Comprehensive Solution for
Rare Diseases
Identify disease-causing variants across all protein-coding regions of the genome with advanced WES technology.
How Does WES Work?
Whole Exome Sequencing step by step
DNA Isolation
DNA is extracted and purified from your blood or saliva sample.
Exome Capture
Protein-coding regions are targeted with specific probes.
Sequencing
High-accuracy sequencing on the Illumina NovaSeq platform.
Analysis & Report
Variants are classified and reported according to ACMG guidelines.
Who Is WES Suitable For?
Comprehensive solution for undiagnosed genetic conditions
Suspected Rare Disease
Ideal for individuals with long-undiagnosed genetic conditions.
Developmental Delay
Developmental delay and intellectual disability in children.
Family History
Families with hereditary disease history and consanguinity.
Our Test Options
Choose the WES test that suits you best
WES Whole Exome Sequencing
ComprehensiveComprehensive genetic test analyzing all protein-coding regions of the genome. Most effective method for rare disease diagnosis.
WES Trio Analysis
Family AnalysisSimultaneous analysis of patient, mother and father for inherited variant detection. High diagnostic yield in familial rare diseases.
WES Rapid Result
Urgent / PriorityPriority processing with results in 2-3 weeks for urgent cases. Suitable for NICU and critical patients.
Frequently Asked Questions
What you wonder about WES testing
How long does the WES test take?
WES results are typically ready within 4-6 weeks. Rush processing is available for urgent cases.
Does WES diagnose all genetic conditions?
WES can identify many genetic conditions, but not all. It covers approximately 85% of known disease-causing variants.
What if the test shows a variant of uncertain significance?
Variants of uncertain significance (VUS) are periodically reclassified as new scientific data becomes available.
Latest Articles
News and insights about genetic testing
WES Test in Newborns and Infants: The Vital Importance of Early Diagnosis
Early diagnosis of genetic diseases in newborns and infants is extremely important for protecting their health and quickly initiating treatment processes.
WES Test and Artificial Intelligence: The Era of AI-Enabled Genetic Diagnosis
The WES (Whole Exome Sequencing) test, a revolutionary step in the diagnosis of genetic diseases, has become one of the most important tools for families and healthcare professionals today.
How to Interpret WES Test Results? Meaning of Variant and Mutation
In medicine, genetic tests are an important tool for understanding an individual's genetic makeup and for detecting potential health issues in advance.
Get Information About WES Testing
Our expert genetic counselors are happy to answer your questions.