{"id":3205,"date":"2025-10-06T05:52:40","date_gmt":"2025-10-06T05:52:40","guid":{"rendered":"https:\/\/genoks.com.tr\/docs\/microarray-analysis-me\/"},"modified":"2026-05-01T21:43:14","modified_gmt":"2026-05-01T21:43:14","password":"","slug":"microarray-analysis-me","status":"publish","type":"docs","link":"https:\/\/genoks.com.tr\/me\/docs\/microarray-analysis-me\/","title":{"rendered":"\u0160ta je mikroarray analiza? Kako se izvodi?"},"content":{"rendered":"<p><!--genoks-intro-me:start--><\/p>\n<p><strong>\u0160ta je mikroarray analiza?<\/strong><\/p>\n<p>Hromozomska mikroarray (CMA \/ array-CGH) je tehnika visoke rezolucije koja detektuje dobitke i gubitke DNK u celom genomu na nivou mikrodelecija i mikroduplikacija veli\u010dine od oko 50-100 kb. Ne zahteva kulturu \u017eivih \u0107elija i daje rezultate u roku od 5-10 dana iz periferne krvi, amnionske te\u010dnosti ili horionskih resica. CMA se preporu\u010duje kao <strong>dijagnosti\u010dki test prvog izbora (ACMG 2010)<\/strong> za neobja\u0161njeno razvojno ka\u0161njenje, intelektualnu ometenost, poreme\u0107aj iz spektra autizma i multiple kongenitalne anomalije.<\/p>\n<p><strong>\u0160ta ne detektuje:<\/strong> balansirane translokacije, ta\u010dkaste mutacije, monogenske bolesti, mozaicizam niskog nivoa i uniparentalnu dizomiju bez informativnih SNP proba. Za specifi\u010dna klini\u010dka pitanja mo\u017ee biti potrebno kariotipiranje ili NGS kao dopuna CMA.<\/p>\n<p><!--genoks-intro-me: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>\u0160ta je mikroarray analiza? Hromozomska mikroarray (CMA \/ array-CGH) je tehnika visoke rezolucije koja detektuje dobitke i gubitke DNK u celom genomu na nivou mikrodelecija i mikroduplikacija veli\u010dine od oko 50-100 kb. Ne zahteva kulturu \u017eivih \u0107elija i daje rezultate<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":[210],"doc_tag":[91,112],"class_list":["post-3205","docs","type-docs","status-publish","hentry","doc_category-genoks-gdhm-genetic-tests-me","doc_tag-array","doc_tag-mikroarray-analizi"],"aioseo_notices":[],"year_month":"2026-05","word_count":661,"total_views":0,"reactions":{"happy":0,"normal":0,"sad":0},"author_info":{"name":"admin","author_nicename":"admin","author_url":"https:\/\/genoks.com.tr\/me\/author\/admin\/"},"doc_category_info":[{"term_name":"Genoks GDHM Genetski testovi","term_url":"https:\/\/genoks.com.tr\/me\/docs-category\/genoks-gdhm-genetic-tests-me\/"}],"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=\"\u0160ta je mikroarray analiza?Hromozomska mikroarray (CMA \/ array-CGH) je tehnika visoke rezolucije koja detektuje dobitke i gubitke DNK u celom genomu na nivou mikrodelecija i mikroduplikacija veli\u010dine od oko 50-100 kb. 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Kako se izvodi? - Genoks Genetics | NIPT, Skrining Nosilaca, Onkogenetika i WES Usluge","description":"\u0160ta je mikroarray analiza?Hromozomska mikroarray (CMA \/ array-CGH) je tehnika visoke rezolucije koja detektuje dobitke i gubitke DNK u celom genomu na nivou mikrodelecija i mikroduplikacija veli\u010dine od oko 50-100 kb. Ne zahteva kulturu \u017eivih \u0107elija i daje rezultate u roku od 5-10 dana iz periferne krvi, amnionske te\u010dnosti ili horionskih resica. 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Kako se izvodi? - Genoks Genetics | NIPT, Skrining Nosilaca, Onkogenetika i WES Usluge","og:description":"\u0160ta je mikroarray analiza?Hromozomska mikroarray (CMA \/ array-CGH) je tehnika visoke rezolucije koja detektuje dobitke i gubitke DNK u celom genomu na nivou mikrodelecija i mikroduplikacija veli\u010dine od oko 50-100 kb. Ne zahteva kulturu \u017eivih \u0107elija i daje rezultate u roku od 5-10 dana iz periferne krvi, amnionske te\u010dnosti ili horionskih resica. 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