{"id":3229,"date":"2025-10-06T05:52:40","date_gmt":"2025-10-06T05:52:40","guid":{"rendered":"https:\/\/genoks.com.tr\/docs\/genoks-panel-ngs-en\/"},"modified":"2026-05-02T05:14:14","modified_gmt":"2026-05-02T05:14:14","password":"","slug":"genoks-panel-ngs-en","status":"publish","type":"docs","link":"https:\/\/genoks.com.tr\/en\/docs\/genoks-panel-ngs-en\/","title":{"rendered":"Genoks Panel (All NGS Disease Panels)"},"content":{"rendered":"<p><!--genoks-intro-en:start--><\/p>\n<p><strong>Genoks Panel \u2014 All NGS Disease Panels.<\/strong> Comprehensive NGS-based diagnostic panels covering hereditary cardiac, neuromuscular, metabolic, immune, ophthalmologic, dermatologic, skeletal, and oncology conditions. Targeted gene-by-gene depth (\u226550\u00d7 coverage) with CNV\/SV detection. Reporting time 4-8 weeks depending on panel. Sample: 2-4 mL EDTA peripheral blood. Variants are interpreted by ACMG\/AMP 2015 criteria; post-test genetic counseling is mandatory.<\/p>\n<p><!--genoks-intro-en:end--><\/p>\n<p style=\"text-align: justify\"><strong>Genoks Panel ( T\u00fcm NGS Hastal\u0131k Panelleri) Nedir ?<\/strong><\/p>\n<p style=\"text-align: justify\">Genoks Panel (T\u00fcm NGS Panelleri) bir genetik hastal\u0131k veya klinik durum ile ili\u015fkili \u00e7ok say\u0131da genin taranmas\u0131na izin veren genetik test panelidir. Literat\u00fcrde belli bir hastal\u0131k ile ili\u015fkilendirilmi\u015f t\u00fcm genlerin ekzon b\u00f6lgeleri yeni nesil dizileme y\u00f6netemi ile analiz edilir, \u00e7e\u015fitli genetik hastal\u0131klar\u0131n belirtilerini ve semptomlar\u0131n\u0131 ortaya \u00e7\u0131karabilecek mutasyonlar\u0131 tespit etmeye \u00e7al\u0131\u015f\u0131r.<\/p>\n<p style=\"text-align: justify\">Genoks Panel, bir\u00e7ok farkl\u0131 hastal\u0131k t\u00fcr\u00fcn\u00fc i\u00e7eren se\u00e7enekler sunar. Bu hastal\u0131k panelleri aras\u0131nda kanser, kalp hastal\u0131klar\u0131, genetik sendromlar, n\u00f6rolojik hastal\u0131klar, metabolik hastal\u0131klar ve daha bir\u00e7ok hastal\u0131k t\u00fcr\u00fc yer alabilir. Genoks Panel, hastal\u0131klar\u0131n te\u015fhis edilmesine, riskin tahmin edilmesine ve tedavi planlar\u0131n\u0131n belirlenmesine yard\u0131mc\u0131 olabilir. Ayr\u0131ca, genetik test sonu\u00e7lar\u0131na dayanarak ki\u015fiye \u00f6zel tedavi yakla\u015f\u0131mlar\u0131 geli\u015ftirilmesine de yard\u0131mc\u0131 olabilir.<\/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>8 Hafta (+\/- 2 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>Genoks Panel \u2014 All NGS Disease Panels. Comprehensive NGS-based diagnostic panels covering hereditary cardiac, neuromuscular, metabolic, immune, ophthalmologic, dermatologic, skeletal, and oncology conditions. Targeted gene-by-gene depth (\u226550\u00d7 coverage) with CNV\/SV detection. Reporting time 4-8 weeks depending on panel. Sample: 2-4<span class=\"excerpt-hellip\"> 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