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Noise-robust assessment of SNP array based CNV calls through local noise estimation of log R ratios.
Cosemans, Nele; Claes, Peter; Brison, Nathalie; Vermeesch, Joris Robert; Peeters, Hilde.
Afiliação
  • Cosemans N; Center for Human Genetics, University Hospital Leuven, KU Leuven, Leuven, Belgium.
  • Claes P; Medical Image Computing, ESAT/PSI, Department of Electrical Engineering, KU Leuven, Leuven, Belgium.
  • Brison N; Medical Imaging Research Center, UZ Leuven, Leuven, Belgium.
  • Vermeesch JR; Center for Human Genetics, University Hospital Leuven, KU Leuven, Leuven, Belgium.
  • Peeters H; Center for Human Genetics, University Hospital Leuven, KU Leuven, Leuven, Belgium.
Stat Appl Genet Mol Biol ; 17(2)2018 04 28.
Article em En | MEDLINE | ID: mdl-29708886
Arrays based on single nucleotide polymorphisms (SNPs) have been successful for the large scale discovery of copy number variants (CNVs). However, current CNV calling algorithms still have limitations in detecting CNVs with high specificity and sensitivity, especially in case of small (<100 kb) CNVs. Therefore, this study presents a simple statistical analysis to evaluate CNV calls from SNP arrays in order to improve the noise-robustness of existing CNV calling algorithms. The proposed approach estimates local noise of log R ratios and returns the probability that a certain observation is different from this log R ratio noise level. This probability can be triggered at different thresholds to tailor specificity and/or sensitivity in a flexible way. Moreover, a comparison based on qPCR experiments showed that the proposed noise-robust CNV calls outperformed original ones for multiple threshold values.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Modelos Estatísticos / Polimorfismo de Nucleotídeo Único / Variações do Número de Cópias de DNA / Modelos Genéticos Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Stat Appl Genet Mol Biol Assunto da revista: BIOLOGIA MOLECULAR / GENETICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Bélgica

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Modelos Estatísticos / Polimorfismo de Nucleotídeo Único / Variações do Número de Cópias de DNA / Modelos Genéticos Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Stat Appl Genet Mol Biol Assunto da revista: BIOLOGIA MOLECULAR / GENETICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Bélgica