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Whole genome

What Is Whole Genome Sequencing? A Simple Explainer (India)

Whole genome sequencing (WGS) reads nearly all your DNA in one test. Here's what it is, how it works, what it reveals, and what it costs in India, in plain English.

The Meridian Clinical Team Medically reviewed by Meridian Medical Review Board 3 min readUpdated 6 July 2026

Whole genome sequencing (WGS) is a test that reads nearly all 3 billion "letters" of your DNA in one go, the entire genetic instruction manual for your body. Unlike cheaper DNA kits that only check a few pre-selected spots, WGS reads the whole thing, so it can estimate your inherited risk for many diseases and be re-analysed for years as science advances.

What is whole genome sequencing?

Think of your DNA as a book written in four letters, A, C, G, and T, running to about 3 billion characters. Small spelling differences, called variants, influence your health. Whole genome sequencing reads essentially the entire book, cover to cover, rather than flipping to a few bookmarked pages. That's the core idea in one sentence.

How does it work?

The process is simpler than it sounds:

  1. Sample. You give a blood or saliva sample; your DNA is extracted from it.
  2. Sequencing. A machine chemically "reads" the order of the letters, covering each stretch of your genome multiple times for accuracy.
  3. Analysis. Software compares your sequence to reference databases and flags meaningful variants.
  4. Interpretation. A doctor explains what those variants mean for your health, the step that turns data into decisions.

What can it detect?

  • Common-disease risk. Your inherited tendency toward heart disease, type 2 diabetes, high blood pressure, and some cancers, expressed as a polygenic risk score.
  • Carrier status. Whether you silently carry recessive conditions relevant to family planning.
  • Medication response. How you metabolise certain common drugs.
  • Rare variants. Well-established single-gene findings a microarray would miss.

Crucially, WGS reports risk and tendency, never a diagnosis or a certainty. A high score is a reason to prevent early, not a prediction that you will get a disease.

WGS vs a consumer DNA kit

Consumer DNA kitWhole genome sequencing
Genome read~600k common variants (<0.1%)~98–100% of genome
Finds rare/novel variantsNoYes
Re-analysable in futureLimitedYes
Doctor includedUsually noYes (with clinical providers)

This is why "I did a DNA test" can mean wildly different things. For a fuller comparison, see our whole genome sequencing guide.

Why sequence once and keep the data

Your DNA doesn't change over your lifetime. So a single high-quality WGS becomes a resource you revisit: as researchers discover new gene-disease links, your existing data can be re-analysed without a new sample. You sequence once and benefit for years.

What it costs in India

Clinical-grade whole genome sequencing in India typically costs around ₹54,999, more than a consumer kit because it reads vastly more of your genome and includes accredited lab work and a doctor's interpretation. Our WGS cost in India guide breaks down exactly what you're paying for.

At Meridian, a whole genome test is ~₹54,999, run at a CAP-grade accredited partner lab, with reports in about 14 working days and a free doctor consultation included.

The bottom line

Whole genome sequencing reads nearly your entire genetic code in one test, revealing inherited risks that narrow DNA kits simply can't see. It's a broad, future-proof baseline, and, interpreted with a doctor, a practical way to act on your risks early rather than late.

This article is for education, not medical diagnosis. Genetic results describe risk and tendencies, not certainty. Always discuss testing and results with a qualified doctor.

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Frequently asked questions

Whole genome sequencing reads almost all 3 billion letters of your DNA in a single test. Instead of checking a few pre-chosen spots like cheaper DNA kits, it reads the whole instruction manual, so it can be analysed for many health questions now and in the future.

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