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A new standard in predictive, preventive, and personalized medicine.

Unlock the potential of your genome for a healthier future.

Our targeted genomic health insights can empower you to make informed decisions.

🔍 25% Silent Carriers

25% of individuals are silent carriers of mutations that cause serious diseases. Don’t let your health be a mystery.

👶 Impact on Births

At 25 million births p.a., we can reduce disease burden by up to 250,000 annually through genomic sequencing while planning families.

🎗️ Cancer Risk

2-3% of healthy individuals carry mutations that significantly increase their lifetime cancer risk. Be proactive with your health.

❤️ Heart Conditions

1 in 500 individuals are at risk for various heart conditions due to genetic mutations. Know your risk and take action.

Take Charge of Your Health Today!

With LifeGenomics Whole Exome Sequencing, gain targeted insights tailored to your genetic profile. Make informed decisions about your health and future.

Your Test Journey

1. Book the Test

Schedule your test via our website, scan the QR code, or call +1 (800) 123-4567.

2. Sample Collection

Our professional team will collect your sample at a convenient time and place.

3. Testing

The sample will be processed in our advanced lab for precise results.

4. Receive Your Report

Get your detailed report with personalized health insights online or by mail.

Why Choose LifeGenomics

Why Choose LifeGenomics Whole Exome Sequencing?

Our comprehensive sequencing service identifies genetic variations that may impact your health. Here’s how we can help you:

Identify Cardiovascular Risks

We will identify genetic factors that influence your risk for heart disease, including arrhythmias and cardiomyopathies.

Assess Cancer Risk

We will assess mutations related to hereditary cancers, such as BRCA1/BRCA2, to inform your health decisions.

Analyze Metabolic Health

We will analyze your genetic predispositions to conditions like diabetes and obesity, guiding your wellness strategies.

Investigate Neurological Conditions

We will investigate genetic causes of neurological diseases, such as Alzheimer’s and Parkinson’s, to provide insights for proactive care.

Tailor Pharmacogenomics

We will tailor your medication plan based on how your genetics affect your response to treatments, ensuring effective care.

Explore your unique genetic profile with LifeGenomics today!

The whole exome consists of all protein-coding regions of the genome, which make up about 1-2% of your DNA but are responsible for about 85% of known disease-related genetic variants.

One of a kind genomic test in India to provide valuable insights into an individual’s health.
Next Generation Sequencing (NGS) technology and proprietary bioinformatics tools are used to extract genetic information.
A large panel DNA Sequencing effort with results for scientifically curated and ACMG approved gene lists (over 250+ disorders) delivered over an easy-to-use software interface.

LifeGenomics