Resolving the chromatin impact of mosaic variants with targeted Fiber-seq.

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作者： Stephanie C,Bohaczuk ^[1] ; Zachary J,Amador ^[2] ; Chang,Li ^[1] ; Benjamin J,Mallory ^[2] ; Elliott G,Swanson ^[2] ; Jane,Ranchalis ^[1] ; Mitchell R,Vollger ^[1] ; Katherine M,Munson ^[2] ; Tom,Walsh ^[1] ; Morgan O,Hamm ^[2] ; Yizi,Mao ^[1] ; Andre,Lieber ^[1] ; Andrew B,Stergachis ^[3]

作者单位： Division of Medical Genetics, University of Washington School of Medicine, Seattle, Washington 98195, USA. ^[1] Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA. ^[2] Division of Medical Genetics, University of Washington School of Medicine, Seattle, Washington 98195, USA; absterga@uw.edu.;Department of Genome Sciences, University of Washington, Seattle, Washington 98195, USA.;Brotman Baty Institute for Precision Medicine, Seattle, Washington 98195, USA. ^[3]

主题词人类(Humans);染色质(Chromatin);启动区, 遗传(Promoter Regions, Genetic);镶嵌现象(Mosaicism);序列分析, DNA(Sequence Analysis, DNA)

DOI 10.1101/gr.279747.124

PMID 39653420

发布时间 2025-01-11

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准确一般字义偏差语意偏离译文作用小提交