Genetic background for cardio vascular disorders in the general Finnish population

Dataset ID Technology Samples
EGAD00001001251 Illumina HiSeq 2000 966

Dataset Description

Low coverage (4-6x) sequencing on samples from population cohorts (Finrisk, Health2000) will be done at Wellcome Trust Sanger Institute (WTSI) using Illumina HiSeq sequencing technology. We will produce 100bp paired end reads. Variants will be called using the 1000 Genomes Project pipeline. The samples have been selected from a national representative set of approximately 30,300 samples and comprises 500 individuals of each gender in the extreme tail of high density lipoprotein (HDL) concentrations. Included individuals were between 25 and 65 years of age. Individuals with a diagnosis of diabetes or BMI>30 were excluded from the study.

Data Use Conditions


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Label Code Version Modifier
general research use and clinical care DUO:0000005 2019-01-07
user specific restriction DUO:0000026 2019-01-07
project specific restriction DUO:0000027 2019-01-07
return to database or resource DUO:0000029 2019-01-07
publication required DUO:0000019 2019-01-07
institution specific restriction DUO:0000028 2019-01-07