MedGenome

MedGenome MedGenome is a global genomics diagnostics company and home to South Asia’s largest CAP-accredited genetic testing lab.

With 1300+ tests across oncology, rare diseases, reproductive health and more, we support accurate diagnosis and better patient care. MedGenome is a global genomics and precision diagnostics company focused on enabling accurate, early and actionable diagnosis through advanced genomic science. We operate South Asia’s largest CAP-accredited genetic testing laboratory and offer a comprehensive test m

enu of more than 1,300 genetic assays across key disease areas. Our diagnostic capabilities span rare inherited disorders, oncology, reproductive health, infectious diseases and preventive wellness. By integrating next-generation sequencing technologies with proprietary assays and AI-enabled bioinformatics platforms, MedGenome delivers high-quality genomic insights that support clinicians in complex clinical decision-making. Founded with a vision to make genomic healthcare affordable and accessible, MedGenome has built deep scientific and clinical expertise backed by extensive research and global collaborations. Our work is supported by a strong research foundation with hundreds of peer-reviewed scientific publications, reflecting our commitment to evidence-based diagnostics and innovation. MedGenome serves clinicians and healthcare institutions across hundreds of locations in India and multiple countries worldwide. Our team of scientists, genome analysts, bioinformaticians and clinical experts works closely with healthcare providers to ensure test accuracy, clinical relevance and timely reporting. We are driven by a commitment to continuous innovation, quality and education. From developing in-house genomics solutions to advancing awareness around genetic testing, MedGenome plays an active role in shaping the future of precision medicine. At MedGenome, every genome decoded strengthens our mission to improve patient outcomes, support clinicians with reliable insights and transform healthcare through the power of genomics.

Read the full blog here: https://tinyurl.com/474jw627Not all patients respond to medications the same way. Pharmacogenom...
27/04/2026

Read the full blog here: https://tinyurl.com/474jw627

Not all patients respond to medications the same way. Pharmacogenomics is helping bridge this gap by enabling clinicians to tailor treatments based on an individual’s genetic profile, improving drug efficacy while minimising adverse reactions.

This blog explores how pharmacogenomics testing works, its growing role in clinical practice, and how it is advancing personalised medicine across therapeutic areas.

Discover how integrating genetics into prescribing decisions can lead to safer, more effective care.

To know more: 🌐https://tinyurl.com/5cdpseb6  📞1800 296 9696Febrile illnesses aren’t always caused by a single infection,...
25/04/2026

To know more: 🌐https://tinyurl.com/5cdpseb6 📞1800 296 9696

Febrile illnesses aren’t always caused by a single infection, and that’s where diagnosis gets complicated. With multiplex RT-PCR, it’s now possible to detect multiple pathogens, including malaria, in one test—delivering high specificity and results in as little as one working day.

Faster answers. Better clinical decisions.

25/04/2026

3 billion letters.
One unique story.
Today we celebrate the code that writes us into existence.

Celebrating the people who make it all possible!At MedGenome's Annual Felicitation Ceremony, hosted off-site in Bangalor...
22/04/2026

Celebrating the people who make it all possible!
At MedGenome's Annual Felicitation Ceremony, hosted off-site in Bangalore on 10th April, we came together to recognize the outstanding contributions of our teams.

Our Elite Awards honoured the exceptional achievements of our sales champions, with around 25 individuals recognised for their remarkable performance and impact.

Our Long Service Awards celebrated the dedication of over 100 team members who have been with us for over 7 years, an inspiring testament to their loyalty, resilience, and shared growth.

These milestones reflect not just individual success, but the collective spirit that drives us forward. Here’s to raising the bar, supporting one another, and continuing to achieve more, together.

Featured on BW Healthcare World for World Hemophilia Day: https://tinyurl.com/49bk89ejDr. Thenral S Geetha, Principal Sc...
17/04/2026

Featured on BW Healthcare World for World Hemophilia Day: https://tinyurl.com/49bk89ej

Dr. Thenral S Geetha, Principal Scientist - Inherited Disease Genomics, MedGenome, discusses the impact of delayed hemophilia diagnosis in children.

Early signs like unexplained bruising or prolonged bleeding are often overlooked, and limited awareness and access to specialised testing further contribute to this gap. Advances in genetic testing are now enabling earlier detection and more timely care.

With increased awareness and the right diagnostic support, earlier detection can significantly improve disease management and quality of life for affected children.

