Mapmygenome now offers Whole Genome Sequencing as a complete solution to healthcare providers, patients and researchers alike. With high-precision reporting, detailed interpretation and easy-to-read clinical reports, this service empowers you to make the right decisions for diagnosis and/or treatment. Whole genome data can be used for clinical interpretation, genetic diagnosis, predictive screening, disease risk assessment, nutrigenomics and pharmacogenomics (drug response) profile.
This includes: -
- Clinical report for genetic diagnosis
- Predictive screening tests (Genomepatri/MyFitGene/MedicaMap) as per client request
- Personalised Genetic Counseling session (~45 mins)
- Recommendations and guidelines from our counsellor. This may include other screening tests if any.
A physician's summary or a genetic counseling session is strongly recommended, to enable accurate analysis and interpretation.
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