Data
199,836 bulk items are available, covering 199,836 participants, encoded using Data-Coding
1.
Notes
Joint variant calling for the first 150,000 participants sequenced in the main phase of the whole genome sequencing project, together with the 50,000 participants sequenced during the Vanguard phase. This joint variant calling was performed by deCODE Genetics using a GraphTyper pipeline. The data is provided in a pVCF format.
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