Article
Using Full Genomic Information to Predict Disease: Breaking Down the Barriers Between Complex and Mendelian Diseases.
Annual review of genomics and human genetics - 31 Aug 2018
Jordan Daniel M, Do Ron
Abstract excerpt
While sequence-based genetic tests have long been available for specific loci, especially for Mendelian disease, the rapidly falling costs of genome-wide genotyping arrays, whole-exome sequencing, and whole-genome sequencing are moving us toward a future where full genomic information might inform the prognosis and treatment of a variety of diseases, including complex disease. Similarly, the availability of large...
Topics
- Genetic Diseases, Inborn
- Genetic Predisposition to Disease
- Genome-Wide Association Study
- Humans
- Exome Sequencing