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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Has reproduction · 92
Large-scale integration of single-cell transcriptomic data captures transitional progenitor states in mouse skeletal muscle regeneration.
PMID 34773081 · PMC8589952 · Communications biology · 2021 · 8 claims · 7 setups
Large-scale integration of 111 sc/snRNAseq datasets captures rare, transitional myogenic progenitor states (commitment and fusion) that are poorly represented in individual datasets.
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Has reproduction · 64
Celline: a flexible tool for one-step retrieval and integrative analysis of public single-cell RNA sequencing data.
PMID 41458999 · PMC12738925 · Frontiers in bioinformatics · 2025 · 8 claims · 6 setups
Celline is a Python package that automates the full scRNA-seq workflow (retrieval, metadata extraction, preprocessing, cell-type annotation, batch correction, trajectory inference) via single-line commands.
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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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Development of a pediatric immune cell atlas and characterization of CD4+ T cells in food allergy.
PMID 42025535 · PMC13105851 · Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2026 · 8 claims · 8 setups
A pediatric single-cell PBMC reference atlas was developed from 57 healthy children across 8 public scRNA-seq studies.
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Single-Cell RNA-Seq Profiling of Transposable Element Expression in Human Peripheral Blood Cells During Viral Infections.
PMID 41683713 · PMC12898442 · International journal of molecular sciences · 2026 · 8 claims · 8 setups
TE expression is significantly higher in PBMCs from viral infection cohorts (and recovered individuals) compared to healthy controls
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TOFU-MAaPO: fast, scalable and reproducible analysis of large metagenome sequence data from the Sequence Read Archive.
PMID 42277027 · PMC13260335 · Nature communications · 2026 · 8 claims · 5 setups
TOFU-MAaPO yields significantly more high-quality MAGs than metaFun, nf-core/mag, and ATLAS due to integration of multiple complementary binning tools with unified MAGScoT refinement
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scDecorr: feature decorrelation based representation learning enables self-supervised alignment of multiple single-cell experiments.
PMID 42056283 · PMC13128840 · Scientific reports · 2026 · 7 claims · 1 setups
scDecorr learns robust cell representations of unlabelled single-cell experiments in a negative-sample-free self-supervised fashion using feature decorrelation
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Metapipeline-DNA: A comprehensive germline and somatic genomics Nextflow pipeline.
PMID 41850291 · PMC13030954 · Cell reports methods · 2026 · 8 claims · 7 setups
Metapipeline-DNA automates germline and somatic DNA sequencing analysis end-to-end, from raw reads through preprocessing, feature detection, QC, and visualization.
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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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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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Processing and population genetic analysis of multigenic datasets with ProSeq3 software.
PMID 19797407 · PMC2778335 · Bioinformatics (Oxford, England) · 2009 · 8 claims · 7 setups
ProSeq3 is a program with a graphic user interface that simplifies preparation and basic population genetic analysis of multigenic DNA polymorphism datasets
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TRED: a transcriptional regulatory element database, new entries and other development.
PMID 17202159 · PMC1899102 · Nucleic acids research · 2007 · 8 claims · 3 setups
TRED collects mammalian cis- and trans-regulatory elements together with experimental evidence, mapped onto assembled genomes
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CERTOMICS: trusted single-cell multiomics pipeline for high-resolution profiling of adoptive cellular immunotherapies.
PMID 41741362 · PMC13008325 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 2 setups
CERTOMICS is a Nextflow-based, CAR-aware pipeline for standardized single-cell multiomics profiling (GEX, V(D)J, ADT) of CAR-engineered cellular immunotherapies
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Developmental convergence and divergence in human stem cell models of autism.
PMID 41611887 · PMC12999519 · Nature · 2026 · 8 claims · 8 setups
Different ASD-associated mutations show the largest mutation-specific transcriptional changes early in hCO differentiation but converge on shared transcriptional changes as development progresses
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pSTIING: a 'systems' approach towards integrating signalling pathways, interaction and transcriptional regulatory networks in inflammation and cancer.
PMID 16381926 · PMC1347407 · Nucleic acids research · 2006 · 8 claims · 3 setups
pSTIING is a publicly accessible web-based knowledgebase integrating protein-protein, protein-lipid, protein-small molecule interactions, transcriptional regulatory associations, ligand-receptor-cell type information, and signal transduction modules, with a focus on inflammation, cell migration and cancer.