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1.
Pharmacogenomics ; 14(4): 391-401, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23438886

RESUMO

BACKGROUND: Genome-wide association studies (GWAS) have had limited success when applied to complex diseases. Analyzing SNPs individually requires several large studies to integrate the often divergent results. In the presence of epistasis, multivariate approaches based on the linear model (including stepwise logistic regression) often have low sensitivity and generate an abundance of artifacts. METHODS: Recent advances in distributed and parallel processing spurred methodological advances in nonparametric statistics. U-statistics for structured multivariate data (µStat) are not confounded by unrealistic assumptions (e.g., linearity, independence). RESULTS: By incorporating knowledge about relationships between SNPs, µGWAS (GWAS based on µStat) can identify clusters of genes around biologically relevant pathways and pinpoint functionally relevant regions within these genes. CONCLUSION: With this computational biostatistics approach increasing power and guarding against artifacts, personalized medicine and comparative effectiveness will advance while subgroup analyses of Phase III trials can now suggest risk factors for adverse events and novel directions for drug development.


Assuntos
Epilepsia/genética , Estudo de Associação Genômica Ampla/estatística & dados numéricos , Redes e Vias Metabólicas/genética , Estatísticas não Paramétricas , Ensaios Clínicos Fase III como Assunto , Epistasia Genética , Humanos , Polimorfismo de Nucleotídeo Único/genética , Proteínas ras/genética
2.
Int. microbiol ; 10(4): 245-251, dic. 2007. ilus, tab
Artigo em En | IBECS | ID: ibc-62538

RESUMO

Microbial populations associated with methanogenic fixed- or floating-bed bioreactors used for anaerobic digestion of lignocellulosic waste were investigated. Fluorescent in situ hybridization (FISH) was used to characterize microorganisms in samples obtained from different heights in the reactors, which were operated in a semi-continuous manner (feeding and mixing once every 2 days). The FISH results showed that Methanosaeta concilii cells were most numerous at the bottom of both reactors. M. concilii cells were more abundant in the fixed-bed reactor (FXBR), which performed better than the floating-bed reactor (FLBR). Species of the Methanosarcina genera (mainly M. barkeri and M. mazei) were also observed in the FLBR but rarely in the FXBR. Methane production in each of the reactors ranged from 0.29 to 0.33 m3 CH(4)/kg COD(rem) (chemical oxygen demand removed). The removal of volatile fatty acids (VFA; 70-75 h) in the FXBR was more efficient than in the FLBR (AU)


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Assuntos
Águas Residuárias/microbiologia , Digestão de Lodos , Methanosarcinales/patogenicidade , Methanosarcina/patogenicidade , Biodegradação Ambiental , Sondas de Oligonucleotídeos/análise , Biocombustíveis , Microbiologia da Água
3.
Int Microbiol ; 10(4): 245-51, 2007 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-18228221

RESUMO

Microbial populations associated with methanogenic fixed- or floating-bed bioreactors used for anaerobic digestion of lignocellulosic waste were investigated. Fluorescent in situ hybridization (FISH) was used to characterize microorganisms in samples obtained from different heights in the reactors, which were operated in a semi-continuous manner (feeding and mixing once every 2 days). The FISH results showed that Methanosaeta concilii cells were most numerous at the bottom of both reactors. M. concilii cells were more abundant in the fixed-bed reactor (FXBR), which performed better than the floating-bed reactor (FLBR). Species of the Methanosarcina genera (mainly M. barkeri and M. mazei) were also observed in the FLBR but rarely in the FXBR. Methane production in each of the reactors ranged from 0.29 to 0.33 m3 CH(4)/kg COD(rem) (chemical oxygen demand removed). The removal of volatile fatty acids (VFA; 70-75 h) in the FXBR was more efficient than in the FLBR.


Assuntos
Anaerobiose/fisiologia , Bactérias Anaeróbias/fisiologia , Reatores Biológicos/microbiologia , Methanosarcina/fisiologia , DNA Bacteriano/análise , Ácidos Graxos Voláteis/metabolismo , Hibridização in Situ Fluorescente , Metano/metabolismo , Methanosarcina/isolamento & purificação , Eliminação de Resíduos Líquidos/métodos
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