{"id":5445,"date":"2021-12-10T08:06:00","date_gmt":"2021-12-10T08:06:00","guid":{"rendered":"https:\/\/genekor.dermtherapy.gr\/2023\/12\/06\/san-antonio-breast-cancer-symposium-2021\/"},"modified":"2024-03-06T10:48:20","modified_gmt":"2024-03-06T10:48:20","slug":"san-antonio-breast-cancer-symposium-2021","status":"publish","type":"post","link":"https:\/\/genekor.com\/ro\/2021\/12\/10\/san-antonio-breast-cancer-symposium-2021\/","title":{"rendered":"San Antonio Breast Cancer Symposium 2021"},"content":{"rendered":"\n<p>Publica\u021bia recent\u0103 a studiului realizat de echipa \u0219tiin\u021bific\u0103 a Genekor <strong>&#8222;Different Copy Number Variations (CNVs) account for 10.4% of pathogenic variants in 1418 patients referred for hereditary breast cancer testing&#8221;<\/strong> a fost prezentat\u0103 la <strong>Simpozionul Cancerului de S\u00e2n de la San Antonio 2021.<\/strong><\/p>\n\n\n\n<p>Simpozionul \u0218tiintific International pentru interac\u021biunea dintre oameni de stiinta \u0219i clinicieni \u00een cancerul de s\u00e2n.<\/p>\n\n\n\n<p>\u00cen acest studiu foarte important au fost testa\u021bi un total de 1.418 de pacien\u021bi pentru a determina predispozi\u021bia la cancerul de s\u00e2n bazat\u0103 pe analiza unui panel de gene folosind metoda de Secven\u021biere de Nou\u0103 Genera\u021bie (NGS).<\/p>\n\n\n\n<p>Rezultatele au ar\u0103tat c\u0103 analiza rearanjamentelor genomice mari (CNV) nu ar trebui s\u0103 se limiteze la genele BRCA 1\/2. Algoritmii de detec\u021bie al CNV pun la dispozi\u021bie o metodologie rentabil\u0103 \u0219i fezabil\u0103 pentru determinarea acestora din datele NGS. Este recomandat ca analizele genetice \u00een cazul cancerului mamar ereditar s\u0103 includ\u0103 secven\u021bierea \u0219i analiza complet\u0103 a CNV-urilor genelor care sunt implicate \u00een deciziile de management medical al pacien\u021bilor.<\/p>\n\n\n\n<p>Vezi aici Poster <\/p>\n\n\n\n<figure class=\"wp-block-image size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"940\" height=\"788\" src=\"https:\/\/genekor.com\/wp-content\/uploads\/2023\/12\/san-antonio-final.png\" alt=\"\" class=\"wp-image-5430\" srcset=\"https:\/\/genekor.com\/wp-content\/uploads\/2023\/12\/san-antonio-final.png 940w, https:\/\/genekor.com\/wp-content\/uploads\/2023\/12\/san-antonio-final-300x251.png 300w, https:\/\/genekor.com\/wp-content\/uploads\/2023\/12\/san-antonio-final-768x644.png 768w\" sizes=\"auto, (max-width: 940px) 100vw, 940px\" \/><\/figure>\n","protected":false},"excerpt":{"rendered":"<p>Publica\u021bia recent\u0103 a studiului realizat de echipa \u0219tiin\u021bific\u0103 a Genekor &#8222;Different Copy Number Variations (CNVs) account for 10.4% of pathogenic variants in 1418 patients referred for hereditary breast cancer testing&#8221; [&hellip;]<\/p>\n","protected":false},"author":4,"featured_media":5428,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[33],"tags":[],"class_list":["post-5445","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorized-ro"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO Premium plugin v24.0 (Yoast SEO v24.0) - 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