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dc.contributor.authorDomingos, Ana L. B.-
dc.contributor.authorGranzotto, Lucas A.-
dc.contributor.authorBelini Junior, Edis-
dc.contributor.authorOliveira, Thiago Y. K.-
dc.contributor.authorDomingos, Ana C. B.-
dc.contributor.authorBonini-Domingos, Claudia R.-
dc.date.accessioned2014-05-20T14:00:38Z-
dc.date.available2014-05-20T14:00:38Z-
dc.date.issued2010-02-01-
dc.identifierhttp://dx.doi.org/10.1590/S1516-84842010000100018-
dc.identifier.citationRevista Brasileira de Hematologia e Hemoterapia. Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea, v. 32, n. 1, p. 78-79, 2010.-
dc.identifier.issn1516-8484-
dc.identifier.urihttp://hdl.handle.net/11449/21434-
dc.description.abstractVariations in the phenotypic expression of heterozygous beta thalassemia reflect the formation of different populations. To better understand the profile of heterozygous beta-thalassemia of the Brazilian population, we aimed at establishing parameters to direct the diagnosis of carriers and calculate the frequency from information stored in an electronic database. Using a Data Mining tool, we evaluated information on 10,960 blood samples deposited in a relational database. Over the years, improved diagnostic technology has facilitated the elucidation of suspected beta thalassemia heterozygote cases with an average frequency of 3.5% of referred cases. We also found that the Brazilian beta thalassemia trait has classic increases of Hb A2 and Hb F (60%), mainly caused by mutations in beta zero thalassemia, especially in the southeast of the country.en
dc.format.extent78-79-
dc.language.isopor-
dc.publisherAssociação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea-
dc.sourceSciELO-
dc.subjectData miningen
dc.subjectbeta thalassemia traiten
dc.subjectBioinformaticsen
dc.subjectGenetic diversityen
dc.titlePerfil de beta talassemia heterozigota obtido a partir de análise data mining em banco de dadospt
dc.title.alternativeThe profile of beta thalassemia obtained by data mining analysis in a databaseen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.description.affiliationUnesp Depto. de Química-
dc.description.affiliationUnesp Depto. de Ciências da Computação-
dc.description.affiliationUSP Hemocentro-
dc.description.affiliationUnesp Programa de Pós-Graduação em Genética-
dc.description.affiliationUnesp Depto. de Biologia-
dc.description.affiliationUnespUnesp Depto. de Química-
dc.description.affiliationUnespUnesp Depto. de Ciências da Computação-
dc.description.affiliationUnespUnesp Programa de Pós-Graduação em Genética-
dc.description.affiliationUnespUnesp Depto. de Biologia-
dc.identifier.doi10.1590/S1516-84842010000100018-
dc.identifier.scieloS1516-84842010000100018-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileS1516-84842010000100018.pdf-
dc.relation.ispartofRevista Brasileira de Hematologia e Hemoterapia-
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