Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens-Reference-Cited by-同舟云学术

Using next-generation sequencing for high resolution multiplex analysis of copy number variation from nanogram quantities of DNA from formalin-fixed paraffin-embedded specimens

Published:2010-06-04 Issue:14 Volume:38 Page:e151-e151
ISSN:1362-4962
Container-title:Nucleic Acids Research
language:en
Short-container-title:

Author:

Wood Henry M.,Belvedere Ornella,Conway Caroline,Daly Catherine,Chalkley Rebecca,Bickerdike Melissa,McKinley Claire,Egan Phil,Ross Lisa,Hayward Bruce,Morgan Joanne,Davidson Leslie,MacLennan Ken,Ong Thian K.,Papagiannopoulos Kostas,Cook Ian,Adams David J.,Taylor Graham R.,Rabbitts Pamela

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/38/14/e151/16767656/gkq510.pdf

Reference30 articles.

1. Systems medicine: the future of medical genomics and healthcare;Auffray;Genome Med.,2009

2. Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing;Campbell;Nat. Genet.,2008

3. High-resolution mapping of copy-number alterations with massively parallel sequencing;Chiang;Nat. Methods,2009

4. CNV-seq, a new method to detect copy number variation using high-throughput sequencing;Xie;BMC Bioinformatics,2009

5. Sensitive and accurate detection of copy number variants using read depth of coverage;Yoon;Genome Res.,2009

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