Latest news with #NIPT
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Business Standard
a day ago
- Health
- Business Standard
Genomic testing sees sharp uptake in India, now growing beyond metros
With 18 per cent CAGR, India's genomic diagnostics market is expanding into Tier 2 and 3 cities as affordability, cancer screening, and personalised care fuel adoption Anjali Singh Mumbai Demand for genomic testing in India has surged significantly over the past two to three years, fuelled by growing clinical awareness, rapid technological advancements and the rising adoption of personalised medicine. From being a niche service concentrated in major metros, genomic diagnostics are now expanding into Tier 2 and Tier 3 cities, reshaping the landscape of preventive and precision healthcare. The Indian genomic diagnostics market is valued at $550 million in 2024 and is projected to grow at a compound annual growth rate (CAGR) of 18 per cent, reaching $2,066.31 million by 2030, according to industry estimates. Key drivers include wider physician adoption, declining test prices, improved accessibility and a shift in consumer behaviour towards proactive and personalised healthcare. Diagnostic majors such as Agilus Diagnostics, Metropolis Healthcare, Dr Lal PathLabs, Mahajan Imaging and Labs, and Redcliffe Labs report double-digit growth in the segment. While metros like Mumbai, Bengaluru and Delhi still contribute the lion's share, growing awareness and infrastructure in cities like Lucknow, Bhubaneswar, Pune, Kochi and Surat are driving demand beyond urban hubs. Test affordability has improved substantially. Prices for routine genomic tests—like BRCA1/2 (used to analyse a person's DNA to identify mutations in genes that increase the risk of breast and ovarian cancer) and NIPT (non-invasive prenatal testing, a blood test performed on pregnant women to assess the risk of certain genetic conditions in the foetus)—have come down by 30–40 per cent, now ranging between Rs 5,000 and Rs 20,000, depending on complexity. While advanced oncology panels and exome sequencing can still cost up to Rs 2 lakh, widespread adoption of high-throughput platforms and in-house test development has made even complex testing more accessible. Experts believe that although demand for genomic testing is rising across multiple segments, increasing cancer incidence and a countrywide focus on cancer detection and reproductive health have been key growth drivers. 'The rapid increase in demand for cancer tests, along with paediatric and reproductive health applications like prenatal testing and carrier testing, are major contributing factors driving growth in genetic testing. The country is also witnessing a rise in testing for rare genetic diseases, driven by India's huge genetic diversity,' said Nilaya Varma, group chief executive officer and co-founder, Primus Partners. 'Genomic testing now contributes 5–7 per cent of our total diagnostics revenue, up from under 2 per cent three years ago,' said Anand K, managing director and chief executive officer, Agilus Diagnostics. Redcliffe Labs pegs this number even higher, at 30–40 per cent, with consistent 20 per cent year-on-year growth in test volumes. 'We've seen a dramatic rise in genomic testing demand over the past five years, especially in oncology, rare diseases and reproductive health. What's encouraging is that Tier 2 and 3 cities like Lucknow, Bhubaneswar and Coimbatore are now actively adopting these tests,' said Himani Pandey, lab head – genomics, Redcliffe Labs. Metropolis Healthcare, which entered the genomics space three years ago, has seen over 50 per cent revenue growth in the segment and plans further expansion through investments in bioinformatics and next-generation sequencing (NGS) platforms. 'We've seen over 50 per cent revenue growth in genomics since our entry into the space three years ago. Genomic testing is increasingly being integrated into routine health check-ups, cancer diagnostics, rare disease screening and personalised treatment planning. We are investing heavily in bioinformatics and NGS platforms to scale further,' said Kirti Chadha, chief scientific and innovation officer, Metropolis Healthcare. Similarly, Dr Lal PathLabs, through its genomics division Genevolve, has launched over 500 tests covering oncogenomics, neurogenomics, rare disease panels and reproductive health. 'With Illumina's NovaSeq X platform at our national reference lab and a focused genomics sales team, we're bringing cutting-edge testing to both metros and smaller towns,' said Shankha Banerjee, chief executive officer, Dr Lal PathLabs. While margins on genomic tests can vary—and in many cases remain lower than routine diagnostics due to high input costs and low volumes—players see genomics as a long-term strategic bet. 'It's not just about margins—it's about clinical value and helping doctors make better treatment decisions,' said Shelly Mahajan, lab director at Mahajan Imaging. A common thread across players is the push for in-house development and Indian population–specific panels, often coupled with global partnerships for specialised tests. Most labs are also investing in AI-driven bioinformatics, advanced molecular labs and automation to enhance scalability. Yet, challenges remain. Despite cost reductions, insurance coverage for genomic tests in India is still extremely limited, creating affordability barriers for patients in lower-income segments. Industry leaders stress that broader insurance inclusion could accelerate adoption, particularly for cancer, rare diseases and reproductive health-related tests. Nonetheless, the momentum is clear: Genomic testing is no longer a fringe offering. With its ability to provide deep molecular insights for early diagnosis, targeted therapy and risk prediction, it is fast becoming a core pillar in India's diagnostics growth strategy.
