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Please use this identifier to cite or link to this item: http://hdl.handle.net/1843/57814
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dc.creatorVladmir Cláudio Cordeiro-de-Limapt_BR
dc.creatorDenis Leonardo Jardimpt_BR
dc.creatorAndreia c Melopt_BR
dc.creatorCelso Abdon Mellopt_BR
dc.creatorClarissa Serodio Baldottopt_BR
dc.creatorMauro Zukinpt_BR
dc.creatorAknar Calabrichpt_BR
dc.creatorAna Gelattipt_BR
dc.creatorGilberto De-castro-jrpt_BR
dc.creatorThiago Bueno De-oliveirapt_BR
dc.creatorMarkus Gifonipt_BR
dc.creatorLuiz Henrique Araújopt_BR
dc.creatorWilliams Barrapt_BR
dc.creatorAnelisa k. Coutinhopt_BR
dc.creatorRenata D?alpino Peixotopt_BR
dc.creatorCarla Rameri De-azevedopt_BR
dc.creatorEduardo Paulinopt_BR
dc.creatorJosé Binespt_BR
dc.creatorRomualdo Barrosopt_BR
dc.creatorDaniel Gimenespt_BR
dc.creatorRafael Aliosha Kalikspt_BR
dc.creatorAndre Poisl Faypt_BR
dc.creatorBernardo Garicocheapt_BR
dc.creatorDiogo Buganopt_BR
dc.creatorPedro Isaacssonpt_BR
dc.creatorCarlos Chiattonept_BR
dc.creatorJorge Vazpt_BR
dc.creatorGuilherme Dufflespt_BR
dc.creatorOtavio Baiocchipt_BR
dc.creatorRafael Schmerling,pt_BR
dc.creatorRodrigo Ramela Munhozpt_BR
dc.creatorRodrigo Guedespt_BR
dc.creatorOlavo Feherpt_BR
dc.creatorVanderson Rochapt_BR
dc.creatorCamilla Akemi Felizardo Yamadapt_BR
dc.creatorCarolina Fittipaldipt_BR
dc.creatorClarissa Maria de Cerqueira Mathiaspt_BR
dc.creatorRenan Orsati Clarapt_BR
dc.creatorAlesssandro Lealpt_BR
dc.creatorMax Manopt_BR
dc.creatorWilliam Nassib Williampt_BR
dc.creatorAline Lauda Freitas Chavespt_BR
dc.creatorGustavo Dos Santos Fernandespt_BR
dc.creatorAngélica Nogueira Rodriguespt_BR
dc.date.accessioned2023-08-14T20:58:21Z-
dc.date.available2023-08-14T20:58:21Z-
dc.date.issued2021-07-30-
dc.citation.volume17pt_BR
dc.citation.spage1pt_BR
dc.citation.epage44pt_BR
dc.identifier.doi10.5935/2526-8732.20210019pt_BR
dc.identifier.issn25268732pt_BR
dc.identifier.urihttp://hdl.handle.net/1843/57814-
dc.description.resumoThere has been a rapid increase in the volume of genomic data gathered from different cancers, this has helped to develop new tumor classifications as well as to select better tailored therapies for the patients. Some of the genomic markers identified are also prognostic and predictive factors. Additionally, many technologies have been used to investigate these alterations, each with different benefits and caveats. The Genomics Committee from the Sociedade Brasileira de Oncologia Clínica (SBOC) put together a group of specialists, from different regions of Brazil that work both in the private and public scenario, to gather and organize the information regarding the utility of somatic mutation testing in solid tumors. This special article summarizes their recommendations on how to better incorporate this information into clinical practice.pt_BR
dc.format.mimetypepdfpt_BR
dc.languageengpt_BR
dc.publisherUniversidade Federal de Minas Geraispt_BR
dc.publisher.countryBrasilpt_BR
dc.publisher.departmentMED - DEPARTAMENTO DE CLÍNICA MÉDICApt_BR
dc.publisher.initialsUFMGpt_BR
dc.relation.ispartofBrazilian Journal Of Oncology-
dc.rightsAcesso Abertopt_BR
dc.subjectSomatic mutation testingpt_BR
dc.subjectPrecision oncologypt_BR
dc.subjectComprehensive genomic profilingpt_BR
dc.subjectGenomic medicinept_BR
dc.subjectOncologypt_BR
dc.subject.otherMedicina Genômicapt_BR
dc.subject.otherOncologiapt_BR
dc.titleImplementing somatic mutation testing in clinical setting: recommendations from a panel of experts.pt_BR
dc.title.alternativeImplementando testes de mutação somática em ambiente clínico: recomendações de um painel de especialistaspt_BR
dc.typeArtigo de Periódicopt_BR
dc.url.externahttp://brazilianjournalofoncology.com.br/details/168/en-US/implementando-testes-de-mutacao-somatica-em-ambiente-clinico--recomendacoes-de-um-painel-de-especialistaspt_BR
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