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 · 90
Systematic clustering algorithm for chromatin accessibility data and its application to hematopoietic cells.
PMID 33253153 · PMC7728210 · PLoS computational biology · 2020 · 7 claims · 5 setups
A systematic clustering algorithm for ATAC-seq data can be built by binarizing the genome into open/closed chromatin (1/0) strings and computing Hamming distances between samples for hierarchical clustering.
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Has reproduction · 62
Application of alternative de novo motif recognition models for analysis of structural heterogeneity of transcription factor binding sites: a case study of FOXA2 binding sites.
PMID 34547062 · PMC8408018 · Vavilovskii zhurnal genetiki i selektsii · 2021 · 8 claims · 4 setups
MultiDeNA pipeline combines PWM, diPWM, BaMM and InMoDe models to train, evaluate, threshold, and classify ChIP-seq peaks for TFBS structural heterogeneity
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Has reproduction · 77
Accurate chromatin marks peak calling with Omnipeak.
PMID 41521664 · PMC12784980 · Nucleic acids research · 2026 · 8 claims · 6 setups
Omnipeak is a universal unsupervised peak-calling algorithm based on a constrained three-state hidden Markov model (zero, noise, signal states)
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Has reproduction · 79
Enriched domain detector: a program for detection of wide genomic enrichment domains robust against local variations.
PMID 24782521 · PMC4066758 · Nucleic acids research · 2014 · 8 claims · 5 setups
EDD is a new algorithm that detects broad (megabase-size) enrichment domains from ChIP-seq data of widely distributed chromatin proteins such as A- and B-type lamins.
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A generic reference defined by consensus peaks for single-cell ATAC-seq data analysis.
PMID 41663439 · PMC12996591 · Nature communications · 2026 · 7 claims · 7 setups
Aggregating peaks from 624 high-quality bulk ATAC-seq datasets defines ~1.4 million observed consensus peaks (cPeaks) covering ~30% of the genome.
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Molecular interactions between HNF4a, FOXA2 and GABP identified at regulatory DNA elements through ChIP-sequencing.
PMID 19822575 · PMC2794179 · Nucleic acids research · 2009 · 8 claims · 6 setups
ChIP-seq identified 3064 GABP peaks, 7266 FOXA2 peaks and 18783 HNF4a peaks in HepG2 cells
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A ligand-centered framework for γδ T cell activation in colorectal cancer revealed by single-cell and transformer-based perturbation.
PMID 41607803 · PMC12835328 · Frontiers in immunology · 2025 · 8 claims · 8 setups
CRC-infiltrating γδ T cells show varied activation levels, with the TRM-like population being the major tumor-infiltrating subtype and exhibiting the lowest effector and exhaustion signature scores.
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Has reproduction · 65
Cancer-predicting transcriptomic and epigenetic signatures revealed for ulcerative colitis in patient-derived epithelial organoids.
PMID 29983891 · PMC6033374 · Oncotarget · 2018 · 7 claims · 6 setups
UC patient-derived organoids histologically phenocopy primary UC tissue, showing disorganized stratified epithelium, reduced mucin/goblet cells, and non-uniform proliferation compared to non-IBD organoids
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Directing stem cell differentiation by chromatin state approximation.
PMID 41734818 · PMC12956330 · Nucleic acids research · 2026 · 8 claims · 8 setups
Greedy selection of culture conditions by chromatin (ATAC-seq) distance to target is a viable optimisation strategy for differentiation protocols
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B-lineage commitment is dependent on a reversible epigenetic switch.
PMID 41266087 · PMC12863259 · Genes & development · 2026 · 8 claims · 8 setups
B-lymphoid commitment is mediated by a transcription factor-dose-dependent epigenetic switch that suppresses inherent T-lineage potential in early lymphoid progenitors
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EpiXFormer: a cross-attention neural network for predicting cell type-specific transcription factor binding sites.
PMID 41527854 · PMC12796812 · Briefings in bioinformatics · 2026 · 8 claims · 8 setups
EpiXFormer achieves high accuracy (mean AUROC ~0.99) predicting binding sites of both TFs and non-sequence-specific DBPs across 199 DBP-cell type pairs
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Single-nucleus multiomic profiling of the aging mouse substantia nigra reveals conserved gene alterations linked to Parkinson's disease.
PMID 41781332 · PMC13138337 · Genome research · 2026 · 8 claims · 7 setups
Single-nucleus multiome (RNA+ATAC) sequencing of mouse substantia nigra across four age stages (2, 6, 12, 18 months) yields a 40,125-cell atlas spanning 27 cell subclasses
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Isoform-specific single-cell perturb-seq reveals distinct functions of alternative promoters in drug response.
PMID 41728950 · PMC12926921 · Nucleic acids research · 2026 · 5 claims · 8 setups
CRISPR-dCas9-based screens exhibit widespread promoter specificity, with untargeted promoters often showing compensatory upregulation to maintain overall gene expression
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Early feature extraction drives model performance in high-resolution chromatin accessibility prediction.
PMID 41526189 · PMC12951969 · Genome research · 2026 · 8 claims · 6 setups
Early feature extraction (via ConvNeXt V2 blocks), rather than downstream architecture type, is the primary determinant of prediction accuracy in high-resolution chromatin accessibility prediction.
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Molecular interactome of HNRNPU reveals regulatory networks in neuronal differentiation and DNA methylation.
PMID 41674383 · PMC12895067 · Nucleic acids research · 2026 · 7 claims · 8 setups
HNRNPU forms extensive protein networks including an association with the mammalian SWI/SNF chromatin-remodeling complex
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PeakPrime: a peak-guided primer design pipeline for target enrichment in 3'-end RNA-seq.
PMID 41919010 · PMC13034549 · Bioinformatics advances · 2026 · 8 claims · 7 setups
PeakPrime is a reproducible Nextflow pipeline that calls 3′ RNA-seq coverage peaks (MACS2), selects exonic windows, designs strand-appropriate primers (Primer3), and screens specificity (Bowtie2)
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GeneExt: a gene model extension tool for enhanced single-cell RNA-seq analysis.
PMID 41769841 · PMC12970594 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 8 setups
Incomplete/inaccurate gene annotations, especially missing or truncated 3' UTRs, cause reads to map to non-genic regions and genes to be under-quantified or missing from scRNA-seq expression matrices in non-model species
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FragmentFinder-a user-friendly, Windows-based tool for identifying and characterizing short RNAs excised from any noncoding RNA.
PMID 41704564 · PMC12907730 · NAR genomics and bioinformatics · 2026 · 6 claims · 1 setups
FragmentFinder (FF) is a user-friendly, Windows-executable tool that identifies and characterizes short RNAs excised from any noncoding RNA precursor, requiring no computational background
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Single-nucleus multiome analysis in the human prefrontal cortex identifies gene expression and cis-regulatory elements associated with aging.
PMID 41832957 · PMC13137218 · Cell reports · 2026 · 8 claims · 8 setups
Generated a single-nucleus multiome (snATAC + gene expression) dataset from 357 human dorsolateral prefrontal cortex samples (ages 15-100, European and African admixed ancestry), yielding over 1.5 million cells as a public resource.
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Has reproduction · 90
The tumour suppressor L(3)mbt inhibits neuroepithelial proliferation and acts on insulator elements.
PMID 21857667 · PMC3173870 · Nature cell biology · 2011 · 8 claims · 8 setups
Brain tumors in l(3)mbt mutants originate from overproliferation of neuroepithelial cells of the optic lobes, not from defects in asymmetric cell division.