Dataset
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
GRU US PS RTN PUB IS
See further information on Data Use Conditions
| 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 |
