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200,004 bulk items are available, covering 200,004 participants, encoded using Data-Coding 1.
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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