Multiplexed direct genomic selection (MDiGS): a pooled BAC capture approach for highly accurate CNV and SNP/INDEL detection-Reference-Cited by-同舟云学术

Multiplexed direct genomic selection (MDiGS): a pooled BAC capture approach for highly accurate CNV and SNP/INDEL detection

Published:2014-03-20 Issue:10 Volume:42 Page:e82-e82
ISSN:1362-4962
Container-title:Nucleic Acids Research
language:en
Short-container-title:

Author:

Alvarado David M.¹,Yang Ping¹,Druley Todd E.²³,Lovett Michael⁴,Gurnett Christina A.¹²⁵

Affiliation:

1. Department of Orthopaedic Surgery, Washington University School of Medicine, 660 S Euclid Ave., St Louis, MO 63110, USA

2. Department of Pediatrics, Washington University School of Medicine, 660 S Euclid Ave., St Louis, MO 63110, USA

3. Department of Genetics, Washington University School of Medicine, 660 S Euclid Ave., St Louis, MO 63110, USA

4. Genome Technology and Systems Biology, NHLI, Imperial College, London, UK

5. Department of Neurology, Washington University School of Medicine, 660 S Euclid Ave., St Louis, MO 63110, USA

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/42/10/e82/25346572/gku218.pdf

Reference24 articles.

1. Direct genomic selection;Bashiardes;Nat. Methods,2005

2. Population-based rare variant detection via pooled exome or custom hybridization capture with or without individual indexing;Ramos;BMC Genomics,2012

3. Accurate and exact CNV identification from targeted high-throughput sequence data;Nord;BMC Genomics,2011

4. Estimating genome-wide copy number using allele-specific mixture models;Wang;J. Comput. Biol.,2008

5. Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives;Zhao;BMC Bioinformatics,2013

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