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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TEAD4 and RXRA Regulate the Function of Nucleus Pulposus Cells in Intervertebral Disc Degeneration Via the TNF-α/NF-κB Pathway: An Integrated Analysis of Single-Cell RNA-Seq, Bulk RNA-Seq, and In Vitro Validation.
PMID 41511606 · PMC12995935 · Applied biochemistry and biotechnology · 2026 · 8 claims · 8 setups
TEAD4 and RXRA play critical roles in IDD progression, likely regulating NP cell behavior and ECM metabolism via the TNF-α/NF-κB pathway
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Single-cell RNA-seq reveals trans-sialidase-like superfamily gene expression heterogeneity in Trypanosoma cruzi populations.
PMID 41945382 · PMC13056360 · eLife · 2026 · 8 claims · 5 setups
Surface protein-coding genes, especially TcS superfamily members, are expressed with greater heterogeneity than single-copy genes.
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Has reproduction · 47
Comprehensive analysis of metastatic gastric cancer tumour cells using single-cell RNA-seq.
PMID 33441952 · PMC7806779 · Scientific reports · 2021 · 8 claims · 6 setups
Carcinoma cell profiles are distinct for each patient, while diverse microenvironmental (nonmalignant) subsets are shared across different patients.
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Dynamics of severity-associated immune remodeling by granulocytes and macrophages in acute lung injury.
PMID 42111184 · PMC13157102 · iScience · 2026 · 7 claims · 7 setups
Granulocytes expand while macrophages are depleted as ALI severity progresses from intermediate to late stage
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A Cross-Species Single-Cell Atlas Reveals Conserved Regulatory Networks and Candidate Hearing Loss Genes in the Cochlea.
PMID 42074555 · PMC13115875 · Genes · 2026 · 8 claims · 8 setups
A cross-species single-cell/single-nucleus RNA-seq atlas of human fetal and mouse postnatal cochlea identifies 19 conserved major cell types
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Cell-type- and chromosome-specific chromatin landscapes and DNA replication programs of Drosophila testis tumor stem cell-like cells.
PMID 41371963 · PMC12758400 · Genome research · 2026 · 8 claims · 6 setups
GSC-like and CySC-like cells isolated from upd tumor testes are transcriptionally comparable to wild-type GSC/early-spermatogonia and CySC clusters, respectively
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CeLLTra: aligning cell names with gene expression via a pathway-informed transformer.
PMID 41652996 · PMC12881829 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 4 setups
Grouping genes into pathway-defined gene sets as Transformer input tokens (instead of using individual genes or discretized bins) mitigates the long-sequence problem and improves representation learning of scRNA-Seq gene expression profiles.
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Pseudotimecascade Visualizes Gene Expression Cascade in Pseudotime Analysis.
PMID 41939293 · PMC13047748 · Computational and structural biotechnology journal · 2026 · 8 claims · 6 setups
Pseudotimecascade jointly analyzes multiple genes to uncover their relative temporal ordering and stage-specific activation patterns along pseudotime.
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Ensemble of Time-Evolving SASP Gene Sets Identifies IGFBP7 and CDKN1A as a Potential Marker Pair for Senescent Fibroblast Subpopulations Across Tissues.
PMID 41977201 · PMC13073673 · International journal of molecular sciences · 2026 · 8 claims · 5 setups
SASP genes are not uniformly expressed in all senescent fibroblasts but only in specific subpopulations, indicating combinatorial and heterogeneous SASP expression.
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scLong: a billion-parameter foundation model for capturing long-range gene context in single-cell transcriptomics.
PMID 41639087 · PMC12982784 · Nature communications · 2026 · 7 claims · 4 setups
scLong performs self-attention across all ~27,874 human genes, including lowly expressed ones, to capture long-range gene dependencies missed by models restricted to highly expressed gene subsets
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Identifying clinically relevant cell state interactions in the tumor microenvironment of IDH-mutant gliomas using CSI-TME.
PMID 41807578 · PMC13230996 · Molecular systems biology · 2026 · 7 claims · 8 setups
CSI-TME is a computational pipeline that deconvolves bulk tumor RNA-seq into cell-type-specific expression (via CODEFACS), infers transcriptional states per cell type via ICA, and identifies IC pairs from two cell types whose joint activity is associated with survival via Cox regression
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Telomerase-Associated Genes as Prognostic Markers in High-Grade Serous Ovarian Cancer.
PMID 42050900 · PMC13137916 · Medical science monitor : international medical journal of experimental and clinical research · 2026 · 8 claims · 8 setups
TAGs are linked to HGSOC progression and yield a candidate prognostic model
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PICDGI: A framework for predicting cancer driver genes through dynamic gene-gene interaction modeling of single-cell data.
PMID 42044093 · PMC13119913 · PLoS computational biology · 2026 · 8 claims · 3 setups
PICDGI is a Bayesian framework that predicts driver-like regulatory genes by integrating dynamic gene-gene interaction modeling with scRNA-seq data, without using DNA mutation calls
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Has reproduction · 53
spliceJAC: transition genes and state-specific gene regulation from single-cell transcriptome data.
PMID 36321549 · PMC9627675 · Molecular systems biology · 2022 · 8 claims · 8 setups
spliceJAC uses unspliced and spliced mRNA count matrices to construct cell state-specific gene-gene regulatory interaction (Jacobian) matrices from scRNA-seq data
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Has reproduction · 51
Cell type-specific eQTL analysis of COVID-19 based on single-cell transcriptomic data.
PMID 41064594 · PMC12501775 · NAR genomics and bioinformatics · 2025 · 8 claims · 8 setups
Single-cell eQTL analysis across eight immune cell types identified 2593 genes whose expression is significantly associated with common genetic polymorphisms, with most genes showing cell type-specific effects
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GeneExt: a gene model extension tool for enhanced single-cell RNA-seq analysis.
PMID 41769841 · PMC12970594 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 8 setups
Incomplete/inaccurate gene annotations, especially missing or truncated 3' UTRs, cause reads to map to non-genic regions and genes to be under-quantified or missing from scRNA-seq expression matrices in non-model species
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Cell type-specific network analysis in Diversity Outbred mice identifies genes potentially responsible for human bone mineral density GWAS associations.
PMID 41811178 · PMC12978698 · eLife · 2026 · 8 claims · 8 setups
Cell type-specific Bayesian and co-expression networks generated from BMSC-OB scRNA-seq data in Diversity Outbred mice can prioritize and contextualize genes underlying human BMD GWAS associations
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Comprehensive analysis for the role of macrophage-driven genes in abdominal aortic aneurysm.
PMID 41815567 · PMC12973086 · Cardiovascular diagnosis and therapy · 2026 · 8 claims · 8 setups
SMU1 is identified as a novel macrophage-related gene associated with AAA development, serving as a potential diagnostic biomarker and therapeutic target
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Single-cell transcriptomics reveals heterogeneous neutrophil populations and diagnostic biomarkers in atherosclerosis.
PMID 41847341 · PMC12989409 · Frontiers in physiology · 2026 · 8 claims · 8 setups
Integration of scRNA-seq data from six human carotid samples identified 16 distinct cell subtypes after batch effect correction with Harmony
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Characterizing gene perturbations in single cells via network divergence analysis.
PMID 41965857 · PMC13249949 · Nature communications · 2026 · 8 claims · 8 setups
scDNS quantifies gene-specific functional perturbations by measuring Jensen-Shannon divergence between condition-specific gene interaction network configurations