Zawya
17-06-2025
- Business
- Zawya
Gulf Scientific Corporation announces strategic partnership with GeneMind Biosciences
DUBAI, United Arab Emirates: Gulf Scientific Corporation (GSC), a leading provider of scientific and laboratory solutions, is pleased to announce a strategic partnership with GeneMind Biosciences, a pioneering developer of DNA sequencing systems. This alliance marks a significant milestone in our ongoing commitment to delivering innovative healthcare solutions and advancing molecular diagnostics. Founded with a focus on research and development, GeneMind Biosciences is a key player in the development of high-performance DNA sequencers - core instruments of modern molecular diagnostics. The company is committed to building a comprehensive precision medical ecosystem by collaborating with genetic testing service providers and medical institutions worldwide. This partnership with GSC represents a shared vision to enhance diagnostic capabilities, support cutting-edge scientific research, and ultimately improve patient outcomes. By combining GSC's extensive network and expertise with GeneMind's innovative sequencing technology, we aim to drive forward the future of healthcare through advanced molecular diagnostics, including non-invasive prenatal testing (NIPT). GSC is proud to represent GeneMind Biosciences in the UAE, Kuwait, Oman, Bahrain, and Qatar, bringing their groundbreaking NIPT technology to healthcare providers and patients across these markets. GeneMind's cutting-edge NIPT technology allows for early and accurate detection of fetal chromosomal abnormalities, reducing the risk of miscarriage and improving pregnancy outcomes. This technology has the potential to revolutionize prenatal care and improve the lives of expectant mothers. "We are excited to collaborate with GeneMind Biosciences, whose innovative DNA sequencing solutions align perfectly with our mission to empower healthcare providers to achieve their scientific objectives by providing innovative and reliable solutions, application support, and comprehensive after-sales services," stated Manaf Afyouni, Managing Director of Gulf Scientific Corporation. "Our partnership will enable us to bring cutting-edge NIPT technology to the region, enhancing prenatal care and improving patient outcomes." As part of this strategic partnership, GSC will be providing comprehensive support and services to healthcare professionals within the region. This collaboration will also facilitate the development of new research initiatives and projects focused on advancing molecular diagnostics and NIPT. We look forward to sharing updates on the groundbreaking initiatives and projects that will result from this strategic partnership. For more information about Gulf Scientific Corporation and our solutions, including GeneMind's NIPT technology, please visit Source: AETOSWire Contact details: Manaf Afyouni Email: marketing@ Website:
Web Release
17-06-2025
- Business
- Web Release
Gulf Scientific Corporation announces strategic partnership with GeneMind Biosciences to advance molecular diagnostics and pioneer non-invasive prenatal testing (NIPT)
Gulf Scientific Corporation (GSC), a leading provider of scientific and laboratory solutions, is pleased to announce a strategic partnership with GeneMind Biosciences, a pioneering developer of DNA sequencing systems. This alliance marks a significant milestone in our ongoing commitment to delivering innovative healthcare solutions and advancing molecular diagnostics. Founded with a focus on research and development, GeneMind Biosciences is a key player in the development of high-performance DNA sequencers – core instruments of modern molecular diagnostics. The company is committed to building a comprehensive precision medical ecosystem by collaborating with genetic testing service providers and medical institutions worldwide. This partnership with GSC represents a shared vision to enhance diagnostic capabilities, support cutting-edge scientific research, and ultimately improve patient outcomes. By combining GSC's extensive network and expertise with GeneMind's innovative sequencing technology, we aim to drive forward the future of healthcare through advanced molecular diagnostics, including non-invasive prenatal testing (NIPT). GSC is proud to represent GeneMind Biosciences in the UAE, Kuwait, Oman, Bahrain, and Qatar, bringing their groundbreaking NIPT technology to healthcare providers and patients across these markets. GeneMind's cutting-edge NIPT technology allows for early and accurate detection of fetal chromosomal abnormalities, reducing the risk of miscarriage and improving pregnancy outcomes. This technology has the potential to revolutionize prenatal care and improve the lives of expectant mothers. 'We are excited to collaborate with GeneMind Biosciences, whose innovative DNA sequencing solutions align perfectly with our mission to empower healthcare providers to achieve their scientific objectives by providing innovative and reliable solutions, application support, and comprehensive after-sales services,' stated Manaf Afyouni, Managing Director of Gulf Scientific Corporation. 'Our partnership will enable us to bring cutting-edge NIPT technology to the region, enhancing prenatal care and improving patient outcomes.' As part of this strategic partnership, GSC will be providing comprehensive support and services to healthcare professionals within the region. This collaboration will also facilitate the development of new research initiatives and projects focused on advancing molecular diagnostics and NIPT. We look forward to sharing updates on the groundbreaking initiatives and projects that will result from this strategic partnership. For more information about Gulf Scientific Corporation and our solutions, including GeneMind's NIPT technology, please visit Source: AETOSWire