Featured on India TV for World Parkinson's Day: https://tinyurl.com/4ywd6s4cDr. Ramesh Menon, Director of Personal Genom...
16/04/2026

Featured on India TV for World Parkinson's Day: https://tinyurl.com/4ywd6s4c

Dr. Ramesh Menon, Director of Personal Genomics and Genomic Medicine at MedGenome, explains how genetics shapes Parkinson’s Disease (PD) risk. While family history plays a role, cases can also often result from a combination of genetic and environmental factors.

In India, an estimated 32–45% of PD cases are early-onset (

Read the full blog here: https://diagnostics.medgenome.com/blog/clonotrack-ngs-clonality-mrd-b-cell-malignancies/ Minima...
13/04/2026

Read the full blog here: https://diagnostics.medgenome.com/blog/clonotrack-ngs-clonality-mrd-b-cell-malignancies/

Minimal Residual Disease (MRD) is no longer just a research metric, it is a critical determinant of prognosis and treatment strategy in B-cell malignancies. With advancements in Next-Generation Sequencing (NGS), detecting residual disease at ultra-low levels (up to10⁻⁶ ) is now possible, enabling earlier intervention and more informed clinical decisions.

MedGenome’s ClonoTrack brings this capability to clinical practice through:

1. High-resolution clonality assessment
2. Longitudinal MRD monitoring
3. Precision-driven care across B-ALL, CLL, MM, and NHL

Explore how NGS-based MRD tracking is reshaping disease management and improving patient outcomes.

Featured in Fortune India: https://tinyurl.com/m5x4s2vtThis World Health Day 2026, we reaffirmed our commitment to scien...
08/04/2026

Featured in Fortune India: https://tinyurl.com/m5x4s2vt

This World Health Day 2026, we reaffirmed our commitment to science-led innovation in healthcare with India’s first prospective study demonstrating the clinical impact of our cost-effective RNA-based NGS in Sarcoma diagnosis.

The study highlights how integrating RNA sequencing into clinical workflows can significantly improve diagnostic accuracy and influence treatment decisions in complex sarcoma cases, marking an important step towards strengthening precision oncology in India, especially in resource-constrained settings.

You can read the study in the Journal of Global Oncology: https://ascopubs.org/doi/10.1200/GO-25-00440

As we move forward, science and collaboration will remain central to improving patient outcomes in rare and challenging cancers.

“MedGenome has always provided a healthy work-life balance and shown great understanding and support when employees face...
30/03/2026

“MedGenome has always provided a healthy work-life balance and shown great understanding and support when employees face health challenges. I’ve seen this not only in my own journey but also in the way the company stood by colleagues during difficult times.
What truly makes me stay is the way the organization recognizes individual talent and provides opportunities to grow. The trust placed in our work, combined with the opportunity to keep learning and contributing to meaningful outcomes for patients and families, keeps me deeply engaged in my role every day. The collaborative environment, empowering culture, focus on innovation, and the impact our work creates for families motivates me to see a long-term future here.”
—Sonakshi Makwana

Featured on BioSpectrum India for World TB Day: https://tinyurl.com/ya4hm24mDr Gunisha Pasricha, Associate Director - Re...
26/03/2026

Featured on BioSpectrum India for World TB Day: https://tinyurl.com/ya4hm24m

Dr Gunisha Pasricha, Associate Director - Research Services, Infectious Disease Genomics, MedGenome, shares five major advancements over the past decade that have transformed tuberculosis management, including rapid molecular testing, better treatment options for drug resistant TB, expanded screening programmes, digital surveillance, and the increasing use of genomics.

These developments are strengthening early detection, improving treatment pathways, and helping public health systems respond more effectively to one of India’s most pressing infectious disease challenges.

To know more: 🌐 https://tinyurl.com/yk9mpn5k or 📞1800 296 9696Accurate and rapid answers can change the course of TB tre...
24/03/2026

To know more: 🌐 https://tinyurl.com/yk9mpn5k or 📞1800 296 9696

Accurate and rapid answers can change the course of TB treatment.

This World TB Day, discover how SPIT SEQ, MedGenome’s NGS-based test, is advancing TB drug resistance detection with speed, accuracy, and comprehensive genomic insights.

Address

MedGenome Labs Ltd. Sy. Nos. 94/1C And 94/2, Tower 1, Ground Floor, Veerasandra Village, Attibele Hobli, Electronic City Phase-1, Electronics City
Bangalore
560100

Opening Hours

Monday 9am - 6pm
Tuesday 9am - 6pm
Wednesday 9am - 6pm
Thursday 9am - 6pm
Friday 9am - 6pm

Telephone

+9118001033691

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