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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Robust characterization and interpretation of rare pathogenic cell populations from spatial omics using GARDEN.
PMID 41547856 · PMC12917120 · Nature communications · 2026 · 8 claims · 8 setups
GARDEN identifies and characterizes rare pathogenic cell populations/regions in spatial omics by embedding graph-based dynamic attention into a spatially-aware graph fusion contrastive model
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Serial Spatial Transcriptomes Reveal Regulatory Transitions in Maize Leaf Development.
PMID 41493197 · PMC13110159 · Plant biotechnology journal · 2026 · 8 claims · 5 setups
An optimised Visium spatial transcriptomics protocol (two-step OCT embedding combined with OCT-Immersion First cryopreservation) preserves high-integrity RNA from fragile plant tissues such as SAM
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Manual validation finds ultra-long-read sequencing best enables faithful, population-level structural variant calling in Drosophila melanogaster euchromatin with nanopore.
PMID 41806374 · PMC13148403 · G3 (Bethesda, Md.) · 2026 · 8 claims · 5 setups
Only ultra-long long-reads (N50 > 50 kb) are capable of accurately calling structural variants of any size in D. melanogaster euchromatin
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Has reproduction · 61
TEMP: a computational method for analyzing transposable element polymorphism in populations.
PMID 24753423 · PMC4066757 · Nucleic acids research · 2014 · 8 claims · 8 setups
TEMP combines pair-end (discordant) read and split (soft-clipped) read information to identify both presence and absence of TE insertions in genomic DNA from heterogeneous/pooled samples.
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Unbalanced chromatin binding of Polycomb complexes drives neurodevelopmental disorders.
PMID 41653922 · PMC13034722 · Molecular cell · 2026 · 8 claims · 8 setups
Heterozygous de novo missense mutations in RING1 and RNF2 are found in individuals with neurodevelopmental/intellectual disability phenotypes
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ANOMALY: a Snakemake pipeline for identifying NuMTs from long-read sequencing data.
PMID 41647924 · PMC12869244 · NAR genomics and bioinformatics · 2026 · 8 claims · 8 setups
ANOMALY is a novel Snakemake pipeline for detecting NuMTs from long-read sequencing data
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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