Clinical Whole Genome Sequencing (WGS)

Whole genome sequencing is performed at a U.S. CAP-accredited and CLIA-certified Laboratory, or at a Hong Kong ISO-certified laboratory.

A non-invasive genetic test analyzing over 20,000 genes and 3 billion base pairs in the entire human genome.

Detects genetic mutations associated with ASD and its comorbidities, including speech delay, intellectual disability, developmental regression, movement disorder, and seizures.

How to prepare your child for WGS

Please refrain from eating and drinking water for at least 3 hours before the screening process to ensure the accuracy of gene swab sample.