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Frequently Asked Questions

  • Why do I see a high sample no call rate in the smaller callsets?
  • What is the cost to filter the VDS?
  • Downloading and Disseminating Genomic Data
  • How can we find the sequencing depth for the WGS data?
  • How do I select specific variants from the Hail MatrixTables or Hail VDS?
  • What reference are the variants called against for the genomic data?
  • Are array data imputed?
  • Recommendations for processing CRAMs with GATK on the Researcher Workbench
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