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).

• RAGER: A user-friendly computational platform for integrated analysis of RNA-Seq and ATAC-seq data.

  PMID 42172220 · PMC13196991 · PloS one · 2026 · 8 claims · 8 setups

  Has reproduction · 63

  RAGER integrates widely-used bioinformatics tools into an automated Snakemake-based pipeline for joint analysis of RNA-seq and ATAC-seq data

  embryonic cd34+ shared promoter rna-seq atac-seq gsea

• HTSstation: a web application and open-access libraries for high-throughput sequencing data analysis.

  PMID 24475057 · PMC3903476 · PloS one · 2014 · 8 claims · 5 setups

  Has reproduction · 66

  HTSstation is a web application suite coupling simple web forms to modular analysis pipelines for ChIP-seq, RNA-seq, 4C-seq and re-sequencing HTS applications, accessible at http://htsstation.epfl.ch.

  embryonic mycobacterium forebrain rna-seq re-sequencing 4c-seq

• WikiPathways App for Cytoscape: Making biological pathways amenable to network analysis and visualization.

  PMID 25254103 · PMC4168754 · F1000Research · 2014 · 8 claims · 7 setups

  Has reproduction · 76

  The open-source WikiPathways app for Cytoscape imports biological pathways from WikiPathways for data visualization and network analysis.

  cardiac cytoscape rna-seq pathway network

• ENCODE whole-genome data in the UCSC Genome Browser.

  PMID 19920125 · PMC2808953 · Nucleic acids research · 2010 · 7 claims · 8 setups

  Full-text index only

  The UCSC ENCODE Data Coordination Center serves as the primary repository for ENCODE experimental results, providing access via Genome Browser, Table Browser, and FTP download.

  lines chip-seq dnase-seq rna-seq

• CircleBase V2: an eccDNA annotation platform across cancers and species.

  PMID 41273082 · PMC12807720 · Nucleic acids research · 2026 · 8 claims · 7 setups

  Full-text index only

  CircleBase V2 provides a 12-fold increase in human eccDNA data, comprising over 3.8 million entries from >300 cell types/tissues

  raw eccdna tissues cancer circle-seq motif gene

• A transcriptome sequence dataset characterizing eggs, nymphs and adults of Oxycarenus hyalinipennis, the cotton seed bug.

  PMID 41717652 · PMC12915258 · Data in brief · 2026 · 8 claims · 8 setups

  Full-text index only

  This dataset provides the first transcriptomic resources for the invasive pest Oxycarenus hyalinipennis

  whole-insect cross assembled global rna-seq differential sequence

• A copula-infused graph neural network for cell type classification in single-cell RNA sequencing data.

  PMID 41940310 · PMC12914865 · Computational and structural biotechnology journal · 2026 · 8 claims · 5 setups

  Full-text index only

  scCopulaGNN combines copula theory with graph neural network representation learning for scRNA-seq cell type classification

  brain pancreas kidney turtle scrna-seq simulated

• scDEBGCL: a deep embedding approach based on bipartite graph contrastive learning for single-cell RNA-seq data.

  PMID 41981652 · PMC13188691 · BMC biology · 2026 · 7 claims · 3 setups

  Full-text index only

  scDEBGCL is a deep embedding method for scRNA-seq data based on bipartite graph contrastive learning, integrating contrastive learning, graph reconstruction, and ZINB-based data reconstruction losses.

  nine yan dpt scrna-seq trajectory

• scGACL: a generative adversarial network with multi-scale contrastive learning for accurate single-cell RNA sequencing imputation.

  PMID 41632596 · PMC12866930 · Briefings in bioinformatics · 2026 · 8 claims · 6 setups

  Full-text index only

  scGACL, a GAN integrated with multi-scale contrastive learning, is proposed to overcome the over-smoothing problem in scRNA-seq imputation

  simulated real-world scrna-seq scrna-seq clustering gene

• SEAseq: a portable and cloud-based chromatin occupancy analysis suite.

  PMID 35193506 · PMC8864840 · BMC bioinformatics · 2022 · 7 claims · 2 setups

  Has reproduction · 94

  SEAseq is a comprehensive, infrastructure-independent pipeline that performs the major analyses needed to process ChIP-Seq/CUT&RUN chromatin binding datasets in a single execution

  any chip-seq cut&run

• A2TEA: Identifying trait-specific evolutionary adaptations.

