{"id":17350,"date":"2022-02-18T20:02:48","date_gmt":"2022-02-18T20:02:48","guid":{"rendered":"https:\/\/cancercentertec100.com\/?p=17350"},"modified":"2022-02-18T20:03:04","modified_gmt":"2022-02-18T20:03:04","slug":"la-secuenciacion-de-nueva-generacion-ngs","status":"publish","type":"post","link":"https:\/\/cancercentertec100.com\/en\/noti-genetica\/la-secuenciacion-de-nueva-generacion-ngs\/","title":{"rendered":"La Secuenciaci\u00f3n de Nueva Generaci\u00f3n (NGS)"},"content":{"rendered":"<p class=\"has-color-4-color has-text-color\">By: Dr. Gildardo Fco. Zafra de la Rosa.<\/p>\n\n\n\n<p>La NGS es una de las nuevas herramientas moleculares que han permitido analizar m\u00faltiples genes simult\u00e1neamente con un menor costo y tiempo.&nbsp;<\/p>\n\n\n\n<p>Es tambi\u00e9n llamada <em>secuenciaci\u00f3n masiva en paralelo,<\/em> debido a que se basa en el ensamblado de secuencias de millones de bases a partir de fragmentos de ADN, lo que permite analizar grandes y complejos genomas, que en general miden 20 pb a 20 Kb. Por lo que es un buen m\u00e9todo para analizar tejidos neopl\u00e1sicos. As\u00ed, en caso de encontrar una variante, se compara con una secuencia de referencia para considerarla normal o patol\u00f3gica.&nbsp;<\/p>\n\n\n\n<p>Para interpretar los resultados y aplicarlos a la cl\u00ednica, es necesario consultar las bases de datos p\u00fablicas que se encuentran disponibles en l\u00ednea. Sin embargo; muchas variantes a\u00fan no est\u00e1n determinadas ni como normales porque no se encuentran en poblaci\u00f3n \u201csana\u201d, ni como patol\u00f3gicas porque no se han publicado casos cl\u00ednicos afectados que tengan dicha variante. En tal caso, se denominan variantes de significado i<em>ncierto<\/em>. De donde resulta relevante hacer trabajos colaborativos, a fin de formar una base de datos, ya que con ello ser\u00e1 posible encontrar variantes comunes en la poblaci\u00f3n estudiada y transformar una variante considerada anteriormente de significado incierto en una variante relacionada con c\u00e1ncer por ejemplo y adem\u00e1s informar en la bibliograf\u00eda los hallazgos a trav\u00e9s de publicaciones en revistas cient\u00edficas.<\/p>\n\n\n\n<p>Especialmente es aplicable a pacientes con c\u00e1ncer, dado que en la mayor\u00eda de los casos un tumor es la resultante de variantes localizadas en diferentes genes, fen\u00f3meno conocido como heterogeneidad gen\u00e9tica, tanto al\u00e9licas, cuando en un mismo gen ocurren diferentes mutaciones que producen un mismo fenotipo, cuanto de locus, cuando diferentes genes producen la misma neoplasia. La aplicaci\u00f3n de la NGS en pacientes con c\u00e1ncer ha resultado de gran valor ya que se han encontrado variantes definidamente patog\u00e9nicas, pudiendo trazar la l\u00ednea de transmisi\u00f3n hereditaria e incluso una mejor orientaci\u00f3n terap\u00e9utica al conocer el defecto b\u00e1sico de la neoplasia.<\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"768\" src=\"https:\/\/cancercentertec100.com\/wp-content\/uploads\/2022\/02\/scientist-examining-dna-sequencing-gel-2021-11-17-05-54-03-utc-1024x768.jpg\" alt=\"\" class=\"wp-image-17351\" srcset=\"https:\/\/cancercentertec100.com\/wp-content\/uploads\/2022\/02\/scientist-examining-dna-sequencing-gel-2021-11-17-05-54-03-utc-1024x768.jpg 1024w, https:\/\/cancercentertec100.com\/wp-content\/uploads\/2022\/02\/scientist-examining-dna-sequencing-gel-2021-11-17-05-54-03-utc-300x225.jpg 300w, https:\/\/cancercentertec100.com\/wp-content\/uploads\/2022\/02\/scientist-examining-dna-sequencing-gel-2021-11-17-05-54-03-utc-768x576.jpg 768w, https:\/\/cancercentertec100.com\/wp-content\/uploads\/2022\/02\/scientist-examining-dna-sequencing-gel-2021-11-17-05-54-03-utc-580x435.jpg 580w, https:\/\/cancercentertec100.com\/wp-content\/uploads\/2022\/02\/scientist-examining-dna-sequencing-gel-2021-11-17-05-54-03-utc-860x645.jpg 860w, https:\/\/cancercentertec100.com\/wp-content\/uploads\/2022\/02\/scientist-examining-dna-sequencing-gel-2021-11-17-05-54-03-utc-1160x870.jpg 1160w, https:\/\/cancercentertec100.com\/wp-content\/uploads\/2022\/02\/scientist-examining-dna-sequencing-gel-2021-11-17-05-54-03-utc.jpg 1320w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/figure>","protected":false},"excerpt":{"rendered":"<p>Por: Dr. Gildardo Fco. Zafra de la Rosa. La NGS es una de las nuevas herramientas moleculares que han permitido analizar m\u00faltiples genes simult\u00e1neamente con un menor costo y tiempo.&nbsp; Es tambi\u00e9n llamada secuenciaci\u00f3n masiva en paralelo, debido a que se basa en el ensamblado de secuencias de millones de bases a partir de fragmentos&#8230;<\/p>","protected":false},"author":1,"featured_media":17352,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[293],"tags":[],"class_list":["post-17350","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-noti-genetica"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>La Secuenciaci\u00f3n de Nueva Generaci\u00f3n (NGS)<\/title>\n<meta name=\"description\" content=\"Por: Dr. Gildardo Fco. Zafra de la Rosa. 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