Generated by All in One SEO v4.9.5.1, this is an llms.txt file, used by LLMs to index the site. # MedGenome - Leading Genetics Diagnostics Lab in India MedGenome - Leading Genetics Diagnostics Lab in India ## Sitemaps - [XML Sitemap](https://diagnostics.medgenome.com/sitemap.xml): Contains all public & indexable URLs for this website. ## Posts - [Blog](https://diagnostics.medgenome.com/blog-listing/) - Stay up-to-date on genetic diagnostics with MedGenome's blog. Uncover the latest discoveries, breakthroughs, and expert insights shaping the landscape of personalized medicine. - [World IVF Day 2026: How Genetic Testing Is Improving IVF Success Rates?](https://diagnostics.medgenome.com/blog/world-ivf-day-how-genetic-testing-is-improving-ivf-success-rates/) - World IVF Day 2026: discover how genetic testing and PGT improve IVF success rates by selecting healthy embryos, lowering miscarriage risk and guiding care. - [Explore The Role of Genetics in Neurological Disorders](https://diagnostics.medgenome.com/explore-the-role-of-genetics-in-neurological-disorders/) - [Types of Genetic Testing in the First Trimester of Pregnancy](https://diagnostics.medgenome.com/blog/first-trimester-genetic-testing-guide/) - [Everything About Chorionic Villus Sampling: A Complete Parent's Manual](https://diagnostics.medgenome.com/blog/what-is-chorionic-villus-sampling-meaning-purpose-and-accuracy/) - Chorionic villus sampling is a prenatal diagnostic test used early in pregnancy to detect chromosomal and inherited genetic conditions. - [Not ‘Cancer Survivors’ but ‘Cancer Challengers’](https://diagnostics.medgenome.com/blog/ngs-based-genetic-testing-transforming-cancer-treatment/) - NGS is transforming cancer care. See how Medgenome’s advanced sequencing enables personalized, precise treatment. Explore what’s possible today. - [When to consider the Carrier Screening Test and why it is important for new couples](https://diagnostics.medgenome.com/blog/when-to-consider-the-carrier-screening-test/) - Preconception: Ideally, carrier screening should be performed before pregnancy or during the early stages of pregnancy planning. This allows couples to fully understand their carrier status and accordingly different reproductive options can be suggested. Assisted reproductive techniques or prenatal screening: Assisted Reproductive Techniques: If both partners are carriers for the same genetic disorder, options - [Genetic Testing for Women: Understanding disease risks and the screening tests available across ages](https://diagnostics.medgenome.com/blog/genetic-testing-for-women-across-ages/) - From fertility to menopause, Medgenome provides key genetic insights tailored to every stage. Empower your health journey. Learn more. - [Spina Bifida Birth Defect](https://diagnostics.medgenome.com/blog/spina-bifida-birth-defects/) - Spina bifida can be detected early. Medgenome’s genetic screening ensures better planning. Every baby deserves a healthy start. - [Decoding NIPT: What Expectant Parents Need to Know](https://diagnostics.medgenome.com/blog/why-expectant-parents-need-nipt/) - Planning a family? Medgenome’s NIPT offers clarity without risks, even in early pregnancy. Discover safer ways to stay informed. Read more. - [5 Most Common Cancers in Men](https://diagnostics.medgenome.com/5-most-common-cancers-in-men/) - [Genetics of Lung Cancer](https://diagnostics.medgenome.com/blog/genetics-of-lung-cancer/) - Every tumor tells a story. Medgenome’s testing helps personalize lung cancer treatment. Tailor therapy with data. Explore now. - [Redefining Bloodstream Infection & amp; Sepsis Diagnosis with cfDNA Metagenomics](https://diagnostics.medgenome.com/blog/redefining-bloodstream-infection-sepsis-diagnosis-with-cfdna-metagenomics/) - [NPM1-MRD Detect: Redefining Precision Monitoring in NPM1-Mutated AML](https://diagnostics.medgenome.com/blog/npm1-mrd-detect-redefining-precision-monitoring-in-npm1-mutated-aml/) - [Genetic Screening for Breast Cancer](https://diagnostics.medgenome.com/blog/genetics-screening-breast-cancer/) - Know your BRCA and beyond. Medgenome offers cutting edge screening for early breast cancer risks. Make informed choices. Start now. - [Spinal Muscular Atrophy: Why Early Genetic Diagnosis Is Critical](https://diagnostics.medgenome.com/blog/spinal-muscular-atrophy-early-genetic-diagnosis-critical/) - [From Family History to Future Health: The Power of Preventive Genetic Screening](https://diagnostics.medgenome.com/blog/from-family-history-to-future-health-the-power-of-preventive-genetic-screening/) - [KaryoSeq Low Pass Whole Genome Sequencing vs.Traditional Karyotyping](https://diagnostics.medgenome.com/blog/karyoseq-low-pass-whole-genome-sequencing-vs-traditional-karyotyping/) - KaryoSeq offers a modern take on genome analysis. Discover how it stacks up against traditional karyotyping. Understand the difference. Read more. - [Benefits of PGT in Improving IVF Success Rates](https://diagnostics.medgenome.com/blog/benefits-of-pgt-in-improving-ivf-success-rates/) - IVF success starts with smarter science. Medgenome’s PGT helps increase success rates and reduce risks. Give your journey the best start. Learn more. - [How Detecting Copy Number Variation (CNVs) Improve Early Diagnosis & Treatment Plans?](https://diagnostics.medgenome.com/blog/copy-number-variations-cnv/) - Copy Number Variations can impact health in surprising ways. Medgenome helps you spot them early. Learn why CNVs matter to you. - [SPIT SEQ and Next-Generation Sequencing Combat Drug-Resistant Tuberculosis](https://diagnostics.medgenome.com/blog/spit-seq-fight-against-drug-resistant-tuberculosis/) - Fighting drug resistant TB just got faster. Medgenome’s SPIT Seq technology is changing the game. Discover how it works today. - [Newborn Screening Tests and What They Detect](https://diagnostics.medgenome.com/blog/benefits-of-newborn-screening-test-for-babies/) - The first few days matter most. Medgenome’s newborn screening gives babies a healthier start. See how early testing can help. - [What Are Neurological Disorders and How Genetics Influences Their