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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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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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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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).
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Bayesian inference of RNA velocity incorporating timepoints, lineage bifurcations, and count data.
PMID 41860983 · PMC13021174 · PLoS computational biology · 2026 · 8 claims · 8 setups
VeloVAE significantly outperforms previous RNA velocity methods in data fit, accuracy of inferred differentiation directions, and transcription rate estimation.
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Has reproduction · 67
HArmonized single-cell RNA-seq Cell type Assisted Deconvolution (HASCAD).
PMID 37907883 · PMC10619225 · BMC medical genomics · 2023 · 6 claims · 4 setups
Removal of batch effects in reference scRNA-seq datasets (via Harmony-Symphony) benefits the task of cell composition deconvolution
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Has reproduction · 100
ChIP-seq Data Processing and Relative and Quantitative Signal Normalization for Saccharomyces cerevisiae.
PMID 40364978 · PMC12067309 · Bio-protocol · 2025 · 8 claims · 6 setups
Spike-in normalization, though semiquantitative, often fails to reliably support comparisons within and between ChIP-seq samples.
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Has reproduction · 50
Viewing RNA-seq data on the entire human genome.
PMID 28979763 · PMC5605993 · F1000Research · 2017 · 8 claims · 3 setups
RNA-Seq Viewer is a web application that visualizes genome-wide RNA-seq expression data pulled from NCBI's SRA and GEO databases using Ideogram.js
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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
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TiRank prioritizes phenotypic niches in tumor microenvironment for clinical biomarker discovery.
PMID 41689080 · PMC12910759 · Genome medicine · 2026 · 7 claims · 4 setups
TiRank is a framework that integrates scRNA-seq, ST, and bulk transcriptomes using an REO-transformation module and multitask transfer learning to align data into a unified embedding space for prioritizing clinically relevant spatial niches
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SeqExpressionAnalyser: An R Package for Automated End-to-End RNA-Seq Analysis From Reads to Differential Expression.
PMID 41602550 · PMC12833196 · Bioinformatics and biology insights · 2026 · 8 claims · 2 setups
SeqExpressionAnalyser is a novel R package/Shiny web application that provides the first R-based, fully integrated interface for interactive end-to-end RNA-Seq differential gene expression analysis, from FASTQ reads to results.
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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