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).

• Strand bias in complementary single-nucleotide polymorphisms of transcribed human sequences: evidence for functional effects of synonymous polymorphisms.

  PMID 16916449 · PMC1559705 · BMC genomics · 2006 · 8 claims · 5 setups

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  Genome-wide, both intronic SNPs (iSNPs) and FFD SNPs show a significant excess of A→G over complementary T→C substitutions, confirming prior transcription-coupled repair (TCR) findings from a single chromosome 7 region.

  autosomal intronic chimpanzee genes comparative human-chimpanzee background

• umite: fast quantification of Smart-seq3 libraries with improved UMI retrieval.

  PMID 41692984 · PMC12989134 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 6 setups

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  umite offers efficient mismatch-tolerant (fuzzy) UMI detection that boosts UMI retrieval by 5%-15% compared to standard position-based matching

  smart-seq3 cd4+ 800-cell umi pipeline gene