{"id":9835,"date":"2025-06-07T06:21:29","date_gmt":"2025-06-07T03:21:29","guid":{"rendered":"https:\/\/medilab.km.ua\/?p=9835"},"modified":"2026-04-20T18:53:43","modified_gmt":"2026-04-20T15:53:43","slug":"dna-sequencing-is-possible-and-its-use","status":"publish","type":"post","link":"https:\/\/medilab.km.ua\/en\/dna-sequencing-is-possible-and-its-use\/","title":{"rendered":"DNA SEQUENCEING: ESSENCE, POSSIBILITIES AND APPLICATIONS"},"content":{"rendered":"<div class=\"kk-star-ratings kksr-auto kksr-align-left kksr-valign-top\"\n    data-payload='{&quot;align&quot;:&quot;left&quot;,&quot;id&quot;:&quot;9835&quot;,&quot;slug&quot;:&quot;default&quot;,&quot;valign&quot;:&quot;top&quot;,&quot;ignore&quot;:&quot;&quot;,&quot;reference&quot;:&quot;auto&quot;,&quot;class&quot;:&quot;&quot;,&quot;count&quot;:&quot;545&quot;,&quot;legendonly&quot;:&quot;&quot;,&quot;readonly&quot;:&quot;&quot;,&quot;score&quot;:&quot;4.9&quot;,&quot;starsonly&quot;:&quot;&quot;,&quot;best&quot;:&quot;5&quot;,&quot;gap&quot;:&quot;5&quot;,&quot;greet&quot;:&quot;Rate this post&quot;,&quot;legend&quot;:&quot;4.9\\\/5 - (545 votes)&quot;,&quot;size&quot;:&quot;24&quot;,&quot;title&quot;:&quot;\u0421\u0415\u041a\u0412\u0415\u041d\u0423\u0412\u0410\u041d\u041d\u042f \u0414\u041d\u041a: \u0421\u0423\u0422\u041d\u0406\u0421\u0422\u042c, \u041c\u041e\u0416\u041b\u0418\u0412\u041e\u0421\u0422\u0406 \u0422\u0410 \u0417\u0410\u0421\u0422\u041e\u0421\u0423\u0412\u0410\u041d\u041d\u042f&quot;,&quot;width&quot;:&quot;139.6&quot;,&quot;_legend&quot;:&quot;{score}\\\/{best} - ({count} {votes})&quot;,&quot;font_factor&quot;:&quot;1.25&quot;}'>\n            \n<div class=\"kksr-stars\">\n    \n<div class=\"kksr-stars-inactive\">\n            <div class=\"kksr-star\" data-star=\"1\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" data-star=\"2\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" data-star=\"3\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" data-star=\"4\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" data-star=\"5\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n    <\/div>\n    \n<div class=\"kksr-stars-active\" style=\"width: 139.6px;\">\n            <div class=\"kksr-star\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n            <div class=\"kksr-star\" style=\"padding-right: 5px\">\n            \n\n<div class=\"kksr-icon\" style=\"width: 24px; height: 24px;\"><\/div>\n        <\/div>\n    <\/div>\n<\/div>\n                \n\n<div class=\"kksr-legend\" style=\"font-size: 19.2px;\">\n            4.9\/5 - (545 votes)    <\/div>\n    <\/div>\n<p data-start=\"60\" data-end=\"88\"><strong data-start=\"60\" data-end=\"88\">What is DNA sequencing?<\/strong><\/p>\n<p data-start=\"90\" data-end=\"411\">DNA sequencing is the process of determining the exact sequence of nucleotides (A, T, C, G) in a DNA molecule. In other words, it is reading the genetic code of a person or any other organism. The method allows you to identify mutations, variations and genetic traits that affect health, disease risks, drug response, etc.<\/p>\n<p data-start=\"413\" data-end=\"453\"><strong data-start=\"413\" data-end=\"453\">History and stages of technology development<\/strong><\/p>\n<ul data-start=\"455\" data-end=\"783\">\n<li data-start=\"455\" data-end=\"549\">\n<p data-start=\"457\" data-end=\"549\"><strong data-start=\"457\" data-end=\"469\">1977<\/strong> \u2014 development of the Sender method, which became the basis for the first genetic decodings.