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Bioinformatics Advance Access originally published online on October 24, 2008
Bioinformatics 2008 24(24):2818-2824; doi:10.1093/bioinformatics/btn548
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© 2008 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Aggressive assembly of pyrosequencing reads with mates

Jason R. Miller 1,*, Arthur L. Delcher 2, Sergey Koren 1, Eli Venter 1, Brian P. Walenz 1, Anushka Brownley 1, Justin Johnson 1, Kelvin Li 1, Clark Mobarry 3 and Granger Sutton 1

1The J. Craig Venter Institute, 9712 Medical Center Drive, Rockville MD 20850, 2Center for Bioinformatics & Computational Biology, University of Maryland, College Park, MD 20742 and 3White Oak Technologies Inc, 1300 Spring St., Ste 320, Silver Spring, MD 20910, USA

*To whom correspondence should be addressed.


   Abstract

Motivation: DNA sequence reads from Sanger and pyrosequencing platforms differ in cost, accuracy, typical coverage, average read length and the variety of available paired-end protocols. Both read types can complement one another in a ‘hybrid’ approach to whole-genome shotgun sequencing projects, but assembly software must be modified to accommodate their different characteristics. This is true even of pyrosequencing mated and unmated read combinations. Without special modifications, assemblers tuned for homogeneous sequence data may perform poorly on hybrid data.

Results: Celera Assembler was modified for combinations of ABI 3730 and 454 FLX reads. The revised pipeline called CABOG (Celera Assembler with the Best Overlap Graph) is robust to homopolymer run length uncertainty, high read coverage and heterogeneous read lengths. In tests on four genomes, it generated the longest contigs among all assemblers tested. It exploited the mate constraints provided by paired-end reads from either platform to build larger contigs and scaffolds, which were validated by comparison to a finished reference sequence. A low rate of contig mis-assembly was detected in some CABOG assemblies, but this was reduced in the presence of sufficient mate pair data.

Availability: The software is freely available as open-source from http://wgs-assembler.sf.net under the GNU Public License.

Contact: jmiller{at}jcvi.org

Supplementary information: Supplementary data are available at Bioinformatics online.

Associate Editor: Dmitrij Frishman


Received on June 20, 2008; revised on October 17, 2008; accepted on October 20, 2008

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