Literature DB >> 23990415

A-clustering: a novel method for the detection of co-regulated methylation regions, and regions associated with exposure.

Tamar Sofer1, Elizabeth D Schifano, Jane A Hoppin, Lifang Hou, Andrea A Baccarelli.   

Abstract

MOTIVATION: DNA methylation is a heritable modifiable chemical process that affects gene transcription and is associated with other molecular markers (e.g. gene expression) and biomarkers (e.g. cancer or other diseases). Current technology measures methylation in hundred of thousands, or millions of CpG sites throughout the genome. It is evident that neighboring CpG sites are often highly correlated with each other, and current literature suggests that clusters of adjacent CpG sites are co-regulated.
RESULTS: We develop the Adjacent Site Clustering (A-clustering) algorithm to detect sets of neighboring CpG sites that are correlated with each other. To detect methylation regions associated with exposure, we propose an analysis pipeline for high-dimensional methylation data in which CpG sites within regions identified by A-clustering are modeled as multivariate responses to environmental exposure using a generalized estimating equation approach that assumes exposure equally affects all sites in the cluster. We develop a correlation preserving simulation scheme, and study the proposed methodology via simulations. We study the clusters detected by the algorithm on high dimensional dataset of peripheral blood methylation of pesticide applicators. AVAILABILITY: We provide the R package Aclust that efficiently implements the A-clustering and the analysis pipeline, and produces analysis reports. The package is found on http://www.hsph.harvard.edu/tamar-sofer/packages/ CONTACT: tsofer@hsph.harvard.edu

Entities:  

Mesh:

Year:  2013        PMID: 23990415      PMCID: PMC3810849          DOI: 10.1093/bioinformatics/btt498

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  18 in total

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7.  Validation of a DNA methylation microarray for 450,000 CpG sites in the human genome.

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8.  Exposure to airborne particulate matter is associated with methylation pattern in the asthma pathway.

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9.  The human colon cancer methylome shows similar hypo- and hypermethylation at conserved tissue-specific CpG island shores.

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10.  Capturing heterogeneity in gene expression studies by surrogate variable analysis.

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2.  Epigenome-wide cross-tissue predictive modeling and comparison of cord blood and placental methylation in a birth cohort.

Authors:  Margherita M De Carli; Andrea A Baccarelli; Letizia Trevisi; Ivan Pantic; Kasey Jm Brennan; Michele R Hacker; Holly Loudon; Kelly J Brunst; Robert O Wright; Rosalind J Wright; Allan C Just
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3.  An evaluation of supervised methods for identifying differentially methylated regions in Illumina methylation arrays.

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4.  PrEMeR-CG: inferring nucleotide level DNA methylation values from MethylCap-seq data.

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Journal:  Bioinformatics       Date:  2014-08-31       Impact factor: 6.937

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6.  Identification of epigenetic modulators in human breast cancer by integrated analysis of DNA methylation and RNA-Seq data.

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Review 7.  Epigenetic epidemiology: promises for public health research.

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8.  Association between sperm mitochondarial DNA copy number and nuclear DNA methylation.

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9.  Early life lead exposure causes gender-specific changes in the DNA methylation profile of DNA extracted from dried blood spots.

Authors:  Arko Sen; Nicole Heredia; Marie-Claude Senut; Matthew Hess; Susan Land; Wen Qu; Kurt Hollacher; Mary O Dereski; Douglas M Ruden
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10.  Multi-generational impacts of arsenic exposure on genome-wide DNA methylation and the implications for arsenic-induced skin lesions.

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Journal:  Environ Int       Date:  2018-07-05       Impact factor: 9.621

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