Health Genomics

In recent years, technological advancements have revolutionized prenatal screening tests, providing expectant parents with accurate and reliable information about their baby’s health. Non-Invasive Prenatal Testing (NIPT) has emerged as a groundbreaking genetic screening option that offers unparalleled insight into an unborn child’s genetic makeup, helping identify potential chromosomal abnormalities. In this blog, we will delve […]

What is personalised genomics ? Personalised genomics is a field of study that involves analysing and interpreting individualised genetic information through genome sequencing to identify genetic variations. This approach allows for the development of patient-specific treatments based on an individual’s genetic profile, leading to maximised therapeutic effectiveness and minimise adverse effects. Personalised genomics is a

CRISPR-Cas9 technology has emerged as a groundbreaking tool in genetic research and medical applications, offering unprecedented opportunities for genome editing. However, along with its immense potential, CRISPR technology also presents significant risks that must be carefully considered. In this detailed blog, we will explore the future frontiers and potential risks associated with CRISPR-Cas9. Future Frontiers

CRISPR-Cas9 technology has revolutionised genome editing, offering immense potential for treating genetic diseases and advancing scientific research. However, along with its promising applications, ethical considerations play a crucial role in guiding the responsible use of this powerful tool. Ethical Considerations in CRISPR Applications CRISPR-Cas9 technology has revolutionised genome editing, offering immense potential for treating genetic

India, a nation celebrated for its cultural diversity, is not merely a melting pot of traditions and languages but also a canvas painted with intricate genetic variations. The GenomeIndia project, a groundbreaking initiative by the Centre for Integrative Biology and Systems Medicine (IBSE) at IIT Madras, endeavors to unravel this complexity through comprehensive whole-genome sequencing