Sealer: a scalable gap-closing application for finishing draft genomes-Reference-Cited by-同舟云学术

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Sealer: a scalable gap-closing application for finishing draft genomes

Published:2015-07-25 Issue:1 Volume:16 Page:
ISSN:1471-2105
Container-title:BMC Bioinformatics
language:en
Short-container-title:BMC Bioinformatics

Author:

Paulino Daniel,Warren René L.,Vandervalk Benjamin P.,Raymond Anthony,Jackman Shaun D.,Birol Inanç

Funder

National Institutes of Health

Genome Canada

British Columbia Cancer Foundation

Genome British Columbia

Publisher

Springer Science and Business Media LLC

Subject

Applied Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Structural Biology

Link

http://link.springer.com/article/10.1186/s12859-015-0663-4/fulltext.html

Reference24 articles.

1. Simpson JT, Wong K, Jackman SD, Schein JE, Jones SJ, Birol I. ABySS: a parallel assembler for short read sequence data. Genome Res. 2009;19:1117–23.

2. Stein LD. The case for cloud computing in genome informatics. Genome Biol. 2010;11:207.

3. 1000 Genomes Project Consortium, Abecasis GR, Altshuler D, Auton A, Brooks LD, Durbin RM, et al. A map of human genome variation from population-scale sequencing. Nature. 2010;467:1061–73.

4. Mardis ER. The $1000 genome, the $100,000 analysis? Genome Med. 2010;2:84.

5. Cancer Genome Atlas Research Network. Genomic and Epigenomic Landscapes of Adult De Novo Acute Myeloid Leukemia. N Engl J Med. 2013;368:2059–74.

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