Difference between revisions of "Delly"
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Revision as of 18:58, 27 November 2017
Description
Delly2 is an integrated structural variant prediction method that can discover, genotype and visualize deletions, tandem duplications, inversions and translocations at single-nucleotide resolution in short-read massively parallel sequencing data. It uses paired-ends and split-reads to sensitively and accurately delineate genomic rearrangements throughout the genome. Structural variants can be visualized using Delly-maze and Delly-suave.
Required Modules
Serial
- delly
System Variables
- HPC_{{#uppercase:delly}}_DIR - installation directory
- HPC_{{#uppercase:delly}}_BIN - executable directory