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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A giant virus forms a specialized subcellular environment within its amoeba host for efficient translation.
PMID 41513996 · PMC12872441 · Nature microbiology · 2026 · 8 claims · 7 setups
The global cellular tRNA pool is not substantially altered during APMV infection, despite the virus encoding its own tRNA genes.
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Genomic instability and mono-parental expression mitigate genomic shock in a cross-subgenus Leishmania hybrid.
PMID 41918820 · PMC13034039 · NAR molecular medicine · 2026 · 7 claims · 8 setups
An in vitro cross between L. infantum and L. tarentolae produced a viable inter-subgenus hybrid, demonstrating genomic compatibility between highly divergent Leishmania species.
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PURE-seq integrates FACS and PIP-seq for single-cell genomics of ultra-rare cells.
PMID 41565684 · PMC12881479 · Nature communications · 2026 · 8 claims · 8 setups
PURE-seq integrates FACS sorting directly into PIP-seq barcoding reaction tubes, minimizing manual handling and cell loss for rare-cell single-cell sequencing.
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Haplotype-resolved and near telomere-to-telomere assembly of the autotetraploid potato genome.
PMID 41634861 · PMC12955163 · Genome biology · 2026 · 8 claims · 8 setups
PHap is a new pipeline that enables haplotype-resolved, near-T2T assembly of autopolyploid genomes using only standard HiFi, ONT-UL, and Hi-C sequencing data
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α4 Integrin blockade impairs CD8+ T cell neuroimmune surveillance following SIV infection.
PMID 41734020 · PMC13078879 · The Journal of clinical investigation · 2026 · 8 claims · 8 setups
α4 blockade preserves CD4+ Th1 cell access to brain parenchyma but impairs CD8 effector recruitment, disrupting antiviral control
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Variation resources at UC Santa Cruz.
PMID 17151077 · PMC1781230 · Nucleic acids research · 2007 · 8 claims · 8 setups
The UCSC Genome Browser variation resources integrate polymorphism data from public collections (dbSNP, HapMap, Affymetrix, Perlegen, SeattleSNPs) into a common format with additional annotations and genomic context.