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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Scalable nonparametric clustering with unified marker gene selection for single-cell RNA-seq data.
PMID 41825449 · PMC13030991 · Cell reports methods · 2026 · 7 claims · 3 setups
NCLUSION matches the performance of state-of-the-art single-cell clustering techniques with significantly reduced runtime
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FLASH-MM: fast and scalable single-cell differential expression analysis using linear mixed-effects models.
PMID 41644528 · PMC12982622 · Nature communications · 2026 · 8 claims · 6 setups
FLASH-MM produces LMM parameter estimates identical to lmer (lme4) up to the sixth decimal place while being 50- to 140-fold faster as sample size increases from 20,000 to 120,000 cells
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Prior-guided factorization for reliable imputation of scRNA-seq data.
PMID 41860953 · PMC13004523 · PLoS computational biology · 2026 · 8 claims · 8 setups
scZN models scRNA-seq counts as a mixture of a two-state (Gamma-Poisson/negative binomial) transcriptional bursting process and dropout, formalized via a zero-inflated negative binomial (ZINB) and solved as constrained nonnegative matrix factorization into a cell-to-cell-type assignment matrix and a cell-type expression matrix
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Bridging unpaired single-cell multimodal data for integrative analyses with SuperMap.
PMID 41650244 · PMC12890892 · Proceedings of the National Academy of Sciences of the United States of America · 2026 · 8 claims · 7 setups
SuperMap learns cross-modal feature mappings directly from unpaired multimodal data without requiring paired training data
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Robust and efficient annotation of cell states through gene signature scoring.
PMID 41708334 · PMC12951948 · Genome research · 2026 · 8 claims · 8 setups
Established scoring methods (Seurat, SCANPY, UCell, JASMINE) fail to provide robust and comparable score distributions across diverse signatures and experimental conditions, precluding accurate unsupervised cell-state annotation.
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Cell neighborhood topology directs rare cell population identification.
PMID 41912521 · PMC13199379 · Nature communications · 2026 · 8 claims · 8 setups
RareQ is a framework that quantifies neighborhood connectivity (Q), a cell-specific measure of kNN-graph cliquishness, to detect rare cell populations from single-cell and spatial omics data
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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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Ultra-precision deconvolution of spatial transcriptomics decodes immune heterogeneity and fate-defining programs in tissues.
PMID 41862467 · PMC13168514 · Nature communications · 2026 · 8 claims · 8 setups
UCASpatial is a novel deconvolution algorithm that uses Shannon entropy-based gene weighting combined with weighted non-negative least squares to estimate cell-type composition from spatial transcriptomics data
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omnideconv: a unifying framework for using and benchmarking single-cell-informed deconvolution of bulk RNA-seq data.
PMID 41582216 · PMC12837286 · Genome biology · 2026 · 8 claims · 6 setups
omnideconv is an R package providing a unified interface to twelve second-generation deconvolution methods (AutoGeneS, BayesPrism, Bseq-SC, Bisque, CDseq, CIBERSORTx, CPM, DWLS, MOMF, MuSiC, SCDC, Scaden)
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Benchmarking tools for deciphering cellular crosstalk in spatially-resolved transcriptomics.
PMID 41952215 · PMC13174004 · Genome biology · 2026 · 8 claims · 5 setups
No prior systematic, quantitative benchmark exists for CCI inference methods specifically developed for spatial transcriptomics across multiple platforms
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DAESC + : high-performance, integrated software for single-cell allele-specific expression data.
PMID 41851619 · PMC13169709 · BMC bioinformatics · 2026 · 8 claims · 6 setups
DAESC+ is a dual-module, end-to-end software package (DAESC-P for preprocessing, DAESC-GPU for differential analysis) for single-cell ASE data
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scMILD: Single-cell multiple instance learning for sample classification and associated subpopulation discovery.
PMID 41907409 · PMC13019583 · iScience · 2026 · 8 claims · 8 setups
scMILD identifies condition-associated cells using only sample-level labels via a dual-branch MIL architecture with a shared encoder