Editorial: Next Generation Sequencing (NGS) for Rare Diseases Diagnosis

被引：1
|
作者：
Yang, Xiu-An [1 ,2 ]
机构：
[1] Chengde Med Univ, Sch Basic Med Sci, Lab Genet Engn & Genom, Chengde, Peoples R China
[2] Chengde Med Univ, Hebei Key Lab Nerve Injury & Repair, Chengde, Peoples R China
来源：
FRONTIERS IN GENETICS | 2021年 / 12卷
关键词：
next generation sequencing; rare diseases diagnosis; whole-exome sequencing; copy number variation; bioinformatics;
D O I：
10.3389/fgene.2021.808042
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页数：2
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