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Repository irissv
Name: irissv
Owner: iuc
Synopsis: Refine insertion sequences
Implement for Refining Insertion Sequences is a tool which corrects the sequences of structural variant calls (currently only insertions). It uses FalconSense to obtain consensus sequences of the reads surrounding each variant and aligns these sequences back to the reference at the insertion site, resulting in an insertion which takes into account the aggregate information of all supporting reads.
Clone this repository: hg clone https://toolshed.g2.bx.psu.edu/repos/iuc/irissv
Type: unrestricted
Revision: 2:b4b6b660293a
This revision can be installed: True
Times cloned / installed: 244

Contents of this repository

Name Description Version Minimum Galaxy Version
Refine insertion sequences 1.0.4+galaxy2 20.01

Categories
Variant Analysis - Tools for single nucleotide polymorphism data such as WGA