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).

• The chromosome-scale genome assembly and annotation of Rosa bracteata (Macartney Rose).

  PMID 41794947 · PMC13096426 · Scientific data · 2026 · 8 claims · 8 setups

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  A chromosome-scale genome assembly of R. bracteata totaling 540.63 Mb with contig N50 of 35.97 Mb was generated, with 501.06 Mb anchored onto seven pseudochromosomes.

  genomic root pacbio young pacbio hi-c rna-seq

• The chromosome-scale genome assembly, annotation of Bischofia polycarpa (H. Lév.) Airy Shaw, Phyllanthaceae.

  PMID 41765919 · PMC13066037 · Scientific data · 2026 · 8 claims · 8 setups

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  B. polycarpa genome was assembled de novo using PacBio HiFi reads and Hi-C data to a size of 585.68 Mb with contig N50 of 12.62 Mb

  polycarpa illumina pacbio hi-c

• Chromosome-scale genome assembly for yellow wood sorrel, Oxalis stricta.

  PMID 41482730 · PMC12958822 · G3 (Bethesda, Md.) · 2026 · 8 claims · 8 setups

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  O. stricta genome assembly is chromosome-scale, 436 Mb, spanning 12 chromosomes across 2 subgenomes

  stricta long-read short-read hi-c

• A chromosome-level reference genome of an endangered plant Craigia yunnanensis.

  PMID 41771874 · PMC13065974 · Scientific data · 2026 · 8 claims · 8 setups

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  A chromosome-level genome assembly of C. yunnanensis was generated using PacBio HiFi sequencing and Hi-C scaffolding

  yunnanensis pacbio hi-c illumina

• A golden age of brain exploration.

  PMID 15660159 · PMC544547 · PLoS biology · 2005 · 8 claims · 3 setups

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  Over 99% of neuroscience literature focuses on only 1% of the ~15,000–16,000 genes expressed in the brain, leaving most brain-expressed genes uncharacterized.

  brain transgenic situ microarray bacterial

• Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.

  PMID 18162506 · PMC7611804 · Diabetes · 2008 · 8 claims · 8 setups

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  Heterozygous INS mutations are a common cause of permanent neonatal diabetes (PNDM) diagnosed before 6 months of age

  peripheral patients mody young-onset pcr microsatellite variant

• Centromere organization and epigenetic regulation in Aristolochia fimbriata.

  PMID 41761339 · PMC13049873 · Genome biology · 2026 · 8 claims · 8 setups

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  A complete gapless telomere-to-telomere (T2T) genome assembly of A. fimbriata was constructed, substantially improving on the previous v1 assembly.

  aristolochia fimbriata pacbio hi-c cenh3

• 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

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  PURE-seq integrates FACS sorting directly into PIP-seq barcoding reaction tubes, minimizing manual handling and cell loss for rare-cell single-cell sequencing.

  hek293t pbmcs melanoma bone single-cell infercnv gene