  PMID 37224329 · PMC10186066 · F1000Research · 2022 · 8 claims · 7 setups

  Has reproduction · 90

  A2TEA integrates gene family expansion analysis with differential expression data across species to identify genes that were targets of evolutionary adaptation to a given stress/treatment

  user-provided multi-species genes sequences rna-seq orthologous phylogenetic

• Partial domain adaptation enables cross domain cell type annotation between scRNA-seq and snRNA-seq.

  PMID 42090457 · PMC13170964 · PLoS computational biology · 2026 · 7 claims · 5 setups

  Full-text index only

  ScNucAdapt is a partial domain adaptation framework that enables cross-domain cell type annotation between paired or unpaired scRNA-seq and snRNA-seq datasets.

  bladder kidney cortex frozen scrna-seq snrna-seq

• scZiva: imputation method for single-cell RNA-seq data with zero-inflated variational autoencoder.

  PMID 41857511 · PMC13122936 · BMC bioinformatics · 2026 · 8 claims · 1 setups

  Full-text index only

  scZiva is a novel VAE-based imputation method for scRNA-seq data using a Zero-Inflated Negative Binomial (ZINB) likelihood.

  simulated scrna-seq

• Integrating and mapping single-cell transcriptomics across the entire gene expression space.

  PMID 42059480 · PMC13130072 · Briefings in bioinformatics · 2026 · 8 claims · 1 setups

  Full-text index only

  scGES is a deep learning framework that corrects batch effects across the entire gene expression space by leveraging information from both HVGs and LVGs

  real scrna-seq

• scSAMAC: saliency-adjusted masking induced attention contrastive learning for single-cell clustering.

  PMID 40131310 · PMC11934584 · Briefings in bioinformatics · 2025 · 8 claims · 1 setups

  Has reproduction · 85

  scSAMAC integrates contrastive learning and negative binomial (NB) losses into a VAE, extracting features via contrastive unit similarity while preserving intrinsic data characteristics to enhance robustness and generalization in clustering.

  scrna-seq scrna-seq

• 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

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  scDecorr learns robust cell representations of unlabelled single-cell experiments in a negative-sample-free self-supervised fashion using feature decorrelation

  datasets scrna-seq

• CellFishing.jl: an ultrafast and scalable cell search method for single-cell RNA sequencing.

  PMID 30744683 · PMC6371477 · Genome biology · 2019 · 8 claims · 5 setups

  Has reproduction · 97

  CellFishing.jl achieves accuracy comparable to state-of-the-art software (scmap-cell) but is markedly faster

  scrna-seq shekhar2016 svd lsh hamming

• pysradb: A Python package to query next-generation sequencing metadata and data from NCBI Sequence Read Archive.

  PMID 31114675 · PMC6505635 · F1000Research · 2019 · 7 claims · 4 setups

  Has reproduction · 90

  pysradb provides a command-line interface to query metadata and download raw sequencing data from NCBI SRA using the SRAdb SQLite database.

  sra-deposited pc3 sra tissues metadata polya assays

• De Novo Assembly and Annotation of the Larval Transcriptome of Two Spadefoot Toads Widely Divergent in Developmental Rate.

  PMID 31217263 · PMC6686947 · G3 (Bethesda, Md.) · 2019 · 8 claims · 8 setups

  Has reproduction · 91

  De novo transcriptome assemblies were generated for larval P. cultripes and S. couchii, providing new genomic resources for spadefoot toads

  whole-body cultripes expression-filtered bulk novo transcriptome

• Eye in a Disk: eyeIntegration Human Pan-Eye and Body Transcriptome Database Version 1.0.

  PMID 31343654 · PMC6660187 · Investigative ophthalmology & visual science · 2019 · 8 claims · 5 setups

  Has reproduction · 94

  EiaD is a reproducible, versioned RNA-seq transcriptome dataset combining 916 healthy human eye samples and 1375 GTEx body samples across 19 eye and 54 body tissues, built with a Snakemake pipeline and served as a single SQLite database.

  gtex eye stem retinal bulk differential single-cell