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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Multimodal-based analysis of single-cell ATAC-seq data enables highly accurate delineation of clinically relevant tumor cell subpopulations.
PMID 41530870 · PMC12888741 · Genome medicine · 2026 · 8 claims · 8 setups
MAAS integrates chromatin accessibility, CNVs, and SNVs from scATAC-seq data to identify functional tumor cell subpopulations
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A multi-omic single-cell landscape of perinatal mouse skin maps lineage specification and reveals shared dynamics in human fetal skin.
PMID 41998142 · PMC13144478 · Experimental & molecular medicine · 2026 · 7 claims · 8 setups
Integrated scATAC/scRNA multi-omics analysis of developing mouse skin identifies gene network axes underlying skin lineage specification
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scCNMF: an integrated analysis model for paired single-cell RNA sequencing and assay for transposase-accessible chromatin sequencing data leveraging cell similarity and cis-regulatory potential.
PMID 41800139 · PMC12962131 · PeerJ · 2026 · 7 claims · 2 setups
scCNMF is an NMF-based model for vertical integration of paired scRNA-seq and scATAC-seq data that jointly incorporates a cell similarity matrix and a cis-regulatory potential (CRP) matrix
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Human-scATAC-Corpus: a comprehensive database of scATAC-seq data.
PMID 41296545 · PMC12807747 · Nucleic acids research · 2026 · 8 claims · 6 setups
Human-scATAC-Corpus is a comprehensive database of human scATAC-seq data comprising 5,407,621 cells from 35 datasets across 37 tissues or cell lines
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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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Dynamics and regulation of mitotic chromatin accessibility bookmarking at single-cell resolution.
PMID 36696508 · PMC9876548 · Science advances · 2023 · 7 claims · 8 setups
Chromatin accessibility continually decreases from mitotic entry until metaphase, then gradually increases as chromosomes segregate.
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Predicting enhancer-gene links from single-cell multi-omics data by integrating prior Hi-C information.
PMID 42100854 · PMC13229940 · Nucleic acids research · 2026 · 8 claims · 6 setups
SCEG-HiC, a weighted graphical lasso (wglasso) method, predicts enhancer-gene links from single-cell multi-omics data by integrating bulk average Hi-C as a prior penalty matrix
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A generic reference defined by consensus peaks for single-cell ATAC-seq data analysis.
PMID 41663439 · PMC12996591 · Nature communications · 2026 · 7 claims · 7 setups
Aggregating peaks from 624 high-quality bulk ATAC-seq datasets defines ~1.4 million observed consensus peaks (cPeaks) covering ~30% of the genome.
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Benchmarking component choices for unpaired single cell RNA and epigenomic integration.
PMID 41987329 · PMC13192178 · Genome biology · 2026 · 7 claims · 8 setups
Gene activity scores (GAS) show limited correlation with actual gene expression but effectively preserve cellular neighborhood structure and support clustering.
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Single-cell multiome and enhancer connectome of human retinal pigment epithelium and choroid nominate causal variants in macular degeneration.
PMID 41528844 · PMC12971065 · Cell reports · 2026 · 8 claims · 8 setups
Generated a single-cell gene expression and chromatin accessibility (multiome) atlas of human RPE and choroid from control and AMD eyes
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GAMMI: graph-guided contrastive and adversarial integration of single-cell and spatial multi-omics data.
PMID 42108634 · PMC13158126 · Briefings in bioinformatics · 2026 · 6 claims · 5 setups
GAMMI consistently outperforms state-of-the-art integration methods (GLUE, Harmony, MIDAS, scMoMaT) in biological conservation and batch correction across five mosaic single-cell multi-omics benchmarks
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Lorentz-regularized interpretable VAE for multi-scale single-cell transcriptomic and epigenomic embeddings.
PMID 41555918 · PMC12812404 · Frontiers in genetics · 2025 · 7 claims · 5 setups
LiVAE, a dual-pathway VAE with Lorentzian geometric regularization between a primary Euclidean pathway and an information-bottleneck pathway, balances local fidelity with global topology coherence in single-cell embeddings
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Geometry-aware graph attention networks to explain single-cell chromatin states and gene expression with SEAGALL.
PMID 42026624 · PMC13238118 · Genome biology · 2026 · 8 claims · 6 setups
SEAGALL combines a geometry-regularised autoencoder (GRAE) to embed cells and build a cell-cell graph with a graph attention network (GAT) classifier and GNNExplainer-based XAI to identify features driving cell type/phenotype.
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Benchmarking LLM-based agents for single-cell omics analysis.
PMID 41742311 · PMC13064268 · Genome biology · 2026 · 8 claims · 8 setups
Introduces a comprehensive benchmarking evaluation system comprising an open-source agent platform, 18 evaluation metrics across four dimensions, and 50 real-world single-cell omics tasks
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Single-cell multiomics uncovers an endothelial mechanosensitive PIEZO1-IL-33 axis driving pulmonary fibrosis.
PMID 41862476 · PMC13004862 · Nature communications · 2026 · 7 claims · 8 setups
Mechanical stress (MS) signaling is significantly elevated in endothelial cells (ECs) from IPF patients and correlates with fibrosis severity and lung function decline
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Evaluating the Utilities of Foundation Models in Single-Cell Data Analysis.
PMID 41869863 · PMC13170260 · Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026 · 8 claims · 8 setups
Among ten/eleven evaluated single-cell FMs, scGPT, Geneformer, and CellFM are the top models considering both performance and user accessibility
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MitoPerturb-Seq identifies gene-specific single-cell responses to mitochondrial DNA depletion and heteroplasmy.
PMID 41922875 · PMC13095666 · Nature structural & molecular biology · 2026 · 8 claims · 6 setups
MitoPerturb-Seq combines pooled CRISPR–Cas9 screening (CROP-seq) with 10x Genomics multiome (scATAC-seq + scRNA-seq) to simultaneously profile mtDNA sequence/copy number/heteroplasmy and the nuclear transcriptome/chromatin accessibility in single heteroplasmic cells
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OTMODE: an optimal transport theory-based framework for identifying differential features in single-cell multi-omics data.
PMID 41335419 · PMC12766913 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 8 setups
OTMODE, using an unbalanced Sinkhorn algorithm and Wald test, improves differential feature identification in single-cell multi-omics data
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Heterochronic transcription factor expression drives cone-dominant retina development in 13-lined ground squirrels.
PMID 41649260 · PMC12880807 · eLife · 2026 · 8 claims · 8 setups
13LGS cone photoreceptors arise from both early-stage and late-stage neurogenic progenitors, unlike mice where cones arise only from early-stage progenitors
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Semi-parametric empirical bayes method for multiplet detection in snATAC-seq with probabilistic multi-omic integration.
PMID 42054434 · PMC13148828 · PLoS computational biology · 2026 · 8 claims · 5 setups
SEBULA models the singlet background directly from observed HCLC (high-coverage locus count) statistics using fragment-level snATAC-seq information, avoiding reliance on synthetic/artificial doublets.