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).

• CellPredX, a computational framework for cross-data type, cross-sample, and cross-protocol cell type annotation through domain adaptation and deep metric learning.

  PMID 41481570 · PMC12758788 · PLoS computational biology · 2026 · 8 claims · 7 setups

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  CellPredX is a unified semi-supervised framework integrating domain adaptation and deep metric learning to align heterogeneous embeddings for cross-modality cell type annotation.

  pbmc fetal pancreas gse149683 matched unmatched cross-protocol

• SexTumorDB: a comprehensive resource of sex-dependent tumor landscape at single-cell resolution.

  PMID 41741497 · PMC13046873 · Scientific data · 2026 · 7 claims · 8 setups

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  SexTumorDB is an integrated resource of RNA-seq profiles of non-reproductive tumors at single-cell resolution, curated, processed, and standardized from published datasets

  acute bladder clear colorectal scrna-seq snrna-seq

• Single-cell RNA-sequencing of dermal fibroblasts demonstrates culture-induced changes and variable persistence of keloid disease features.

  PMID 42058918 · PMC13123497 · iScience · 2026 · 7 claims · 6 setups

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  Fibroblast culture leads to subtype assimilation, with in vivo heterogeneity persisting only minimally by passage 4

  dermal mesenchymal stromal patient-matched single-cell bulk qpcr

• Single-cell spatial transcriptomic analysis of human skin anatomy.

  PMID 41872488 · PMC13083264 · Nature genetics · 2026 · 8 claims · 6 setups

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  MERFISH-based spatial atlas of ~1.2 million cells resolves 45 cell types across 114 samples and 15 anatomic sites in normal human skin

  normal skin gtex matched merfish scrna-seq bulk

• SysPIMP: the web-based systematical platform for identifying human disease-related mutated sequences from mass spectrometry.

  PMID 19036792 · PMC2686442 · Nucleic acids research · 2009 · 8 claims · 7 setups

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  SysPIMP is a web-based platform integrating disease mutation databases with X!Tandem and BLAST to identify disease-related mutated proteins from MS results

  omim pmd swissprot msipi database sequence tandem