The mission of the Miller lab is to reduce the burden of undiagnosed genetic diseases on patients and their families by improving the efficiency and effectiveness of genetic testing, and to better understand human genetic disease through the identification and characterization of novel disease-causing variation. To do this, the Miller lab uses new technologies, such as long-read DNA and RNA sequencing to improve clinical genetic testing options, identify novel mechanisms of disease, reduce the time required to make a genetic diagnosis, and lower barriers to obtaining comprehensive clinical genetic testing. Clinically, Dr. Miller cares for patients in both general genetics and skeletal dysplasia clinics. More information can be found on his lab website at www.millerlaboratory.com.