Cytogenomics

Investigate genetic variations at the chromosomal level for comprehensive understanding of chromosomal structure and its impact on health.

Cytogenomics combines the traditional cytogenetic techniques with high-throughput genomic methods to explore the relationship between chromosomal structures and genomic information. It identifies chromosomal abnormalities, translocations, and copy number variations that can lead to genetic disorders and developmental abnormalities providing a detailed understanding of the structural and functional aspects of chromosomes and how they impact genomic variations and disease pathogenesis.

Cytogenomics is a rapidly evolving field that utilizes state-of-the-art technologies and has revolutionized the field of clinical genetics by enabling early diagnosis and personalized treatment of genetic disorders.