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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Full-text index only
Cell atlases and the developmental foundations of the phenotype.
PMID 41662466 · PMC12904592 · PLoS computational biology · 2026 · 8 claims · 6 setups
There is a proportional relationship between average developmental similarity (⟨simD⟩) and average phenotypic similarity (⟨simP⟩) across genes, supporting the D–P rule on average
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Full-text index only
MultiSP deciphers tissue structure and multicellular communication from spatial multi-omics data.
PMID 41650976 · PMC13174227 · Cell genomics · 2026 · 7 claims · 5 setups
MultiSP outperforms existing spatial and single-cell multi-omics integration methods in detecting biologically accurate spatial domains across multiple spatial multi-omics technologies and tissue types
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Full-text index only
Multiomics and deep learning dissect regulatory syntax in human development.
PMID 41951735 · PMC13216069 · Nature · 2026 · 8 claims · 8 setups
The Human Development Multiomic Atlas (HDMA) is a single-cell atlas of chromatin accessibility and gene expression from 817,740 fetal cells across 12 organs, spanning 203 cell types
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Has reproduction · 67
Sequencing mRNA from cryo-sliced Drosophila embryos to determine genome-wide spatial patterns of gene expression.
PMID 23951250 · PMC3741199 · PloS one · 2013 · 8 claims · 8 setups
Cryosectioning single blastoderm-stage D. melanogaster embryos along the A–P axis and sequencing mRNA from each slice yields reliable genome-wide spatial expression patterns.
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Has reproduction · 87
High-resolution mapping of transcriptional dynamics across tissue development reveals a stable mRNA-tRNA interface.
PMID 25122613 · PMC4216921 · Genome research · 2014 · 8 claims · 7 setups
mRNA codon and amino acid pools are highly stable across mouse development and across tissues, simply reflecting the genomic background distribution of any possible transcriptome.