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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Single-cell epigenomics uncovers heterochromatin instability and transcription factor dysfunction during mouse brain aging.
PMID 41824460 · PMC13189690 · Cell reports · 2026 · 8 claims · 6 setups
Aging causes widespread, concordant changes in chromatin accessibility and gene expression across neuronal and glial cell types in the mouse brain
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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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Single-nucleus multiple-organ chromatin accessibility landscape in the adult rat.
PMID 41632074 · PMC12954174 · GigaScience · 2026 · 8 claims · 5 setups
Generated a multi-organ snATAC-seq atlas of 9 adult rat organs comprising 25 libraries and over 110,000 cells
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Single-nucleus ATAC-seq analysis resolves chromatin and transcriptional features of fibrolamellar carcinoma.
PMID 41865105 · PMC13144680 · Scientific reports · 2026 · 8 claims · 5 setups
snATAC-seq resolves cell-type specific chromatin accessibility, microRNA activity, transcription factor networks, and super enhancer usage in FLC tumors versus non-malignant liver (NML).
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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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Discovery of key regulators in classical monocyte phenotypes linked to COVID-19 severity using single-cell multi-omics sequencing.
PMID 41732268 · PMC12925236 · iScience · 2026 · 8 claims · 8 setups
Two severity-associated classical monocyte (cMono) subtypes, IL7R+ and CD163+, exist with distinct transcriptional and epigenetic landscapes.
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Single-cell profiling of trabecular meshwork identifies mitochondrial dysfunction in a glaucoma model that is protected by vitamin B3 treatment.
PMID 41556506 · PMC12818872 · eLife · 2026 · 8 claims · 8 setups
Mouse TM contains three molecularly distinct, reproducible cell subtypes (TM1, TM2, TM3) identified by scRNA-seq and validated by IF/ISH
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Single-cell spatiotemporal dissection of the human maternal-fetal interface.
PMID 41951740 · PMC13149032 · Nature · 2026 · 8 claims · 8 setups
Generated a comprehensive single-cell multiomic and spatial atlas of the human maternal-fetal interface from early gestation to term
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A longitudinal single-cell and spatial multiomic atlas of pediatric high-grade glioma.
PMID 42030938 · PMC13198283 · Cell reports. Medicine · 2026 · 8 claims · 8 setups
A multiomic (snRNA-seq, snATAC-seq, WGS, CODEX) atlas defines a core set of pHGG neoplastic cell states shared across molecular subtypes
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Single-cell transcriptomics and chromatin accessibility profiling elucidate the kidney-protective mechanism of mineralocorticoid receptor antagonists.
PMID 37906287 · PMC10760974 · The Journal of clinical investigation · 2024 · 8 claims · 8 setups
Mineralocorticoid effects are established through open chromatin and target gene expression primarily in principal and connecting tubule cells, and to a lesser extent in distal convoluted tubule cells
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Genetics and environment distinctively shape the human immune cell epigenome.
PMID 41593234 · PMC12900638 · Nature genetics · 2026 · 8 claims · 6 setups
Exposure-associated differentially methylated regions (eDMRs) and genotype-associated DMRs (gDMRs) show distinct genomic distributions: eDMRs are enriched at enhancers/regulatory regions, while gDMRs are predominantly found in gene bodies.