DocumentCode
140626
Title
Exploring regulatory elements in low-methylated regions for gene expression prediction
Author
Hong Hu ; Yang Dai
Author_Institution
Dept. of Bioeng., Univ. of Illinois at Chicago, Chicago, IL, USA
fYear
2014
fDate
26-30 Aug. 2014
Firstpage
4763
Lastpage
4766
Abstract
Recent studies on methylomes have indicated that low-methylated regions (LMRs) are related to potential active distal regulatory regions. To further investigate the potential relation between LMRs and gene expression regulation, we propose a penalized logistic regression model to predict gene expression directional change based on computationally analyzed transcription factor binding sites in LMRs that are distinctive between two cell types. We evaluated this approach using the whole genome bisulphite sequencing and RNA-seq data of two cell types: adipose-derived stem cells and iPSCs of adipose-derived stem cells. For Differentially Expressed (DE) genes with LMRs in their intergenic and/or genebody regions, our model obtained a 10-fold cross-validated AUC value of 0.88 for prediction of expression directional change. For DE genes with only LMRs in intergenic regions the corresponding AUC value is 0.84.
Keywords
RNA; cellular biophysics; genetics; genomics; regression analysis; RNA-seq data; active distal regulatory regions; adipose-derived stem cells; computationally analyzed transcription factor binding sites; differentially expressed genes; gene expression directional change prediction; genebody regions; iPSC; intergenic regions; low-methylated regions; methylomes; penalized logistic regression model; ten-fold cross-validated AUC value; whole genome bisulphite sequencing; Bioinformatics; DNA; Gene expression; Genomics; Logistics; Predictive models; Pulse width modulation;
fLanguage
English
Publisher
ieee
Conference_Titel
Engineering in Medicine and Biology Society (EMBC), 2014 36th Annual International Conference of the IEEE
Conference_Location
Chicago, IL
ISSN
1557-170X
Type
conf
DOI
10.1109/EMBC.2014.6944689
Filename
6944689
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