Increasing access to aprecise genetic diagnosis
Participant LoginWhat is SeqFirst?
SeqFirst is a research study. We want to know if doing a genetic test called “whole genome sequencing” as soon as a child is found to have a health condition is more useful than standard testing and referral to specialists.
What is a precise genetic diagnosis?
If someone has a precise genetic diagnosis, it means that they have specific genetic differences that explain their health condition. Finding a precise genetic diagnosis for a child can help to plan for their future needs and take advantage of new treatments. Learn more about SeqFirst and the importance of a precise genetic diagnosis in the video below.
Where can I learn more?
You can learn more about genetics and genetic testing in our Learning Center.
We’ve made some short modules to help explain what being a part of this study looks like for families. These modules are part of the sign-up process for families in the SeqFirst “Newborns” program.
Participant Tasks
Learn more about what it looks like to be a participant in the SeqFirst “Newborns” program.
Our team
The SeqFirst team is comprised of multiple experts in genetics, pediatrics, health economics, and bioethics, uniting to better serve families facing genetic related health conditions.
Michael Bamshad, MD
Principal Investigator
Professor and Head of Genetic Medicine in the Department of Pediatrics at the University of Washington and Seattle Children’s Hospital.
Tara Wenger, MD, PhD
Co-Investigator
Associate Professor and Associate Medical Director for Inpatient Services in the Department of Pediatrics at the University of Washington and Seattle Children’s Hospital.
Katrina Dipple, MD, PhD
Co-Investigator
Professor and Associate Division Head of the Division of Genetic Medicine and Medical Director for Genetics in the Department of Pediatrics at the University of Washington and Seattle Children’s Hospital.
SeqFirst is working with:
