Whole Genome Sequencing

Advanced genetic testing used to analyse an individual’s complete genomic DNA sequence, covering coding and non-coding regions of the genome. Whole Genome Sequencing can help identify genetic variants associated with inherited conditions and support personalised health assessment and clinical decision-making.

Key Services:

• Whole Genome Sequencing (WGS)
• Comprehensive Genomic Variant Analysis
• Single Nucleotide Variant (SNV) Detection
• Insertion and Deletion (Indel) Analysis
• Copy Number Variant (CNV) Analysis
• Structural Variant Analysis
• Inherited Disease Screening
• Rare Genetic Disorder Analysis
• Pharmacogenomic Variant Analysis
• Carrier Status Assessment
• Genetic Risk Assessment
• Clinical Genomic Interpretation and Reporting