{"id":33790,"date":"2022-11-26T11:09:53","date_gmt":"2022-11-26T11:09:53","guid":{"rendered":"https:\/\/gyncentrum.pl\/badanie-wes\/"},"modified":"2024-02-21T10:43:25","modified_gmt":"2024-02-21T10:43:25","slug":"wes-test","status":"publish","type":"servies","link":"https:\/\/gyncentrum.pl\/en\/wes-test\/","title":{"rendered":"WES test"},"content":{"rendered":"\n
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WES study<\/h3>\n
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The most extensive genetic testing on the market<\/p>\n<\/h3>\n

Whole-exome sequencing – WES is the most extensive test of the coding portions of the genome available on the market today, with up to 20,000 genes being analyzed.<\/strong> A change in any of them can lead to the development of a genetic disease, such as those manifested by autism spectrum disorders. Since the WES test checks many thousands of genes simultaneously, it significantly shortens the diagnostic process and reduces its cost.<\/strong> If the test detects a specific disease, the patient has a chance to get into the care of specialists and start effective treatment sooner.<\/p>\n<\/div>\n \n <\/div>\n

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Get your genes tested and find out the cause of your health problems!<\/p>\n<\/h3>\n

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What does the WES study consist of?<\/p>\n<\/h3>\n

The<\/strong> Whole Exome Sequencing (WES) test<\/strong> involves sequencing the coding regions of genes in the human body, i.e., whole exome sequencing<\/strong>, where mutations can impinge on the formation of defective proteins and result in genetic disorders. The test involves analyzing 20,000 genes for mutations in them. Detection of such mutations allows the implementation of appropriate therapy at an early stage of the disease or identification of a disease entity<\/strong> that often cannot be determined by other diagnostic tests.<\/p>\n

The test material is DNA isolated from blood. The test is based on<\/strong> the Next Generation Sequencing ( NGS) technique<\/strong>, which makes it possible to precisely identify sequences of coding genes in which mutations can cause genetic diseases.<\/strong><\/p>\n<\/span>\n <\/div>\n <\/div>\n\n <\/div>\n<\/section>\n\n\n\n

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WES TRIO study<\/p>\n<\/h3>\n

The WES TRIO test differs from the standard WES test in that it offers the possibility of including genetic material from the patient’s parents in the analysis as well.<\/strong> The DNA of all test subjects is first sequenced and then compared with each other for the presence of the same gene variations. Checking the genes of the parents makes it easier to make the right diagnosis. It also makes it possible to determine whether a disease is hereditary, and if so, from which parent the sick patient inherited the defective gene.<\/strong> The result of the WES TRIO test thus provides valuable information on the patient’s health status, as well as that of his immediate family members.<\/p>\n<\/span>\n <\/div>\n <\/div>\n\n <\/div>\n<\/section>\n\n\n\n

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WES examination – indications<\/h3>\n

The WES examination is intended for both children and adults who present with various worrisome symptoms and health problems, including those of unknown cause, such as:<\/p>\n