The Science Behind HEALTHSTRING

Precision Genomics.
Designed for Human Diversity.

We combine next-generation DNA sequencing with proprietary AI-driven interpretation to deliver clinical-grade, population-agnostic genetic insights.

18+Years of Genomics Expertise
94.89%Clinical Sensitivity
100%Privacy Protection
Trusted technology. Clinically grounded insights.
Designed for diverse populations, including India.
01
Deep, Clinically Relevant DNA Sequencing

Comprehensive exome sequencing enriched with mitochondrial DNA and curated non-coding markers, covering the most clinically relevant regions of the genome.

  • >99% Coverage of genes
  • Detection of rare, actionable mutations
  • Built on Illumina sequencing

Why it matters: Focus on what's clinically relevant — without unnecessary noise.

02
AI-Powered, Population-Agnostic Interpretation

Our proprietary ML engine ensures accurate results across ethnicities.

  • 94.89% sensitivity in detection
  • Unbiased ACMG classification
  • Prioritises clinically meaningful findings

Why it matters: Most tests are less accurate outside Western populations. This isn't.

03
From Data to Clinical Insight

The reports are designed to drive preventive and clear clinical actions.

  • Evidence backed genetic findings
  • Clinically interpretable reports
  • Enables early detection and preventive, precision care

Why it matters: Not just data — clear guidance you and your doctor can rely on.

The Future of Healthcare Starts From Your DNA.

Genetic diseases are often progressive and can be worsened by lifestyle or environmental factors. The future of healthcare lies in the ability to detect diseases at the DNA level, enabling targeted surveillance, preventive measures, and precise clinical intervention.

Genetic risk awareness enables proactive and preventive healthcare.
DNA based diagnosis can help in precision treatment of many diseases.
Genetic insights can help identify medications best suited to you.
DNA screening can help prevent inherited diseases in children.
What We Cover

HEALTHSTRING analyses genetic factors associated with over 6,000 health conditions, including cancers, heart diseases, and many others.

Blood Disorders
Bone Disorders
Cancers
Complex Genetic Diseases
Connective Tissue Disorders
Developmental Delays
Digestive System Diseases
Hearing Disorders
Heart Diseases
Hormonal Disorders
Immune System Disorders
Blood Disorders
Bone Disorders
Cancers
Complex Genetic Diseases
Connective Tissue Disorders
Developmental Delays
Digestive System Diseases
Hearing Disorders
Heart Diseases
Hormonal Disorders
Immune System Disorders
Blood Disorders
Bone Disorders
Cancers
Complex Genetic Diseases
Connective Tissue Disorders
Developmental Delays
Digestive System Diseases
Hearing Disorders
Heart Diseases
Hormonal Disorders
Immune System Disorders
Joint Disorders
Kidney Disorders
Liver Disorders
Metabolic Disorders
Muscular Diseases
Neurological Diseases
Reproductive Disorders
Respiratory Diseases
Skin and Hair Disorders
Vision Disorders
Joint Disorders
Kidney Disorders
Liver Disorders
Metabolic Disorders
Muscular Diseases
Neurological Diseases
Reproductive Disorders
Respiratory Diseases
Skin and Hair Disorders
Vision Disorders
Joint Disorders
Kidney Disorders
Liver Disorders
Metabolic Disorders
Muscular Diseases
Neurological Diseases
Reproductive Disorders
Respiratory Diseases
Skin and Hair Disorders
Vision Disorders
100 Hereditary Cancers

HEALTHSTRING analyses over 800 cancer-causing genes and their mutations, offering the most comprehensive preventive cancer screening available globally. Covers organs including Breast, Lung, Blood, Thyroid, Stomach, Ovary, Prostate, Liver, Brain, Pancreas, Skin, Kidney, Colon, and more. Conditions include Lynch Syndrome, Li-Fraumeni Syndrome, Hereditary Breast-Ovarian Cancer, Hereditary Colorectal Cancer, Von Hippel-Lindau Syndrome, Retinoblastoma, and 94 more.

Choose the Right Medication. Personalised From Your DNA.

Your genes determine how your body metabolises drugs. The same dose that heals one person can cause serious harm to another. Healthstring screens across every major prescribing category.

Personalise your medication plan
Reduce risk of side effects
Improve treatment effectiveness
58
drugs
Oncology
47
drugs
Cardiology
40
drugs
Neurology
157
drugs
Other

We adhere to international guidelines, ensuring clinical accuracy.

ASCO
ACMG
NCCN
ACC
CPIC

Not all genetic tests are the same

Most consumer tests — including many you may have heard of — use SNP chip technology. They test a fixed set of pre-selected markers. For rare inherited disease mutations, they are clinically unreliable.

SNP chip tests
Most consumer DNA products
HEALTHSTRING
Whole-exome sequencing
Technology
500–2,000 fixed markers
All 20,000 protein-coding genes
Rare variant detection
Misses most
High — monogenic diseases
Sensitivity
<40% sensitivity
94.89% sensitivity
Clinical use
Not recommended
ACMG-classified findings
BMJ study, 50,000 individuals: SNP chip tests detected BRCA cancer mutations with only 34.6% sensitivity and 4.2% positive predictive value. Most dangerous variants go undetected.

Take Control of Your Health,
Before Symptoms Begin

One test. A lifetime of genetic clarity. Understand your risks, act early, and get guided support every step of the way.

No prior medical knowledge needed.

This test provides risk assessment and is not a diagnostic tool.
Please consult a qualified healthcare professional for medical decisions.