Detecting methylation signatures in neurodegenerative disease by density-based clustering of applications with reducing noise

Abstract There have been numerous genetic and epigenetic datasets generated for the study of complex disease including neurodegenerative disease. However, analysis of such data often suffers from detecting the outliers of the samples, which subsequently affects the extraction of the true biological...

Full description

Bibliographic Details
Main Authors: Saurav Mallik, Zhongming Zhao
Format: Article
Language:English
Published: Nature Publishing Group 2020-12-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-020-78463-3
id doaj-cac7be4a73e04b479ecf1dc9a2db5591
record_format Article
spelling doaj-cac7be4a73e04b479ecf1dc9a2db55912020-12-20T12:31:48ZengNature Publishing GroupScientific Reports2045-23222020-12-0110111410.1038/s41598-020-78463-3Detecting methylation signatures in neurodegenerative disease by density-based clustering of applications with reducing noiseSaurav Mallik0Zhongming Zhao1Center for Precision Health, School of Biomedical Informatics, The University of Texas Health Science Center at HoustonCenter for Precision Health, School of Biomedical Informatics, The University of Texas Health Science Center at HoustonAbstract There have been numerous genetic and epigenetic datasets generated for the study of complex disease including neurodegenerative disease. However, analysis of such data often suffers from detecting the outliers of the samples, which subsequently affects the extraction of the true biological signals involved in the disease. To address this critical issue, we developed a novel framework for identifying methylation signatures using consecutive adaptation of a well-known outlier detection algorithm, density based clustering of applications with reducing noise (DBSCAN) followed by hierarchical clustering. We applied the framework to two representative neurodegenerative diseases, Alzheimer’s disease (AD) and Down syndrome (DS), using DNA methylation datasets from public sources (Gene Expression Omnibus, GEO accession ID: GSE74486). We first applied DBSCAN algorithm to eliminate outliers, and then used Limma statistical method to determine differentially methylated genes. Next, hierarchical clustering technique was applied to detect gene modules. Our analysis identified a methylation signature comprising 21 genes for AD and a methylation signature comprising 89 genes for DS, respectively. Our evaluation indicated that these two signatures could lead to high classification accuracy values (92% and 70%) for these two diseases. In summary, this framework will be useful to better detect outlier-free genetic and epigenetic signatures in various complex diseases and their developmental stages.https://doi.org/10.1038/s41598-020-78463-3
collection DOAJ
language English
format Article
sources DOAJ
author Saurav Mallik
Zhongming Zhao
spellingShingle Saurav Mallik
Zhongming Zhao
Detecting methylation signatures in neurodegenerative disease by density-based clustering of applications with reducing noise
Scientific Reports
author_facet Saurav Mallik
Zhongming Zhao
author_sort Saurav Mallik
title Detecting methylation signatures in neurodegenerative disease by density-based clustering of applications with reducing noise
title_short Detecting methylation signatures in neurodegenerative disease by density-based clustering of applications with reducing noise
title_full Detecting methylation signatures in neurodegenerative disease by density-based clustering of applications with reducing noise
title_fullStr Detecting methylation signatures in neurodegenerative disease by density-based clustering of applications with reducing noise
title_full_unstemmed Detecting methylation signatures in neurodegenerative disease by density-based clustering of applications with reducing noise
title_sort detecting methylation signatures in neurodegenerative disease by density-based clustering of applications with reducing noise
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2020-12-01
description Abstract There have been numerous genetic and epigenetic datasets generated for the study of complex disease including neurodegenerative disease. However, analysis of such data often suffers from detecting the outliers of the samples, which subsequently affects the extraction of the true biological signals involved in the disease. To address this critical issue, we developed a novel framework for identifying methylation signatures using consecutive adaptation of a well-known outlier detection algorithm, density based clustering of applications with reducing noise (DBSCAN) followed by hierarchical clustering. We applied the framework to two representative neurodegenerative diseases, Alzheimer’s disease (AD) and Down syndrome (DS), using DNA methylation datasets from public sources (Gene Expression Omnibus, GEO accession ID: GSE74486). We first applied DBSCAN algorithm to eliminate outliers, and then used Limma statistical method to determine differentially methylated genes. Next, hierarchical clustering technique was applied to detect gene modules. Our analysis identified a methylation signature comprising 21 genes for AD and a methylation signature comprising 89 genes for DS, respectively. Our evaluation indicated that these two signatures could lead to high classification accuracy values (92% and 70%) for these two diseases. In summary, this framework will be useful to better detect outlier-free genetic and epigenetic signatures in various complex diseases and their developmental stages.
url https://doi.org/10.1038/s41598-020-78463-3
work_keys_str_mv AT sauravmallik detectingmethylationsignaturesinneurodegenerativediseasebydensitybasedclusteringofapplicationswithreducingnoise
AT zhongmingzhao detectingmethylationsignaturesinneurodegenerativediseasebydensitybasedclusteringofapplicationswithreducingnoise
_version_ 1724376529072291840