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Stay updated with OneDNA media highlights, press releases, and news coverage featuring advancements in genomics, innovation, and preventive healthcare solutions
OneDNA is committed to making clinically relevant and affordable genomic testing accessible to individuals, clinicians, and healthcare partners across India. Our portfolio spans preventive genomics, pharmacogenomics, clinical genetics, microbiome analysis, maternal screening, and newborn screening, enabling informed health decisions across the life continuum.

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Read real patient stories from OneDNA showcasing how genetic testing supports early detection, preventive care, and better health outcomes for all patients.
OneDNA is committed to making clinically relevant and affordable genomic testing accessible to individuals, clinicians, and healthcare partners across India. Our portfolio spans preventive genomics, pharmacogenomics, clinical genetics, microbiome analysis, maternal screening, and newborn screening, enabling informed health decisions across the life continuum.

Have questions about DNA or genetic testing? OneDNA's expert consultation team in Hyderabad is always ready to guide you. Contact us today for quick support!
OneDNA is committed to making clinically relevant and affordable genomic testing accessible to individuals, clinicians, and healthcare partners across India. Our portfolio spans preventive genomics, pharmacogenomics, clinical genetics, microbiome analysis, maternal screening, and newborn screening, enabling informed health decisions across the life continuum.

Newborn screening by OneDNA helps detect genetic and metabolic disorders early, enabling timely treatment and better long-term health outcomes for your baby.
Newborn screening is a simple, safe heel-prick blood test performed within the first 24–72 hours after birth to detect serious but treatable congenital and metabolic disorders, often before any symptoms appear. The test uses a Dried Blood Spot (DBS) card collected via heel prick and is analysed using advanced technologies including ELISA, TMS, GC-MS, and LC-MSMS at ISO-certified laboratories.

Maternal Cell Contamination (MCC) testing detects maternal DNA in fetal samples to ensure accurate prenatal genetic results and prevent diagnostic errors.
Maternal Cell Contamination (MCC) occurs when maternal cells mix with fetal or placental tissue during prenatal procedures like CVS or amniocentesis. Since maternal and fetal DNA are ~50% similar, even small amounts of maternal cells can mask fetal mutations or cause false results potentially leading to misdiagnosis of aneuploidy if undetected.

View OneDNA awards and recognitions highlighting excellence in genetic testing, innovation, and contributions to advanced genomics and preventive healthcare.
OneDNA is committed to making clinically relevant and affordable genomic testing accessible to individuals, clinicians, and healthcare partners across India. Our portfolio spans preventive genomics, pharmacogenomics, clinical genetics, microbiome analysis, maternal screening, and newborn screening, enabling informed health decisions across the life continuum.