{"database":"EVA","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Vcf":["ftp://ftp.ebi.ac.uk/pub/databases/eva/PRJEB15197/decode_variants_2016_08_12.garys.sorted.without_chr_in_contigname.fixed.vcf.gz"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":{"citationCount":0,"reanalysisCount":0,"viewCount":0,"searchCount":0},"additional":{"dataset_type":["Whole Genome Sequencing"],"omics_type":["Genomics"],"submitter":["deCODE Genetics"],"instrument_platform":["Illumina HiSeq 2500, Illumina Genome Analyzer IIx, Illumina HiSeq 2000"],"species":["Homo Sapiens"],"full_dataset_link":["https://www.ebi.ac.uk/eva/?eva-study=PRJEB15197"],"repository":["EVA"],"name_synonyms":["whole genome, heredity, Genomes."],"description_synonyms":["sequence, whole genome, primary structure of sequence macromolecule, Genomes."],"citation_count":["0"],"additional_accession":[]},"is_claimable":false,"name":"deCODE Genetics whole-genome sequencing variants 2","description":"Sequence variants identified in deCODE's whole-genome sequencing of 15,220 Icelanders","dates":{"publication":"2017-01-01"},"accession":"PRJEB15197","cross_references":{"TAXONOMY":["9606"]}}