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Whole Genome Sequencing

Whole Genome Sequencing
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Mapmygenome now offers Whole Genome Sequencing to aid the practice of 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.

This includes:
- Primary Genotype Report
- Personalised Genetic Counseling session (~45 mins)
- Recommendations and guidelines from our counselor. This may include other screening tests if any.
A physician's summary or a genetic counseling session is necessary before purchase.


$ 1799

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Why WGS is right for you:

  • Extensive coverage- this is bigger than the exome! Covers 95% to 98% of the genome, instead of just exonic (coding) regions.

  • WGS offers more comprehensive view of your entire genome, with longer reads and better detection of CNVs

  • Sanger confirmation of pathogenic variants and extended clinical reports are available as an add-on package.

  • Expert counseling provided after the delivery of the report


  • Platform: Next Generation Sequencing (Illumina HiSeq)

  • Coverage: 30X

  • Sample type: 2 ml Blood (EDTA) (or) 1 ug purified genomic DNA

  • TAT: 10 weeks

  • Deliverables: Clinical report with diagnostic findings, as per client/physician's indications. Variants file available on request.

Call : 1800-102-4595 write to :
Toll Free Number 1800-102-4595 | Email | © 2019 Mapmygenome™ - Know Yourself
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