Whole-Exome Sequencing
Whole-Exome Sequencing (WES)
What is Whole-Exome Sequencing (WES)
What is an exome and why is it important to study it
Inside each cell of the body lies an instruction that determines how it develops, functions, and interacts with others. This instruction is encoded in the DNA molecule — a long chain consisting of four chemical bases: A, T, C, and G (adenine, thymine, cytosine, and guanine).
These bases connect in a specific sequence, passed from parents to children. In this form, genetic information becomes interpretable for cellular function.
The human body is made up of cells, each containing DNA. Genes carry instructions for synthesizing all proteins in the body.
The entire set of a person’s genetic information is called the genome and includes over 3.2 billion bases. However, only about 1% of this sequence (approximately 30 million nucleotide pairs) constitutes the exome — the DNA region containing protein-coding genes.
85% of all clinically significant mutations are located in the exome.
How to take the test
You can take the test at our collection point at:
Tashkent, 1st Rakatboshi passage, 17
Blood collection takes no more than 10 minutes. Results are available online or in print.
Whole-Exome Sequencing in the Genscreen Laboratory
International experience
Experts with years of practice in genetics, laboratory diagnostics and bioinformatics.
Confidentiality guarantee
We strictly follow the privacy policy: information is not shared with third parties without consent.
Personal consultation
Online consultation is available to explain results after the study.
Reliability and control
Every research stage is under strict supervision and multiple checks.
Technological leadership
Modern equipment and international diagnostic standards.
Transparent pricing
Clear costs without hidden fees, with the option to choose the most suitable test.