SVM 2 : an improved paired-end-based tool for the detection of small genomic structural variations using high-throughput single-genome resequencing data-Reference-Cited by-同舟云学术

SVM 2 : an improved paired-end-based tool for the detection of small genomic structural variations using high-throughput single-genome resequencing data

Published:2012-06-25 Issue:18 Volume:40 Page:e145-e145
ISSN:1362-4962
Container-title:Nucleic Acids Research
language:en
Short-container-title:

Author:

Chiara Matteo¹,Pesole Graziano¹¹¹,Horner David S.¹

Affiliation:

1. Department of Biomolecular Sciences and Biotechnology, University of Milan, Milan 20133, 2 Institute of Biomembranes and Bioenergetics, National Research Council, 3 Department of Biosciences, Biotechnology and Pharmacological Sciences, University of Bari and 4 Center of Excellence in Genomics (CEGBA), Bari 70125, Italy

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/40/18/e145/25347888/gks606.pdf

Reference40 articles.

1. Next-generation DNA sequencing;Shendure;Nat. Biotechnol.,2008

2. A map of human genome variation from population-scale sequencing;1000 Genomes Project Consortium;Nature,2010

3. Detection of large-scale variation in the human genome;Iafrate;Nat. Genet.,2004

4. Large-scale copy number polymorphism in the human genome;Sebat;Science,2004

5. Fine-scale structural variation of the human genome;Sharp;Nat. Genet.,2005

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