{"id":3201,"date":"2025-10-06T05:52:40","date_gmt":"2025-10-06T05:52:40","guid":{"rendered":"https:\/\/genoks.com.tr\/docs\/microarray-analysis-en\/"},"modified":"2026-05-01T21:43:14","modified_gmt":"2026-05-01T21:43:14","password":"","slug":"microarray-analysis-en","status":"publish","type":"docs","link":"https:\/\/genoks.com.tr\/en\/docs\/microarray-analysis-en\/","title":{"rendered":"What is Microarray Analysis? How is it Performed?"},"content":{"rendered":"<p><!--genoks-intro-en:start--><\/p>\n<p><strong>What is Microarray Analysis?<\/strong><\/p>\n<p>Chromosomal microarray (CMA \/ array-CGH) is a high-resolution technique that detects gains and losses of DNA across the entire genome at the level of microdeletions and microduplications down to ~50-100 kb. It does not require live cell culture and produces results in 5-10 days from peripheral blood, amniotic fluid, or chorionic villi. CMA is the recommended <strong>first-tier diagnostic test (ACMG, 2010)<\/strong> for unexplained developmental delay, intellectual disability, autism spectrum disorder, and multiple congenital anomalies.<\/p>\n<p><strong>What it does not detect:<\/strong> balanced translocations, point mutations, single-gene disorders, low-level mosaicism, and uniparental disomy without informative SNP probes. Karyotyping or NGS may be needed to complement CMA in specific clinical questions.<\/p>\n<p><!--genoks-intro-en:end--><\/p>\n<p style=\"text-align: justify\"><strong>Mikroarray Analizi Nedir?<\/strong><br \/>\nMikroarray analizi, bir\u00e7ok genin ifadesini ayn\u0131 anda belirlemek i\u00e7in kullan\u0131lan bir y\u00fcksek-throughput teknolojisidir. Bu teknoloji\u00a0bir\u00e7ok genin DNA veya RNA \u00f6rneklerinin hibridizasyon yoluyla ayn\u0131 anda analiz edilmesine olanak tan\u0131r.<\/p>\n<p style=\"text-align: justify\">Mikroarray analizi, bir\u00e7ok farkl\u0131 ara\u015ft\u0131rma alan\u0131nda kullan\u0131lmaktad\u0131r. \u00d6rne\u011fin, bu teknoloji, bir organizman\u0131n gen ekspresyon profillerinin incelenmesi, hastal\u0131klar\u0131n molek\u00fcler nedenlerinin anla\u015f\u0131lmas\u0131, ila\u00e7 ke\u015ffi, t\u0131bbi te\u015fhis, kanser te\u015fhisi ve tedavisi gibi bir\u00e7ok alanda kullan\u0131lmaktad\u0131r.<\/p>\n<p style=\"text-align: justify\">Mikroarray analizi, \u00f6nce bir\u00e7ok genin DNA veya RNA&#8217;s\u0131n\u0131n bir \u00e7ip \u00fczerine yerle\u015ftirilmesiyle ba\u015flar. Daha sonra, bu \u00e7ipler, \u00f6rneklerle hibridize edilir ve floresan etiketleri veya di\u011fer detekt\u00f6r sistemleri kullan\u0131larak gen ifadesi \u00f6l\u00e7\u00fcl\u00fcr. Bu y\u00f6ntem, binlerce hatta milyonlarca geni ayn\u0131 anda analiz etmeyi m\u00fcmk\u00fcn k\u0131lar.<\/p>\n<p style=\"text-align: justify\">Mikroarray analizi sonu\u00e7lar\u0131, gen ifadesi profilini veya genetik varyasyonlar\u0131 belirlemek i\u00e7in kullan\u0131labilir. Bu y\u00f6ntem, gen ifadesi profilinin zaman i\u00e7indeki de\u011fi\u015fimleri, farkl\u0131 dokular aras\u0131ndaki farkl\u0131l\u0131klar veya bir hastal\u0131k durumunda farkl\u0131 gen ifadesi d\u00fczeyleri gibi bir\u00e7ok farkl\u0131 fakt\u00f6r\u00fcn incelenmesine olanak tan\u0131r.