Enhanced depth and coverage to detect variants missed by standard exomes.Optimized for rare disease diagnosis.
Access structural variants, non-coding regions, and deeper genomic signals beyond exome reach. The strongest option for complex cases.
Quickly surface the most clinically relevant variants with AI-powered prioritizationbuilt for medical geneticists and diagnostic labs.
Compare coverage, sample types, strengths,and best-use scenarios to choose the most suitable option for your patient.