BGI’s Whole Clinical Exome Sequencing examines the DNA sequence of over 180,000 exons across 22,000 genes, screening for more than 4000 monogenic diseases.
Why Choose Whole Clinical Exome Sequencing?
Accurately provides a straightforward and cost effective approach for identifying the genetic variants responsible for a wide range of genetic disorders, thereby assisting clinical diagnosis. Many genetic disorders are amenable to effective treatment upon timely diagnosis. Early detection and intervention can lead to more favorable clinical outcomes.
Conditions Screened: Sequencing of over 180,000 exons across 22,000 genes for more than 4000 monogenic diseases. Contact us for more information.
Suitable for: Intended for use in conjunction with the clinical presentation and other markers of disease progression for the management of patients with rare genetic disorders.
TA Time: 50 working days Sample: Peripheral blood, DNA
Technology: High coverage NGS
We care for your samples from the start through to the result reporting. Highly experienced laboratory professionals follow strict quality procedures to ensure the integrity of your results.
Search for genes of interest and associated mutations, and confirm whether the Xome test is suitable for your requirements.