Early access to long-read whole genome sequencing

GeneDx’s long-read whole genome sequencing (lrWGS) expands our diagnostic capabilities for cases that still need answers.

Long-read sequencing can reveal complex genetic variation, including certain structural variants and repeat expansions, that may go undetected with traditional short-read sequencing. GeneDx pairs this expanded detection with rich phenotypic data and deep clinical interpretation to help close diagnostic gaps.

Contact us to learn more about our early access program.