Delly is a structural variant detection method for the discovery of germline and somatic genomic rearrangements. Delly can detect deletions, tandem duplications, inversions and translocations at single-nucleotide resolution in short-read massively parallel sequencing data.

Funding:

Neither development nor maintenance funded by de.NBI.

Homepage: 

https://github.com/dellytools/delly

BioTools: 

https://bio.tools/delly2

Bioconda: 

https://bioconda.github.io/recipes/delly/README.html

Contact: 

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