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Whole Genome

Sequence once. Benefit for life.

Whole genome sequencing reads ~30x across nearly all of your DNA. From one simple home sample you get your raw data file, a clear report, and free re-reading for life as the science grows.

Whole genome (~30x) ~4 weeks Counseling available Encrypted & private
Who it's for

Built for people who want to get ahead.

People who want the most complete picture of their DNA

Those who value owning their raw genomic data

Anyone planning for decades of health insight

Why it helps

The problems it helps you solve.

Honest about what genetics can and can't do, focused on where it genuinely moves the needle.

01

Tests that expire

Targeted tests answer one question. A whole genome answers questions you haven't asked yet.

02

Re-testing later

Sequence once. As research advances, we re-read the same data, no new sample needed.

03

Owning your data

Your encrypted raw genome is yours, with clear control over access and deletion.

What you'll learn

Insight you can actually act on.

Inherited risk across heart, metabolic, medication and more

Carrier status for family planning

Your complete medication-response profile

Free re-reading as the science grows

In your report

Whole genome (~30x) analysed for you

A clear High, Moderate or Average risk score

Clinically validated risk models

A doctor-ready PDF and a plain-language plan

Benefits

Why it's worth doing now.

The outcomes that matter, not the science for its own sake.

See it early

Understand inherited risk years before symptoms, when prevention works best.

A plan that fits you

Turn results into specific, personal next steps, not generic advice.

Decide with your doctor

Guideline-backed findings you can share at your next appointment.

Insight for life

Your DNA doesn't change, so your report keeps paying off as science grows.

How it works

From order to insight, in four steps.

01

Order your test

Choose what you want to learn online in minutes. We ship a simple kit to your door.

02

Give a sample

A quick, painless sample at home. Seal it and mail it back in the prepaid kit.

03

Receive insights

Your encrypted, plain-language report lands in your secure dashboard in a few weeks.

04

Take action

A clear, personal plan you can act on, and share with your doctor when it counts.

Your result

A clear number, not a maybe.

Your report places you in one of three genetic-risk bands, with what each means and what to do next.

Risk band

Average

Inherited risk in line with the general population. Stay on top of the basics and re-check as the science grows.

Risk band

Moderate

A meaningful genetic tilt. Small, specific changes now compound into a very different decade ahead.

Risk band

High

A strong inherited signal. The best time to act is well before any symptom appears.

Pricing
₹54,999one-time

Includes your full Whole Genome Sequencing report, a personal action plan, and a secure dashboard for life.

What's included

  • Your Whole Genome Sequencing testClinical-grade DNA analysis
  • Home sample pickup & dropA trained phlebotomist comes to you
  • A plain-language reportYour result, with a personal action plan
  • A free doctor consultationWalk through your result with a doctor, on us
A Meridian doctor
Included free

A free consultation with a doctor.

Your result is never just a number. A qualified doctor walks you through what it means for you and your next steps, at no extra cost.

30-minute session One-on-one No extra cost
Questions

Good to know.

A home sample collection, ~30x whole genome sequencing, your downloadable raw data file (VCF), a plain-language report, and free re-reading for life. About four weeks after your sample reaches the lab, your data is ready.

Have questions before you decide?

Book a free 15-minute call with the team and we'll answer them, no pressure, so you can order with confidence.

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Your DNA won't change.
The decisions you make can.

The most personalized health plan you'll ever have is already inside you. Explore the tests and turn it into a longer, healthier life.