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DC Field | Value | Language |
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dc.contributor.author | Domingos, Ana L. B. | - |
dc.contributor.author | Granzotto, Lucas A. | - |
dc.contributor.author | Belini Junior, Edis | - |
dc.contributor.author | Oliveira, Thiago Y. K. | - |
dc.contributor.author | Domingos, Ana C. B. | - |
dc.contributor.author | Bonini-Domingos, Claudia R. | - |
dc.date.accessioned | 2014-05-20T14:00:38Z | - |
dc.date.available | 2014-05-20T14:00:38Z | - |
dc.date.issued | 2010-02-01 | - |
dc.identifier | http://dx.doi.org/10.1590/S1516-84842010000100018 | - |
dc.identifier.citation | Revista 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.issn | 1516-8484 | - |
dc.identifier.uri | http://hdl.handle.net/11449/21434 | - |
dc.description.abstract | Variations 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.extent | 78-79 | - |
dc.language.iso | por | - |
dc.publisher | Associação Brasileira de Hematologia e Hemoterapia e daSociedade Brasileira de Transplante de Medula Óssea | - |
dc.source | SciELO | - |
dc.subject | Data mining | en |
dc.subject | beta thalassemia trait | en |
dc.subject | Bioinformatics | en |
dc.subject | Genetic diversity | en |
dc.title | Perfil de beta talassemia heterozigota obtido a partir de análise data mining em banco de dados | pt |
dc.title.alternative | The profile of beta thalassemia obtained by data mining analysis in a database | en |
dc.type | outro | - |
dc.contributor.institution | Universidade Estadual Paulista (UNESP) | - |
dc.contributor.institution | Universidade de São Paulo (USP) | - |
dc.description.affiliation | Unesp Depto. de Química | - |
dc.description.affiliation | Unesp Depto. de Ciências da Computação | - |
dc.description.affiliation | USP Hemocentro | - |
dc.description.affiliation | Unesp Programa de Pós-Graduação em Genética | - |
dc.description.affiliation | Unesp Depto. de Biologia | - |
dc.description.affiliationUnesp | Unesp Depto. de Química | - |
dc.description.affiliationUnesp | Unesp Depto. de Ciências da Computação | - |
dc.description.affiliationUnesp | Unesp Programa de Pós-Graduação em Genética | - |
dc.description.affiliationUnesp | Unesp Depto. de Biologia | - |
dc.identifier.doi | 10.1590/S1516-84842010000100018 | - |
dc.identifier.scielo | S1516-84842010000100018 | - |
dc.rights.accessRights | Acesso aberto | - |
dc.identifier.file | S1516-84842010000100018.pdf | - |
dc.relation.ispartof | Revista Brasileira de Hematologia e Hemoterapia | - |
Appears in Collections: | Artigos, TCCs, Teses e Dissertações da Unesp |
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