In the practice of precision medicine, the accurate filtering of common and rare missense variants of benign consequence remains an unsolved problem. Sundaram et. al. using an identity by state model attempt to infer a variants clinical importance by using their prevalence in the genomes of our close relatives, non-human primate (NHP) species. In human, […]
Review of Sundaram et. al. Nature Genetics 2018
![](https://icts-precisionhealth.wustl.edu/files/2018/08/NIH-thumb-350x233.png)