Description

30× 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, inherited, or undiagnosed conditions.

Unlike targeted genetic tests, WGS evaluates genetic variation across coding and non-coding regions, providing a broad view of an individual’s DNA to support clinical evaluation, diagnosis, and decision-making.

For Comprehensive Genetic Analysis

30× WGS provides genome-wide sequencing coverage and can identify a broad range of genetic variants that may not be captured by targeted genetic testing.

Analyzes coding, non-coding, intronic, regulatory, and intergenic regions
Detects SNVs and small insertions/deletions
Provides genomic information for rare, complex, atypical, or previously undiagnosed conditions
Supports evaluation of inherited genetic variants across the genome
Enables future reanalysis as new genes, variants, and scientific knowledge become available
Why 30× WGS?

With approximately 30× average sequencing depth, the test provides high-quality genome-wide sequencing data suitable for comprehensive assessment of genetic variation.

30× WGS offers a practical balance between broad genomic coverage and sequencing depth, making it suitable for many applications where a comprehensive assessment of the genome is desired.