IAnnotateSV

From UFRC
Revision as of 15:30, 19 March 2018 by Maxprok (talk | contribs) (Created page with "Category:SoftwareCategory:BiologyCategory:Phylogenetics {|<!--CONFIGURATION: REQUIRED--> |{{#vardefine:app|iannotatesv}} |{{#vardefine:url|https://github.com/rhsha...")
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search

Description

iannotatesv website  

iAnnotateSV is a Python library and command-line software toolkit to annotate and visualize structural variants detected from Next Generation DNA sequencing data. This works for majority is just re-writing of a tool called dRanger_annotate written in matlab by Mike Lawrence at Broad Institue. But it also has some additional functionality and control over the annotation w.r.t the what transcripts to be used for annotation. It is designed for use with hybrid capture, including both whole-exome and custom target panels, and short-read sequencing platforms such as Illumina.

Environment Modules

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

System Variables

  • HPC_{{#uppercase:iannotatesv}}_DIR - installation directory
  • HPC_{{#uppercase:iannotatesv}}_BIN - executable directory




Citation

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

https://github.com/rhshah/iAnnotateSV#Citation