Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion-Reference-Cited by-同舟云学术

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Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion

Published:2011-11-07 Issue:46 Volume:108 Page:E1128-E1136
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Xi R.,Hadjipanayis A. G.,Luquette L. J.,Kim T.-M.,Lee E.,Zhang J.,Johnson M. D.,Muzny D. M.,Wheeler D. A.,Gibbs R. A.,Kucherlapati R.,Park P. J.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference58 articles.

1. FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

2. Strong Association of De Novo Copy Number Mutations with Autism

3. Rare chromosomal deletions and duplications increase risk of schizophrenia

4. Large recurrent microdeletions associated with schizophrenia

5. A new highly penetrant form of obesity due to deletions on chromosome 16p11.2

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