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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The 1000 Chinese Pangenome empowers medical and population genetics.
PMID 41922767 · PMC13233627 · Nature · 2026 · 8 claims · 8 setups
1,116 diploid genome assemblies (55 de novo, 1,061 pangenome-informed) were generated as part of the 1KCP project
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An integrative single-nucleus multiomic atlas of the human left ventricle identifies gene regulatory network dynamics across cardiac development, aging, and disease.
PMID 41937210 · PMC13067603 · Genome biology · 2026 · 8 claims · 8 setups
Constructed an integrated multiomic atlas of the human left ventricle combining ~2.3M snRNA-seq nuclei from 299 donors and ~690K snATAC-seq nuclei from 106 donors
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Chromosome-level genome assembly of the blackchin tilapia (Sarotherodon melanotheron).
PMID 41942530 · PMC13234295 · Scientific data · 2026 · 7 claims · 7 setups
A chromosome-level genome assembly of blackchin tilapia was generated with total length 1,027.41 Mb and scaffold N50 of 38.87 Mb, with 93.42% of sequence anchored to 22 chromosomes.
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Chemotherapy-induced reactive myelopoiesis promotes expansion of immunosuppressive neutrophil-like monocytes in mice and humans.
PMID 41945895 · PMC13232731 · JCI insight · 2026 · 8 claims · 8 setups
Monocytes from lymphoma patients receiving CTX-containing chemotherapy show variable, often chemotherapy-induced or -enhanced, immunosuppressive activity against T cells
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Single cell multiomics revealed fibrotic trajectories of endometrial cells and interaction with the pro-fibrotic macrophages in intrauterine adhesion.
PMID 41947225 · PMC13188631 · Genome medicine · 2026 · 8 claims · 8 setups
Human IUA endometrium contains a novel ACTA2+KRT8+ myofibrotic-epithelial subpopulation and an ACTA2+CD31+ myofibrotic-endothelial subpopulation, in addition to myofibroblasts
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Linear RAG scanning mediates editing of Igκ variable region repertoires.
PMID 41986707 · PMC13190342 · Nature · 2026 · 8 claims · 7 setups
Cer/Sis deletion converts primary diffusion-based Vκ-to-Jκ1 joining into a one-loop-based linear RAG-scanning mechanism
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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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The long non-coding RNA landscape of endurance exercise training.
PMID 42019922 · PMC13158426 · Molecular metabolism · 2026 · 8 claims · 8 setups
759 unique lncRNAs are differentially expressed across 18 rat tissues in response to 8 weeks of endurance training
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TBL1X/TBL1XR1 govern β-cell identity through a PAX6-containing gene regulatory network.
PMID 42020373 · PMC13102947 · Nature communications · 2026 · 8 claims · 8 setups
TBL/R1 are crucial regulators of β-cell identity and determinants of diabetes development and progression
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Haplotype-resolved genome assemblies of BJ and IMR-90 human fibroblast cell lines reveal extensive structural variation and enable reanalysis of historical sequencing data.
PMID 42049241 · PMC13124242 · Nucleic acids research · 2026 · 8 claims · 8 setups
Chromosome-level, phased diploid genome assemblies were generated for BJ and IMR-90 fibroblast cell lines spanning 5.9 and 6.0 Gbp with diploid QV exceeding 60
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GLYATL1 is associated with metabolic and epigenetic changes and with endocrine resistance in luminal breast cancer.
PMID 42050691 · PMC13126711 · Clinical epigenetics · 2026 · 8 claims · 8 setups
GLYATL1 expression is upregulated in AI-resistant breast cancer cell models and in patients undergoing AI therapy
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Sensitive detection of somatic mutations in GC-rich cancer gene promoters.
PMID 42088607 · PMC13136893 · NAR cancer · 2026 · 8 claims · 8 setups
Gene promoters, due to high GC content (CpG islands, ~70% of promoters), are systematically undersampled and have poor coverage in whole cancer genomes, causing missed somatic mutation calls
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pmid-42118837
PMID 42118837 · PMC13187773 · 8 claims · 8 setups
Gene expression and regulatory modules strongly separate metapodials from phalanges, and separate tissues to a lesser extent along the anterior-posterior axis or between limb types
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Given the complexity of the human genome, can 'personalised medicine' or 'individualised drug therapy' ever be achieved?
PMID 19706359 · PMC3525196 · Human genomics · 2009 · 7 claims · 3 setups
The human genome is far too complex, given current understanding, for personalised medicine or individualised drug therapy to be realised in the near term
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Tipping the balance in autoimmune disease.
PMID 18001485 · PMC2246277 · Genome biology · 2007 · 8 claims · 8 setups
Human autoimmune diseases are fundamentally diseases of immune dysfunction, evidenced by predisposing genes being immune-function genes, some shared and some unique across MS, T1D, SLE, CD and RA
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Improved RNA-DNA interaction calling suggests RNA-based gene regulation of phenotypic transitions.
PMID 42258536 · PMC13244158 · Nucleic acids research · 2026 · 7 claims · 8 setups
RADIAnT is a reads-to-interactions computational pipeline for analyzing RNA–DNA ligation data
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A haplotype-resolved genome assembly of the bocaccio rockfish, Sebastes paucispinis.
PMID 40323688 · PMC12584591 · The Journal of heredity · 2025 · 6 claims · 8 setups
This paper presents the first de novo, haplotype-resolved reference-quality genome assembly of Sebastes paucispinis (bocaccio rockfish).
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Protein structure and function by the sea.
PMID 11983051 · PMC139342 · Genome biology · 2002 · 8 claims · 8 setups
High-throughput structural genomics (X-ray crystallography and NMR) can rapidly expand the number of solved protein structures far beyond what is currently in the Protein Data Bank.
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In silico meets in vivo.
PMID 18304380 · PMC2374716 · Genome biology · 2008 · 8 claims · 8 setups
About 10% of positions in multiple sequence alignments of the human genome with other vertebrate genomes are likely incorrect.
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ENCODE whole-genome data in the UCSC Genome Browser.
PMID 19920125 · PMC2808953 · Nucleic acids research · 2010 · 7 claims · 8 setups
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.