Choose a service
Select one of the available genetic testing services to view its explanation, sample requirements, clinical use, and next steps.
Whole Exome Sequencing (WES)
Whole Exome Sequencing (WES) is an advanced genetic test that analyzes the protein-coding regions of the genome to help investigate unexplained symptoms, rare diseases,...
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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...
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Single Gene Sequencing
Single Gene Sequencing focuses on analyzing a specific gene when clinical findings strongly suggest a particular inherited condition.
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Specific Panels
Specific Panels analyze a selected group of genes associated with a particular disease, symptom, or clinical specialty, providing a focused and efficient testing approach.
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Familial Variant Test
Familial Variant Testing helps determine whether relatives carry a previously identified genetic variant that has already been detected within the family.
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Reproductive Carrier Screening
Reproductive Carrier Screening helps identify whether prospective parents carry genetic variants associated with inherited conditions that could be passed to their children.
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Cancer Carrier Screen Test
Cancer Carrier Screening helps identify inherited genetic variants associated with an increased risk of developing certain types of cancer.
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Proactive Carrier Screen Test
Proactive Carrier Screening helps healthy individuals identify inherited genetic risks before symptoms appear, supporting informed healthcare and family planning decisions.
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Sample Collection Coordination
Mass Diagnostics provides sample collection coordination and logistics support to help patients and physicians access advanced genetic testing services through trusted international laboratory partners.
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