coMET: visualisation of regional epigenome-wide association scan results and DNA co-methylation patterns.
coMET: visualisation of regional epigenome-wide association scan results and DNA co-methylation patterns.
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DOI:
10.1186/s12859-015-0568-2
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发表时间:
2015-04-28
影响因子:
3
通讯作者:
Bell JT
中科院分区:
文献类型:
--
作者:
Martin TC;Yet I;Tsai PC;Bell JT
Epigenome-wide association scans (EWAS) are an increasingly powerful and widely-used approach to assess the role of epigenetic variation in human complex traits. However, this rapidly emerging field lacks dedicated visualisation tools that can display features specific to epigenetic datasets. We developed coMET, an R package and online tool for visualisation of EWAS results in a genomic region of interest. coMET generates a regional plot of epigenetic-phenotype association results and the estimated DNA methylation correlation between CpG sites (co-methylation), with further options to visualise genomic annotations based on ENCODE data, gene tracks, reference CpG-sites, and user-defined features. The tool can be used to display phenotype association signals and correlation patterns of microarray or sequencing-based DNA methylation data, such as Illumina Infinium 450k, WGBS, or MeDIP-seq, as well as other types of genomic data, such as gene expression profiles. The software is available as a user-friendly online tool from http://epigen.kcl.ac.uk/cometand as an R Bioconductor package. Source code, examples, and full documentation are also available from GitHub. Our new software allows visualisation of EWAS results with functional genomic annotations and with estimation of co-methylation patterns. coMET is available to a wide audience as an online tool and R package, and can be a valuable resource to interpret results in the fast growing field of epigenetics. The software is designed for epigenetic data, but can also be applied to genomic and functional genomic datasets in any species.
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影响因子:
48
作者:
Huber W;Carey VJ;Gentleman R;Anders S;Carlson M;Carvalho BS;Bravo HC;Davis S;Gatto L;Girke T;Gottardo R;Hahne F;Hansen KD;Irizarry RA;Lawrence M;Love MI;MacDonald J;Obenchain V;Oleś AK;Pagès H;Reyes A;Shannon P;Smyth GK;Tenenbaum D;Waldron L;Morgan M
通讯作者:
Morgan M
DOI:
10.1038/nrg3000
发表时间:
2011-07-12
期刊:
Nature reviews. Genetics
影响因子:
--
作者:
通讯作者:
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影响因子:
9.8
作者:
Grundberg, Elin;Meduri, Eshwar;Deloukas, Panos
通讯作者:
Deloukas, Panos
DOI:
10.1093/bioinformatics/btq419
发表时间:
2010-09-15
期刊:
Bioinformatics (Oxford, England)
影响因子:
--
作者:
Pruim RJ;Welch RP;Sanna S;Teslovich TM;Chines PS;Gliedt TP;Boehnke M;Abecasis GR;Willer CJ
通讯作者:
Willer CJ
影响因子:
46.9
作者:
通讯作者:
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