Difference between revisions of "Novoalign"

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and the results of the analyses must published in peer-reviewed journals as
 
and the results of the analyses must published in peer-reviewed journals as
 
requested by the software manufacturer [http://www.novocraft.com/wiki/tiki-view_faq.php?faqId=1#q23 in Novoalign FAQ].
 
requested by the software manufacturer [http://www.novocraft.com/wiki/tiki-view_faq.php?faqId=1#q23 in Novoalign FAQ].
 
 
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==Required Modules==
 
==Required Modules==
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===Serial===
 
===Serial===
 
*{{#var:app}}
 
*{{#var:app}}
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==System Variables==
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* HPC_{{#uppercase:{{#var:app}}}}_DIR - installation directory
 
* HPC_NOVOALIGN_BIN - executable directory
 
* HPC_NOVOALIGN_BIN - executable directory
 
* HPC_NOVOALIGN_DOC - documentation directory
 
* HPC_NOVOALIGN_DOC - documentation directory

Revision as of 19:22, 10 August 2012

Description

novoalign website  

Novoalign is a highly accurate program for mapping next-generation sequencing reads to a reference database. It is an aligner for single-ended and paired-end reads from the Illumina Genome Analyser. Novoalign finds global optimum alignments using full Needleman-Wunsch algorithm with affine gap penalties.

Limited functionality and single-threaded performance are available without a paid license. Novoalign must only be used for academic/non-profit research and the results of the analyses must published in peer-reviewed journals as requested by the software manufacturer in Novoalign FAQ.

Required Modules

modules documentation

Serial

  • novoalign

System Variables

  • HPC_{{#uppercase:novoalign}}_DIR - installation directory
  • HPC_NOVOALIGN_BIN - executable directory
  • HPC_NOVOALIGN_DOC - documentation directory