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).

• 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

  Has reproduction · 62

  MultiDeNA pipeline combines PWM, diPWM, BaMM and InMoDe models to train, evaluate, threshold, and classify ChIP-seq peaks for TFBS structural heterogeneity

  foxa2 genomic frequency chip-seq novo threshold

• Lift&Add-rapid and robust addition of new species to alignments of conserved non-coding sequences.

  PMID 42203687 · PMC13224966 · Bioinformatics (Oxford, England) · 2026 · 7 claims · 5 setups

  Full-text index only

  Lift&Add, a Snakemake/bash workflow combining UCSC liftOver, Liftoff, and MAFFT, enables rapid addition of new genome sequences to existing multi-species alignments of conserved elements without requiring new whole-genome alignments.

  mm10 opossum newly vertebrate phastcons ucsc liftoff

• Beyond blacklists: a critical assessment of exclusion set generation strategies and alternative approaches.

  PMID 41826793 · PMC13020910 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 8 setups

  Full-text index only

  Pre-generated Blacklist exclusion sets were difficult to reproduce due to sensitivity to input BAM data, aligner choice, and read length

  hg38 gm12878 gse235167 syo-1 chip-seq rna-seq atac-seq

• TSniffer: unbiased de novo identification of RNA editing sites and quantification of editing activity in RNA-seq data.

  PMID 41549280 · PMC12838065 · Genome biology · 2026 · 8 claims · 6 setups

  Full-text index only

  TSniffer is a novel tool that uses a rolling window Fisher's exact test approach to identify RNA editing sites (TsRegions) de novo in RNA-seq data without relying on editing databases or two-sample differential comparison.

  type hela mm10 brain rna-seq genomic database

• Boolean logic links chromatin accessibility states to gene expression variability across cell types.

  PMID 41909952 · PMC13148175 · Nucleic acids research · 2026 · 7 claims · 4 setups

  Full-text index only

  ocrRBBR infers interpretable Boolean rules from combinations of accessible OCRs that explain gene expression variability across cell types

  immune genes atac-seq bulk hi-c

• Data-driven projections of candidate enhancer-activating SNPs in immune regulation.

  PMID 40011812 · PMC11863423 · BMC genomics · 2025 · 7 claims · 7 setups

  Has reproduction · 57

  A data-driven computational protocol combining motif scanning, open-chromatin filtering, gene proximity, dbSNP validation, spacing, and cross-species conservation can prioritize SNPs likely to create functional GAS motifs.

  genome pbmc lung il4-stimulated motif chip-seq bulk

• Long non-coding RNA profiling of hypertrophic cardiomyopathy in mice.

  PMID 41942516 · PMC13230700 · Scientific data · 2026 · 6 claims · 8 setups

  Full-text index only

  This study presents a transcriptome-wide RNA-Seq dataset delineating differentially expressed lncRNAs in left ventricle of the TNNT2 ∆160 HCM mouse model (n=31 TG, n=33 nTG).

  left fastq rna-seq lncrna bulk fastqc read

• E3RC: A step-by-step computational protocol for exploring enhancer RNA expression and regulation using conventional RNA-seq data.

  PMID 40716058 · PMC12318280 · STAR protocols · 2025 · 6 claims · 3 setups

  Has reproduction · 62

  E3RC is a computational framework for identifying and quantifying eRNAs and characterizing their expression and transcriptional regulation using conventional RNA-seq data.

  preimplantation genome erna bulk computational motif

• Highly efficient chromatin conformation capture with post-enrichment in single cells by HiChew.

  PMID 42036683 · PMC13112749 · Genome biology · 2026 · 8 claims · 8 setups

  Full-text index only

  HiChew achieves approximately 50% valid pair ratios compared to about 8% for unenriched methods like Dip-C

  hek293t chromosome gm12878 hichew dip-c sequencing