Brad A. Perkins

Identification of misclassified ClinVar variants using disease population prevalence

Amalio Telenti, C Thomas Caskey, N. Shah, 2016, bioRxiv.

Deep sequencing of 10,000 human genomes

Levi C. T. Pierce, Ahmed Moustafa, Amalio Telenti, 2016, Proceedings of the National Academy of Sciences.

Precision medicine screening using whole-genome sequencing and advanced imaging to identify disease risk in adults

Anders M. Dale, James B. Brewer, Victor Lavrenko, 2017, Proceedings of the National Academy of Sciences.

Precision medicine integrating whole-genome sequencing, comprehensive metabolomics, and advanced imaging

E. Kirkness, J. Venter, J. Venter, 2020, Proceedings of the National Academy of Sciences.

Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites

Amalio Telenti, C Thomas Caskey, Nicholas J Schork, 2017, Nature Genetics.