{
  "id": 17338663,
  "title": "CNVSIM: an interpretable copy-number reference atlas for cancer subtyping",
  "url": "https://urgent.news/2026/10/30/cnvsim-an-interpretable-copy-number-reference-atlas-for-cancer",
  "topic": "health",
  "section": "Health & Medicine",
  "published": "2026-10-30T00:00:00.000Z",
  "source": {
    "name": "bioRxiv",
    "slug": "biorxiv",
    "url": "https://www.biorxiv.org/content/10.64898/2026.10.26.761332v1?rss=1"
  },
  "original_language": "en",
  "account": null,
  "summary": "Background: Genome-wide copy-number variation (CNV) profiles provide a structural representation of cancer genomes, but interpreting new profiles within a reusable reference remains challenging. Results: We developed CNVSIM, which organizes CNV profiles into cancer root-specific reference spaces and defines reference subtypes annotated with chromosome-scale and gene-level signatures. Applied to…",
  "key_points": [],
  "editors_take": null,
  "illustration": null,
  "coverage": {
    "outlets": 1,
    "also_reported_by": []
  },
  "ai_generated": true,
  "disclaimer": "Summaries, key points and the editor’s take are written by software from other outlets’ reporting and may contain errors — always check the linked original."
}