<\/p>\n<div id=\"attachment_1579\" style=\"width: 2570px\" class=\"wp-caption alignnone\"><img loading=\"lazy\" decoding=\"async\" aria-describedby=\"caption-attachment-1579\" class=\"size-full wp-image-1579\" src=\"https:\/\/genoks.com.tr\/wp-content\/uploads\/2023\/04\/biotechnology-specialist-laboratory-conducting-experiments-scaled.jpg\" alt=\"Mikroarray Analizi\" width=\"2560\" height=\"1707\" \/><p id=\"caption-attachment-1579\" class=\"wp-caption-text\">Mikroarray Analizi<\/p><\/div>\n<p style=\"text-align: justify\"><strong>Y\u00fcksek-throughput Teknolojisi Nedir?<\/strong><br \/>\n&#8220;Y\u00fcksek-throughput teknolojisi&#8221;, b\u00fcy\u00fck miktarda veri \u00fcretmek ve i\u015flemek i\u00e7in kullan\u0131lan bir dizi otomatize edilmi\u015f y\u00f6ntemi ifade eder. Bu teknoloji, bir\u00e7ok disiplinde geni\u015f \u00e7apta kullan\u0131lmaktad\u0131r, \u00f6zellikle de biyoteknoloji, farmakoloji, molek\u00fcler biyoloji, genetik, proteomik ve di\u011fer biyolojik bilimlerde.<\/p>\n<p style=\"text-align: justify\">Y\u00fcksek-throughput teknolojisi, bir\u00e7ok \u00f6rnek veya veri noktas\u0131 ayn\u0131 anda i\u015flenebilen otomatik ve robotik sistemler kullanarak b\u00fcy\u00fck veri setleri olu\u015fturmay\u0131 m\u00fcmk\u00fcn k\u0131lar. Bu teknoloji, \u00f6zellikle genetik, genomik, proteomik ve di\u011fer biyolojik bilimlerde, bir\u00e7ok veri noktas\u0131n\u0131n analiz edilmesi gereken durumlarda yararl\u0131d\u0131r.<\/p>\n<p style=\"text-align: justify\">\u00d6rnek olarak, y\u00fcksek-throughput teknolojisi, mikroarray analizi, RNA dizileme (RNA-seq), protein dizileme, h\u00fccre taramada kullan\u0131labilir. Ayr\u0131ca proteom analizi, genomik tarama, metabolom analizi gibi bir\u00e7ok teknikte kullan\u0131labilir. Bu teknolojiler, ayn\u0131 anda binlerce hatta milyonlarca veri noktas\u0131n\u0131 analiz edebilir, bu da \u00e7ok say\u0131da bilgi elde etmeyi ve anlamaya yard\u0131mc\u0131 olur.<\/p>\n<p style=\"text-align: justify\">Y\u00fcksek-throughput teknolojisi, veri \u00fcretim h\u0131z\u0131n\u0131 art\u0131rarak ara\u015ft\u0131rmac\u0131lar\u0131n daha h\u0131zl\u0131 sonu\u00e7lar almas\u0131na, daha kapsaml\u0131 bilgi edinmelerine ve daha iyi sonu\u00e7lar elde etmelerine yard\u0131mc\u0131 olur. Bu teknoloji, bir\u00e7ok alanda b\u00fcy\u00fck veri setleri \u00fcretmek i\u00e7in temel bir ara\u00e7 haline gelmi\u015ftir.<\/p>\n<table>\n<tbody>\n<tr>\n<td><strong>Y\u00f6ntem :<\/strong><\/td>\n<td>Mikroarray<\/td>\n<\/tr>\n<tr>\n<td><strong>Raporlama S\u00fcresi :<\/strong><\/td>\n<td>4-6 Hafta<\/td>\n<\/tr>\n<tr>\n<td><strong><strong>Prenatal\/ Postnatal:<\/strong><\/strong><\/td>\n<td>Postnatal<\/td>\n<\/tr>\n<tr>\n<td><strong>Gerekli Numune<\/strong>:<\/td>\n<td>EDTA&#8217;l\u0131 Kan (2-4 ml)<\/td>\n<\/tr>\n<tr>\n<td><strong>Saklamama \/ Ta\u015f\u0131ma S\u0131cakl\u0131\u011f\u0131:<\/strong><\/td>\n<td>+ 4C\u00b0\/ + 24C\u00b0<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>T\u00fcm genetik testlerimiz <strong>&#8220;Hasta Onam Formu&#8221;<\/strong> ve <strong>&#8220;KVKK Formu&#8221;<\/strong>nun imzalanmas\u0131n\u0131n ard\u0131ndan \u00e7al\u0131\u015f\u0131lmaya ba\u015flan\u0131r.<\/p>\n<hr \/>\n<p><strong>Detayl\u0131 Bilgi Almak \u0130\u00e7in Bize Mesaj Atabilirsiniz.<\/strong><\/p>\n<table>\n<tbody>\n<tr>\n<td>[contact-form-7 id=&#8221;710&#8243; title=&#8221;genetik ba\u015fvuru&#8221;]<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>Genoks Genetik Hastal\u0131klar De\u011ferlendirme Merkezi T.C. Sa\u011fl\u0131k Bankanl\u0131\u011f\u0131nca denetlenen ve GHDM-SM\/06.15\/01 ruhsat numaras\u0131 ile hizmet veren sa\u011fl\u0131k kurulu\u015fudur. genoks.com.tr web sayfas\u0131nda bulunan bilgiler, genetik de\u011ferlendirme ve\/veya tan\u0131-te\u015fhis ama\u00e7l\u0131 kullan\u0131lmamal\u0131d\u0131r. T\u00fcm i\u00e7erikler bilgilendirme ama\u00e7l\u0131d\u0131r.