{"id":1557,"date":"2025-11-11T02:54:25","date_gmt":"2025-11-10T23:54:25","guid":{"rendered":"https:\/\/fideshealth.com\/fertijin\/?page_id=1557"},"modified":"2025-11-27T11:26:12","modified_gmt":"2025-11-27T08:26:12","slug":"ngs","status":"publish","type":"page","link":"https:\/\/fideshealth.com\/fertijin\/hizmetlerimiz\/ngs\/","title":{"rendered":"NGS"},"content":{"rendered":"\n<h2 class=\"wp-block-heading\"><strong>NGS (Next Generation Sequencing) Nedir?<\/strong><\/h2>\n\n\n\n<p><strong>NGS (Yeni Nesil Dizileme \u2013 Next Generation Sequencing)<\/strong>, <strong>Preimplantasyon Genetik Tarama (PGT-A)<\/strong> y\u00f6ntemleri aras\u0131nda yer alan <strong>en kapsaml\u0131 kromozom analiz teknolojilerinden biridir.<\/strong><br>Embriyo transferi \u00f6ncesinde yap\u0131lan bu test sayesinde, embriyolardaki olas\u0131 genetik bozukluklar <strong>gebelik s\u00fcreci ba\u015flamadan<\/strong> tespit edilebilir.<\/p>\n\n\n\n<p>NGS y\u00f6ntemi, <strong>t\u00fcm 24 kromozomun<\/strong> (22 otozomal kromozom + X ve Y cinsiyet kromozomlar\u0131) detayl\u0131 taramas\u0131n\u0131 sa\u011flar.<br>Bu sayede hem <strong>kromozom say\u0131s\u0131ndaki anormallikler (an\u00f6ploidi)<\/strong> hem de <strong>translokasyon gibi yap\u0131sal de\u011fi\u015fiklikler<\/strong>g\u00fcvenilir \u015fekilde belirlenebilir.<\/p>\n\n\n\n<p>\u0130stanbul\u2019daki <strong>FertiJin Kad\u0131n Sa\u011fl\u0131\u011f\u0131 ve T\u00fcp Bebek Merkezi<\/strong>, ileri genetik laboratuvar teknolojileriyle <strong>NGS testini y\u00fcksek ba\u015far\u0131 oran\u0131yla uygulayan<\/strong> say\u0131l\u0131 merkezlerden biridir.<\/p>\n\n\n\n<p><a href=\"#randevu-al\">\ud83d\udc49 <strong>\u00dccretsiz \u00f6n g\u00f6r\u00fc\u015fme i\u00e7in hemen randevu al\u0131n<\/strong><\/a><\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>NGS (Yeni Nesil Dizileme) Nas\u0131l \u00c7al\u0131\u015f\u0131r?<\/strong><\/h2>\n\n\n\n<p>NGS teknolojisi, embriyodan al\u0131nan h\u00fccre \u00f6rneklerindeki DNA\u2019n\u0131n dizilimini \u00e7\u0131kararak <strong>t\u00fcm kromozomlar\u0131 tek tek analiz eder.<\/strong><br>Bu y\u00f6ntem, klasik genetik testlere g\u00f6re <strong>\u00e7ok daha y\u00fcksek \u00e7\u00f6z\u00fcn\u00fcrl\u00fckte ve g\u00fcvenilir<\/strong> sonu\u00e7lar sunar.<\/p>\n\n\n\n<p>NGS testi ile:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>24 kromozomun tamam\u0131 taran\u0131r,<\/li>\n\n\n\n<li>Kromozom eksiklikleri veya fazlal\u0131klar\u0131 (an\u00f6ploidi) tespit edilir,<\/li>\n\n\n\n<li>Translokasyon gibi yap\u0131sal bozukluklar analiz edilir,<\/li>\n\n\n\n<li>Sa\u011fl\u0131kl\u0131 embriyolar objektif verilerle se\u00e7ilir.<\/li>\n<\/ul>\n\n\n\n<p>\ud83d\udca1 Bu sayede embriyo transferi \u00f6ncesinde genetik olarak en uygun embriyo belirlenir, gebelik ba\u015far\u0131s\u0131 artar ve d\u00fc\u015f\u00fck riski azal\u0131r.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>NGS Hangi Hastalara Uygulanabilir?