<\/p>\n<\/li>\n<li data-start=\"550\" data-end=\"632\">\n<p data-start=\"552\" data-end=\"632\"><strong data-start=\"552\" data-end=\"564\">2003<\/strong> \u2014 completion of the Human Genome Project: complete human DNA decoded.<\/p>\n<\/li>\n<li data-start=\"633\" data-end=\"783\">\n<p data-start=\"635\" data-end=\"783\"><strong data-start=\"635\" data-end=\"647\">Today<\/strong> \u2014 used <a href=\"https:\/\/medilab.km.ua\/en\/sequencing-of-the-new-generation-of-ngs-answers-to-the-main-question\/\">next generation sequencing<\/a> (NGS), which allows the analysis of thousands of genes simultaneously with high speed and accuracy.<\/p>\n<\/li>\n<\/ul>\n<p data-start=\"785\" data-end=\"808\"><strong data-start=\"785\" data-end=\"808\">Sequencing methods<\/strong><\/p>\n<ol data-start=\"810\" data-end=\"1158\">\n<li data-start=\"810\" data-end=\"897\">\n<p data-start=\"813\" data-end=\"897\"><strong data-start=\"813\" data-end=\"837\">Sender sequencing<\/strong> \u2014 a classic method, still relevant for short fragments.<\/p>\n<\/li>\n<li data-start=\"898\" data-end=\"1047\">\n<p data-start=\"901\" data-end=\"1047\"><strong data-start=\"901\" data-end=\"937\">NGS (Next Generation Sequencing)<\/strong> \u2014 high-throughput technology used for whole-genome, exome, and panel sequencing.<\/p>\n<\/li>\n<li data-start=\"1048\" data-end=\"1158\">\n<p data-start=\"1051\" data-end=\"1158\"><strong data-start=\"1051\" data-end=\"1096\">Third generation (PacBio, Oxford Nanopore)<\/strong> \u2014 capable of reading long stretches of DNA in real time.<\/p>\n<\/li>\n<\/ol>\n<p><img decoding=\"async\" class=\"alignnone size-full wp-image-9837\" src=\"https:\/\/medilab.km.ua\/wp-content\/uploads\/2025\/06\/999-1.jpg\" alt=\"DNA nucleotide sequence on the monitor screen\" width=\"1200\" height=\"667\" srcset=\"https:\/\/medilab.km.ua\/wp-content\/uploads\/2025\/06\/999-1.jpg 1200w, https:\/\/medilab.km.ua\/wp-content\/uploads\/2025\/06\/999-1-150x83.jpg 150w, https:\/\/medilab.km.ua\/wp-content\/uploads\/2025\/06\/999-1-600x334.jpg 600w, https:\/\/medilab.km.ua\/wp-content\/uploads\/2025\/06\/999-1-300x167.jpg 300w, https:\/\/medilab.km.ua\/wp-content\/uploads\/2025\/06\/999-1-1024x569.jpg 1024w, https:\/\/medilab.km.ua\/wp-content\/uploads\/2025\/06\/999-1-768x427.jpg 768w\" sizes=\"(max-width: 1200px) 100vw, 1200px\" \/><\/p>\n<p data-start=\"1160\" data-end=\"1200\"><strong data-start=\"1160\" data-end=\"1200\">Indications for sequencing<\/strong><\/p>\n<ul data-start=\"1202\" data-end=\"1396\">\n<li data-start=\"1202\" data-end=\"1225\">\n<p data-start=\"1204\" data-end=\"1225\">Hereditary diseases<\/p>\n<\/li>\n<li data-start=\"1226\" data-end=\"1251\">\n<p data-start=\"1228\" data-end=\"1251\">Oncological diagnostics<\/p>\n<\/li>\n<li data-start=\"1252\" data-end=\"1287\">\n<p data-start=\"1254\" data-end=\"1287\">Prenatal genetic testing<\/p>\n<\/li>\n<li data-start=\"1288\" data-end=\"1334\">\n<p data-start=\"1290\" data-end=\"1334\">Individualization of treatment (pharmacogenetics)<\/p>\n<\/li>\n<li data-start=\"1335\" data-end=\"1396\">\n<p data-start=\"1337\" data-end=\"1396\">Unspecified conditions (e.g., developmental delay, epilepsy)<\/p>\n<\/li>\n<\/ul>\n<p data-start=\"1398\" data-end=\"1430\"><strong data-start=\"1398\" data-end=\"1430\">Examples from medical practice<\/strong><\/p>\n<ul data-start=\"1432\" data-end=\"1706\">\n<li data-start=\"1432\" data-end=\"1507\">\n<p data-start=\"1434\" data-end=\"1507\"><strong data-start=\"1434\" data-end=\"1475\">Patient with suspected Marfan syndrome<\/strong> \u2014 a mutation was detected in the FBN1 gene.