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>What is Microarray Analysis? Chromosomal microarray (CMA \/ array-CGH) is a high-resolution technique that detects gains and losses of DNA across the entire genome at the level of microdeletions and microduplications down to ~50-100 kb. It does not require live<span class=\"excerpt-hellip\"> [\u2026]<\/span><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"closed","template":"","meta":{"footnotes":""},"doc_category":[204],"doc_tag":[91,112],"class_list":["post-3201","docs","type-docs","status-publish","hentry","doc_category-genoks-gdhm-genetic-tests","doc_tag-array","doc_tag-mikroarray-analizi"],"aioseo_notices":[],"year_month":"2026-05","word_count":652,"total_views":0,"reactions":{"happy":0,"normal":0,"sad":0},"author_info":{"name":"admin","author_nicename":"admin","author_url":"https:\/\/genoks.com.tr\/en\/author\/admin\/"},"doc_category_info":[{"term_name":"Genoks GDHM Genetic Tests","term_url":"https:\/\/genoks.com.tr\/en\/docs-category\/genoks-gdhm-genetic-tests\/"}],"doc_tag_info":[{"term_name":"array","term_url":"https:\/\/genoks.com.tr\/docs-tag\/array\/"},{"term_name":"Mikroarray Analizi","term_url":"https:\/\/genoks.com.tr\/docs-tag\/mikroarray-analizi\/"}],"aioseo_head":"\n\t\t<!-- All in One SEO Pro 4.9.5.2 - aioseo.com -->\n\t<meta name=\"description\" content=\"What is Microarray Analysis?Chromosomal microarray (CMA \/ array-CGH) is a high-resolution technique that detects gains and losses of DNA across the entire genome at the level of microdeletions and microduplications down to ~50-100 kb. 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It does not require live cell culture and produces results in 5-10 days from peripheral blood, amniotic fluid, or chorionic villi.","inLanguage":"en-US","isPartOf":{"@id":"https:\/\/genoks.com.tr\/en\/#website"},"breadcrumb":{"@id":"https:\/\/genoks.com.tr\/en\/docs\/microarray-analysis-en\/#breadcrumblist"},"author":{"@id":"https:\/\/genoks.com.tr\/en\/author\/admin\/#author"},"creator":{"@id":"https:\/\/genoks.com.tr\/en\/author\/admin\/#author"},"datePublished":"2025-10-06T05:52:40+00:00","dateModified":"2026-05-01T21:43:14+00:00"},{"@type":"WebSite","@id":"https:\/\/genoks.com.tr\/en\/#website","url":"https:\/\/genoks.com.tr\/en\/","name":"Genoks Genetics | NIPT, Carrier Screening, Oncogenetics and WES Services","description":"Shedding Light on Your Genes!","inLanguage":"en-US","publisher":{"@id":"https:\/\/genoks.com.tr\/en\/#organization"}}]},"og:locale":"en_US","og:site_name":"Genoks Genetics | NIPT, Carrier Screening, Oncogenetics and WES Services - Shedding Light on Your Genes!","og:type":"article","og:title":"What is Microarray Analysis? 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How is it Performed? - Genoks Genetics | NIPT, Carrier Screening, Oncogenetics and WES Services","twitter:description":"What is Microarray Analysis?Chromosomal microarray (CMA \/ array-CGH) is a high-resolution technique that detects gains and losses of DNA across the entire genome at the level of microdeletions and microduplications down to ~50-100 kb. 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