Combined Low-Pass Whole-Genome and Targeted Sequencing Identifies Causative Mutations and Associated Genomic Scarring Indicative of Homologous Recombination Deficiency

被引：0

作者：

An, J. ^{[1
]}

Belbin, G. ^{[2
]}

Mazur, C. ^{[2
]}

Li, J. ^{[2
]}

Pickrell, J. ^{[2
]}

Metzger, D. ^{[1
]}

Gao, S. ^{[1
]}

Van Roey, E. ^{[1
]}

Seager, R. ^{[1
]}

Pabla, S. ^{[1
]}

Dash, D. ^{[1
]}

Conroy, J. ^{[1
]}

机构：

[1] OmniSeq Labcorp, Buffalo, NY USA

[2] Gencove, New York, NY USA

来源：

JOURNAL OF MOLECULAR DIAGNOSTICS | 2022年 / 24卷 / 10期

关键词：

D O I：

暂无

中图分类号：

R36 [病理学];

学科分类号：

100104 ;

摘要：

ST060

引用

页码：S109 / S110

页数：2

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