Whole-genome variant detection in long-read sequencing data from ultra-low input patient samples.
利用超低输入量患者样本的长读长测序数据进行全基因组变异检测
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doi:10.1101/2025.07.25.25332067
Wang Katherine, Lee Hayan, Aex Cera J, Finot Lucas, Zhu Kevin, Chang Julianna R, Horning Aaron M, Rowell William J, Li Philip, Kingan Sarah B, Snyder Michael P, Erwin Graham S
