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Registro Completo |
Biblioteca(s): |
Embrapa Recursos Genéticos e Biotecnologia. |
Data corrente: |
23/01/2012 |
Data da última atualização: |
10/11/2016 |
Tipo da produção científica: |
Documentos |
Autoria: |
SALOMAO, A. N. |
Afiliação: |
ANTONIETA NASSIF SALOMAO, CENARGEN. |
Título: |
Manual de Curadores de Germoplasma - Vegetal: Glossário. |
Ano de publicação: |
2010 |
Fonte/Imprenta: |
Brasília, DF: Embrapa Recursos Genéticos e Biotecnologia, 2010. |
Páginas: |
14 p. |
Série: |
(Embrapa Recursos Genéticos e Biotecnologia. Documentos, 326). |
Idioma: |
Português |
Palavras-Chave: |
Glossário; Recurso genético vegetal. |
Thesagro: |
Conservação. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/149795/1/doc326.pdf
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Marc: |
LEADER 00532nam a2200157 a 4500 001 1913203 005 2016-11-10 008 2010 bl uuuu u0uu1 u #d 100 1 $aSALOMAO, A. N. 245 $aManual de Curadores de Germoplasma - Vegetal$bGlossário.$h[electronic resource] 260 $aBrasília, DF: Embrapa Recursos Genéticos e Biotecnologia$c2010 300 $a14 p. 490 $a(Embrapa Recursos Genéticos e Biotecnologia. Documentos, 326). 650 $aConservação 653 $aGlossário 653 $aRecurso genético vegetal
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Embrapa Recursos Genéticos e Biotecnologia (CENARGEN) |
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Registro Completo
Biblioteca(s): |
Embrapa Gado de Leite. |
Data corrente: |
26/12/2018 |
Data da última atualização: |
24/01/2023 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
B - 3 |
Autoria: |
RIBEIRO, I. M.; BORGES, C. C. H.; SILVA, B. Z.; ARBEX, W. A. |
Afiliação: |
WAGNER ANTONIO ARBEX, CNPGL. |
Título: |
A genetic programming model for association studies to detect epistasis in low heritability data. |
Ano de publicação: |
2018 |
Fonte/Imprenta: |
Revista de Informática Teórica e Aplicada, v. 25, n. 2, p. 85-92, 2018. |
Idioma: |
Inglês |
Conteúdo: |
Abstract The genome-wide associations studies (GWAS) aims to identify the most influential markers in relation to the phenotype values. One of the substantial challenges is to find a non-linear mapping between genotype and phenotype, also known as epistasis, that usually becomes the process of searching and identifying functional SNPs more complex. Some diseases such as cervical cancer, leukemia and type 2 diabetes have low heritability. The heritability of the sample is directly related to the explanation defined by the genotype, so the lower the heritability the greater the influence of the environmental factors and the less the genotypic explanation. In this work, an algorithm capable of identifying epistatic associations at different levels of heritability is proposed. The developing model is a aplication of genetic programming with a specialized initialization for the initial population consisting of a random forest strategy. The initialization process aims to rank the most important SNPs increasing the probability of their insertion in the initial population of the genetic programming model. The expected behavior of the presented model for the obtainment of the causal markers intends to be robust in relation to the heritability level. The simulated experiments are case-control type with heritability level of 0.4, 0.3, 0.2 and 0.1 considering scenarios with 100 and 1000 markers. Our approach was compared with the GPAS software and a genetic programming algorithm without the initialization step. The results show that the use of an efficient population initialization method based on ranking strategy is very promising compared to other models. MenosAbstract The genome-wide associations studies (GWAS) aims to identify the most influential markers in relation to the phenotype values. One of the substantial challenges is to find a non-linear mapping between genotype and phenotype, also known as epistasis, that usually becomes the process of searching and identifying functional SNPs more complex. Some diseases such as cervical cancer, leukemia and type 2 diabetes have low heritability. The heritability of the sample is directly related to the explanation defined by the genotype, so the lower the heritability the greater the influence of the environmental factors and the less the genotypic explanation. In this work, an algorithm capable of identifying epistatic associations at different levels of heritability is proposed. The developing model is a aplication of genetic programming with a specialized initialization for the initial population consisting of a random forest strategy. The initialization process aims to rank the most important SNPs increasing the probability of their insertion in the initial population of the genetic programming model. The expected behavior of the presented model for the obtainment of the causal markers intends to be robust in relation to the heritability level. The simulated experiments are case-control type with heritability level of 0.4, 0.3, 0.2 and 0.1 considering scenarios with 100 and 1000 markers. Our approach was compared with the GPAS software and a genetic programming algorithm without... Mostrar Tudo |
Palavras-Chave: |
Computational Modeling; Genetic Programming; GWAS; Mathematical Modeling; Random Forest; SNP. |
Thesaurus NAL: |
Bioinformatics. |
Categoria do assunto: |
X Pesquisa, Tecnologia e Engenharia |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/189322/1/Artigo-RevInfTeorApl.pdf
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Marc: |
LEADER 02397naa a2200241 a 4500 001 2102526 005 2023-01-24 008 2018 bl uuuu u00u1 u #d 100 1 $aRIBEIRO, I. M. 245 $aA genetic programming model for association studies to detect epistasis in low heritability data.$h[electronic resource] 260 $c2018 520 $aAbstract The genome-wide associations studies (GWAS) aims to identify the most influential markers in relation to the phenotype values. One of the substantial challenges is to find a non-linear mapping between genotype and phenotype, also known as epistasis, that usually becomes the process of searching and identifying functional SNPs more complex. Some diseases such as cervical cancer, leukemia and type 2 diabetes have low heritability. The heritability of the sample is directly related to the explanation defined by the genotype, so the lower the heritability the greater the influence of the environmental factors and the less the genotypic explanation. In this work, an algorithm capable of identifying epistatic associations at different levels of heritability is proposed. The developing model is a aplication of genetic programming with a specialized initialization for the initial population consisting of a random forest strategy. The initialization process aims to rank the most important SNPs increasing the probability of their insertion in the initial population of the genetic programming model. The expected behavior of the presented model for the obtainment of the causal markers intends to be robust in relation to the heritability level. The simulated experiments are case-control type with heritability level of 0.4, 0.3, 0.2 and 0.1 considering scenarios with 100 and 1000 markers. Our approach was compared with the GPAS software and a genetic programming algorithm without the initialization step. The results show that the use of an efficient population initialization method based on ranking strategy is very promising compared to other models. 650 $aBioinformatics 653 $aComputational Modeling 653 $aGenetic Programming 653 $aGWAS 653 $aMathematical Modeling 653 $aRandom Forest 653 $aSNP 700 1 $aBORGES, C. C. H. 700 1 $aSILVA, B. Z. 700 1 $aARBEX, W. A. 773 $tRevista de Informática Teórica e Aplicada$gv. 25, n. 2, p. 85-92, 2018.
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