Whole Exome Sequencing (WES)
Whole Exome Sequencing (WES) is aimed to sequence all the protein-coding regions or exons in a genome, collectively known as exome. There are approximately 180,000 exons which represent less than 2% of the human genome. As most of the disease-related variants are found in the exons, WES is thought to be an efficient way to understand the genetic cause of diseases or conditions. We provide a very cost-effective, high quality WES service.
Identify coding variants
Discovery of novel disease-causing genetic mutations
Rare variant mapping