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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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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Evaluating imputation methods for accurate estimation of cell population fractions in single-cell RNA sequencing.
PMID 41503159 · PMC12770975 · NAR genomics and bioinformatics · 2026 · 8 claims · 6 setups
Eight prominent imputation methods (MAGIC, SAVER, scVI, DCA, scBiG, kNN-smoothing, scImpute, ALRA) were systematically evaluated for their ability to recover the true non-zero expression fraction using simulated and real-world scRNA-seq data
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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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PreTSA: computationally efficient modeling of temporal and spatial gene expression patterns.
PMID 41673899 · PMC12998178 · Genome biology · 2026 · 7 claims · 8 setups
PreTSA dramatically reduces computational time and memory versus GAM (Monocle, TSCAN) and PseudotimeDE for identifying temporally variable genes (TVGs) while producing highly similar results
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scTWAS: a powerful statistical framework for single-cell transcriptome-wide association studies.
PMID 41820391 · PMC13121454 · Nature communications · 2026 · 8 claims · 5 setups
scTWAS uses a latent-variable expression-measurement model combined with a moment-based regression to more accurately estimate genetic regulation of gene expression from single-cell data, improving GReX prediction across cell types and datasets
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scComm: a contrastive learning framework for deciphering cell-cell communications at single-cell resolution.
PMID 41877186 · PMC13134144 · Genome biology · 2026 · 8 claims · 7 setups
scComm infers cell-cell communications at single-cell resolution using a data-adaptive L-R weighting module and supervised contrastive learning (SupCon loss) to distinguish significant CCC events from background noise
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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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scGACL: a generative adversarial network with multi-scale contrastive learning for accurate single-cell RNA sequencing imputation.
PMID 41632596 · PMC12866930 · Briefings in bioinformatics · 2026 · 8 claims · 6 setups
scGACL, a GAN integrated with multi-scale contrastive learning, is proposed to overcome the over-smoothing problem in scRNA-seq imputation
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ScLRTC: imputation for single-cell RNA-seq data via low-rank tensor completion.
PMID 34844559 · PMC8628418 · BMC genomics · 2021 · 8 claims · 8 setups
scLRTC imputes dropout entries closest to the original expression values on simulated datasets, outperforming other state-of-the-art methods by SSE and PCC.
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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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FUNCellA: A Tool for Single-Sample Enrichment Analysis and Relative Pathway Activity Estimation in Single-Cell RNA Sequencing Data.
PMID 42021835 · PMC13096679 · Computational and structural biotechnology journal · 2026 · 7 claims · 8 setups
FUNCellA integrates 7 single-sample enrichment algorithms with novel relative activation thresholding methods to identify active, inactive, and intermediate cellular states in scRNA-Seq data
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A copula-infused graph neural network for cell type classification in single-cell RNA sequencing data.
PMID 41940310 · PMC12914865 · Computational and structural biotechnology journal · 2026 · 8 claims · 5 setups
scCopulaGNN combines copula theory with graph neural network representation learning for scRNA-seq cell type classification
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Hypergraph representations of single-cell RNA sequencing data for improved cell clustering.
PMID 41896196 · PMC13070707 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 6 setups
Unipartite network projections (e.g. cell/gene co-expression networks) of scRNA-seq data lose higher-order information and are an inefficient, inflated representation of sparse transcriptomic data
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Compact and informative representation learning for scRNA-seq data clustering with masked information bottleneck.
PMID 41917934 · PMC13162528 · BMC biology · 2026 · 6 claims · 4 setups
scMIB achieves state-of-the-art and more stable clustering performance across diverse scRNA-seq datasets compared with ten baseline methods
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scZiva: imputation method for single-cell RNA-seq data with zero-inflated variational autoencoder.
PMID 41857511 · PMC13122936 · BMC bioinformatics · 2026 · 8 claims · 1 setups
scZiva is a novel VAE-based imputation method for scRNA-seq data using a Zero-Inflated Negative Binomial (ZINB) likelihood.
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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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Trajectory-guided dimensionality reduction for multi-sample single-cell RNA-seq data reveals biologically relevant sample-level heterogeneity.
PMID 42024616 · PMC13188987 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 6 setups
MUSTARD is a trajectory-guided dimensionality reduction method for multi-sample, multi-condition scRNA-seq data that simultaneously captures gene expression variation along pseudotime and across samples
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scSurvival: Single-Cell Survival Analysis of Clinical Cancer Cohort Data at Cellular Resolution.
PMID 42013315 · PMC13133615 · Cancer discovery · 2026 · 8 claims · 7 setups
scSurvival, an attention-based multiple-instance Cox regression framework, models each tumor sample as an ensemble of cells to predict survival outcomes at both patient and single-cell levels
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Single-cell omics data-driven decoding of tumor clonal evolution through reinforcement learning.
PMID 41998716 · PMC13224513 · Genome medicine · 2026 · 8 claims · 3 setups
scRevol is an RL-based model that infers tumor clonal evolution from scRNA-seq-derived CNV profiles via a label assignment learning strategy.
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scSurv: a deep generative model for single-cell survival analysis.
PMID 41429574 · PMC12797213 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 6 setups
scSurv combines a Cox proportional hazards model with a deep generative model (VAE) of single-cell transcriptomes to estimate individual cellular contributions to clinical outcomes