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Robust group fused lasso for multisample copy number variation detection under uncertainty.
Sharifi Noghabi, Hossein; Mohammadi, Majid; Tan, Yao-Hua.
Afiliação
  • Sharifi Noghabi H; The Center of Excellence of Soft Computing and Intelligent Information Processing (SCIIP), Ferdowsi University of Mashhad, Iran. hossein1990@gmail.com.
  • Mohammadi M; Department of Technology, Policy and Management, Delft University of Technology, Netherlands.
  • Tan YH; Department of Technology, Policy and Management, Delft University of Technology, Netherlands.
IET Syst Biol ; 10(6): 229-236, 2016 Dec.
Article em En | MEDLINE | ID: mdl-27879477
ABSTRACT
One of the most important needs in the post-genome era is providing the researchers with reliable and efficient computational tools to extract and analyse this huge amount of biological data, in which DNA copy number variation (CNV) is a vitally important one. Array-based comparative genomic hybridisation (aCGH) is a common approach in order to detect CNVs. Most of methods for this purpose were proposed for one-dimensional profiles. However, slightly this focus has moved from one- to multi-dimensional signals. In addition, since contamination of these profiles with noise is always an issue, it is highly important to have a robust method for analysing multi-sample aCGH profiles. In this study, the authors propose robust group fused lasso which utilises the robust group total variations. Instead of l2,1 norm, the l1 - l2 M-estimator is used which is more robust in dealing with non-Gaussian noise and high corruption. More importantly, Correntropy (Welsch M-estimator) is also applied for fitting error. Extensive experiments indicate that the proposed method outperforms the state-of-the art algorithms and techniques under a wide range of scenarios with diverse noises.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hibridização Genômica Comparativa / Variações do Número de Cópias de DNA Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hibridização Genômica Comparativa / Variações do Número de Cópias de DNA Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article