|EGAD00010000234||Illumina HumanExome-12v1_A-GenCall, zCall||12241|
No access to download
Please log in before attempting to download data from the EGA. If you do not have an EGA account and want to request access, contact information for the DAC responsible for access to this data is on the right under the heading 'Who controls access to this dataset'.
This dataset is featured in 2 studies
Studies are experimental investigations of a particular phenomenon. e.g. case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients. Click on one of the Study Accessions below to find out more.
|Study Accession||Study Title|
|EGAS00001000584||Assessing the impact of low frequency coding variants on disease risk using the Exomechip|
|EGAS00000000115||Association studies using the Metabochip array - Samples analysed by the WTCCC (1958 British Birth Cohort (58BC), Hypertension cohort (HT), Type 2 Diabetes Cohort (T2D) and Coronary Artery Disease (CAD) cohort)|
Who controls access to this dataset
For each dataset that requires access control, there is a corresponding Data Access Committee (DAC) who determine access permissions. Data access requests are reviewed by the relevant DAC, not by the EGA. If you need to request access to this data set, please contact:
Wellcome Trust Case Control Consortium Data Access Committee
Access information: https://www.wtccc.org.uk/info/access_to_data_samples.shtml
Contact Person: Giselle Kerry