Development](https://diagnostics.medgenome.com/what-are-neurological-disorders-and-how-genetics-influences-their-development/) - [Difference Between Genetic Testing and Genetic Screening: What You Need to Know](https://diagnostics.medgenome.com/difference-between-genetic-testing-and-genetic-screening-what-you-need-to-know/) - [Rh Incompatibility In Pregnancy – How MedGenome Rhesus D Track Can Help Expecting Mothers](https://diagnostics.medgenome.com/rh-incompatibility-in-pregnancy-how-medgenome-rhesus-d-track-can-help-expecting-mothers/) - [The Human Genome Can Fill 800 Dictionaries or 10,000 Novels!](https://diagnostics.medgenome.com/blog/what-is-genome/) - What exactly is a genome and why does it matter? Medgenome makes complex science simple. Understand your body’s blueprint. Start here. - [Unlocking Insights: Genetic Tests Every Woman Should Consider](https://diagnostics.medgenome.com/blog/types-of-genetic-testing/) - Not all tests are the same. Medgenome breaks down types of genetic testing with clarity. Choose smarter with expert insights. Read more. - [Medgenome’s CNS Tumour Methylation Classifier – A Breakthrough In Brain Tumour Diagnostics](https://diagnostics.medgenome.com/medgenomes-cns-tumour-methylation-classifier-a-breakthrough-in-brain-tumour-diagnostics/) - [Genetic Tests for a Healthy Baby: Empowering Choices for Future Parents](https://diagnostics.medgenome.com/blog/prenatal-diagnosis/) - From NIPT to amnio, prenatal testing options can be confusing. Medgenome helps simplify your choices. Get clarity. Explore now. - [How to Detect Sickle Cell Disease in Time!](https://diagnostics.medgenome.com/blog/sickle-cell-anemia-diagnosis/) - Early sickle cell diagnosis can change lives. Medgenome brings fast, accurate results. Don’t wait for symptoms. Screen early. - [Hypertension – A Silent Killer Why Hypertension is More Dangerous than You Think](https://diagnostics.medgenome.com/blog/hypertension/) - Genetics play a silent role in hypertension. Medgenome’s tools help you detect it early. Understand your risk. Start today. - [Pharmacogenomics a clinical tool for a personalized medicine](https://diagnostics.medgenome.com/pharmacogenomics-a-clinical-tool-for-personalized-medicine/) - [Genetic Testing for a Healthier Tomorrow](https://diagnostics.medgenome.com/blog/benefits-of-genetic-testing-for-health/) - Prevention starts with understanding. Medgenome’s genetic tests reveal what your body’s hiding. Invest in proactive health. Read more. - [Genetic Testing Before & During Pregnancy: What Every Parent Needs to Know](https://diagnostics.medgenome.com/blog/genetic-testing-before-during-pregnancy/) - https://diagnostics.medgenome.com/wp-admin/profile.php - [Comprehensive Tumor Gene Panel: Experience of a Cancer Survivor](https://diagnostics.medgenome.com/blog/precision-medicine-targeted-therapy-lung-cancer-survivor-story/) - Medgenome’s targeted approach helped a cancer survivor thrive. See how precision medicine changes lives. Read this inspiring story now. - [Mother’s Day Spotlight: Why Reproductive Genetic Testing Matters](https://diagnostics.medgenome.com/blog/reproductive-genetics/) - Your fertility journey deserves precision. Medgenome offers expert led reproductive genetics support. Take the guesswork out. Explore now. - [Pancreatic Cancer – Important Facts](https://diagnostics.medgenome.com/blog/genetics-of-pancreatic-cancer/) - Pancreatic cancer is complex. Genes make it clearer. Medgenome explains how. Understand your risks before it’s too late. - [Diabetes is a Growing Burden in the Society – Latest Scientific Advances Can Help Us Manage it Better](https://diagnostics.medgenome.com/blog/genetic-testing-in-diabetes/) - Diabetes risk often hides in your DNA. Medgenome’s testing can reveal it early. Prevent what’s possible. Get tested today. - [Unite to End TB: Advancing Diagnosis with SPIT SEQ](https://diagnostics.medgenome.com/unite-to-end-tb-advancing-diagnosis-with-spit-seq/) - [Symptoms of Ovarian Cancer You Shouldn’t Ignore](https://diagnostics.medgenome.com/symptoms-of-ovarian-cancer-you-shouldnt-ignore/) - [NIPT for Twins: What You Should Know](https://diagnostics.medgenome.com/blog/nipt-for-twins/) - Expecting twins? Get peace of mind with Medgenome’s NIPT—safe, accurate and twin friendly. Secure your prenatal insights now. - [Carrier Screening vs. NIPT: Which Genetic Tests Should You Consider During Pregnancy?](https://diagnostics.medgenome.com/blog/genetic-carrier-screening-vs-nipt/) - [Febrile Neutropenia Panel: Advanced Pathogen Detection for Better Patient Care](https://diagnostics.medgenome.com/blog/febrile-neutropenia-panel-advanced-pathogen-detection-patient-care/) - [Genetic Testing for Women's Health: A Lifeline for Early Detection](https://diagnostics.medgenome.com/genetic-testing-for-womens-health-a-lifeline-for-early-detection/) - [Is Breast Cancer Hereditary? Understand the Role of Family History in Breast Cancer Risk](https://diagnostics.medgenome.com/blog/is-breast-cancer-hereditary/) - [How Genetic Testing is Transforming the Future of Maternal and Newborn Health](https://diagnostics.medgenome.com/how-genetic-testing-is-transforming-the-future-of-maternal-and-newborn-health/) - [What Are Ovarian Cancer Causes at Young Age?](https://diagnostics.medgenome.com/blog/ovarian-cancer-causes/) - [Role of Antimicrobial Resistance in Sepsis: Challenges & Solutions](https://diagnostics.medgenome.com/blog/antimicrobial-resistance-in-sepsis-challenges-solutions/) - [Changing Face of Lung Cancer Diagnosis: Why Genomic Testing is Now Essential](https://diagnostics.medgenome.com/blog/lung-cancer-genomic-testing-essential-diagnosis/) - [Beyond Risk for Down Syndrome: What Else Can NIPT Detect?](https://diagnostics.medgenome.com/blog/beyond-down-syndrome-modern-nipt-detection/) - [What is Down Syndrome? Why It Happens, Clinical Features, and How It Is Detected](https://diagnostics.medgenome.com/blog/what-is-down-syndrome-causes-features-and-diagnosis/) - Down syndrome stems from an extra chromosome, affecting physical and cognitive development, and is diagnosed through prenatal or postnatal tests. - [Pharmacogenomics Testing: How Genes Affect Drug