Hans India
14-06-2025
- Health
- Hans India
Fatherhood redefined: Strength, sensitivity, and science
Fatherhood is evolving. Today, more men are stepping beyond the traditional roles of provider or protector to become deeply involved in the emotional and physical well-being of their families. From hands-on parenting to supporting their partners, modern men are redefining what it means to be a father – active, nurturing, and fully engaged in the journey of raising a family. As fathers take on more holistic roles in parenting, there's also a growing recognition of the importance of understanding family health history and genetics to ensure their family's well-being. Each of us inherits half of our genes from each parent, creating a unique genetic blueprint that not only shapes our physical traits, behaviors, and health conditions but also influences what we pass on to the next generation. With rising awareness of inherited health conditions and the importance of early intervention, many are now taking steps that were once considered to be solely in the domain of maternal healthcare. From preconception planning to active co-parenting and prenatal support to taking proactive measures for their own health, this Father's Day, let us look at the ways men are actively participating in the parenthood journey to help ensure a healthier future for their families. Fatherhood and Family Health Traditionally, pregnancy and childcare have been associated with women in most Indian families. However, with rising awareness around inherited diseases and greater access to genetic counseling and testing, men are increasingly stepping into more active roles, particularly during the preconception and prenatal stages. Genetic tests offer valuable insights not only into an individual's health but also into potential hereditary risks for children inheriting health conditions from their parents. Role of the Father in the Pregnancy Journey Planning for pregnancy A simple blood test for couples planning to have children can reveal if they are both carriers of the same condition and their offspring are at risk of inheriting it. Some conditions may not show symptoms, but identifying whether an individual carries genetic mutations for specific inherited disorders such as thalassemia, spinal muscular atrophy (SMA), or cystic fibrosis helps couples make informed decisions about potential use of prenatal testing or other reproductive options. Carrier screening can help prevent or manage the potential emotional and financial challenges for the family. Supporting and Making Informed Pregnancy Decisions Understanding and actively supporting screenings during the pregnancy journey is a vital part of being a supportive partner and an involved expectant father. Encouraging and supporting Non-Invasive Prenatal Testing (NIPT), which screens common chromosomal abnormalities early in pregnancy, ensures better management of a child's genetic health and early intervention wherever possible. Fathers can help in making thoughtful, evidence-based decisions during this critical stage, laying the foundation for a healthier future for both the child and the family. Understanding and Managing Own Health Men with a family history of chronic conditions such as cancer, cardiovascular disease, or diabetes can undergo genetic predisposition tests that provide insights into inherited risks of developing these conditions. These insights can empower individuals to take proactive steps through targeted lifestyle changes and personalized medical interventions. Taking charge of their own health fosters a culture of preventive care and informed decision-making regarding the health and well-being of the entire family. Driving the Cultural Shift Becoming more aware of the early health options available today is not just a medical decision, but a reflection of proactive fatherhood. It signifies foresight, accountability, and care. In this journey, genetic counselors play a critical role in guiding individuals and couples through these tests, interpreting results, and offering next steps in line with their goals. This Father's Day, let's celebrate not just the role, but the responsibility of fatherhood – one that's informed, involved, and inspired by science. (The writer is a, Senior Director, Lab Operations, MedGenome)
Economist
11-06-2025
- Health
- Economist
A routine test for fetal abnormalities could improve a mother's health
WHEN NON-INVASIVE prenatal testing (NIPT) arrived in 2011, it transformed pregnancy. With a simple blood test, scientists could now sweep a mother's bloodstream for scraps of placental DNA, uncovering fetal genetic defects and shedding light on the health of the unborn baby. But the potential to monitor the mother's health went largely unappreciated.
