Whole Exome Sequencing

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


Learn more about our Next Generation Sequencing services:

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