We work to identify individual genetic profiles that influence diagnosis and management of disease. These include:

• Genetic variant discovery in rare diseases
• Genetic variant discovery impacting therapeutic decision making
  (pharmacogenetics)

If you are a clinician at NCSU interested in identifying the genetic cause of a rare
condition, please fill out this questionnaire. Instructions on obtaining and submitting DNA can be found in the hospital shared drive.

If you belong to a breed club and are interested in mapping a genetic condition that
affects your breed please e-mail our laboratory at: NCSUPrecisionMedicine@ncsu.edu

If you are interested in the genetics surrounding drug response in a patient, please
email our laboratory at: NCSUPrecisionMedicine@ncsu.edu