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  • Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis

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Original article
Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis

Authors

  • Bo Zhou Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California, USA Department of Genetics, Stanford University School of Medicine, Stanford, California, USA PubMed articlesGoogle scholar articles
  • Steve S Ho Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California, USA Department of Genetics, Stanford University School of Medicine, Stanford, California, USA PubMed articlesGoogle scholar articles
  • Xianglong Zhang Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California, USA Department of Genetics, Stanford University School of Medicine, Stanford, California, USA PubMed articlesGoogle scholar articles
  • Reenal Pattni Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California, USA Department of Genetics, Stanford University School of Medicine, Stanford, California, USA PubMed articlesGoogle scholar articles
  • Rajini R Haraksingh Department of Life Sciences, The University of the West Indies, Saint Augustine, Trinidad and Tobago PubMed articlesGoogle scholar articles
  • Alexander E Urban Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California, USA Department of Genetics, Stanford University School of Medicine, Stanford, California, USA Program on Genetics of Brain Function, Stanford Center for Genomics and Personalized Medicine, Tasha and John Morgridge Faculty Scholar, Stanford Child Health Research Institute, Stanford University, Stanford, California, USA PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Alexander E Urban, Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA 94305, USA; aeurban{at}stanford.edu
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Citation

Zhou B, Ho SS, Zhang X, et al
Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis
Journal of Medical Genetics 2018;55:735-743.

Publication history

  • Received January 18, 2018
  • Revised May 16, 2018
  • Accepted June 26, 2018
  • First published July 30, 2018.
Online issue publication 
October 26, 2018

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© Author(s) (or their employer(s)) 2018. No commercial re-use. See rights and permissions. Published by BMJ.