Description
100× Whole Genome Sequencing (WGS) is a comprehensive genetic test that analyzes nearly an individual’s entire genome to help identify genetic causes of rare, complex, or undiagnosed conditions.
Unlike targeted genetic tests, WGS evaluates genetic variation across coding and non-coding regions, providing a comprehensive view of an individual’s DNA to support clinical evaluation, diagnosis, and decision-making.
Why 100× WGS? With approximately 100× average sequencing depth, the test provides high-resolution genomic data designed to support sensitive and reliable detection of genetic variation across the genome. The comprehensive nature of WGS makes it particularly valuable when previous genetic testing has been inconclusive or when a patient’s clinical presentation is complex, multisystem, or not easily explained by a targeted genetic test.
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