
Exome-seq

Exome sequencing is a widely used and cost-effective targeted sequencing method. The application is used to enrich, sequence, and analyze the coding and regulatory regions of the genome, allowing the detection of disease-causing candidate variants (including SNPs, insertions and deletions), population genetics, and more.
Before submitting samples for exome-seq, please review our samples delivery instructions and send us your sample submission form.
The sequencing data is sent via Illumina Basespace cloud. Please open an account and indicate the email address associated with your account in the sample submission form. Instructions on how to open an account and manage your data in the cloud.
For additional information, please contact:
Liat Linde, Head
Rappaport Building: 073-3785452
Emerson Building: 073-3785168
Nitsan Fourier, Lab manager