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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bayesReact: expression-coupled regulatory motif analysis detects microRNA activity across cancers, tissues, and at the single-cell level.
PMID 41657247 · PMC12884093 · Nucleic acids research · 2026 · 8 claims · 6 setups
bayesReact is a novel fully Bayesian generative model for inferring regulatory motif (e.g., miRNA) activity from bulk or single-cell expression data
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Identification of novel DNA sequence motifs that modulate transcription in T cells.
PMID 41514212 · PMC12879379 · BMC genomics · 2026 · 8 claims · 8 setups
Identified 2,036 novel DNA motifs enriched in regulatory regions of T-cell-specific genes
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Differentiation in the human urothelia is defined by distinct alternative polyadenylation.
PMID 41533515 · PMC12937501 · Cell reports · 2026 · 8 claims · 8 setups
APA introduces a major layer of transcriptomic diversity during urothelial differentiation, largely independent of changes in mRNA levels
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Has reproduction · 32
Integrated analysis of post-transcriptional regulations reveals insights into acute myeloid leukemia.
PMID 41407883 · PMC12712020 · Communications biology · 2025 · 8 claims · 6 setups
PTRs computed from integrated transcriptomic/proteomic data of 44 AML samples are highly conserved across AML subtypes and with 29 other human tissues, indicating broadly conserved post-transcriptional mechanisms.
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Integrative analysis of RUNX1 downstream pathways and target genes.
PMID 18671852 · PMC2529319 · BMC genomics · 2008 · 7 claims · 8 setups
Integrating gene expression profiles from three independent RUNX1 perturbation platforms (FPD-AML patient cell lines, RUNX1/CBFβ overexpression in HeLa cells, Runx1 knockout mouse embryos) identifies RUNX1-regulated genes and downstream pathways
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Single-Nucleus Multi-Omics Reveals Hypoxia-Driven Angiogenic Programs and Their Epigenetic Control in Sinonasal Squamous Cell Carcinoma.
PMID 41498635 · PMC12948189 · Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026 · 8 claims · 8 setups
Five distinct malignant cell populations exist in SNSCC, with hypoxic (TC1) and proliferative (TC2) subtypes associated with adverse clinical outcomes.
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Comparative single-cell landscape of immune cells in human livers affected HBV and non-viral cirrhosis.
PMID 41815278 · PMC12971635 · Frontiers in medicine · 2025 · 8 claims · 7 setups
Macrophage-PLCG2 (anti-inflammatory) and CD8+ T-FABP5 subsets are expanded in HBV cirrhosis compared to non-viral cirrhosis
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A comprehensive toolkit for analyzing cell-free DNA genomic sequencing data in liquid biopsy.
PMID 42111187 · PMC13157187 · iScience · 2026 · 8 claims · 8 setups
cfDNAanalyzer integrates feature extraction, feature processing/selection, and machine learning model building into a single one-command-line toolkit for cfDNA genomic sequencing data
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Single-cell epigenetic and transcriptomic states across the continuum of monoclonal B cell lymphocytosis to chronic lymphocytic leukemia.
PMID 41987205 · PMC13192028 · Genome biology · 2026 · 8 claims · 6 setups
The HC-MBL to CLL transition shows subclonal, epigenetic and transcriptomic stability, consistent with a continuous disease spectrum rather than distinct evolutionary phases.
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Surfactant protein B gene variations enhance susceptibility to squamous cell carcinoma of the lung in German patients.
PMID 12107845 · PMC2376109 · British journal of cancer · 2002 · 8 claims · 1 setups
The SP-B intron 4 gene variant is significantly more frequent in squamous cell lung carcinoma (SCC) patients (25.0%) than in matched controls, OR=3.2, P=0.016
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Has reproduction · 80
DMN-seq enriches DNA hypomethylated regions for biomarker discovery using 5-methylcytosine glycosylase.
PMID 41673887 · PMC13097799 · Genome biology · 2026 · 8 claims · 9 setups
DMN-seq (DMN+) uses DME to nick DNA specifically at 5mC sites, enabling 5mC detection at single-base resolution via selective adaptor ligation