DNA Test | Whole Exome Sequencing - WES
Mapmygenome now offers Whole Exome 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.
Genetic counseling | Physician support
- In order to be HIPPA compliant and in order to protect YOU, we require a doctor's/physician's summary or a genetic counseling session before purchase
- You can either book a session with MapMyGenome directly, or choose to see your own genetic counselor or doctor before ordering this test
- Before sending you the test kit, we'll request a copy of the report or proof of the session
MY DNA CHOICES. likes
- The most genetic information available in one test
- Ideal for understanding complex conditions
Benefits | Features
- Primary Genotype Report
- Personalised Genetic Counseling session (~45 mins)
- Recommendations and guidelines from our counselor or a genetic counselor of your choice
- Next Generation Sequencing on Illumina Novaseq
- ~23000 genes sequenced at 70-100x average coverage
- 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
- 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.
- TRIO package available - exome analysis for the affected individual (proband) and two family members
*Large deletions/duplications, copy number variations, and mt-DNA analysis are beyond the scope of this test.
Why is Whole Exome Sequencing right for you?
- Thousands of genetic variants are uncovered every day - extensive coverage and mapping with reference databases is a key part of our analysis
- Sanger confirmation of pathogenic variants and extended clinical reports are available as an add-on package
- Ideal for targeted management of complex syndromes, epilepsy, ASDs, neuropathy, heterogenous phenotypes
- Expert counseling provided after the delivery of the report or you can select your own practitioner
Benefits | Features - The Science behind this test
Platform: Next Generation Sequencing (Illumina HiSeq)
1 ug purified genomic sample ( i.e. 2 x Buccal swab)