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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Aligned cross-modal integration and regulatory heterogeneity characterization of single-cell multiomic data with deep contrastive learning.
PMID 41588477 · PMC12833949 · Genome medicine · 2026 · 8 claims · 4 setups
scMDCF outperforms existing state-of-the-art scMulti-omics integration and clustering models across various types of scMulti-omics datasets, including robustness against batch effects
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BiCLUM: Bilateral contrastive learning for unpaired single-cell multi-omics integration.
PMID 41632825 · PMC12904586 · PLoS computational biology · 2026 · 8 claims · 5 setups
BiCLUM consistently outperforms or matches existing integration methods across multiple RNA+ATAC and RNA+protein datasets in visualization and quantitative benchmarks
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Has reproduction · 85
Protocol for transcriptomic and epigenomic analysis of JAK inhibitor sensitivity in IFN-γ-primed human macrophages using ATAC-seq and RNA-seq.
PMID 41313685 · PMC12702366 · STAR protocols · 2025 · 7 claims · 7 setups
Integrated ATAC-seq and RNA-seq protocol to profile JAK inhibitor sensitivity in IFN-γ-primed human macrophages
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Prediction of myeloid malignant cells in Fanconi anemia using machine learning.
PMID 41557613 · PMC12818649 · PloS one · 2026 · 6 claims · 7 setups
A DNN classifier trained on AML scRNA-seq data accurately predicts AML-like transcriptional profiles at single-cell resolution
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singIST: An integrative method for comparative single-cell transcriptomics between disease models and humans.
PMID 41838773 · PMC13008255 · PLoS computational biology · 2026 · 8 claims · 7 setups
singIST provides explainable quantitative measures of disease model similarity to a human reference at the pathway, cell type, and gene levels
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Single-cell ATAC-seq analysis of human embryoid bodies reveals crucial transcription factor networks involved in early germ layer specification.
PMID 41906160 · PMC13154528 · Cell & bioscience · 2026 · 7 claims · 7 setups
scATAC-seq of human EBs can classify cells into the three germ layers and, via pseudotime analysis, identify 'early committed cells' at the onset of each germ layer.
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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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Has reproduction · 67
GEMmaker: process massive RNA-seq datasets on heterogeneous computational infrastructure.
PMID 35501696 · PMC9063052 · BMC bioinformatics · 2022 · 6 claims · 3 setups
GEMmaker, an nf-core compliant Nextflow workflow, can quantify gene expression from small to massive RNA-seq datasets while remaining reproducible via versioned containerized software.
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Has reproduction · 62
Comprehensive Transcriptome Analysis Reveals Genome-Wide Changes Associated with Endoplasmic Reticulum (ER) Stress in Potato (Solanum tuberosum L.).
PMID 36430273 · PMC9696714 · International journal of molecular sciences · 2022 · 8 claims · 3 setups
TM treatment of potato leaves produces widespread, time-dependent differential gene expression associated with ER stress and the UPR
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Has reproduction · 90
PrimerSeq: Design and visualization of RT-PCR primers for alternative splicing using RNA-seq data.
PMID 24747190 · PMC4411361 · Genomics, proteomics & bioinformatics · 2014 · 8 claims · 3 setups
PrimerSeq is a user-friendly stand-alone software with a GUI for systematic design and visualization of RT-PCR primers for alternative splicing analysis using user-provided RNA-seq data.
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Genome-wide nucleosome and transcription factor responses to genetic perturbations reveal chromatin-mediated mechanisms of transcriptional regulation.
PMID 41365655 · PMC12758391 · Genome research · 2026 · 8 claims · 3 setups
A factor-agnostic MNase-seq chromatin occupancy profiling (COP) approach can simultaneously capture genome-wide TF and nucleosome occupancy at near-nucleotide resolution from a single assay
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Improved reconstruction of transcripts and coding sequences from RNA-seq data.
PMID 41700087 · PMC12910111 · Nucleic acids research · 2026 · 7 claims · 3 setups
GeMoSeq combines combinatorial enumeration of candidate transcripts, splitting heuristics, and likelihood-based (EM) quantification for transcript reconstruction from RNA-seq data
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Interactive analysis of single-cell trajectories in 3D space with Cell Journey.
PMID 41773942 · PMC13042281 · GigaScience · 2026 · 7 claims · 3 setups
Cell Journey is an interactive platform for computing and visualizing RNA velocity-based single-cell trajectories in 3D space.
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Revealing transcriptomic responses in Escherichia coli during early antibiotic exposure.
PMID 41805196 · PMC13098195 · mSystems · 2026 · 8 claims · 3 setups
E. coli's early antibiotic response follows an integrated three-phase model: an immediate/sustained primary stress response, a transient secondary redox-restoring response, and a tertiary response supporting long-term survival via metabolic remodeling and antibiotic-specific defenses.
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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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AutoGERN: single-cell RNA-seq gene regulatory network inference via explicit link modeling and adaptive architectures.
PMID 41871930 · PMC13064981 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 3 setups
AutoGERN explicitly models regulatory information in the message-passing space via learned link (edge) embeddings, which are scored by a lightweight MLP to infer TF–target interactions.
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Harvesting more reads from single-cell combinatorial barcoding data with scarecrow.
PMID 41967853 · PMC13125751 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 3 setups
scarecrow screens a subsample of reads to generate position-specific barcode profiles, then flexibly identifies barcode sequences in reads while accounting for positional jitter
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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 · 68
Loss of CD4(+) T cell-intrinsic arginase 1 accelerates Th1 response kinetics and reduces lung pathology during influenza infection.
PMID 37572656 · PMC10576612 · Immunity · 2023 · 8 claims · 8 setups
Arg1 is highly and specifically induced in lung CD4+ T cells during in vivo influenza infection
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Agent-based modeling of cellular dynamics in adoptive cell therapy.
PMID 41673469 · PMC13004971 · Communications biology · 2026 · 7 claims · 7 setups
ABMACT, an agent-based model of adoptive cell therapy, recapitulated cellular dynamics in two cancer preclinical models (lymphoma and glioblastoma mouse models).