Response](https://diagnostics.medgenome.com/blog/pharmacogenomics-testing-medication-response/) - Discover how pharmacogenomics testing analyzes genetic variations to predict drug response, improve treatment effectiveness, and reduce medication side effects. - [ClonoTrack: NGS-Based Clonality & MRD Monitoring in B-Cell Malignancies](https://diagnostics.medgenome.com/blog/clonotrack-ngs-clonality-mrd-b-cell-malignancies/) - Explore ClonoTrack NGS testing for precise B-cell clonality detection and MRD monitoring to support diagnosis and treatment of hematologic malignancies. - [Why Genetic Testing Matters in Pediatric Rare Disease Diagnosis?](https://diagnostics.medgenome.com/blog/pediatric-genetic-testing-rare-disease-diagnosis/) - Understand the importance of pediatric genetic testing in diagnosing rare diseases early in children. Learn how it enables accurate treatment, better outcomes, and informed care decisions. - [Understanding Rare Genetic Syndrome in Children: Symptoms and Testing](https://diagnostics.medgenome.com/blog/rare-genetic-syndromes-in-children-symptoms-and-testing/) - Learn about rare genetic syndromes in children, their key symptoms, and how genetic testing helps in early and accurate diagnosis for better treatment outcomes. - [Unlocking the Blueprint: The Multitude Power of Whole Genome Sequencing](https://diagnostics.medgenome.com/blog/unlocking-power-of-whole-genome-sequencing/) - Discover the power of whole genome sequencing in decoding genetic information, enabling accurate diagnosis, personalized treatment, and insights into complex diseases. - [Hypertension – A Silent Killer Why Hypertension is More Dangerous than You Think](https://diagnostics.medgenome.com/hypertension-a-silent-killer-why-hypertension-is-more-dangerous-than-you-think-2/) - Discover why hypertension is more dangerous than you think. Medgenome makes early detection easier than ever. Take charge of your health. Learn more. - [Role of Antimicrobial Resistance in Sepsis: Challenges & Solutions](https://diagnostics.medgenome.com/blog/antimicrobial-resistance-in-sepsis-challenges-solutions/) - Sepsis is evolving and so is resistance. Medgenome uncovers smarter ways to combat AMR. Read how innovation is saving lives. - [World Immunization Day](https://diagnostics.medgenome.com/blog/world-immunisation-day/) - Celebrate World Immunisation Day with a genetic twist. See how genes and vaccines work together. Dive into the science. Read more. - [Gene Therapy: a promising potential treatment modality for LCA](https://diagnostics.medgenome.com/blog/gene-therapy-potential-treatment-modality-lca/) - Hope for inherited blindness is here. Medgenome explores gene therapy’s promise for LCA. See what the future looks like. Read on. - [Prenatal Screening In Covid Times](https://diagnostics.medgenome.com/blog/prenatal-screening-in-covid-times/) - COVID changed everything including prenatal care. See how Medgenome adapted testing during uncertain times. Parent with peace of mind. ## Pages - [Home](https://diagnostics.medgenome.com/) - We operate South Asia’s largest CAP-accredited genetic testing lab with 10+ years of genomic expertise, offering clinically validated assays powered by AI/ML-driven bioinformatics. - [Trio Exome Sequencing](https://diagnostics.medgenome.com/rare-inherited-disorders/trio-exome-sequencing-test/) - Our NGS-based Trio Exome Sequencing test analyses thousands of genes in the child and compares them with both parents to identify disease-causing genetic variants and improve the diagnosis of genetic disorders. - [TumorTrack Advance - Comprehensive Tumor Profiling (Tissue Biopsy)](https://diagnostics.medgenome.com/oncology/tumour-track-advance/) - TumorTrack Advance is a tissue biopsy–based comprehensive tumor panel offering genomic profiling of over 500 cancer genes, detecting SNVs, CNVs, InDels, fusions, TMB, MSI, and HRD through a single assay. - [Lung Cancer Panel](https://diagnostics.medgenome.com/oncology/lung-cancer-panel/) - MedGenome’s NGS-based Lung Cancer Panel Test identifies mutations in genes such as EGFR, KRAS, ALK, ROS1, BRAF, and MET in lung cancer cells. Coverage includes SNVs, InDels, CNVs, and fusions. - [Neuro Genetics](https://diagnostics.medgenome.com/rare-inherited-disorders/neuro-genetic-testing/) - MedGenome offers a comprehensive neurology panel to accurately diagnose a wide range of genetic neurological disorders, including epileptic, neurocutaneous, neuromuscular, neurodegenerative, neurometabolic, movement, and mitochondrial disorders. - [BabySecure - Newborn Screening](https://diagnostics.medgenome.com/rare-inherited-disorders/babysecure-newborn-screening-tests/) - MedGenome’s Newborn Screening Test (NBS test) uses advanced TMS and GCMS technologies to identify serious genetic disorders that may be undetected and untreated in newborns. Performed 24 hours after birth. - [Genetic Counselling](https://diagnostics.medgenome.com/genetic-counselling/) - Genetic Counselling Support- Expert pre- and post-test genetic counselling is available to help clinicians and patients understand test results and next steps. - [OncoTrack MRD Test (Molecular Residual Disease)](https://diagnostics.medgenome.com/oncology/molecular-residual-disease-testing/) - [Oncology](https://diagnostics.medgenome.com/oncology/) - Cutting-edge genetic and molecular testing solutions for the diagnosis and management of haematological malignancies and solid tumours. - [About Us](https://diagnostics.medgenome.com/about-us/) - We are South Asia’s largest genetic testing laboratory operating in India, Offering 1,300+ advanced genetic tests across rare inherited diseases, reproductive health, oncology, infectious diseases, and preventive wellness. - [Non-Invasive Prenatal Testing](https://diagnostics.medgenome.com/reproductive-health/non-invasive-prenatal-testing-nipt/) - MedGenome offers NIPT/NIPS, including Advanced and Twins options, for all pregnant women. These tests screen for Trisomy 21, 18, 13, sex chromosome abnormalities, and other chromosomal aneuploidies, with results in 7 days. - [Reproductive Health](https://diagnostics.medgenome.com/reproductive-health/) - Comprehensive