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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Has reproduction · 100
Charting and probing the activity of ADARs in human development and cell-fate specification.
PMID 39537590 · PMC11561244 · Nature communications · 2024 · 8 claims · 6 setups
RNA editing (AEI) and ADAR/ADARB1/ADARB2 expression show organ-specific dynamic shifts across fetal-to-adult developmental stages in human forebrain, hindbrain, heart, liver, kidney, and testis
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Full-text index only
nf-core/proteinfamilies: a scalable pipeline for the generation of protein families.
PMID 41563008 · PMC12950615 · GigaScience · 2026 · 8 claims · 3 setups
nf-core/proteinfamilies is a scalable, parametrizable, open-source Nextflow pipeline that generates new protein families or assigns sequences to existing families using profile HMMs and MSAs
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Full-text index only
umite: fast quantification of Smart-seq3 libraries with improved UMI retrieval.
PMID 41692984 · PMC12989134 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 6 setups
umite offers efficient mismatch-tolerant (fuzzy) UMI detection that boosts UMI retrieval by 5%-15% compared to standard position-based matching
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Full-text index only
Genomic analysis of the Ixworth chicken: insights into a local dual-purpose breed.
PMID 41814148 · PMC13064311 · BMC genomics · 2026 · 6 claims · 8 setups
The Ixworth chicken is genetically distinct from red junglefowl, commercial broilers, and commercial layers.
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Has reproduction
Accelerating rare disease diagnostics by linking DNA and RNA through an explainable and interactive RNA-guided workflow.
PMID 41685349 · PMC12891912 · NAR genomics and bioinformatics · 2026 · 8 claims · 6 setups
A streamlined RNA-guided workflow combining OUTRIDER, FRASER, Borzoi, and MOLGENIS VIP was developed to identify gene-disease associations by linking outlier gene expression/splicing to prioritized patient-level variants
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Has reproduction · 45
Identifying and classifying trait linked polymorphisms in non-reference species by walking coloured de bruijn graphs.
PMID 23536903 · PMC3607606 · PloS one · 2013 · 8 claims · 9 setups
Bubbleparse detects sequence variants directly from NGS reads without a reference genome, using the coloured de Bruijn graph implementation of Cortex plus a new depth-first bubble-finding module.