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Whole Genome Sequencing

Regular price
Rs. 89,000.00
Regular price
Sale price
Rs. 89,000.00
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Whole Genome Sequencing
Whole Genome Sequencing - Mapmygenome
Whole Genome Sequencing - Mapmygenome
Whole Genome Sequencing - Mapmygenome
Whole Genome Sequencing - Mapmygenome
BENEFITS +

Decodes 100% of your DNA across 3.2 billion base pairs
Clinical-grade 30x depth of coverage using Next-Generation Sequencing (NGS)
Covers hereditary disease risks, cancer screening, pharmacogenomics, carrier status, and wellness traits
NABL-accredited laboratory (MC-6120) with strict quality controls
Includes expert genetic counselling session post-report
Bank-level data encryption — your data is never shared or sold
Available with or without raw genomic data (FASTQ, BAM, VCF files)

WHAT'S INCLUDED +

Hereditary Disease Risk Panel
Hereditary Cancer Screening Panel
Pharmacogenomics (Drug Response) Panel
Carrier Screening Panel
Wellness & Traits Panel
Ancestry & Haplogroup Analysis

SAMPLE TYPE +

  • Blood
  • Saliva

TESTING TECHNIQUE +

Whole Genome Sequencing (WGS) using Illumina Next-Generation Sequencing (NGS) platforms at 30x depth of coverage. Reads all 3.2 billion base pairs across both coding (exons) and non-coding (introns) regions of the genome. Processed in an NABL-accredited genomics facility (MC-6120) under strict quality controls.

Decodes 100% of your DNA across 3.2 billion base pairs
Clinical-grade 30x depth of coverage using Next-Generation Sequencing (NGS)
Covers hereditary disease risks, cancer screening, pharmacogenomics, carrier status, and wellness traits
NABL-accredited laboratory (MC-6120) with strict quality controls
Includes expert genetic counselling session post-report
Bank-level data encryption — your data is never shared or sold
Available with or without raw genomic data (FASTQ, BAM, VCF files)

Features

  • Personalized and Actionable

  • Pan India Shipping

  • Digital Reports

  • Secure Personal Data

FAQs

Who can benefit from this test ?

Any looking for a comprehensive genomic analysis for preventive health or for accurate clinical genetic diagnosis

How do we analyze?

Whole Genome Sequencing using advanced NGS techniques at 30x coverage

How long does it take to get the report?

56 days