{"id":63582,"date":"2025-12-08T11:18:05","date_gmt":"2025-12-08T09:18:05","guid":{"rendered":"https:\/\/www.clinica-sante.com\/ro\/analize\/testare-panel-somatic-ngs-personalizat-101-3000-gene\/"},"modified":"2026-03-24T11:43:52","modified_gmt":"2026-03-24T09:43:52","slug":"testare-panel-somatic-ngs-personalizat-101-3000-gene","status":"publish","type":"product","link":"https:\/\/www.clinica-sante.com\/ro\/analize-diagnostic-genetic\/testare-panel-somatic-ngs-personalizat-101-3000-gene\/","title":{"rendered":"Testare panel somatic NGS personalizat (101- 3000 gene)"},"content":{"rendered":"<p>Testul utilizeaz\u0103 tehnologia avansat\u0103 NGS pentru identificarea muta\u021biilor somatice (SNV, <strong>indel<\/strong>, CNV \u0219i fuziuni genice) \u00een ADN-ul extras din probe tisulare. Panelul acoper\u0103 un spectru larg de gene asociate proceselor neoplazice, displazice sau degenerative, oferind o viziune molecular\u0103 detaliat\u0103 asupra patologiei investigate.<\/p>\n<p>Prin personalizarea con\u021binutului (101\u20133000 gene), analiza poate fi direc\u021bionat\u0103 c\u0103tre paneluri tematice (oncologie solid\u0103, hematologic\u0103, neuro-oncologic\u0103 etc.) sau complet integrativ\u0103, sus\u021bin\u00e2nd medicina de precizie \u0219i strategiile terapeutice \u021bintite.<\/p>\n<p><strong>Afec\u021biuni sau simptome asociate<\/strong><\/p>\n<ul>\n<li>tumori solide (carcinom, sarcom, melanom, tumori cerebrale etc.)<\/li>\n<li>neoplazii hematologice (leucemii, limfoame, mielodisplazii)<\/li>\n<li>procese proliferative sau degenerative cu substrat genetic somatic complex<\/li>\n<li>evaluarea r\u0103spunsului sau rezisten\u021bei la terapii moleculare<\/li>\n<\/ul>\n<p><strong>Cui se adreseaz\u0103<\/strong><\/p>\n<p><strong>Medicilor<\/strong> oncologi, hematologi, geneticieni, anatomopatologi \u0219i altor speciali\u0219ti implica\u021bi \u00een diagnosticul, prognosticul \u0219i managementul terapeutic al pacien\u021bilor cu suspiciune sau confirmare de boal\u0103 somatic\u0103 cu component\u0103 genetic\u0103.<\/p>\n<p><strong>Metodologie de testare<\/strong><\/p>\n<p>Secven\u021biere de genera\u021bie urm\u0103toare (NGS) cu acoperire extins\u0103, aplicat\u0103 pe ADN extras din probe tisulare proaspete sau fixate (\u00een func\u021bie de disponibilitate). Panelul este configurabil \u0219i poate include \u00eentre 101 \u0219i 3000 de gene, selectate \u00een func\u021bie de nevoile clinice \u0219i de scopul investiga\u021biei.<\/p>\n<p><strong>Beneficii \u0219i importan\u021b\u0103 clinic\u0103<\/strong><\/p>\n<ul>\n<li>permite caracterizarea molecular\u0103 detaliat\u0103 a leziunilor somatice<\/li>\n<li>ofer\u0103 informa\u021bii predictive, prognostice \u0219i terapeutice esen\u021biale pentru medicina personalizat\u0103<\/li>\n<li>detecteaz\u0103 simultan muta\u021bii, dele\u021bii, amplific\u0103ri, fuziuni \u0219i alte varia\u021bii structurale<\/li>\n<li>faciliteaz\u0103 identificarea \u021bintelor terapeutice specifice \u0219i op\u021biunilor de tratament inovatoare<\/li>\n<li>panelul larg reduce necesitatea efectu\u0103rii mai multor teste secven\u021biale<\/li>\n<\/ul>\n<p><strong>Particularit\u0103\u021bi \u0219i limit\u0103ri<\/strong><\/p>\n<ul>\n<li>analiza vizeaz\u0103 exclusiv varia\u021biile somatice; nu include interpretarea muta\u021biilor germinale<\/li>\n<li>calitatea rezultatelor depinde de integritatea ADN-ului \u0219i de reprezentativitatea probei<\/li>\n<li>personalizarea este posibil\u0103 \u00een limita genelor disponibile \u0219i validate tehnic pentru panel<\/li>\n<li>interpretarea variantelor rare sau de semnifica\u021bie incert\u0103 poate necesita corelare clinic\u0103 \u0219i histologic\u0103<\/li>\n<\/ul>\n<p><strong>Tip prob\u0103<\/strong><\/p>\n<p>Biopsie tisular\u0103 proasp\u0103t\u0103 sau, \u00een unele cazuri, \u021besut fixat \u00een parafin\u0103 (FFPE), conform protocolului laboratorului.<\/p>\n<p><strong>Recoltare<\/strong><\/p>\n<p>Proba se colecteaz\u0103 \u00een condi\u021bii sterile \u0219i se transport\u0103 rapid la laborator. Pentru \u021besutul FFPE, blocul parafinat sau sec\u021biunile reprezentative trebuie \u00eenso\u021bite de raport <strong>histopatologic<\/strong>.<\/p>\n<p><strong>Condi\u021bii<\/strong><\/p>\n<p>Respectarea strict\u0103 a protocolului de recoltare, manipulare \u0219i transport pentru men\u021binerea calit\u0103\u021bii ADN-ului. Probele degradate pot limita acurate\u021bea detec\u021biei muta\u021biilor.<\/p>\n<p><strong>Analize asociate recomandate<\/strong><\/p>\n<ul>\n<li>testare germinal\u0103 (din s\u00e2nge) pentru diferen\u021bierea variantelor ereditare de cele somatice<\/li>\n<li>analize de expresie genic\u0103 sau transcriptomic\u0103 pentru completarea profilului molecular<\/li>\n<li>teste imunohistochimice \u0219i FISH pentru validarea muta\u021biilor de interes terapeutic<\/li>\n<li>monitorizare ulterioar\u0103 prin paneluri de rezisten\u021b\u0103 sau recuren\u021b\u0103 tumoral\u0103<\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>Analiz\u0103 genetic\u0103 complex\u0103, realizat\u0103 prin secven\u021biere de nou\u0103 genera\u021bie (NGS), care permite investigarea simultan\u0103 a unui num\u0103r extins de gene (101\u20133000) implicate \u00een mecanismele somatice ale bolilor, \u00een special ale tumorilor. Panelul este complet personalizabil, adaptat tipului de \u021besut \u0219i suspiciunii clinice.<\/p>\n","protected":false},"featured_media":0,"template":"","meta":{"_acf_changed":false,"inline_featured_image":false},"product_brand":[],"product_cat":[1209,3166,2876],"product_tag":[],"class_list":["post-63582","product","type-product","status-publish","product_cat-analize","product_cat-diagnostic-genetic","product_cat-serviciu-laborator","first","instock","sale","virtual","purchasable","product-type-simple"],"acf":[],"aioseo_notices":[],"aioseo_head":"\n\t\t<!-- All in One SEO Pro 5.0.0.1 - aioseo.com -->\n\t<meta name=\"description\" content=\"Panel somatic NGS personalizat - test genetic pe 101\u20133000 gene pentru evaluarea variantelor implicate in afectiuni oncologice si medicina personalizata. 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