<\/p>\n<\/li>\n<li data-start=\"1508\" data-end=\"1619\">\n<p data-start=\"1510\" data-end=\"1619\"><strong data-start=\"1510\" data-end=\"1533\">In a child with autism<\/strong> \u2014 exome sequencing allowed us to detect a de novo mutation that was not known in the family.<\/p>\n<\/li>\n<li data-start=\"1620\" data-end=\"1706\">\n<p data-start=\"1622\" data-end=\"1706\"><strong data-start=\"1622\" data-end=\"1639\">In a cancer patient<\/strong> \u2014 NGS testing revealed a BRCA1 mutation, which changed the treatment plan.<\/p>\n<\/li>\n<\/ul>\n<p data-start=\"1708\" data-end=\"1733\"><strong data-start=\"1708\" data-end=\"1733\">Advantages and limitations<\/strong><\/p>\n<p data-start=\"1735\" data-end=\"1748\"><strong data-start=\"1735\" data-end=\"1748\">Advantages:<\/strong><\/p>\n<ul data-start=\"1749\" data-end=\"1962\">\n<li data-start=\"1749\" data-end=\"1781\">\n<p data-start=\"1751\" data-end=\"1781\">high accuracy and sensitivity;<\/p>\n<\/li>\n<li data-start=\"1782\" data-end=\"1838\">\n<p data-start=\"1784\" data-end=\"1838\">the ability to analyze tens of thousands of genes at a time;<\/p>\n<\/li>\n<li data-start=\"1839\" data-end=\"1901\">\n<p data-start=\"1841\" data-end=\"1901\">informativeness for diagnosing rare and complex diseases;<\/p>\n<\/li>\n<li data-start=\"1902\" data-end=\"1962\">\n<p data-start=\"1904\" data-end=\"1962\">prognostic capabilities (identification of predispositions to diseases).<\/p>\n<\/li>\n<\/ul>\n<p data-start=\"1964\" data-end=\"1978\"><strong data-start=\"1964\" data-end=\"1978\">Limitation:<\/strong><\/p>\n<ul data-start=\"1979\" data-end=\"2221\">\n<li data-start=\"1979\" data-end=\"2025\">\n<p data-start=\"1981\" data-end=\"2025\">difficulty in interpreting some results;<\/p>\n<\/li>\n<li data-start=\"2026\" data-end=\"2087\">\n<p data-start=\"2028\" data-end=\"2087\">the probability of detecting \u201cvariants of uncertain significance\u201d;<\/p>\n<\/li>\n<li data-start=\"2088\" data-end=\"2124\">\n<p data-start=\"2090\" data-end=\"2124\">high cost in some cases;<\/p>\n<\/li>\n<li data-start=\"2125\" data-end=\"2221\">\n<p data-start=\"2127\" data-end=\"2221\">ethical dilemmas (e.g., whether to inform the patient of findings unrelated to his complaints).<\/p>\n<\/li>\n<\/ul>\n<p data-start=\"2223\" data-end=\"2267\"><strong data-start=\"2223\" data-end=\"2267\">Comparison table of sequencing methods<\/strong><\/p>\n<div class=\"_tableContainer_16hzy_1\">\n<div class=\"_tableWrapper_16hzy_14 group flex w-fit flex-col-reverse\">\n<table class=\"w-fit min-w-(--thread-content-width)\" data-start=\"2269\" data-end=\"2710\">\n<thead data-start=\"2269\" data-end=\"2353\">\n<tr data-start=\"2269\" data-end=\"2353\">\n<th data-start=\"2269\" data-end=\"2287\" data-col-size=\"sm\">Method<\/th>\n<th data-start=\"2287\" data-end=\"2298\" data-col-size=\"sm\">Precision<\/th>\n<th data-start=\"2298\" data-end=\"2310\" data-col-size=\"sm\">Speed<\/th>\n<th data-start=\"2310\" data-end=\"2327\" data-col-size=\"sm\">Read length<\/th>\n<th data-start=\"2327\" data-end=\"2341\" data-col-size=\"sm\">Data volume<\/th>\n<th data-start=\"2341\" data-end=\"2353\" data-col-size=\"sm\">Cost<\/th>\n<\/tr>\n<\/thead>\n<tbody data-start=\"2438\" data-end=\"2710\">\n<tr