HMM-DM: identifying differentially methylated regions using a hidden Markov model

被引:29
作者
Yu, Xiaoqing [1 ]
Sun, Shuying [2 ]
机构
[1] Yale Univ, Dept Biostat, New Haven, CT 06511 USA
[2] Texas State Univ, Dept Math, San Marcos, TX 78666 USA
关键词
bisulfite sequencing; cancer; differential methylation; hidden Markov model; DNA METHYLATION; METHYLOME ANALYSIS; ACCURATE; PLURIPOTENT; PIPELINE; ALIGNER; PACKAGE; READS; LOCI; RRBS;
D O I
10.1515/sagmb-2015-0077
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA methylation is an epigenetic modification involved in organism development and cellular differentiation. Identifying differential methylations can help to study genomic regions associated with diseases. Differential methylation studies on single-CG resolution have become possible with the bisulfite sequencing (BS) technology. However, there is still a lack of efficient statistical methods for identifying differentially methylated (DM) regions in BS data. We have developed a new approach named HMM-DM to detect DM regions between two biological conditions using BS data. This new approach first uses a hidden Markov model (HMM) to identify DM CG sites accounting for spatial correlation across CG sites and variation across samples, and then summarizes identified sites into regions. We demonstrate through a simulation study that our approach has a superior performance compared to BSmooth. We also illustrate the application of HMM-DM using a real breast cancer dataset.
引用
收藏
页码:69 / 81
页数:13
相关论文
共 43 条
[1]  
Akalin A, 2012, GENOME BIOL, V13, DOI [10.1186/gb-2012-13-10-R87, 10.1186/gb-2012-13-10-r87]
[2]   DNA Methylation Dynamics during In Vivo Differentiation of Blood and Skin Stem Cells [J].
Bock, Christoph ;
Beerman, Isabel ;
Lien, Wen-Hui ;
Smith, Zachary D. ;
Gu, Hongcang ;
Boyle, Patrick ;
Gnirke, Andreas ;
Fuchs, Elaine ;
Rossi, Derrick J. ;
Meissner, Alexander .
MOLECULAR CELL, 2012, 47 (04) :633-647
[3]   PASS-bis: a bisulfite aligner suitable for whole methylome analysis of Illumina and SOLiD reads [J].
Campagna, Davide ;
Telatin, Andrea ;
Forcato, Claudio ;
Vitulo, Nicola ;
Valle, Giorgio .
BIOINFORMATICS, 2013, 29 (02) :268-270
[4]   BS Seeker: precise mapping for bisulfite sequencing [J].
Chen, Pao-Yang ;
Cokus, Shawn J. ;
Pellegrini, Matteo .
BMC BIOINFORMATICS, 2010, 11
[5]   Using beta-binomial regression for high-precision differential methylation analysis in multifactor whole-genome bisulfite sequencing experiments [J].
Dolzhenko, Egor ;
Smith, Andrew D. .
BMC BIOINFORMATICS, 2014, 15
[6]   DNA methylation profiling of human chromosomes 6, 20 and 22 [J].
Eckhardt, Florian ;
Lewin, Joern ;
Cortese, Rene ;
Rakyan, Vardhman K. ;
Attwood, John ;
Burger, Matthias ;
Burton, John ;
Cox, Tony V. ;
Davies, Rob ;
Down, Thomas A. ;
Haefliger, Carolina ;
Horton, Roger ;
Howe, Kevin ;
Jackson, David K. ;
Kunde, Jan ;
Koenig, Christoph ;
Liddle, Jennifer ;
Niblett, David ;
Otto, Thomas ;
Pettett, Roger ;
Seemann, Stefanie ;
Thompson, Christian ;
West, Tony ;
Rogers, Jane ;
Olek, Alex ;
Berlin, Kurt ;
Beck, Stephan .
NATURE GENETICS, 2006, 38 (12) :1378-1385
[7]   A Bayesian hierarchical model to detect differentially methylated loci from single nucleotide resolution sequencing data [J].
Feng, Hao ;
Conneely, Karen N. ;
Wu, Hao .
NUCLEIC ACIDS RESEARCH, 2014, 42 (08) :e69
[8]   SAMPLING-BASED APPROACHES TO CALCULATING MARGINAL DENSITIES [J].
GELFAND, AE ;
SMITH, AFM .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 1990, 85 (410) :398-409
[9]   Preparation of reduced representation bisulfite sequencing libraries for genome-scale DNA methylation profiling [J].
Gu, Hongcang ;
Smith, Zachary D. ;
Bock, Christoph ;
Boyle, Patrick ;
Gnirke, Andreas ;
Meissner, Alexander .
NATURE PROTOCOLS, 2011, 6 (04) :468-481
[10]   Genome-scale DNA methylation mapping of clinical samples at single-nucleotide resolution [J].
Gu, Hongcang ;
Bock, Christoph ;
Mikkelsen, Tarjei S. ;
Jaeger, Natalie ;
Smith, Zachary D. ;
Tomazou, Eleni ;
Gnirke, Andreas ;
Lander, Eric S. ;
Meissner, Alexander .
NATURE METHODS, 2010, 7 (02) :133-U69