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{ | ||
"creators": [ | ||
{ | ||
"orcid": "0000-0001-5773-5620", | ||
"affiliation": "European Molecular Biology Laboratory (EMBL)", | ||
"name": "Rausch, Tobias" | ||
} | ||
], | ||
"title": "DELLY: structural variant discovery by integrated paired-end and split-read analysis.", | ||
"upload_type": "software", | ||
"access_right": "open", | ||
"description": "<a href=\"https://github.com/dellytools/delly\">Delly</a> is an integrated structural variant (SV) prediction method that can discover and genotype deletions, insertions, duplications, inversions and translocations at single-nucleotide resolution in short-read and long-read massively parallel sequencing data. It uses paired-ends, split-reads and read-depth to sensitively and accurately delineate genomic rearrangements throughout the genome.", | ||
"keywords": [ | ||
"structural-variants", | ||
"genomic-rearrangements", | ||
"cancer-genomics", | ||
"genomics", | ||
"short-reads", | ||
"long-reads", | ||
"sequencing" | ||
] | ||
} |