data-start=\"2438\" data-end=\"2522\">\n<td data-start=\"2438\" data-end=\"2456\" data-col-size=\"sm\">Sanger<\/td>\n<td data-start=\"2456\" data-end=\"2467\" data-col-size=\"sm\">High<\/td>\n<td data-start=\"2467\" data-end=\"2479\" data-col-size=\"sm\">Slow<\/td>\n<td data-start=\"2479\" data-end=\"2496\" data-col-size=\"sm\">Up to 1000 pairs<\/td>\n<td data-start=\"2496\" data-end=\"2510\" data-col-size=\"sm\">Little<\/td>\n<td data-start=\"2510\" data-end=\"2522\" data-col-size=\"sm\">Medium<\/td>\n<\/tr>\n<tr data-start=\"2523\" data-end=\"2622\">\n<td data-start=\"2523\" data-end=\"2541\" data-col-size=\"sm\">NGS<\/td>\n<td data-start=\"2541\" data-end=\"2555\" data-col-size=\"sm\">Very high<\/td>\n<td data-start=\"2555\" data-end=\"2564\" data-col-size=\"sm\">High<\/td>\n<td data-start=\"2564\" data-end=\"2594\" data-col-size=\"sm\">Short snippets (150\u2013300)<\/td>\n<td data-start=\"2594\" data-end=\"2604\" data-col-size=\"sm\">Great<\/td>\n<td data-start=\"2604\" data-end=\"2622\" data-col-size=\"sm\">1 gene lower<\/td>\n<\/tr>\n<tr data-start=\"2623\" data-end=\"2710\">\n<td data-start=\"2623\" data-end=\"2641\" data-col-size=\"sm\">Third generation<\/td>\n<td data-start=\"2641\" data-end=\"2652\" data-col-size=\"sm\">Medium<\/td>\n<td data-start=\"2652\" data-end=\"2666\" data-col-size=\"sm\">Very high<\/td>\n<td data-start=\"2666\" data-end=\"2683\" data-col-size=\"sm\">Up to 1 million pairs<\/td>\n<td data-start=\"2683\" data-end=\"2698\" data-col-size=\"sm\">Very large<\/td>\n<td data-start=\"2698\" data-end=\"2710\" data-col-size=\"sm\">High<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<div class=\"sticky end-(--thread-content-margin) h-0 self-end select-none\">\n<div class=\"absolute end-0 flex items-end\"><\/div>\n<\/div>\n<\/div>\n<\/div>\n<p data-start=\"2712\" data-end=\"2753\"><strong data-start=\"2712\" data-end=\"2753\">Relevance for the future of medicine<\/strong><\/p>\n<p data-start=\"2755\" data-end=\"3145\">DNA sequencing is gradually becoming a standard not only in complex clinical cases but also in personalized medicine. It is used in the selection of biological therapies, immunotherapy in oncology, risk prediction for diabetes, heart disease, neurological conditions. Genetic tests are becoming increasingly available, including commercial products for identifying ancestry or food intolerances.<\/p>\n<p data-start=\"2755\" data-end=\"3145\">DNA sequencing opens a new era in medicine, when treatment and prevention become individual, and the accuracy of diagnosis is maximized. It is not just an analysis - it is a map of our biological essence.<\/p>","protected":false},"excerpt":{"rendered":"<p>What is DNA sequencing? DNA sequencing is the process of determining the exact sequence of nucleotides (A, T, C, G) in a DNA molecule.<\/p>","protected":false},"author":627,"featured_media":9836,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-9835","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorized"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>\u0421\u0435\u043a\u0432\u0435\u043d\u0443\u0432\u0430\u043d\u043d\u044f \u0414\u041d\u041a: \u043c\u043e\u0436\u043b\u0438\u0432\u043e\u0441\u0442\u0456, \u043c\u0435\u0442\u043e\u0434\u0438 \u0442\u0430 \u043f\u0440\u0438\u043a\u043b\u0430\u0434\u0438 \u0437\u0430\u0441\u0442\u043e\u0441\u0443\u0432\u0430\u043d\u043d\u044f<\/title>\n<meta name=\"description\" content=\"\u0429\u043e 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