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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Improved chromosome-level genome assembly of the American cockroach, Periplaneta americana.
PMID 41123565 · PMC12774602 · G3 (Bethesda, Md.) · 2026 · 8 claims · 7 setups
Produced the first chromosome-level genome assembly of P. americana, scaffolded into 17 chromosome-scale scaffolds consistent with karyotype
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Has reproduction · 99
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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The chromosomal genome sequence of the common sea fan, Gorgonia ventalina (Linnaeus, 1758) (Malacalcyonacea: Gorgoniidae).
PMID 41625986 · PMC12856254 · Wellcome open research · 2026 · 7 claims · 6 setups
A chromosome-level genome assembly was produced for Gorgonia ventalina with a total length of 339.18 Mb
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The genome sequence of the Sage Skipper, Muschampia proto (Ochsenheimer, 1808) (Lepidoptera: Hesperiidae).
PMID 41938270 · PMC13049433 · Wellcome open research · 2026 · 8 claims · 8 setups
A chromosome-level genome assembly was produced for Muschampia proto, with 99.67% of haplotype 1 scaffolded into 30 chromosomal pseudomolecules including the Z sex chromosome.
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FEDRANN: effective long-read overlap detection based on dimensionality reduction and approximate nearest neighbors.
PMID 42102720 · PMC13201080 · GigaScience · 2026 · 8 claims · 6 setups
A pipeline combining IDF transformation, sparse random projection (SRP), and NNDescent (the FEDRANN strategy) enables accurate overlap detection across diverse long-read datasets
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Multi-context seeds enable fast and high-accuracy read mapping.
PMID 41764549 · PMC13059148 · Genome biology · 2026 · 7 claims · 5 setups
Multi-context seeds (MCS) allow storage of seeds with different lengths in the same index structure by splitting hash bits among strobes, enabling full and partial matches
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Whole-genome sequencing with AVITI and NovaSeq X Plus reveals comparable performance with contextual biases.
PMID 42206012 · PMC13202175 · NAR genomics and bioinformatics · 2026 · 8 claims · 7 setups
AVITI and NovaSeq X Plus are highly comparable overall for variant-calling performance in WGS