomic Analysis Pipeline for Gene Signature Discovery in Natural Killer Cells Linked to Remission Outcomes in Chronic Myeloid Leukemia.
PMID 41972591 · PMC13072394 · Biology · 2026 · 8 claims · 7 setups
GAFA integrates latent-space representation, pseudotime trajectory modeling, GRN inference, and machine learning-based gene panel discovery into a single coherent pipeline, unlike existing workflows that treat these steps independently.
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Has reproduction · 50
huSA: a comprehensive database for multi-dimensional resolution of bulk, single cell and spatial transcription profiles in skin diseases.
PMID 41719583 · PMC12923168 · Database : the journal of biological databases and curation · 2026 · 7 claims · 8 setups
huSA is a comprehensive, publicly accessible database integrating bulk RNA-seq, scRNA-seq, and spatial transcriptomics data across 17 skin diseases and 63 independent datasets
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Gene regulatory network determinants of rapid recall in human memory CD4(+) T cells.
PMID 41865369 · PMC13207208 · Cell reports · 2026 · 8 claims · 6 setups
Memory CD4+ T cells show enhanced chromatin accessibility proximal to rapid-recall genes compared to naive cells
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A new chromosome-level genome assembly for western painted turtle Chrysemys picta bellii, a model for extreme physiological adaptations.
PMID 41792601 · PMC13077969 · BMC genomics · 2026 · 6 claims · 8 setups
A new haplotype-resolved, chromosome-level reference genome assembly (SLU_Cpb5.0) was generated for C. picta bellii using combined PacBio HiFi, 10x Genomics Chromium, Hi-C, and Bionano optical mapping data from a single individual.
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scDenorm: a denormalization tool for integrating single-cell transcriptomics data.
PMID 41915012 · PMC13142155 · GigaScience · 2026 · 8 claims · 7 setups
Inconsistent delta-method normalization across datasets introduces biases (e.g., B-cell separation) that persist even after integration with Harmony, scanorama, or BBKNN.
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Integrative Learning of Disentangled Representations from Single-Cell RNA-Sequencing Datasets.
PMID 41971949 · PMC13068006 · Computational and structural biotechnology journal · 2026 · 8 claims · 6 setups
spVIPES decomposes unpaired scRNA-seq datasets with nonmatching features into shared and private latent representations using a Product of Experts framework
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Genetic alternative splicing regulation mapping of cartilage and synovium reveals tissue-specific mechanisms of joint-related traits.
PMID 41820402 · PMC13121699 · Nature communications · 2026 · 8 claims · 8 setups
Generated a splicing quantitative trait loci (sQTL) resource for human cartilage and synovium from over 200 donors
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Hi-Compass: a depth-aware deep learning framework for predicting cell-type-specific 3D genome organization from single-cell to spatial resolution.
PMID 41980945 · PMC13250166 · Nature communications · 2026 · 8 claims · 8 setups
Hi-Compass predicts cell-type-specific Hi-C contact maps using only ATAC-seq as cell-type-specific input, plus DNA sequence and a generalized CTCF binding profile
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PURE-seq integrates FACS and PIP-seq for single-cell genomics of ultra-rare cells.
PMID 41565684 · PMC12881479 · Nature communications · 2026 · 8 claims · 8 setups
PURE-seq integrates FACS sorting directly into PIP-seq barcoding reaction tubes, minimizing manual handling and cell loss for rare-cell single-cell sequencing.
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GRNFormer: accurate gene regulatory network inference using graph transformer.
PMID 41883144 · PMC13069479 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 8 setups
GRNFormer is a generalizable graph transformer framework for GRN inference from single-cell or bulk transcriptomics data across species, cell types, and platforms without cell-type annotations or prior regulatory information
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Spatial multi-omics unveils the monoclonal origin, neuroendocrine plasticity, and microenvironment niches in combined small-cell lung cancer.
PMID 41966692 · PMC13130634 · Cell reports. Medicine · 2026 · 8 claims · 6 setups
Different histologic components within cSCLC tumors share a monoclonal origin
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The UCSC Genome Browser Database: update 2009.
PMID 18996895 · PMC2686463 · Nucleic acids research · 2009 · 8 claims · 6 setups
The UCSC Genome Browser Database (GBD) is a publicly available, integrated collection of genome assembly sequences and annotations across many organisms, including extensive comparative-genomic resources.
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Has reproduction · 66
Caloric Restriction Reprograms Adipose Tissues in Rhesus Monkeys.
PMID 41042069 · PMC12686577 · Aging cell · 2025 · 8 claims · 8 setups
At baseline, SAT and VAT transcriptomes are highly similar, with only ~1% of genes (30 genes, adjusted p<0.05) differentially expressed between depots in Controls