Overview:
IGB offers whole genome sequencing (WGS) solutions designed to provide a complete view of the genome, covering both coding and non-coding regions. These solutions enable comprehensive analysis of genomic variation, including regulatory regions, introns, structural variants, and mitochondrial DNA—going beyond the scope of exome sequencing.
By capturing a broader spectrum of genetic information, WGS supports deeper insights into complex diseases, rare genetic conditions, and traits that may not be explained by coding regions alone. With advancements in sequencing technologies and data analysis, WGS is increasingly being adopted across clinical and research applications for high-resolution genomic discovery.
Features:
• Covers billions of bases for complete genome analysis
• Comprehensive detection of variants across coding and noncoding regions
• Enables retrospective analysis as new biomarkers are discovered
• Supports identification of structural variants and mitochondrial DNA changes
• Applicable to rare disease research, population genomics, and functional genomics
Assay Options:
