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Pathogenic variant burden in the ExAC database: an empirical approach to evaluating population data for clinical variant interpretation.

Yuya KobayashiShan YangKeith NykampJohn GarciaStephen E LincolnScott E Topper
Published in: Genome medicine (2017)
The observations made in this study suggest that, with certain caveats, a very low allele frequency threshold can be adopted to more accurately interpret sequence variants.
Keyphrases
  • electronic health record
  • copy number
  • gene expression
  • emergency department
  • machine learning
  • dna methylation
  • deep learning