Service Profile

Genetic Testing Service

Whole Genome Sequencing (WGS)

Whole Genome Sequencing (WGS) analyzes nearly all genetic material to provide a comprehensive view of the genome for complex diagnostic investigations and unresolved medical cases.

Simple Explanation

What this service helps with

Whole Genome Sequencing (WGS) analyzes nearly all genetic material to provide a comprehensive view of the genome for complex diagnostic investigations and unresolved medical cases.

Clinical Use

How it supports the diagnostic journey

WGS may help identify genetic variants across the genome, supporting diagnosis, rare disease investigations, and clinical decision-making in complex cases.
More Details

Additional information

Whole Genome Sequencing (WGS) is one of the most comprehensive genetic testing approaches available today. Unlike targeted tests that focus on specific genes or selected regions, WGS examines nearly the entire genome, providing a broader view of genetic variation that may contribute to disease.

WGS may be considered in complex diagnostic situations where previous investigations have not provided clear answers, or when physicians require a more complete genomic assessment. By analyzing coding and non-coding regions of DNA, WGS can help identify genetic variants that may be associated with inherited disorders, rare diseases, neurological conditions, and other unexplained clinical presentations.

At Mass Diagnostics, WGS testing is coordinated through trusted international partner laboratories, with support for test selection, sample collection, logistics, and report delivery. Our goal is to help patients and physicians access advanced genomic technologies while maintaining clarity throughout the testing journey.

Need help with Whole Genome Sequencing (WGS)?

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