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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Optimizing Single-Cell Long-Read Sequencing for Enhanced Isoform Detection in Pancreatic Islets.
PMID 41563441 · PMC13007207 · Diabetes · 2026 · 8 claims · 7 setups
5′ single-cell library preparation protocols outperform 3′ protocols for transcript identification and read length
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Haplotype-resolved genome assemblies of BJ and IMR-90 human fibroblast cell lines reveal extensive structural variation and enable reanalysis of historical sequencing data.
PMID 42049241 · PMC13124242 · Nucleic acids research · 2026 · 8 claims · 8 setups
Chromosome-level, phased diploid genome assemblies were generated for BJ and IMR-90 fibroblast cell lines spanning 5.9 and 6.0 Gbp with diploid QV exceeding 60
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Has reproduction · 76
Organelle Genomes and Transcriptomes of Nymphaea Reveal the Interplay between Intron Splicing and RNA Editing.
PMID 34576004 · PMC8466565 · International journal of molecular sciences · 2021 · 8 claims · 8 setups
Both cis- and trans-splicing group II introns in Nymphaea organelle genomes are spliced in random order, generating diverse co-existing intermediates rather than following a fixed splicing sequence.
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Flamenco plasticity tunes somatic piRNAs and rewires isoforms, with implications for heritable transposon spread.
PMID 42009568 · PMC13097621 · Life science alliance · 2026 · 8 claims · 8 setups
Springer drives host gene expression changes via promoter-proximal intronic insertions at an AT-rich motif, with its 5′ LTR initiating transcription that splices into downstream host exons to create hybrid isoforms without adding coding sequence
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Alternative splicing-triggered mRNA decay informs splice-switching targets for neurodevelopmental disorders.
PMID 41678398 · PMC13078869 · The Journal of clinical investigation · 2026 · 7 claims · 12 setups
EANMD, a new computational tool, identifies AS-NMD exons using the 50 nt rule plus additional transcript-level features and outperforms existing tools (SpliceTools, NMD Classifier)
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Isoform-specific single-cell perturb-seq reveals distinct functions of alternative promoters in drug response.
PMID 41728950 · PMC12926921 · Nucleic acids research · 2026 · 5 claims · 8 setups
CRISPR-dCas9-based screens exhibit widespread promoter specificity, with untargeted promoters often showing compensatory upregulation to maintain overall gene expression