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Whole Genome Sequencing

Whole Genome Sequencing
In Stock

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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Reviews & Comments

★★★★★
★★★★★

K Ganapathi

Outstanding service. I have a family history of multiple cancers and was extremely concerned. I got our entire family to get this done to see which mutations were passed on and not. The counseling was fabulous and the recommendations she gave were shared with our oncologist. The oncologist liked the recommendations report and the whole genome report.

For fun I also wanted to get all the data and I got it - It is massive.

Avijit

I had already done a Genomepatri earlier as I am very happy with Mapmygenome's service. I decide to go for a Whole Genome Sequencing as this was the ultimate test.
The pricing was very competitive and the whole process took between 7-8 weeks to get the report, counseling an a action plan.

I liked the regular updates they keep sending me.

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  • Next Generation Sequencing on Illumina Novaseq

  • 95-98% of the entire genome sequenced, with 30x depth

  • Variant identification for rare diseases, congenital defects, inherited/hereditary syndromes, cancer diagnosis, neuromuscular disorders, metabolic disease, epilepsy, ASDs, neuropathy, etc

  • Reporting as per ACMG and ACOG guidelines

  • Predictive tests (Genomepatri/MyFitGene/MedicaMap) feasible on whole genome data (as per client request)

  • Expert counseling provided after the delivery of the report

  • 2 ml Blood (EDTA) sample (or) 1 ug purified genomic DNA (or) 10 dried blood spots required

  • Turnaround time of 8-10 weeks

  • Final deliverables include Clinical report with diagnostic findings, as per client profile or physician/counsellor indications. Raw data available on request.

Call : 1800-102-4595 write to : info@mapmygenome.in
Toll Free Number 1800-102-4595 | Email info@mapmygenome.in | © 2019 Mapmygenome™ - Know Yourself
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