Genetic background for the major psychiatric disorders in the general Finnish population

Dataset ID Technology Samples
EGAD00001001250 Illumina HiSeq 2000 731

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 8028 samples from persons of 30 years or older, which were screened for psychotic and bipolar disorders using the Composite International Diagnostic Interview, self-reported diagnoses, medical examination, and national registers.

Data Use Conditions


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Label Code Version Modifier
obsolete 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