Difference between revisions of "WhatsHap"

From UFRC
Jump to navigation Jump to search
(Created page with "Category:SoftwareCategory:BiologyCategory:Phylogenetics {|<!--CONFIGURATION: REQUIRED--> |{{#vardefine:app|whatshap}} |{{#vardefine:url|https://bitbucket.org/whats...")
 
m (Text replacement - "#uppercase" to "uc")
 
Line 24: Line 24:
 
Run <code>module spider {{#var:app}}</code> to find out what environment modules are available for this application.
 
Run <code>module spider {{#var:app}}</code> to find out what environment modules are available for this application.
 
==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 21:29, 6 December 2019

Description

whatshap website  

WhatsHap is a software for phasing genomic variants using DNA sequencing reads, also called read-based phasing or haplotype assembly. It is especially suitable for long reads, but works also well with short reads.

Environment Modules

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

System Variables

  • HPC_WHATSHAP_DIR - installation directory




Citation

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

https://whatshap.readthedocs.io/en/latest/howtocite.html