A survey of tools for variant analysis of next-generation genome sequencing data-Reference-Cited by-同舟云学术

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A survey of tools for variant analysis of next-generation genome sequencing data

Published:2013-01-21 Issue:2 Volume:15 Page:256-278
ISSN:1467-5463
Container-title:Briefings in Bioinformatics
language:en
Short-container-title:Briefings in Bioinformatics

Author:

Pabinger S.,Dander A.,Fischer M.,Snajder R.,Sperk M.,Efremova M.,Krabichler B.,Speicher M. R.,Zschocke J.,Trajanoski Z.

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Information Systems

Link

http://academic.oup.com/bib/article-pdf/15/2/256/556047/bbs086.pdf

Reference150 articles.

1. Human Genome Sequencing in Health and Disease

2. Targeted capture and massively parallel sequencing of 12 human exomes

3. Genome-wide in situ exon capture for selective resequencing

4. An integrated semiconductor device enabling non-optical genome sequencing

5. Oxford Nanopore announcement sets sequencing sector abuzz

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