Search Site
Our Tests

CLINICAL EXOME SEQUENCING

CLINICAL EXOME SEQUENCING

Clinical Exome Sequencing tests focus on the coding regions of genes associated with known clinical phenotypes, thus reducing additional costs, increasing diagnostic accuracy, and reducing ambiguous and random results because they do not cover genomic regions not related to diseases in the literature. This test is the largest and fastest NGS test available, covering all 4500+ genes identified with Mendelian diseases and OMIM diseases.

WHY CHOOSE CENTOGENE?
  • Test
    Clinical Exome Sequencing
  • Method
    Next Generation Sequencing
  • Analysis Time
    4-5 weeks
  • Sample Type
    Blood, Bone Marrow, Blood Card
  • Sample Tube
    Purple Cap (EDTA), Antiseptic swap
  • Storage Conditions
    +4 C’de 1 hafta
  • Conditions of Carriage
    The same day; At room temperature
  • Rejection Criteria
    Hemolyzed, Lipemic, Icteric samples are not accepted

The main groups of Clinical Exome Sequencing Panels studied at DNA Laboratories Genetic Diseases Evaluation Center are as follows;

  • Hematology Panels
  • Gastroenterology Panels
  • Endocrinology Panels
  • Dermatology Panels
  • Cardiology Panels
  • Ear-Nose-Throat Panels
  • Ophthalmology Panels
  • Pulmonology Panels
  • Hereditary Cancer Panels
  • Immunology Panels
  • Malformation Panels
  • Neurology Panels
  • Nephrology Panels
  • Metabolic Diseases Panels

There are approximately 250 different Clinical Exome Sequencing Panels within these main panel groups.

DNA Image

Discover Your Genetic Heritage

You can contact us to get information about our genetic tests, consultancy services and more.

Contact us

ONCOSEQ DNALAB (Cancer Genetics)

PRIMIS Non-Invasive Prenatal Test

Preimplantation Genetic Diagnosis (PGD)

Whole Exome Sequencing

Clinical Exome Sequencing

Rare Diseases

Carrier Panels - SMARİS