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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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The NIDDK Information Network (dkNET) serves the needs of basic and clinical investigators by providing seamless access to large pools of data and research resources relevant to the mission of The National Institute of Diabetes Digestive and Kidney Diseases (NIDDK). dkNET is hosted at University of California San Diego, and is supported by NIH NIDDK grant 2U24DK097771-09.
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