Dear users, we have installed a new software: Delly 1.1.5:
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Delly: Delly/1.1.5
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Description:
Delly is an integrated structural variant (SV) 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, split-reads and read-depth to sensitively and accurately delineate genomic rearrangements throughout the genome.
You will need to load all module(s) on any one of the lines below before the "Delly/1.1.5" module is available to load.
GCC/11.3.0
Help:
Description
===========
Delly is an integrated structural variant (SV) 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, split-reads and
read-depth to sensitively and accurately delineate genomic rearrangements
throughout the genome.
More information
================
- Homepage: https://github.com/dellytools/delly/
Best,
HPC team