range of testing solutions, including genetic tests and other diagnostic services to support reproductive care. - [Infectious Diseases](https://diagnostics.medgenome.com/infectious-diseases/) - State-of-the-art genetic and molecular testing solutions for a wide range of infectious diseases. - [Inherited Disorders](https://diagnostics.medgenome.com/rare-inherited-disorders/) - Advanced testing solutions to diagnose and manage a wide range of rare hereditary conditions. - [Nephro Genetics](https://diagnostics.medgenome.com/rare-inherited-disorder/nephro-genetic-testing/) - We offers advanced nephrogenetics testing using NGS and MLPA technologies to identify genetic causes of renal disorders, including cystic and interstitial diseases, tubular and glomerular disorders, nephrolithiasis, CAKUT, cystic kidney diseases, and family history of kidney disease. - [Newsletter](https://diagnostics.medgenome.com/newsletter/) - [KaryoSeq](https://diagnostics.medgenome.com/reproductive-health/karyoseq-chromosomal-abnormalities-test/) - KaryoSeq-Chromosomal Abnormalities & CNV Detection Test is a comprehensive genome-wide test that uses low-pass whole genome sequencing, which analyses to detect aneuploidies, CNVs ≥50 kb, and triploidy, supporting prenatal and postnatal assessment. - [Meningoencephalitis Panel](https://diagnostics.medgenome.com/infectious-diseases/meningoencephalitis-panel-multiplex-rt-pcr-test/) - Meningoencephalitis Panel detects multiple pathogens in a single test to help identify conditions affecting the brain and spinal cord. It is applicable for CNS infections and autoimmune or infectious neuroinflammatory disorders. - [Prosthetic Joint Panel](https://diagnostics.medgenome.com/infectious-diseases/prosthetic-joint-multiplex-pcr-panel-test/) - Prosthetic Joint Panel Test helps identify pathogens causing prosthetic joint infections (PJI) in people with joint replacements experiencing pain, redness, swelling, or movement difficulty. - [Comprehensive Transplant Infection Panel](https://diagnostics.medgenome.com/infectious-diseases/post-transplant-infection-test/) - Transplant Panel Test supports post-transplant monitoring by detecting early infections and antimicrobial resistance genes in kidney, liver, heart, lung, or bone marrow transplant recipients. - [Gastrointestinal Pathogen Panel](https://diagnostics.medgenome.com/infectious-diseases/gastrointestinal-pathogen-panel-multiplex-pcr-test/) - Gastrointestinal Pathogen Panel is detect and differentiate 9 species/groups of bacteria, 4 parasites and 5 viruses that can all cause gastroenteritis in humans. - [CMV Drug Resistance Test](https://diagnostics.medgenome.com/infectious-diseases/cmv-drug-resistance-ngs-test/) - Cytomegalovirus (CMV) testing is recommended for transplant recipients with persistent CMV, immunocompromised patients such as those with cancer or HIV, and newborns with congenital CMV infections. - [Tropical Fever Panel](https://diagnostics.medgenome.com/infectious-diseases/tropical-fever-multiplex-rt-pcr-panel/) - MedGenome’s Tropical fever panel is recommended for Patients with symptoms like severe fatigue, joint pain, or jaundice, and Individuals exposed to mosquitoes, floodwaters, or poor sanitation, and more - [SPIT SEQ - Drug-Resistant TB Test Using WGS](https://diagnostics.medgenome.com/infectious-diseases/spit-seq-tb-drug-resistance-test/) - SPIT-SEQ is a whole-genome sequencing (WGS) test for tuberculosis that detects drug resistance in MDR-TB, Pre-XDR, XDR-TB, and rifampicin-resistant TB, helping clinicians select faster and targeted treatment. - [HIV Genotyping and Drug Resistance Testing](https://diagnostics.medgenome.com/infectious-diseases/hiv-genotyping-drug-resistance-test/) - NGS-based HIV Genotyping Test for detecting MRVs and major resistance mutations in treatment failure and high-risk exposure cases - [Respiratory Pathogen Panel](https://diagnostics.medgenome.com/infectious-diseases/respiratory-pathogen-multiplex-rt-pcr-test/) - MedGenome's Respiratory Pathogen Panel identifies viruses, bacteria, and fungi causing respiratory infections such as pneumonia, bronchitis, flu, and other lung infections. - [TORCH Panel Test](https://diagnostics.medgenome.com/infectious-diseases/torch-panel-multiplex-rt-pcr-test/) - TORCH panel test detects infections passed from mother to baby during pregnancy, helping prevent complications such as birth defects, developmental delays, organ damage, miscarriage, and neonatal sepsis. - [Sepsis AMR Panel](https://diagnostics.medgenome.com/infectious-diseases/sepsis-amr-multiplex-pcr-panel-test/) - Sepsis-AMR Panel is a qualitative RT-PCR test that detects 22 bacterial and fungal pathogens and 8 antimicrobial resistance genes directly from whole blood. - [Febrile Neutropenia Panel](https://diagnostics.medgenome.com/infectious-diseases/febrile-neutropenia-multiplex-rt-pcr-panel/) - The Febrile Neutropenia Panel detects bacteria, viruses, fungi, and antimicrobial resistance genes and is recommended for cancer patients, transplant recipients, and those with weakened immunity. - [MetaSeq Powered by DISQVER®](https://diagnostics.medgenome.com/infectious-diseases/metaseq-cfdna-metagenomic-test/) - A cfDNA metagenomic NGS test that detects microbes directly from blood without culture, aiding diagnosis of sepsis, meningitis, pneumonia, endocarditis, and other serious infections. - [Thankyou](https://diagnostics.medgenome.com/thankyou/) - [ClonoTrack (B-Cell Clonality & MRD)](https://diagnostics.medgenome.com/oncology/clonotrack-ngs-b-cell-clonality-mrd-test/) - [HRR Track - Homologous Recombination Repair Test](https://diagnostics.medgenome.com/oncology/hrr-track-test/) - MedGenome’s HRR Track Test screens for mutations (SNVs & InDels) in 15 HRR pathway genes, including BRCA1/2, and is recommended for breast, ovarian, pancreatic, and prostate cancer patients, especially with a family history. - [Endometrial Cancer Panel](https://diagnostics.medgenome.com/oncology/endometrial-cancer-panel/) - Endometrial Cancer Panel Test supports patients diagnosed with or at risk of endometrial cancer and is