Statistical Genetics
Mostrando 1-12 de 78 artigos, teses e dissertações.
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1. The effect of mutation status, pathological features and tumor location on prognosis ın patients with colorectal cancer
SUMMARY OBJECTIVE: Colorectal cancer is the most common malignancy of the gastrointestinal tract. It is the third most common tumor in both genders and the second reason of cancer-related deaths. In recent years, tumor location has gained importance as a prognostic indicator. In this study, we aimed to analyze if there was a prognostic effect of tumor locat
Rev. Assoc. Med. Bras.. Publicado em: 2021-02
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2. Acute pancreatitis and recurrent acute pancreatitis: an exploration of clinical and etiologic factors and outcomes,
RESUMO Objetivo: Descrever a epidemiologia e as características clínicas da pancreatite aguda e da pancreatite aguda recorrente em crianças. Métodos: Estudo observacional e retrospectivo com um componente analítico. Os pacientes foram classificados em dois grupos: pancreatite aguda e pancreatite recorrente. A relação com cada parâmetro obtido foi a
J. Pediatr. (Rio J.). Publicado em: 25/11/2019
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3. Development and applications of the SWAN rating scale for assessment of attention deficit hyperactivity disorder: a literature review
This study reviewed the use of the Strengths and Weaknesses of Attention-Deficit/Hyperactivity-symptoms and Normal-behaviors (SWAN) rating scale in diagnostic and evolutive approaches to attention deficit hyperactivity disorder (ADHD) and in correlational studies of the disorder. A review of articles published in indexed journals from electronic databases wa
Braz J Med Biol Res. Publicado em: 25/08/2015
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4. Prevalence of scoliosis in Williams-Beuren syndrome patients treated at a regional reference center
OBJECTIVE:This study assessed the prevalence of scoliosis and the patterns of scoliotic curves in patients with Williams-Beuren syndrome. Williams-Beuren syndrome is caused by a chromosome 7q11.23 deletion in a region containing 28 genes, with the gene encoding elastin situated approximately at the midpoint of the deletion. Mutation of the elastin gene leads
Clinics. Publicado em: 2014-07
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5. Impact of a chromosome X STR Decaplex in deficiency paternity cases
Deficiency paternity cases, characterized by the absence of the alleged father, are a challenge for forensic genetics. Here we present four cases with a female child and a deceased alleged father in which the analysis of a set of 21 or 22 autosomal STRs (AS STRs) produced results within a range of doubt when genotyping relatives of the alleged father. Aiming
Genet. Mol. Biol.. Publicado em: 2013
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6. Mantel test in population genetics
The comparison of genetic divergence or genetic distances, estimated by pairwise F ST and related statistics, with geographical distances by Mantel test is one of the most popular approaches to evaluate spatial processes driving population structure. There have been, however, recent criticisms and discussions on the statistical performance of the Mantel test
Genet. Mol. Biol.. Publicado em: 2013
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7. Modelo hierárquico bayesiano na determinação de associação entre marcadores e QTL em uma população F2 / Bayesian hierarchical model in the determination of association between markers and QTL in a F2 population
O objetivo do mapeamento de QTL (Quantitative Trait Loci ) e identificar sua posição no genoma, isto e, identificar em qual cromossomo esta e qual sua localização nesse cromossomo, bem como estimar seus efeitos genéticos. Uma vez que as localizações dos QTL não são conhecidas a priori, marcadores são usados frequentemente para auxiliar no seu mapea
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 13/04/2012
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8. Método de Haseman-Elston e suas modificações no estudo de genes controladores de característica quantitativa / Haseman-Elston methodology and modifications on the study genes underlining quantitative trait loci
QTL mapping allows to study loci that play a role in complex traits, as well to determine their chromosomal locations. For this purpose, a set of methods useful for the study of quantitative traits are those based on Haseman-EIston regression, that is quite used in human genetics. These are robustness regression methods for linkage analysis that can be used
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 27/01/2012
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9. Desempenho de 79 progênies de soja na geração F6 e correlações fenotípicas, genotípicas e ambientais / Performance of 79 soybean progeny of F6 generation and their phenotypic, genotypic and environmental correlations
Soybean farmers have interest on increasingly early highly productive cultivars has stimulated the development of new genotypes for breeding soy programs. So that, this study aimed to evaluate the agronomic characteristics of 79 progenies of ten biparental crosses Program Soybean Breeding in Federal University of Uberlândia. The experiment was conducted at
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 30/06/2011
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10. A.N. Kolmogorov's defence of Mendelism
In 1939 N.I. Ermolaeva published the results of an experiment which repeated parts of Mendel's classical experiments. On the basis of her experiment she concluded that Mendel's principle that self-pollination of hybrid plants gave rise to segregation proportions 3:1 was false. The great probability theorist A.N. Kolmogorov reviewed Ermolaeva's data using a t
Genetics and Molecular Biology. Publicado em: 2011
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11. Mapeamento genético de cana-de-açúcar (Saccharum spp.) por associação empregando marcadores SSR e AFLP / Genetic mapping of sugar cane (Saccharum spp.) by association using SSR and AFLP markers
A cultura da cana-de-açúcar (Saccharum spp.) possui uma importância histórica e econômica para o Brasil. O agronegócio sucroalcooleiro vem experimentando forte expansão na última década não só no Brasil como também em todo o mundo em função, principalmente, da demanda por fontes de energia menos agressivas ao ambiente. Para atender a uma maior
Publicado em: 2011
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12. Aplicação de modelos estatísticos e desenvolvimento de algoritmos para estudo genético de doenças neuro-psiquiátricas / Statistical models application and algorithm development for genetic studies in neuropsychiatric diseases
Fatores genéticos têm sido descritos para diversas doenças do sistema nervoso central. Uma etapa importante na identificação de genes responsáveis por estas doenças são os estudos de mapeamento genético. Além disso, devido às novas tecnologias de aquisição de dados de genótipos dos indivíduos, é necessário o estudo e desenvolvimento de progr
Publicado em: 2011