Leveraging Novel Newborn Whole Genome Sequencing to Enable Screening & Diagnosis of Disease
Time: 11:30 am
day: Day 2 Track C AM
Details:
- Accelerating treatment of over 500 diseases by leveraging newborn sequencing technologies
- Achieving faster molecular diagnosis using whole genome sequencing
- Bridging bioinformatics, data science, genomics and molecular sciences to bring newborn screening practices up to speed
