Genomics | |
DMRFusion: A differentially methylated region detection tool based on the ranked fusion method | |
Ehsan Shams Davodly^11  Mehdi Heidari^12  Maryam Yassi^13  Afsaneh Mojtabanezhad Shariatpanahi^14  Mahdieh Dayyani^15  | |
[1] Canada's Michael Smith Genome Sciences Center, BC Cancer Agency, Vancouver, British Columbia, Canada^2;Cancer Genetics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran^4;Cancer Genetics Research Unit, Reza Radiotherapy and Oncology Center, Mashhad, Iran^1;Department of Computer Engineering, Mashhad Branch, Islamic Azad University, Mashhad, Iran^3;Department of Medical Genetics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran^5 | |
关键词: DNA methylation; Epigenetic; Differentially methylated regions; Reduced representation bisulfite sequencing; Filter method; | |
DOI : 10.1016/j.ygeno.2017.12.006 | |
学科分类:医学(综合) | |
来源: Academic Press | |
【 摘 要 】
DNA methylation is an important epigenetic modification involved in many biological processes and diseases. Computational analysis of differentially methylated regions (DMRs) could explore the underlying reasons of methylation. DMRFusion is presented as a useful tool for comprehensive DNA methylation analysis of DMRs on methylation sequencing data. This tool is designed base on the integration of several ranking methods; Information gain, Between versus within Class scatter ratio, Fisher ratio, Z-score and Welch's t-test. In this study, DMRFusion on reduced representation bisulfite sequencing (RRBS) data in chronic lymphocytic leukemia cancer displayed 30 nominated regions and CpG sites with a maximum methylation difference detected in the hypermethylation DMRs. We realized that DMRFusion is able to process methylation sequencing data in an efficient and accurate manner and to provide annotation and visualization for DMRs with high fold difference score (p-value and FDR < 0.05 and type I error: 0.04).
【 授权许可】
CC BY
【 预 览 】
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