{"id":3261,"date":"2025-10-06T05:52:40","date_gmt":"2025-10-06T05:52:40","guid":{"rendered":"https:\/\/genoks.com.tr\/docs\/genomeseq-wgs-me\/"},"modified":"2026-05-02T05:14:17","modified_gmt":"2026-05-02T05:14:17","password":"","slug":"genomeseq-wgs-me","status":"publish","type":"docs","link":"https:\/\/genoks.com.tr\/me\/docs\/genomeseq-wgs-me\/","title":{"rendered":"\u0160ta je GenoMESeq KOMPLETNO SEKVENCIRANJE GENOMA?"},"content":{"rendered":"<p><!--genoks-intro-me:start--><\/p>\n<p><strong>GenoMESeq kompletno sekvenciranje genoma (WGS).<\/strong> Sekvencira \u010ditav ~3 milijarde bp ljudski genom uklju\u010duju\u0107i kodiraju\u0107e, nekodiraju\u0107e, regulatorne i strukturne regije, sa uniformnom ~30\u00d7 pokriveno\u0161\u0107u. Otkriva SNV, male indele, CNV, strukturne varijante i tandem ponavljanja u jednom testu. Najve\u0107i dijagnosti\u010dki prinos za neobja\u0161njenu Mendelovu bolest (~40-50%). Izvje\u0161taj: 8-16 nedjelja. Indikovan kada WES nije dijagnosti\u010dan ili se sumnja na specifi\u010dne strukturne\/ponavljaju\u0107e poreme\u0107aje. Uklju\u010duje analizu mtDNA.<\/p>\n<p><!--genoks-intro-me:end--><\/p>\n<p style=\"text-align: justify\"><strong>GenoMESeq T\u00fcm Genom Sekanslama Nedir?<\/strong><br \/>\nT\u00fcm genom sekanslama (whole genome sequencing &#8211; WGS), bir organizman\u0131n t\u00fcm genomunun DNA dizilimini belirlemek i\u00e7in kullan\u0131lan bir genetik analiz y\u00f6ntemidir. Bu y\u00f6ntem, bir organizman\u0131n t\u00fcm DNA&#8217;s\u0131n\u0131 analiz etti\u011finden, genomda yer alan t\u00fcm genetik materyali, genlerin yan\u0131 s\u0131ra aralar\u0131ndaki bo\u015fluklar\u0131 da i\u00e7erir.<\/p>\n<p style=\"text-align: justify\">WGS, DNA dizilimleme y\u00f6ntemlerinin en kapsaml\u0131 olan\u0131d\u0131r ve herhangi bir organizman\u0131n t\u00fcm genetik bilgisini elde etmek i\u00e7in kullan\u0131labilir. Bu y\u00f6ntem, \u00f6zellikle insan geneti\u011fi, t\u0131p, tar\u0131m ve evrimsel biyoloji gibi bir\u00e7ok alanda ara\u015ft\u0131rmalarda kullan\u0131l\u0131r.<\/p>\n<p style=\"text-align: justify\">WGS verileri, bireysel hastalarda meydana gelen mutasyonlar\u0131 ve genetik de\u011fi\u015fiklikleri tan\u0131mlamak, hastal\u0131klar\u0131n nedenlerini ve tedavi y\u00f6ntemlerini anlamak, t\u00fcrlerin evrimini ve ili\u015fkilerini belirlemek, tar\u0131msal \u00fcretimde kullan\u0131lan bitkilerin ve hayvanlar\u0131n genetik \u00e7e\u015fitlili\u011fini de\u011ferlendirmek gibi bir\u00e7ok farkl\u0131 ama\u00e7 i\u00e7in kullan\u0131labilir. Ancak, WGS y\u00f6ntemi, t\u00fcm genomun analiz edilmesi nedeniyle daha pahal\u0131 ve zaman al\u0131c\u0131d\u0131r.<\/p>\n<table>\n<tbody>\n<tr>\n<td><strong>Y\u00f6ntem :<\/strong><\/td>\n<td>NGS<\/td>\n<\/tr>\n<tr>\n<td><strong>Raporlama S\u00fcresi :<\/strong><\/td>\n<td>12 Hafta &#8211; 16 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>Saklama \/ 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>GenoMESeq kompletno sekvenciranje genoma (WGS). Sekvencira \u010ditav ~3 milijarde bp ljudski genom uklju\u010duju\u0107i kodiraju\u0107e, nekodiraju\u0107e, regulatorne i strukturne regije, sa uniformnom ~30\u00d7 pokriveno\u0161\u0107u. Otkriva SNV, male indele, CNV, strukturne varijante i tandem ponavljanja u jednom testu. Najve\u0107i dijagnosti\u010dki prinos za<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":[],"class_list":["post-3261","docs","type-docs","status-publish","hentry","doc_category-genoks-gdhm-genetic-tests-me"],"aioseo_notices":[],"year_month":"2026-05","word_count":377,"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":[],"aioseo_head":"\n\t\t<!-- All in One SEO Pro 4.9.5.2 - aioseo.com -->\n\t<meta name=\"description\" content=\"GenoMESeq kompletno sekvenciranje genoma (WGS). 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Sekvencira \u010ditav ~3 milijarde bp ljudski genom uklju\u010duju\u0107i kodiraju\u0107e, nekodiraju\u0107e, regulatorne i strukturne regije, sa uniformnom ~30\u00d7 pokriveno\u0161\u0107u. Otkriva SNV, male indele, CNV, strukturne varijante i tandem ponavljanja u jednom testu. Najve\u0107i dijagnosti\u010dki prinos za neobja\u0161njenu Mendelovu bolest (~40-50%). Izvje\u0161taj: 8-16 nedjelja. 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