Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing-Reference-Cited by-同舟云学术

Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing

Published:2011-12-18 Issue:1 Volume:30 Page:61-68
ISSN:1087-0156
Container-title:Nature Biotechnology
language:en
Short-container-title:Nat Biotechnol

Author:

Reumers Joke,De Rijk Peter,Zhao Hui,Liekens Anthony,Smeets Dominiek,Cleary John,Van Loo Peter,Van Den Bossche Maarten,Catthoor Kirsten,Sabbe Bernard,Despierre Evelyn,Vergote Ignace,Hilbush Brian,Lambrechts Diether,Del-Favero Jurgen

Publisher

Springer Science and Business Media LLC

Subject

Biomedical Engineering,Molecular Medicine,Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Link

http://www.nature.com/articles/nbt.2053.pdf

Reference50 articles.

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2. Cirulli, E.T. & Goldstein, D.B. Uncovering the roles of rare variants in common disease through whole-genome sequencing. Nat. Rev. Genet. 11, 415–425 (2010).

3. DePristo, M.A. et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat. Genet. 43, 491–498 (2011).

4. Anonymous. The sequence is dead: long live the genome. Nat. Biotechnol. 29, 463 (2011).

5. Lee, W. et al. The mutation spectrum revealed by paired genome sequences from a lung cancer patient. Nature 465, 473–477 (2010).

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