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).

• Genome modelling and design across all domains of life with Evo 2.

  PMID 41781614 · PMC13128491 · Nature · 2026 · 8 claims · 8 setups

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  Evo 2 accurately predicts functional impacts of genetic variation, from noncoding pathogenic mutations to clinically significant BRCA1 variants, without task-specific fine-tuning

  gene prokaryotic species proteins zero-shot mutational stop

• Mutation spectrum of homogentisic acid oxidase (HGD) in alkaptonuria.

  PMID 19862842 · PMC2830005 · Human mutation · 2009 · 8 claims · 6 setups

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  Mutations in HGD, which encodes homogentisate dioxygenase, cause AKU by blocking conversion of homogentisic acid to maleylacetoacetic acid in the tyrosine catabolic pathway

  aku hgd recombinant hgd missense splice

• Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population.

  PMID 16460646 · PMC3525152 · Human genomics · 2006 · 8 claims · 8 setups

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  GJB2 (connexin 26) mutations account for hearing loss in only 17 of 156 families (11%), a smaller fraction than reported in other populations.

  palestinian genomic probands lymphoblasts targeted sanger pcr

• tRNA-derived RNA processing in sperm transmits non-genetically inherited phenotypes to offspring in C. elegans.

  PMID 41833931 · PMC13136342 · Nature communications · 2026 · 8 claims · 5 setups

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  tDRs accumulate endogenously and are enriched in C. elegans sperm relative to whole males, analogous to mammalian sperm

  elegans small crispr-cas9 gene