URL: https://tobiasrausch.com/delly/
Proper Citation: DELLY (RRID:SCR_004603)
Description: Integrated structural variant prediction software that can detect 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 genome.
Abbreviations: DELLY
Synonyms: DELLY, Structural variant discovery by integrated paired-end and split-read analysis
Resource Type: software resource
Defining Citation: PMID:22962449, DOI:10.1093/bioinformatics/bts378
Keywords: structural variant, genomic rearrangement, deletion, tandem duplication, inversion, translocation, bio.tools
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