Stanford inventors have developed a series of methods which can identify genetic variants and medical genotypes through the phasing of genetic data with the use of Mendelian inheritance as quality control.
Stanford researchers have developed three novel human reference genome sequences, which will significantly improve the interpretation of the growing genetic data stemming from the human genome project and other related draft sequences.
Stanford researchers have developed a novel method that enlarges the search space for disease-gene relationships. The main barrier to genome interpretation is the inherent difficulty in prioritizing the millions of genetic variants in known genes.
Stanford researchers have developed a method for estimating the risk for disease on a genome-wide scale while incorporating population and familial haplotype phasing.