especially useful for aggressive or recurrent cases, helping guide personalised treatment decisions. - [HRD Track - Homologous Recombination Deficiency Test](https://diagnostics.medgenome.com/oncology/hrd-track-test/) - MedGenome’s HRD Track Test identifies homologous recombination deficiency by detecting gene mutations and genomic instability, guiding PARP inhibitor therapy. Analyses BRCA1/2 and 13 HRR genes in ovarian, breast, pancreatic, and prostate cancers. - [ThyroTrack - Thyriod Nodule Prognistication Test by NGS](https://diagnostics.medgenome.com/oncology/thyrotrack-thyroid-tumor-test/) - MedGenome's ThyroTrack is NGS-based test to detect genomic biomarkers in thyroid nodules, performed on FNAC fluid for nodule prognostication and on FFPE tissue block for clinical management. - [Multiple Myeloma Test](https://diagnostics.medgenome.com/oncology/multiple-myeloma-test/) - MedGenome’s Multiple Myeloma Genetic Test helps detect abnormal M protein, assess bone marrow involvement, and identify genetic abnormalities that influence prognosis and treatment in plasma cell–related blood cancer. - [BCR-ABL1 Test](https://diagnostics.medgenome.com/oncology/bcr-abl1-test/) - BCR-ABL1 gene kinase domain analysis helps assess TKI resistance and is recommended for patients with CML or Ph+ ALL showing rising BCR-ABL1 levels after treatment. - [Gastrointestinal Stromal Tumors Test](https://diagnostics.medgenome.com/oncology/gastrointestinal-stromal-tumor-test/) - MedGenome’s NGS-based GIST Test screens actionable gene mutations as per NCCN guidelines, helping identify tumour-driving genetic changes for precise diagnosis and targeted treatment. - [CNS Tumor Methylation Classifier](https://diagnostics.medgenome.com/oncology/cns-tumor-methylation-classifier-test/) - CNS Tumor Methylation Classifier a cutting-edge, genome-wide methylation test that analyses specific patterns in the tumor’s DNA, known as methylation patterns. DNA methylation is a natural process that influences the function of genes. - [Comprehensive Myeloid & Lymphoid Panel](https://diagnostics.medgenome.com/oncology/comprehensive-myeloid-and-lymphoid-panel/) - NGS-based leukemia genetic testing to detect mutations, gene fusions, chromosomal changes, and CNVs across AML, MDS, MPN, CML, JMML, B-ALL, T-ALL, Ph-like ALL, and CLL. - [Hereditary Cancer Panel](https://diagnostics.medgenome.com/oncology/hereditary-cancer-panel-testing/) - MedGenome’s Hereditary Cancer Panel detects inherited mutations linked to cancer risk through analysis of 158 genes and deletion/duplication testing of 30 genes, including BRCA1, BRCA2, HRR, and other high-risk genes. - [Liquid Biopsy Test](https://diagnostics.medgenome.com/oncology/liquid-biopsy-cancer-testing/) - MedGenome’s liquid biopsy tests detect multiple cancer types through a simple blood test, including lung, breast, and colorectal cancers, along with the HRR Genes Liquid Biopsy Panel for breast, ovarian, prostate, and pancreatic cancers. - [ExomeMAX - Enhanced Whole Exome Sequencing](https://diagnostics.medgenome.com/rare-inherited-disorder/exomemax-advanced-exome-sequencing-test/) - ExomeMAX: Advanced WES test covering 20,000+ genes & 210,000 exons. Detects disorders in cardiology, neurology, metabolism, endocrinology & more, including cystic fibrosis, muscular dystrophy & hereditary cancers. 30%higher diagnosis rate. - [Cardio Genetics](https://diagnostics.medgenome.com/rare-inherited-disorders/cardio-genetics/) - Our comprehensive test panels provide genetic testing for heart problems and cardiovascular diseases using advanced NGS and MLPA technologies. This helps diagnose conditions such as congenital heart disease cardiac channelopathies, CPVT, cardiomyopathies, and FH. - [Rapid Exome Sequencing](https://diagnostics.medgenome.com/rare-inherited-disorders/rapid-exome-sequencing-test/) - Our Rapid Exome Sequencing Test analyses critically ill infants with suspected genetic disorders admitted to NICU & PICU, helping clinicians quickly determine whether a genetic condition is causing the patient’s symptoms. - [Ophthalmic Genetic Test](https://diagnostics.medgenome.com/rare-inherited-disorders/ophthalmic-genetic-test/) - Our Comprehensive ophthalmic panels cover 721+ genes linked to inherited retinal diseases, including retinitis pigmentosa, Stargardt disease, LCA, cone-rod dystrophy, congenital cataract, and more - [Endocrine Genetics](https://diagnostics.medgenome.com/rare-inherited-disorders/endocrine-genetic-testing/) - MedGenome offers advanced genetic testing for endocrine disorders to identify hereditary causes and assess familial risk, including diabetes (MODY), CAH, obesity, and other endocrine conditions - [KaryoTrack Chromosomal Microarray (CMA)](https://diagnostics.medgenome.com/rare-inherited-disorders/karyotrack-chromosomal-testing/) - MedGenome’s advanced chromosomal analysis test detects aneuploidies and structural abnormalities, supporting diagnosis of genetic disorders, pregnancy loss, infertility, and congenital conditions across multiple disease areas. - [Whole Exome Sequencing](https://diagnostics.medgenome.com/rare-inherited-disorders/whole-exome-sequencing/) - Our NGS-based WES Test provides comprehensive analysis to identify rare gene mutation–related diseases. It covers all protein-coding regions, intron–exon boundaries of ~23,000 genes, and mitochondrial genes. - [Clinical Exome Sequencing](https://diagnostics.medgenome.com/rare-inherited-disorders/clinical-exome-sequencing-genetic-test/) - Our Clinical Exome Sequencing Test identifies genetic causes of complex, heterogeneous diseases and resolves diagnostic odysseys by detecting specific genes that inherited from family history. - [Targeted Variant Testing](https://diagnostics.medgenome.com/reproductive-health/prenatal-sanger-sequencing-test/) - Our Targeted testing is a specialised genetic test performed during pregnancy to detect specific inherited conditions in the fetus. Its identifying genetic changes that are already known in the family. Book now. - [Carrier Screening](https://diagnostics.medgenome.com/reproductive-health/carrier-screening-test/) - Carrier