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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Spatiotemporal dynamics of spermatogenesis: insights from high-resolution spatial transcriptomics and pseudotime trajectories in mouse testes.
PMID 41602862 · PMC12832764 · Frontiers in reproductive health · 2025 · 8 claims · 7 setups
Salus-STS (1 μm resolution) combined with the Salus Cellbins Algorithm enables accurate subcellular segmentation of individual testicular cells in dense tissue
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Oxidative stress-associated genes TPPP3 and VEGFA in COPD revealed by bulk and single-cell sequencing analysis.
PMID 41620539 · PMC12916760 · Scientific reports · 2026 · 8 claims · 9 setups
76 overlapping genes were identified between COPD-associated DEGs and oxidative stress-related genes.
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Molecular interactome of HNRNPU reveals regulatory networks in neuronal differentiation and DNA methylation.
PMID 41674383 · PMC12895067 · Nucleic acids research · 2026 · 7 claims · 8 setups
HNRNPU forms extensive protein networks including an association with the mammalian SWI/SNF chromatin-remodeling complex
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Lactate metabolism-related interaction perturbation network enables robust stratification of hepatocellular carcinoma.
PMID 41689750 · PMC13009326 · Discover oncology · 2026 · 8 claims · 8 setups
An LM-related gene interaction perturbation network can stratify HCC into four robust molecular subtypes (Cluster1-4)
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Bridging cancer cell-intrinsic driver genes and -extrinsic cell-cell communication with Driver2Comm.
PMID 41701761 · PMC12928580 · PLoS computational biology · 2026 · 8 claims · 5 setups
Driver2Comm is a computational framework that identifies intrinsic-extrinsic (IE) pathways functionally connecting cancer cell driver genes with their associated CCC signatures in the TME using single-cell transcriptomics data.
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Single-cell epigenetic profiling reveals a tumor-intrinsic interferon response program in ccRCC tied to poor prognosis and BAP1 loss.
PMID 41719400 · PMC12922754 · Science advances · 2026 · 8 claims · 8 setups
Subclustering of ccRCC tumor cells reveals four shared epigenetic programs (C0-C3) recurrent across patients, cohorts, and disease stages
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Unravelling Synaptic and Metabolic Mechanisms of Cognitive Resilience in Asymptomatic Alzheimer's Disease Across Two Alzheimer's Disease Cohorts.
PMID 41723778 · PMC12996523 · Cellular and molecular neurobiology · 2026 · 6 claims · 6 setups
Integrating DEG, DET, and DUT analyses (rather than DEGs alone) provides a more comprehensive view of the molecular mechanisms of AsymAD, since some genes/transcripts are only detected by transcript-level methods.
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Discovery of key regulators in classical monocyte phenotypes linked to COVID-19 severity using single-cell multi-omics sequencing.
PMID 41732268 · PMC12925236 · iScience · 2026 · 8 claims · 8 setups
Two severity-associated classical monocyte (cMono) subtypes, IL7R+ and CD163+, exist with distinct transcriptional and epigenetic landscapes.
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RUMINA: high-throughput deduplication of unique molecular identifiers for amplicon and whole-genome sequencing with enhanced error correction.
PMID 41734278 · PMC12975283 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 4 setups
RUMINA improves detection accuracy of ultra-low frequency SNVs (0.01%-1%) compared to UMI-tools and UMICollapse
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Rare variant analyses provide insights into the genetic architecture of endometriosis.
PMID 41736152 · PMC13001359 · Human genomics · 2026 · 7 claims · 8 setups
Gene-based burden testing of rare LoF and deleterious missense variants identifies SOGA1 as significantly associated with endometriosis after Bonferroni correction
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A cell atlas of multiple liver organoids and the fetal liver based on scRNA-seq.
PMID 41736863 · PMC12927097 · iScience · 2026 · 8 claims · 8 setups
A unified liver organoid cell atlas of 217,025 high-quality cells was constructed by integrating scRNA-seq data from 15 organoid samples across 9 studies with human fetal liver data (5-19 weeks gestation)
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Assessment of dispersion metrics for estimating single-cell transcriptional variability.
PMID 41770747 · PMC12970974 · PLoS computational biology · 2026 · 7 claims · 4 setups
The variance-to-mean ratio (VMR/Fano factor) scales approximately linearly with increasing dispersion and is independent of dataset size.
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AmalgaMo: flexible DNA motif merging.
PMID 41768281 · PMC12947577 · Bioinformatics advances · 2026 · 7 claims · 7 setups
AmalgaMo is a flexible command-line tool for merging highly similar DNA/RNA motifs, using five tunable parameters (t, m, r, s, a), accepting HOCOMOCO/JASPAR/MEME/CisBP formats.
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TRAP5 Inhibition Targeting Scar-Associated Macrophages Ameliorates Acute Kidney Injury to Chronic Kidney Disease Transition.
PMID 41773735 · PMC13159109 · Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026 · 8 claims · 8 setups
A distinct scar-associated macrophage (SM) subset marked by high Acp5/TRAP5, Ctsk, Mmp9, and Spp1 emerges and predominates during the renal remodeling/CKD phase after AAI-induced AKI
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The chromosome-scale genome assembly and annotation of Rosa bracteata (Macartney Rose).
PMID 41794947 · PMC13096426 · Scientific data · 2026 · 8 claims · 8 setups
A chromosome-scale genome assembly of R. bracteata totaling 540.63 Mb with contig N50 of 35.97 Mb was generated, with 501.06 Mb anchored onto seven pseudochromosomes.
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MIRit: an integrative R framework for the identification of impaired miRNA-mRNA regulatory networks in complex diseases.
PMID 41800385 · PMC12961272 · Bioinformatics advances · 2026 · 8 claims · 5 setups
MIRit is a comprehensive, open-source R/Bioconductor framework for integrative miRNA–mRNA analysis that supports both paired and unpaired datasets using statistically appropriate methods.
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Cell type-specific epigenetic regulatory circuitry of coronary artery disease loci.
PMID 41807385 · PMC12979833 · Nature communications · 2026 · 8 claims · 8 setups
Integration of CAD GWAS summary statistics with epigenetic data from 45 cell types identifies 1580 candidate CAD genes
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Multi-omics feature engineering driven by biomedical foundation models improves drug response prediction for inflammatory bowel disease patients.
PMID 41844950 · PMC13129071 · Scientific reports · 2026 · 8 claims · 7 setups
FM (MAMMAL)-derived drug-target binding affinity (BA) inference can be used to rank/select biologically relevant protein targets and their associated genes/SNPs for a drug of interest without knowledge of protein structure or active sites
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Molecular profiling of breast cancer in native American women reveals distinct genomic and transcriptomic features.
PMID 41844957 · PMC13144316 · NPJ precision oncology · 2026 · 8 claims · 6 setups
This is the first multi-omics (mutation, CNV, RNA-seq) characterization of breast tumors from Native American women, providing a resource for future studies
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Identification and validation of hub genes involved in papillary thyroid carcinoma progression.
PMID 41851690 · PMC13126906 · BMC cancer · 2026 · 8 claims · 8 setups
1550 overlapping DEGs (1149 upregulated, 401 downregulated) were identified in PTC compared to normal thyroid tissues