Subread: Difference between revisions

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Created page with "Category:SoftwareCategory:BiologyCategory:SequencingCategory:SNP {|<!--CONFIGURATION: REQUIRED--> |{{#vardefine:app|subread}} |{{#vardefine:url|http://bioinf.w..."
 
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[[Category:Software]][[Category:Biology]][[Category:Sequencing]][[Category:SNP]]
[[Category:Software]][[Category:Biology]][[Category:Sequencing]][[Category:Variant Calling]]
{|<!--CONFIGURATION: REQUIRED-->
{|<!--CONFIGURATION: REQUIRED-->
|{{#vardefine:app|subread}}
|{{#vardefine:app|subread}}
|{{#vardefine:url|http://bioinf.wehi.edu.au/subread-package/}}
|{{#vardefine:url|http://subread.sourceforge.net/}}
<!--CONFIGURATION: OPTIONAL (|1}} means it's ON)-->
<!--CONFIGURATION: OPTIONAL (|1}} means it's ON)-->
|{{#vardefine:conf|}}          <!--CONFIGURATION-->
|{{#vardefine:conf|}}          <!--CONFIGURATION-->
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<!--Modules-->
<!--Modules-->
==Required Modules==
==Environment Modules==
 
Run <code>module spider {{#var:app}}</code> to find out what environment modules are available for this application.
===Serial===
* {{#var:app}}
<!--
===Parallel (OpenMP)===
* intel
* {{#var:app}}
===Parallel (MPI)===
* intel
* openmpi
* {{#var:app}}
-->
==System Variables==
==System Variables==
* HPC_{{#uppercase:{{#var:app}}}}_DIR - installation directory
* HPC_{{uc:{{#var:app}}}}_DIR - installation directory
<!--Configuration-->
<!--Configuration-->
{{#if: {{#var: conf}}|==Configuration==
{{#if: {{#var: conf}}|==Configuration==

Latest revision as of 12:57, 15 August 2022

Description

subread website  

The Subread package: a tool kit for processing next-gen sequencing data

Environment Modules

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

System Variables

  • HPC_SUBREAD_DIR - installation directory




Citation

If you publish research that uses subread you have to cite it as follows:

If you use the Subread or Subjunc aligners, please cite: Liao Y, Smyth GK and Shi W (2013). The Subread aligner: fast, accurate and scalable read mapping by seed-and-vote. Nucleic Acids Research, 41(10):e108

If you use the featureCounts program, please cite: Liao Y, Smyth GK and Shi W (2014). featureCounts: an efficient general purpose program for assigning sequence reads to genomic features. Bioinformatics, 30(7):923-30