Screening Panel: Test over 2,000 genes for autosomal recessive and X-linked disorders. Recommended for those planning a pregnancy, undergoing IVF, with a history of pregnancy loss, or in consanguineous marriages. Book now! - [Chromosomal Microarray Analysis](https://diagnostics.medgenome.com/reproductive-health/chromosomal-microarray-analysis-test/) - CMA is a high-resolution genetic test that helps identify genetic causes of developmental delays, intellectual disabilities, autism spectrum disorders, and certain birth defects, including during pregnancy. - [Cytogenetic Testing](https://diagnostics.medgenome.com/reproductive-health/cytogenetic-testing-fish-karyotyping/) - We offers advanced cytogenetic tests to detect numerical and structural chromosomal changes, including aneuploidies, deletions, duplications, and translocations, helping assess fetal genetic health during pregnancy. - [Preimplantation Genetic Testing](https://diagnostics.medgenome.com/reproductive-health/preimplantation-genetic-testing/) - MedGenome’s advanced PGT testing identifies chromosomal abnormalities, helping select healthy embryos for transfer and improve the chances of a successful pregnancy and a healthy baby. Book a test now - [Rhesus D Track](https://diagnostics.medgenome.com/reproductive-health/non-invasive-rhd-testing/) - MedGenome offers a highly reliable fetal RhD test using advanced PCR technology. Designed for RhD-negative pregnant women with singleton pregnancies and a history of Rh incompatibility. Book now. - [Maternal Cell Contamination Testing](https://diagnostics.medgenome.com/reproductive-health/maternal-cell-contamination-test/) - We offers high-precision MCC testing to accurately detect maternal DNA contamination in fetal samples. its ensures that only fetal DNA is analysed, reducing the risk of false-positive/negative results in prenatal diagnostics. - [Prenatal Exome Sequencing](https://diagnostics.medgenome.com/reproductive-health/prenatal-exome-sequencing-test/) - MedGenome provides prenatal exome sequencing to identify genetic disorders in the fetus and support reproductive planning and recurrence risk assessment. Book now - [Maternal Serum Screening](https://diagnostics.medgenome.com/reproductive-health/maternal-serum-screening/) - MSS test assesses the risk of genetic disorders, including neural tube defects and chromosomal conditions like Down syndrome this test can be done in 1st trimester(9-13w6) or 2nd trimester (15-21w6d). - [Advanced Genomics](https://diagnostics.medgenome.com/centre-of-advanced-genomics/) - [Routine Diagnostics](https://diagnostics.medgenome.com/routine-diagnostics/) - [Franchisee](https://diagnostics.medgenome.com/franchisee/) - Join the MedGenome Franchise Program If you’re a lab owner, run a diagnostic center, or have a strong doctor network, this is your opportunity to revolutionize healthcare and elevate your business to new heights. - [Patient Stories](https://diagnostics.medgenome.com/patient-stories/) - Patient Stories - MedGenome: From Diagnosis to Hope – Real Journeys with Genetic Breakthroughs in Oncology, Rare Diseases, and Reproductive Health - [Research Service](https://diagnostics.medgenome.com/research-service/) - MedGenome's Multiomics services enable precision medicine by providing comprehensive view of biological systems for personalised therapies. - [Life at Medgenome](https://diagnostics.medgenome.com/life/) - [Contact Us](https://diagnostics.medgenome.com/contact-us/) - Connect with MedGenome Labs for expert assistance and inquiries. Our team is ready to provide consultations and more information on advanced diagnostic solutions. - [Careers](https://diagnostics.medgenome.com/career/) - Interested in working with us? Join a team of creative, driven and passionate people who are re-shaping the way the world understands data - [Videos](https://diagnostics.medgenome.com/videos/) - MedGenome Video Library: In-Depth Genetic Testing Explanations, Inspiring Patient Stories, Doctor Expert Insights, Transformative Genomics, and Much More - [Brouchers](https://diagnostics.medgenome.com/brouchers/) - Explore our latest MedGenome Brochures. Connect with our Expert for more - [Test Menu New](https://diagnostics.medgenome.com/test-menu-new/) - Delivering trusted, high-quality genetic diagnostic services to support better healthcare decisions. Find you Right Test Today. - [Publications](https://diagnostics.medgenome.com/publication/) - [CNS Tumor Methylation Classifier](https://diagnostics.medgenome.com/oncology/cns-tumor-methylation-classifier/) - [Cookie Policy Eu](https://diagnostics.medgenome.com/cookie-policy-eu/) - This Cookie Policy was last updated on February 21, 2024 and applies to citizens and legal permanent residents of the European Economic Area and Switzerland. 1. Introduction Our website, https://stgdiagnostics.wpengine.com (hereinafter: “the website”) uses cookies and other related technologies (for convenience all technologies are referred to as “cookies”). Cookies are also placed by third parties we have - [Become Business Partner](https://diagnostics.medgenome.com/franchisee/) - [Refund Policy](https://diagnostics.medgenome.com/refund-policy/) - Refund of fees for any reason has to be claimed by the Patient or the guardians of the Patients within 90 days from the date of delivery of report. - [Request Test](https://diagnostics.medgenome.com/test-menu-new/) - [Endorince Genetics](https://diagnostics.medgenome.com/endorince-genetics/) - [Genetic Testing Heart Disease](https://diagnostics.medgenome.com/genetic-testing-heart-disease/) - Genetic testing for heart disease reveals inherited risk early. Book today with MedGenome to protect your heart. Stay one step ahead of heart risks. - [Test Enquiry](https://diagnostics.medgenome.com/test-enquiry/) - Inquire about MedGenome's diagnostic tests today. Our expert team will help you choose the right test and guide you through the process. Contact us now to learn more. - [Grievance redressal](https://diagnostics.medgenome.com/grievance-redressal/) - We strongly believe that our stakeholder's (communities/ customers/ employees/ third party