<\/strong><\/h2>\n\n\n\n<p>NGS (Yeni Nesil Dizileme) testi, a\u015fa\u011f\u0131daki durumlarda s\u0131kl\u0131kla tercih edilir:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Daha \u00f6nce <strong>ba\u015far\u0131s\u0131z t\u00fcp bebek (IVF)<\/strong> denemesi olan \u00e7iftlerde<\/li>\n\n\n\n<li><strong>38 ya\u015f \u00fczeri anne adaylar\u0131nda<\/strong><\/li>\n\n\n\n<li><strong>Tekrarlayan d\u00fc\u015f\u00fck \u00f6yk\u00fcs\u00fc<\/strong> bulunan kad\u0131nlarda<\/li>\n\n\n\n<li><strong>Translokasyon veya genetik karyotip de\u011fi\u015fimi<\/strong> saptanan bireylerde<\/li>\n\n\n\n<li><strong>Embriyo dondurma planlayan<\/strong> \u00e7iftlerde<\/li>\n\n\n\n<li><strong>Cinsiyet kromozomu bozukluklar\u0131n\u0131<\/strong> d\u0131\u015flamak isteyen ailelerde<\/li>\n<\/ul>\n\n\n\n<p>\ud83d\udcac FertiJin\u2019de her \u00e7iftin \u00f6zel durumuna g\u00f6re, NGS veya di\u011fer genetik tarama y\u00f6ntemleri (PGT, FISH PGD, aCGH vb.) birlikte planlan\u0131r.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>NGS Uygulamas\u0131 Nas\u0131l Yap\u0131l\u0131r?<\/strong><\/h2>\n\n\n\n<p>NGS i\u015flemi, t\u00fcp bebek (IVF) tedavisiyle elde edilen embriyolar \u00fczerinde ger\u00e7ekle\u015ftirilir.<br>D\u00f6llenme sonras\u0131 embriyolardan <strong>biyopsi y\u00f6ntemiyle birka\u00e7 h\u00fccre al\u0131n\u0131r<\/strong> ve genetik analiz i\u00e7in laboratuvara g\u00f6nderilir.<\/p>\n\n\n\n<p>G\u00fcn\u00fcm\u00fczde en g\u00fcvenilir y\u00f6ntem olarak kabul edilen <strong>5. veya 6. g\u00fcn trofektoderm biyopsisi<\/strong> uygulan\u0131r.<br>Bu y\u00f6ntem sayesinde:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li><strong>Mozaizm riski (kar\u0131\u015f\u0131k kromozom yap\u0131s\u0131)<\/strong> \u00f6nemli \u00f6l\u00e7\u00fcde azal\u0131r,<\/li>\n\n\n\n<li>Embriyonun geli\u015fimi korunur,<\/li>\n\n\n\n<li>Daha g\u00fcvenilir sonu\u00e7lar elde edilir.<\/li>\n<\/ul>\n\n\n\n<p>Embriyolar\u0131n genetik analizi tamamland\u0131ktan sonra, <strong>genetik olarak sa\u011fl\u0131kl\u0131 olan embriyolar<\/strong> se\u00e7ilerek anne aday\u0131na transfer edilir.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><strong>NGS Testinin Avantajlar\u0131<\/strong><\/h2>\n\n\n\n<figure class=\"wp-block-table\"><table class=\"has-fixed-layout\"><thead><tr><th>Avantaj<\/th><th>A\u00e7\u0131klama<\/th><\/tr><\/thead><tbody><tr><td><strong>T\u00fcm kromozomlar analiz edilir<\/strong><\/td><td>24 kromozomun tamam\u0131 detayl\u0131 olarak taran\u0131r.<\/td><\/tr><tr><td><strong>Y\u00fcksek do\u011fruluk oran\u0131<\/strong><\/td><td>NGS y\u00f6ntemi, genetik tan\u0131da en g\u00fcvenilir teknolojidir.<\/td><\/tr><tr><td><strong>Translokasyon tespiti yap\u0131labilir<\/strong><\/td><td>Kromozom yap\u0131sal bozukluklar\u0131 belirlenebilir.<\/td><\/tr><tr><td><strong>Gebelik ba\u015far\u0131s\u0131n\u0131 art\u0131r\u0131r<\/strong><\/td><td>Sa\u011fl\u0131kl\u0131 embriyolar\u0131n se\u00e7imiyle ba\u015far\u0131 oran\u0131 y\u00fckselir.<\/td><\/tr><tr><td><strong>D\u00fc\u015f\u00fck riskini azalt\u0131r<\/strong><\/td><td>Genetik sorunlar \u00f6nceden saptand\u0131\u011f\u0131 i\u00e7in d\u00fc\u015f\u00fck olas\u0131l\u0131\u011f\u0131 azal\u0131r.<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p>\ud83d\udca1 FertiJin T\u00fcp Bebek Merkezi\u2019nde NGS uygulamalar\u0131, <strong>uluslararas\u0131 genetik laboratuvar standartlar\u0131nda<\/strong>, <strong>uzman genetik dan\u0131\u015fmanl\u0131k e\u015fli\u011finde<\/strong> y\u00fcr\u00fct\u00fclmektedir.