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research article
A Bayesian deconvolution strategy for immunoprecipitation-based DNA methylome analysis
Authors
A Barski
A Bird
+64 more
A Schumacher
AS Cheng
B Khulan
BE Bernstein
C Gebhard
D Zilberman
Daniel J Turner
David K Jackson
DH Yasui
Eleni M Tomazou
Eugene Kulesha
Ewan Birney
F Eckhardt
FV Jacinto
GS Slater
HD Morgan
Heng Li
I Keshet
I Sandovici
J Reinders
Javier Herrero
JM Flanagan
JM Ordway
John C Marioni
Kevin L Howe
L Shen
Liselotte Bäckdahl
M Bibikova
M Frommer
M Weber
M Weber
Marcos M Miretti
Marlis Herberth
MJ Oberley
Natalie P Thorne
Nathan Johnson
P Adorjan
P Flicek
Paul Flicek
R Illingworth
R Mukhopadhyay
R Tompa
RA Irizarry
RA Rollins
Richard Durbin
RS Gitan
S Beck
SD Fouse
Simon Tavaré
SJ Cokus
Stefan Gräf
Stephan Beck
T Rauch
TH Bestor
Thomas A Down
Tim J P Hubbard
TS Mikkelsen
TT Ching
Vardhman K Rakyan
VK Rakyan
VK Rakyan
X Zhang
Y Qi
Z Lippman
Publication date
1 July 2008
Publisher
Nature Publishing Group
Doi
View
on
PubMed
Abstract
DNA methylation is an indispensible epigenetic modification required for regulating the expression of mammalian genomes. Immunoprecipitation-based methods for DNA methylome analysis are rapidly shifting the bottleneck in this field from data generation to data analysis, necessitating the development of better analytical tools. In particular, an inability to estimate absolute methylation levels remains a major analytical difficulty associated with immunoprecipitation-based DNA methylation profiling. To address this issue, we developed a cross-platform algorithm - Bayesian tool for methylation analysis (Batman) - for analyzing methylated DNA immunoprecipitation (MeDIP) profiles generated using oligonucleotide arrays (MeDIP-chip) or next-generation sequencing (MeDIP-seq). We developed the latter approach to provide a high-resolution whole-genome DNA methylation profile (DNA methylome) of a mammalian genome. Strong correlation of our data, obtained using mature human spermatozoa, with those obtained using bisulfite sequencing suggest that combining MeDIP-seq or MeDIP-chip with Batman provides a robust, quantitative and cost-effective functional genomic strategy for elucidating the function of DNA methylation. © 2008 Nature Publishing Group.Fil: Down, Thomas A.. Wellcome Trust Sanger Institute; Reino UnidoFil: Rakyan, Vardhman K.. Institute of Cell and Molecular Science; Reino UnidoFil: Turner, Daniel J.. Wellcome Trust Sanger Institute; Reino UnidoFil: Flicek, Paul. European Bioinformatics Institute; Reino UnidoFil: Li, Heng. Wellcome Trust Sanger Institute; Reino UnidoFil: Kulesha, Eugene. European Bioinformatics Institute; Reino UnidoFil: Gräf, Stefan. European Bioinformatics Institute; Reino UnidoFil: Johnson, Nathan. European Bioinformatics Institute; Reino UnidoFil: Herrero, Javier. European Bioinformatics Institute; Reino UnidoFil: Tomazou, Eleni M.. Wellcome Trust Sanger Institute; Reino UnidoFil: Thorne, Natalie P.. University of Cambridge; Reino UnidoFil: Bäckdahl, Liselotte. University College London; Reino UnidoFil: Herberth, Marlis. University of Cambridge; Reino UnidoFil: Howe, Kevin L.. University of Cambridge; Reino UnidoFil: Jackson, David K.. Wellcome Trust Sanger Institute; Reino UnidoFil: Miretti, Marcos Mateo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Nordeste. Instituto de Biología Subtropical. Universidad Nacional de Misiones. Instituto de Biología Subtropical; Argentina. Wellcome Trust Sanger Institute; Reino UnidoFil: Marioni, John C.. University of Cambridge; Reino UnidoFil: Birney, Ewan. European Bioinformatics Institute; Reino UnidoFil: Hubbard, Tim J. P.. Wellcome Trust Sanger Institute; Reino UnidoFil: Durbin, Richard. Wellcome Trust Sanger Institute; Reino UnidoFil: Tavaré, Simon. University of Cambridge; Reino UnidoFil: Beck, Stephan G.. University College London; Reino Unid
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