Copy‐Number Variants Detection by Low‐Pass Whole‐Genome Sequencing-Reference-Cited by-同舟云学术

Copy‐Number Variants Detection by Low‐Pass Whole‐Genome Sequencing

Published:2017-07 Issue:1 Volume:94 Page:
ISSN:1934-8266
Container-title:Current Protocols in Human Genetics
language:en
Short-container-title:Current Protocols in Human Genetics

Author:

Dong Zirui¹²³,Xie Weiwei³⁴,Chen Haixiao³⁴,Xu Jinjin³⁴,Wang Huilin¹²⁵,Li Yun³⁴,Wang Jun³⁴,Chen Fang³⁴,Choy Kwong Wai¹²⁶,Jiang Hui³⁴

Affiliation:

1. Department of Obstetrics and Gynaecology, The Chinese University of Hong Kong Hong Kong China

2. Shenzhen Research Institute, The Chinese University of Hong Kong Shenzhen China

3. BGI‐Shenzhen Shenzhen China

4. China National Genebank‐Shenzhen, BGI‐Shenzhen Shenzhen China

5. Bao'an Maternal and Child Health Hospital Shenzhen China

6. The Chinese University of Hong Kong‐Baylor College of Medicine Joint Center for Medical Genetics Hong Kong China

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cphg.43

Reference17 articles.

1. A global reference for human genetic variation

2. Searching online Mendelian inheritance in man (OMIM) for information on genetic loci involved in human disease;Baxevanis A. D.;Current Protocols in Human Genetics,2012

3. Contribution of genomic copy-number variations in prenatal oral clefts: a multicenter cohort study

4. The impact of human copy number variation on a new era of genetic testing

5. Interpretation of Genomic Copy Number Variants Using DECIPHER

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