2012
DOI: 10.1186/1743-422x-9-58
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Human polyomaviruses identification by logic mining techniques

Abstract: BackgroundDifferences in genomic sequences are crucial for the classification of viruses into different species. In this work, viral DNA sequences belonging to the human polyomaviruses BKPyV, JCPyV, KIPyV, WUPyV, and MCPyV are analyzed using a logic data mining method in order to identify the nucleotides which are able to distinguish the five different human polyomaviruses.ResultsThe approach presented in this work is successful as it discovers several logic rules that effectively characterize the different fi… Show more

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Cited by 15 publications
(10 citation statements)
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References 13 publications
(24 reference statements)
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“…A mathematical model of HBV transmission was used to predict future chronic hepatitis B (CHB) prevalence in the New Zealand Tongan population with different infection control strategies in literature (Thornley, Bullen & Roberts, 2008). Other studies have been performed with supervised methods for predicting viruses and pathologies (Weitschek et al, 2012; Weitschek, Cunial & Felici, 2015; Polychronopoulos et al, 2014). …”
Section: Introductionmentioning
confidence: 99%
“…A mathematical model of HBV transmission was used to predict future chronic hepatitis B (CHB) prevalence in the New Zealand Tongan population with different infection control strategies in literature (Thornley, Bullen & Roberts, 2008). Other studies have been performed with supervised methods for predicting viruses and pathologies (Weitschek et al, 2012; Weitschek, Cunial & Felici, 2015; Polychronopoulos et al, 2014). …”
Section: Introductionmentioning
confidence: 99%
“…, ; Weitschek et al . , ,b; van Velzen et al . ), and the analysis of numerical data such as gene expression profiles (Arisi et al .…”
Section: Feature Selectionmentioning
confidence: 99%
“…The early region of BKPyV transcribes three transforming proteins called T antigens; LT antigen, ST antigen, and Truncated T antigen, whereas JCPyV early region encodes five T antigens; LT antigen, ST antigen, T’135, T’136 and T’165 antigens [10, 11]. The late region of both BKPyV and JCPyV encodes four proteins VP1, VP2, VP3 and agnoprotein.…”
Section: Introductionmentioning
confidence: 99%