Introduction

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.

For more information about Delly, visit the Delly official website.

Programming language: C++

Brief description: an integrated structural variant (SV) prediction method