<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/PRJEB6042/GEEVS_aggregation_v2.EVA.eva_1.vcf.gz</Vcf></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>0</viewCount><searchCount>0</searchCount></scores><additional><dataset_type>Exome Sequencing</dataset_type><omics_type>Genomics</omics_type><submitter>Center for Genomic Regulation - CRG (Barcelona); Institute of Human Genetics - Helmholtz Zentrum (Munich)</submitter><instrument_platform>Illumina HiSeq 2000, Illumina HiSeq 2500</instrument_platform><species>Homo Sapiens</species><full_dataset_link>https://www.ebi.ac.uk/eva/?eva-study=PRJEB6042</full_dataset_link><repository>EVA</repository><name_synonyms>other disease, human disease, Occidental, familial, disorders, white, genetic, non-neoplastic, disease, Caucasian, diseases, Whites, European, Diseases, disease or disorder, condition, disorder, White, diseases and disorders, Homo sapiens disease, medical condition., inherited genetic, constitutitional genetic, hereditary, Caucasoid, Caucasians</name_synonyms><description_synonyms>Genetic Variations, Individual Health, other disease, Variations, Arts, familial, disorders, white, Diversities, medical condition, Normalcy, Normalcies, Northern Europe, Caucasian, diseases, European, Diseases, Western Europe, Genetic Diversities, disease or disorder, condition, diseases and disorders, Individual, Southern Europe, Caucasoid, Caucasians, Normalities, average, human disease, Industrial, Occidental, Diversity, Industrial Arts, Genetic, Normality, Programs., Genetic Diversity, genetic, non-neoplastic, disease, Health, Whites, disorder, White, Homo sapiens disease, inherited genetic, constitutitional genetic, hereditary, Variation</description_synonyms><citation_count>0</citation_count></additional><is_claimable>false</is_claimable><name>GEUVADIS: Genetic European Variation in Disease</name><description>GEUVADIS: Genetic European Variation in Disease, is a European Medical Sequencing Consortium aiming at sharing capacity across Europe in high-throughput sequencing technology to explore genetic variation in health and disease. It is funded by the European Commission 7th framework program under the Coordination and Support Action scheme. It started on the 1st October 2010, and ended on 31st December 2013.</description><dates><publication>2014-10-20</publication></dates><accession>PRJEB6042</accession><cross_references><TAXONOMY>9606</TAXONOMY></cross_references></HashMap>