کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5905108 1159829 2016 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Gene expression classification using epigenetic features and DNA sequence composition in the human embryonic stem cell line H1
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی ژنتیک
پیش نمایش صفحه اول مقاله
Gene expression classification using epigenetic features and DNA sequence composition in the human embryonic stem cell line H1
چکیده انگلیسی


- A new machine learning method is developed to classify gene expression.
- Epigenetic and genetic features are both considered to construct the classifier.
- The predictive accuracy can be markedly improved when the epigenetic features are considered.

Epigenetic factors are known to correlate with gene expression in the existing studies. However, quantitative models that accurately classify the highly and lowly expressed genes based on epigenetic factors are currently lacking. In this study, a new machine learning method combines histone modifications, DNA methylation, DNA accessibility, transcription factors, and trinucleotide composition with support vector machines (SVM) is developed in the context of human embryonic stem cell line (H1). The results indicate that the predictive accuracy will be markedly improved when the epigenetic features are considered. The predictive accuracy and Matthews correlation coefficient of the best model are as high as 95.96% and 0.92 for 10-fold cross-validation test, and 95.58% and 0.92 for independent dataset test, respectively. Our model provides a good way to judge a gene is either highly or lowly expressed gene by using genetic and epigenetic data, when the expression data of the gene is lacking. And a web-server GECES for our analysis method is established at http://202.207.14.87:8032/fuwu/GECES/index.asp, so that other scientists can easily get their desired results by our web-server, without going through the mathematical details.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Gene - Volume 592, Issue 1, 30 October 2016, Pages 227-234
نویسندگان
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