计算生物学
甲基化
CpG站点
表观遗传学
基因组
表观遗传学
差异甲基化区
生物
作者
T.J. Gorrie-Stone,Melissa C. Smart,Ayden Saffari,Karim Malki,Eilis Hannon,Joe Burrage,Jonathan Mill,Meena Kumari,Leonard C. Schalkwyk
出处
期刊:Bioinformatics
[Oxford University Press]
日期:2019-03-15
卷期号:35 (6): 981-986
被引量:26
标识
DOI:10.1093/bioinformatics/bty713
摘要
Motivation: The datasets generated by DNA methylation analyses are getting bigger. With the release of the HumanMethylationEPIC micro-array and datasets containing thousands of samples, analyses of these large datasets using R are becoming impractical due to large memory requirements. As a result there is an increasing need for computationally efficient methodologies to perform meaningful analysis on high dimensional data.
Results: Here we introduce the bigmelon R package, which provides a memory efficient workflow that enables users to perform the complex, large scale analyses required in epigenome wide association studies (EWAS) without the need for large RAM. Building on top of the CoreArray Genomic Data Structure file format and libraries packaged in the gdsfmt package, we provide a practical workflow that facilitates the reading-in, preprocessing, quality control and statistical analysis of DNA methylation data.
We demonstrate the capabilities of the bigmelon package using a large dataset consisting of 1193 human blood samples from the Understanding Society: UK Household Longitudinal Study, assayed on the EPIC micro-array platform.
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