delly 0.8.3 Integrated structural variant prediction method
Delly is an integrated structural variant prediction method that can discover and genotype 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.
- Retejo: https://github.com/dellytools/delly
- Permesilo: GPL 3+
- Fontkodo de la pako: bioinformatics.scm
- Flikaĵoj: snippet
- Versioj: x86_64-linux, aarch64-linux, powerpc64le-linux, i686-linux, armhf-linux, i586-gnu