Difference between revisions of "Subread"
Jump to navigation
Jump to search
(Created page with "Category:SoftwareCategory:BiologyCategory:SequencingCategory:SNP {|<!--CONFIGURATION: REQUIRED--> |{{#vardefine:app|subread}} |{{#vardefine:url|http://bioinf.w...") |
Moskalenko (talk | contribs) m (Text replacement - "#uppercase" to "uc") |
||
Line 35: | Line 35: | ||
--> | --> | ||
==System Variables== | ==System Variables== | ||
− | * HPC_{{ | + | * HPC_{{uc:{{#var:app}}}}_DIR - installation directory |
<!--Configuration--> | <!--Configuration--> | ||
{{#if: {{#var: conf}}|==Configuration== | {{#if: {{#var: conf}}|==Configuration== |
Revision as of 21:24, 6 December 2019
Description
The Subread package: a tool kit for processing next-gen sequencing data
Required Modules
Serial
- subread
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