hWGS is a powerful tool to comprehensively describe an individual’s complete genetic makeup and characterize the entire human genome. It provides a holistic view of an individual’s genetic landscape. Alternatively, hWES serves as a cost-effective choice to hWGS by focusing on the most functionally relevant portions of the genome by selectively targeting the protein-coding regions (exons) of the genome.

In this webinar, Novogene will give you a comprehensive demonstration of the two pipelines to help you decide which one is ideal for your project. In addition, standard analysis as well as advanced analysis niched for cancer and genetic disease research will also be displayed, which utilizes mainstream software and mature in-house pipelines to ensure your hard work produces publishable data. On top of that, a Novogene-powered literature case study will be reviewed to give you a better understanding of how genome sequencing services can support your study.

• Get an overview of hWGS and hWES services.
• Learn Novogene’s solutions based on genome sequencing.
• Discover the standard analysis and advanced analysis of genome sequencing.
• Interpret a Novogene-powered literature case study.