archive:bioinformatic_tools:sharcgs
Table of Contents
SHARCGS
Overview
SHARCGS[1] stands for SHort read Assembler based on Robust Contig extension for Genome Sequencing.
SHARCGS is a de novo DNA assembly program that uses 25-40mers and deep sequence coverage to assemble genomes. It was used for de novo sequencing from Solexa sequencing data of Helicobacter acinonychis[2].
Website
Source and Documentation
References
1.
a
Juliane C. Dohm, Claudio Lottaz, Tatiana Borodina, and Heinz Himmelbauer. SHARCGS, a fast and highly accurate short-read assembly algorithm for de novo genomic sequencing. Genome Res. November 2007 17: 1697-1706; Published in Advance October 1, 2007, doi:10.1101/gr.6435207.
2.
a
Juliane C. Dohm, Claudio Lottaz, Tatiana Borodina, and Heinz Himmelbauer. Substantial biases in ultra-short read data sets from high-throughput DNA sequencing. Nucleic Acids Research Advance Access published on July 26, 2008, doi:10.1093/nar/gkn425
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archive/bioinformatic_tools/sharcgs.txt · Last modified: 2015/07/28 06:26 by ceisenhart
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