Literature DB >> 27879477

Robust group fused lasso for multisample copy number variation detection under uncertainty.

Hossein Sharifi Noghabi1, Majid Mohammadi2, Yao-Hua Tan2.   

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.

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Mesh:

Year:  2016        PMID: 27879477      PMCID: PMC8687376          DOI: 10.1049/iet-syb.2015.0081

Source DB:  PubMed          Journal:  IET Syst Biol        ISSN: 1751-8849            Impact factor:   1.615


  18 in total

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2.  Robust and stable gene selection via Maximum-Minimum Correntropy Criterion.

Authors:  Majid Mohammadi; Hossein Sharifi Noghabi; Ghosheh Abed Hodtani; Habib Rajabi Mashhadi
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4.  A fused lasso latent feature model for analyzing multi-sample aCGH data.

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Journal:  Biostatistics       Date:  2011-06-03       Impact factor: 5.899

Review 5.  Comparing CNV detection methods for SNP arrays.

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Journal:  Brief Funct Genomic Proteomic       Date:  2009-09-08

6.  Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives.

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7.  Genomic and transcriptional aberrations linked to breast cancer pathophysiologies.

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Journal:  Cancer Cell       Date:  2006-12       Impact factor: 31.743

8.  Multisample aCGH data analysis via total variation and spectral regularization.

Authors:  Xiaowei Zhou; Can Yang; Xiang Wan; Hongyu Zhao; Weichuan Yu
Journal:  IEEE/ACM Trans Comput Biol Bioinform       Date:  2013 Jan-Feb       Impact factor: 3.710

Review 9.  Progress from genome-wide association studies and copy number variant studies in epilepsy.

Authors:  Costin Leu; Antonietta Coppola; Sanjay M Sisodiya
Journal:  Curr Opin Neurol       Date:  2016-04       Impact factor: 5.710

10.  Using graphical adaptive lasso approach to construct transcription factor and microRNA's combinatorial regulatory network in breast cancer.

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Journal:  IET Syst Biol       Date:  2014-06       Impact factor: 1.615

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