The paper introduces cellSTAAR, a novel statistical framework designed to improve the discovery of rare genetic variants within noncoding regions of the human genome. By integrating single-cell epigenetic data with whole-genome sequencing, the method identifies functional associations that are often masked in traditional bulk tissue studies. The tool specifically addresses the difficulty of linkin...去小宇宙查看完整单集简介
前往小宇宙评论区与主播互动
前往小宇宙评论区与主播互动
Fler avsnitt av Paper Talk
Visa alla avsnitt av Paper TalkPaper Talk med 淼淼Elva finns tillgänglig på flera plattformar. Informationen på denna sida kommer från offentliga podd-flöden.
