Low-coverage genome sequencing is an efficient approach for the detection of clinically relevant copy-number variants and mtDNA variants

被引：0
|
作者：
Pajusalu, Sander [1 ,2 ]
Oja, Kaisa Teele [1 ,2 ]
Samarina, Ustina [2 ]
Tooming, Mikk [1 ,2 ]
Kahre, Tiina [1 ,2 ]
Ounap, Katrin [1 ,2 ]
机构：
[1] Univ Tartu, Inst Clin Med, Dept Clin Genet, Tartu, Estonia
[2] Tartu Univ Hosp, Dept Clin Genet, United Labs, Tartu, Estonia
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2023年 / 31卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
P17.011.A
引用
收藏
页码：592 / 592
页数：1
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