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\">NGS Testi Fiyatlar\u0131 \u2013 \u0130stanbul<\/h2>\n\n\n\n<p>NGS testi fiyat\u0131; incelenecek <strong>embriyo say\u0131s\u0131<\/strong>, <strong>laboratuvar y\u00f6ntemi<\/strong> ve <strong>tedavi plan\u0131na dahil edilen ek analizlere<\/strong> g\u00f6re de\u011fi\u015fiklik g\u00f6sterebilir.<br>\u0130stanbul \u015ei\u015fli\u2019deki <strong>FertiJin Kad\u0131n Sa\u011fl\u0131\u011f\u0131 ve T\u00fcp Bebek Merkezi<\/strong>, <strong>eri\u015filebilir fiyat politikas\u0131<\/strong> ve <strong>g\u00fcvenilir sonu\u00e7 garantisi<\/strong> ile hizmet vermektedir.<\/p>\n\n\n\n<p>\ud83d\udcde Bilgi ve fiyat dan\u0131\u015fmanl\u0131\u011f\u0131 i\u00e7in:<br>\ud83d\udcac WhatsApp: +90 542 386 52 34<br><a href=\"#randevu-al\">\ud83d\udc49 <strong>\u00dccretsiz \u00f6n g\u00f6r\u00fc\u015fme i\u00e7in hemen randevu al\u0131n<\/strong><\/a><\/p>\n\n\n\n<h2 class=\"wp-block-heading\">S\u0131k Sorulan Sorular<\/h2>\n\n\n\n<h3 class=\"wp-block-heading\"><strong>NGS testi a\u011fr\u0131l\u0131 m\u0131d\u0131r?<\/strong><\/h3>\n\n\n\n<p>Hay\u0131r. NGS, laboratuvarda embriyo h\u00fccreleri \u00fczerinde yap\u0131lan bir genetik analizdir. Anne veya baba aday\u0131na do\u011frudan i\u015flem uygulanmaz.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">NGS testi ile hangi hastal\u0131klar tespit edilir?<\/h3>\n\n\n\n<p>NGS, kromozom say\u0131sal bozukluklar\u0131n\u0131 (an\u00f6ploidi), translokasyonlar\u0131 ve yap\u0131sal anomalileri tespit eder. Ayr\u0131ca embriyo cinsiyetini de belirleyebilir.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\"><strong>NGS mi, FISH PGD mi tercih edilmelidir?<\/strong><\/h3>\n\n\n\n<p>NGS \u00e7ok daha kapsaml\u0131 ve y\u00fcksek do\u011fruluk oran\u0131na sahiptir. Ancak teknik veya mali nedenlerle FISH PGD y\u00f6ntemi de uygun bir alternatif olabilir.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>NGS (Next Generation Sequencing) Nedir? NGS (Yeni Nesil Dizileme \u2013 Next Generation Sequencing), Preimplantasyon Genetik Tarama (PGT-A) y\u00f6ntemleri aras\u0131nda yer alan en kapsaml\u0131 kromozom analiz teknolojilerinden biridir.Embriyo transferi \u00f6ncesinde yap\u0131lan bu test sayesinde, embriyolardaki olas\u0131 genetik bozukluklar gebelik s\u00fcreci ba\u015flamadan tespit edilebilir. NGS y\u00f6ntemi, t\u00fcm 24 kromozomun (22 otozomal kromozom + X ve Y cinsiyet [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":1467,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-1557","page","type-page","status-publish","hentry"],"acf":[],"_links":{"self":[{"href":"https:\/\/fideshealth.com\/fertijin\/wp-json\/wp\/v2\/pages\/1557","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/fideshealth.com\/fertijin\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/fideshealth.com\/fertijin\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/fideshealth.com\/fertijin\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/fideshealth.com\/fertijin\/wp-json\/wp\/v2\/comments?post=1557"}],"version-history":[{"count":0,"href":"https:\/\/fideshealth.com\/fertijin\/wp-json\/wp\/v2\/pages\/1557\/revisions"}],"up":[{"embeddable":true,"href":"https:\/\/fideshealth.com\/fertijin\/wp-json\/wp\/v2\/pages\/1467"}],"wp:attachment":[{"href":"https:\/\/fideshealth.com\/fertijin\/wp-json\/wp\/v2\/media?parent=1557"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}