Hprc banner tamu.png

SW:Delly

From TAMU HPRC
Jump to: navigation, search

Delly

GCATemplates available: ada

Delly homepage

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. Structural variants can be visualized using Delly-maze and Delly-suave.

module spider Delly

Delly primarily parallelizes on the sample level. Hence, OMP_NUM_THREADS should be always smaller or equal to the number of input samples.

If you have 5 samples, for example, you would use the following in your job script along with the appropriate #SBATCH values:

export OMP_NUM_THREADS=5