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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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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.

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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.

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