workers/ others) feedback/ complaints/ suggestions are important for an organisation to implement policies and procedures at all levels and are precursor to growth of the organisation. We are here to hear any feedback/complaint/suggestion. Write to us at grievance.redressal-mgind@medgenome.com We will get in touch with you - [Terms Conditions](https://diagnostics.medgenome.com/terms-conditions/) - DELIVERY OF SERVICES Subject to receipt of the fees, MedGenome Labs Limited (“MedGenome”) shall carry out the test(s) as requested in this Test Requisition Form (“Test(s)”) in conformity with the applicable industry standards. REPORTS The Report shall be generated within such Turn-Around-Time (“TAT”) as mentioned in this Test Requisition Form(s). However, such TAT may vary - [Privacy policy](https://diagnostics.medgenome.com/privacy-policy/) - 1. Acknowledgment and Acceptance of Terms MedGenome Labs Ltd. is committed to protecting your privacy. This privacy statement sets forth our current privacy practices with regard to the information we collect when you interact with diagnostics.medgenome.com website. By accessing diagnostics.medgenome.com, you acknowledge and fully understand our privacy statement and freely consent to the information collection - [Enquiry](https://diagnostics.medgenome.com/enquiry/) - [Enquiry Page](https://diagnostics.medgenome.com/enquiry-page/) - [Media](https://diagnostics.medgenome.com/media/) - [Videos](https://diagnostics.medgenome.com/videos/) - Watch informative videos about MedGenome's diagnostic tests and services. Our experts discuss various genetic disorders and advancements in genomics. Visit us to learn more. - [Press](https://diagnostics.medgenome.com/press/) - Stay up-to-date with the latest news and press releases from MedGenome Diagnostics. Read about our advancements in genetic testing, research collaborations, and more. - [Kardiogen](https://diagnostics.medgenome.com/kardiogen/) - KardioGen is a Polygenic Risk Score (PRS) , This is a once in a lifetime simple blood test that can predict your genetic risk of developing Coronary Artery Disease. - [About Us](https://diagnostics.medgenome.com/about-us-old/) - MedGenome, a founding member of Genome Asia 100K, initiated to sequence 100,000 genomes in the Asian population to create gene-pool data for higher research purposes. - [Career](https://diagnostics.medgenome.com/career/) - Interested in working with us? Join a team of creative, driven and passionate people who are re-shaping the way the world understands data ## Stories - [Ravi & Swati's Story](https://diagnostics.medgenome.com/stories/ravi-swatis-story-how-carrier-screening-helped-them-in-getting-a-healthy-baby/) - One test changed everything for this couple. Medgenome’s carrier screening brought them hope. Learn how the right test matters. - [The Journey of Mr. Arjun and Ms. Shilpa](https://diagnostics.medgenome.com/stories/premarital-testing-matching-the-genes/) - A Medgenome patient shares how genetic testing changed their care path. Real insights. Real results. Read their story. - [Story of Ms. Savitha](https://diagnostics.medgenome.com/stories/nipt-detects-variant-of-turner-syndrome-not-detectable-by-fish/) - This real case shows how Medgenome’s NIPT revealed what others missed. Discover the power of precision. - [Mr. and Mrs. Swamy’s Journey to Parenthood](https://diagnostics.medgenome.com/stories/baby-conceived-using-ivf-in-combination-with-pgs/) - A healthy baby through IVF and PGS. Medgenome made it possible. See what science and love can achieve. Read the story. - [Gujarat Family’s Journey Through Cancer Prevention](https://diagnostics.medgenome.com/stories/six-members-of-a-family-diagnosed-with-familial-adenomatous-polyposis-fap-an-inherited-disorder-in-gujarat/) - Six lives changed through one diagnosis. Medgenome identified a hereditary disorder in time. Know your family history. Read more. - [Vinay & Saroja's Journey with Family Planning](https://diagnostics.medgenome.com/stories/genetic-testing-provides-hope-for-couple-with-family-history-of-hearing-loss/) - MedGenome is the leading solution provider of clinical genomics for Physicians and Healthcare providers across India. - [Amit & Akhil's Genetic Testing Journey](https://diagnostics.medgenome.com/stories/medgenomes-comprehensive-testing-covers-the-entire-hbb-gene-for-β-thalassemia/) - Medgenome’s full gene sequencing covers what others may miss in β thalassemia. Get accurate diagnosis from the start. - [Arjun’s Battle with Leukemia](https://diagnostics.medgenome.com/stories/genetic-testing-at-baseline-and-post-induction-chemotherapy-helps-in-informed-treatment-decision-for-a-leukemia-patient/) - Master Arjun (name changed), a 5-year-old boy presented with fever, fatigue, chest discomfort, weight loss & loss of appetite had consulted Dr Mahadev Swamy, a leading Hemato-Oncologist based at Goa, for further clinical examination as referred by a General Physician from a community hospital. Basic workup on blood sample revealed suspected acute leukemia, which was - [Ramdev and Savita’s Fight Against Thalassemia](https://diagnostics.medgenome.com/stories/thalassemia-a-story-of-love-hope-and-perseverance-cancer-genetic-test-in-india/) - MedGenome Labs Ltd offers carrier testing for various recessive disorders and provides genetic counselling services. Thalassemia is an autosomal recessive disorder and is characterized by defective formation of hemoglobin. Test helps healthcare provider to understand the nature of cancer genetic test in india. - [Premarital genetic carrier testing: Matching the genes](https://diagnostics.medgenome.com/stories/premarital-genetic-carrier-testing-matching-the-genes/) - Mr. Arjun (name changed) and Ms. Shilpa (name changed) are maternal cousins. They are planning to get married. There is no significant clinical history suggestive of any genetic disorder in the family apart from hypertension in their grandparents. Pre-marital genetic counselling was done, explaining to them the risk of genetic disorder in their children ,since - [Genetic testing reveals multiple actionable mutations impacting the course of