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MatchMyGenome Premium

MatchMyGenome Premium
In Stock

This is Mapmygenome’s advanced couple carrier screening test.

Ideal for preconception screening, MatchMyGenome can be used to determine the carrier status of common recessive genetic disorders in both the partners to estimate the risk of disease in their future children. Reporting is as per guidelines set down by the American College of Medical Genetics (ACMG), and the report is supplemented with pre-test and post-test genetic counselling to further the value of the test for the customer.

Over 2000+ genes associated with known autosomal recessive and X-linked recessive diseases can be analyzed for comprehensive carrier screening.

Apart from the customers, this test also empowers health practitioners to be able to provide suitable reproductive counseling and options.

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Features of MatchMyGenome Premium:

Technology: Next Generation Sequencing (Illumina Hiseq), average coverage of 70-100x, minimum depth of 10x. All OMIM genes and clinically relevant genes are covered.

Sample type: EDTA blood (2 ml per partner) or purified genomic DNA or dried blood spots (on filter card)

Turnaround Time: 8-10 weeks

Flexible analysis and reporting for any significant family history of mendelian diseases.

Can also include personal risk profile for non-mendelian / complex diseases based on family history (eg: Cleft lip and palate, autism spectrum disorders etc)

Illumina Hiseq with Illumina Novaseq.

Access to your genetic data at no additional cost.

Free pre-test and post-test genetic counseling sessions with board certified genetic counselors.

"Additional reporting on specific conditions in either partner's clinical history"

Call : 1800-102-4595 write to : info@mapmygenome.in
Toll Free Number 1800-102-4595 | Email info@mapmygenome.in | © 2018 Mapmygenome™ - Know Yourself
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