Difference between revisions of "SHARCGS"

From UFRC
Jump to navigation Jump to search
(Created page with "Category:SoftwareCategory:biologyCategory:NGSCategory:de novo assembly {|<!--CONFIGURATION: REQUIRED--> |{{#vardefine:app|sharcgs}} |{{#vardefine:url|http://sh...")
 
Line 58: Line 58:
 
{{#if: {{#var: citation}}|==Citation==
 
{{#if: {{#var: citation}}|==Citation==
 
If you use the programs or Helicobacter Solexa data for a publication please cite:
 
If you use the programs or Helicobacter Solexa data for a publication please cite:
   Dohm JC, Lottaz C, Borodina T, Himmelbauer H
+
   Dohm JC, Lottaz C, Borodina T, Himmelbauer H SHARCGS, a fast and highly accurate short-read assembly algorithm for de novo genomic sequencing. Genome Research 2007 17: 1697-1706.
  SHARCGS, a fast and highly accurate short-read assembly algorithm
 
  for de novo genomic sequencing. Genome Research 2007 17: 1697-1706.
 
 
If you use Beta vulgaris Solexa data for a publication please cite:
 
If you use Beta vulgaris Solexa data for a publication please cite:
   Dohm JC, Lottaz C, Borodina T, Himmelbauer H
+
   Dohm JC, Lottaz C, Borodina T, Himmelbauer H Substantial biases in ultra-short read data sets from high-throughput DNA sequencing. Nucleic Acids Res. 2008 Jul 26.[Epub ahead of print]
  Substantial biases in ultra-short read data sets from high-throughput
 
  DNA sequencing. Nucleic Acids Res. 2008 Jul 26.[Epub ahead of print]
 
  
 
|}}
 
|}}

Revision as of 15:28, 7 February 2018

Description

sharcgs website  

SHort-read Assembler based on Robust Contig-extension for Genomic Sequencing.

Environment Modules

Run module spider sharcgs to find out what environment modules are available for this application.

System Variables

  • HPC_{{#uppercase:sharcgs}}_DIR - installation directory
  • HPC_{{#uppercase:sharcgs}}_DATA - Sample data directory




Citation

If you use the programs or Helicobacter Solexa data for a publication please cite:

  Dohm JC, Lottaz C, Borodina T, Himmelbauer H SHARCGS, a fast and highly accurate short-read assembly algorithm for de novo genomic sequencing. Genome Research 2007 17: 1697-1706.

If you use Beta vulgaris Solexa data for a publication please cite:

  Dohm JC, Lottaz C, Borodina T, Himmelbauer H Substantial biases in ultra-short read data sets from high-throughput DNA sequencing. Nucleic Acids Res. 2008 Jul 26.[Epub ahead of print]