Using XHMM Software to Detect Copy Number Variation in Whole‐Exome Sequencing Data-Reference-Cited by-同舟云学术

Using XHMM Software to Detect Copy Number Variation in Whole‐Exome Sequencing Data

Published:2014-04 Issue:1 Volume:81 Page:
ISSN:1934-8266
Container-title:Current Protocols in Human Genetics
language:en
Short-container-title:Current Protocols in Human Genetics

Author:

Fromer Menachem¹²³,Purcell Shaun M.¹²³

Affiliation:

1. Division of Psychiatric Genomics and Icahn Institute for Genomics and Multiscale Biology, Icahn School of Medicine at Mount Sinai, New York New York

2. Stanley Center for Psychiatric Research and Medical and Population Genetics Program, Broad Institute of MIT and Harvard Cambridge Massachusetts

3. Analytic and Translational Genetics Unit Psychiatric and Neurodevelopmental Genetics Unit, Massachusetts General Hospital Boston Massachusetts

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/0471142905.hg0723s81

Reference15 articles.

1. A copy number variation morbidity map of developmental delay

2. A framework for variation discovery and genotyping using next-generation DNA sequencing data

3. Discovery and Statistical Genotyping of Copy-Number Variation from Whole-Exome Sequencing Depth

4. Rare chromosomal deletions and duplications increase risk of schizophrenia

5. De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

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