treatment in a patient with lung cancer](https://diagnostics.medgenome.com/stories/genetic-testing-reveals-multiple-actionable-mutations-impacting-the-course-of-treatment-in-a-patient-with-lung-cancer/) - 63-year-old Santosh Khurrana (name changed) felt the symptoms related to lung cancer and went for a consultation with Dr. Shyam Aggarwal. Before starting the therapy, he decided to test Santhosh for presence of genetic mutation/s. 63-year-old Santosh Khurrana (name changed) felt the symptoms related to lung cancer and went for a consultation with Dr. Shyam - [Amar's Journey to Recovery](https://diagnostics.medgenome.com/stories/genetic-testing-can-go-a-long-way-in-determining-the-treatment-and-outcome-of-a-disease-in-a-patient/) - A single test by Medgenome led to a life changing treatment decision. Explore the impact of genetic precision. Read more. - [Sushila’s Journey with Genetic Testing](https://diagnostics.medgenome.com/stories/genetic-testing-provides-hope-to-the-couple-with-family-history-of-liver-failures-2/) - Medgenome gave this family hope despite a history of liver failures. Your genes don’t define you. Read their journey. - [19-Year-Old's Life-Saving Diagnosis](https://diagnostics.medgenome.com/stories/genetic-testing-can-go-a-long-way-in-determining-the-treatment-and-outcome-of-a-disease-in-a-patient-2/) - Medgenome helped redefine a treatment journey through actionable results. See how one test changed everything. - [Ahmed’s Story of Hope](https://diagnostics.medgenome.com/stories/early-diagnosis-is-a-way-to-beat-rare-genetic-disorders/) - Early detection is hope. Medgenome’s testing identifies rare genetic disorders at the right time. Act early. Read why it matters. - [Story of Rukhsar](https://diagnostics.medgenome.com/stories/next-generation-sequencing-ngs-based-multigene-panel-testing-in-clinical-decision-making-and-management-of-an-aml-patient/) - Medgenome’s NGS panel made all the difference in AML case management. Explore how genomics guides better outcomes. - [7-Year-Old Kiara's DBA Diagnosis](https://diagnostics.medgenome.com/stories/genetic-testing-based-accurate-diagnosis-helps-clinician-decide-on-a-course-of-action/) - Medgenome supports clinicians with data backed decisions via genetic testing. See why doctors trust us. Learn more. - [Mr. Aswathanarayan's Battle with Leukemia](https://diagnostics.medgenome.com/stories/personalized-medicine-aids-in-treatment-of-a-leukaemia-patient/) - Personalized care isn't a buzzword. See how Medgenome helped a leukemia patient beat the odds. Precision that saves. Read their story. - [Story of Seven-Year-Old John](https://diagnostics.medgenome.com/stories/seven-year-old-boy-treated-for-a-rare-genetic-disease/) - A rare condition diagnosed early. Medgenome helped rewrite a child’s health journey. See how timing saves lives. - [Ahana’s CML Diagnosis](https://diagnostics.medgenome.com/stories/genetic-testing-critical-for-complete-evaluation-of-chronic-myeloid-leukaemia-patient/) - Medgenome’s genetic panel provided clarity in a complex leukemia case. See how precision led to progress. Learn more. - [Story of Santosh Khurrana](https://diagnostics.medgenome.com/stories/genetic-testing-reveals-multiple-actionable-mutations-impacting-the-course-of-treatment-in-a-patient-with-lung-cancer-2/) - Genetic testing reveals multiple actionable mutations impacting the course of treatment in a patient with lung cancer. Genetic testing reveals a mutation that renders resistance to third generation TKIs - [Creed’s Fight Against Blindness](https://diagnostics.medgenome.com/stories/creed-pettits-story/) - Story of a a 9 year boy from Miami, Florida had been slowly going blind since the day he was born. - [Suvarna's Journey with Preventive Diagnostics](https://diagnostics.medgenome.com/stories/brca-testing-helps-a-young-lady-understand-the-risk-of-hereditary-cancer-running-in-the-family/) - Mutation in BRCA1 gene helped a young woman understand the genetic basis of hereditary cancer running in her family and helped her with precise course of treatment. - [31-Year-Old Identified at High Risk for Heart Disease](https://diagnostics.medgenome.com/stories/polygenic-risk-score-test/) - Patient information A 31-year-old man felt sudden chest pain while at work. His colleagues on noticing his discomfort rushed him to the hospital. He was diagnosed with Myocardial Infarction and underwent Coronary Artery Bypass Graft (CABG). He and his family members were suggested to undergo Coronary Artery Disease -Polygenic Risk Score (CAD-PRS) Test to determine - [Early Detection of CAD in 14-Year-Old](https://diagnostics.medgenome.com/stories/polygenic-risk-score-test-14-years/) - Patient information A 14-year-old female had heart attack/MI and underwent anterior wall Myocardial Infarction on 06.10.2020. She is currently on antiplatelet, statins and heparin medication. She was suggested to undergo Coronary Artery Disease -Polygenic Risk Score Test to find out whether she was at high risk of getting Coronary Artery Disease. Genetic History No ## Careers - [Zonal Business Manager](https://diagnostics.medgenome.com/careers/zonal-business-manager/) - Zonal Business Manager - [Manager - Scientific Affairs](https://diagnostics.medgenome.com/careers/manager-scientific-affairs/) - Scientific Affairs Manager - [Area Sales Manager](https://diagnostics.medgenome.com/careers/area-sales-manager/) ## Categories - [Infectious Diseases](https://diagnostics.medgenome.com/category/infectious-diseases/) - [Reproductive Health](https://diagnostics.medgenome.com/category/reproductive-health/) - [Rare Inherited Disorders](https://diagnostics.medgenome.com/category/rare-inherited-disorders/) - [Oncology](https://diagnostics.medgenome.com/category/oncology/) - [Research Services](https://diagnostics.medgenome.com/category/research-services/) - [MedGenome](https://diagnostics.medgenome.com/category/medgenome/) ## Tags - [Cancer Genetic Test](https://diagnostics.medgenome.com/tag/cancer-genetic-test/) - [Genetic Companies](https://diagnostics.medgenome.com/tag/genetic-companies/) - 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