Exome sequencing data analysis to characterize copy number variants involved in m.14487T>C mutation
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https://www.ncbi.nlm.nih.gov/sra/SRP199417
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资源简介：
In this study, we analyze DNA whole-exome sequencing (WES) data from 3 patients with m.14487T>C mutation to detect rare candidate SNVs. Overall design: Examination of EDTA blood of each patient or their biological parents (trio) with m.14487T>C mutation by deep sequencing
创建时间：
2020-05-20
