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