.zenodo.json

{
  "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"
  ]
}