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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Benchmarking methods for genome annotation using nanopore direct RNA in a non-model crop plant.
PMID 41800382 · PMC12967217 · Bioinformatics advances · 2026 · 6 claims · 8 setups
Annotation tools show substantial variation in isoform detection, structural completeness, splicing classification, and handling of 5' read truncation when applied to plant dRNA-seq data.
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Single-oocyte full-length isoform sequencing unveils the impact of transposable elements on RNA diversity and stability.
PMID 41946711 · PMC13233917 · Nature communications · 2026 · 8 claims · 8 setups
Single-oocyte full-length (PacBio long-read) isoform sequencing systematically profiles isoform diversity across human (GV, MI, MII) and mouse (GV, GVBD, MI, MII) oocyte maturation stages
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The circadian isoform landscape of mouse livers.
PMID 41987907 · PMC13076092 · NAR genomics and bioinformatics · 2026 · 5 claims · 6 setups
R2C2 long-read nanopore sequencing generates highly accurate, full-length cDNA reads suitable for quantitative detection of circadian oscillations
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isoSeQL: comparing long-read isoforms across multiple datasets.
PMID 41452740 · PMC12790818 · Bioinformatics (Oxford, England) · 2026 · 8 claims · 4 setups
isoSeQL enables comparison of long-read isoform profiles across multiple datasets by consolidating SQANTI3-annotated samples into a unified SQLite database with consistent isoform IDs
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Long-read assembly reveals vast transcriptional complexity in the placenta associated with metabolic and endocrine function.
PMID 41927596 · PMC13219539 · Nature communications · 2026 · 8 claims · 8 setups
Long-read RNA-seq of 72 term placentas yields a high-confidence reference of 37,661 isoforms across 12,302 genes, including thousands of previously unannotated isoforms and genes
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Phenotypic variation meets systems biology.
PMID 19664197 · PMC2745761 · Genome biology · 2009 · 8 claims · 8 setups
Cellular differentiation states are constrained by complex networks with substantial positive and negative regulation, challenging the concept of single 'master regulators'
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Targeted long-read RNA sequencing for rare disease diagnosis and variant interpretation.
PMID 41984969 · PMC13082330 · Science advances · 2026 · 8 claims · 6 setups
STRIPE enables deep, haplotype-resolved sequencing of full-length transcripts for customized disease-specific gene panels to detect transcript aberrations and sequence variants