TileProbe: modeling tiling array probe effects using publicly available data

被引:10
作者
Judy, Jennifer Toolan [2 ]
Ji, Hongkai [1 ]
机构
[1] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Biostat, Baltimore, MD 21205 USA
[2] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Mental Hlth, Baltimore, MD 21205 USA
关键词
CHROMATIN-STRUCTURE; DNA METHYLATION; CHIP-CHIP; OLIGONUCLEOTIDE; HUMAN-CHROMOSOME-21; IDENTIFICATION; NORMALIZATION;
D O I
10.1093/bioinformatics/btp425
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Individual probes on an Affymetrix tiling array usually behave differently. Modeling and removing these probe effects are critical for detecting signals from the array data. Current data processing techniques either require control samples or use probe sequences to model probe-specific variability, such as with MAT. Although the MAT approach can be applied without control samples, residual probe effects continue to distort the true biological signals. Results: We propose TileProbe, a new technique that builds upon the MAT algorithm by incorporating publicly available data sets to remove tiling array probe effects. By using a large number of these readily available arrays, TileProbe robustly models the residual probe effects that MAT model cannot explain. When applied to analyzing ChIP-chip data, TileProbe performs consistently better than MAT across a variety of analytical conditions. This shows that TileProbe resolves the issue of probe-specific effects more completely.
引用
收藏
页码:2369 / 2375
页数:7
相关论文
共 26 条
[21]   High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays [J].
Urban, AE ;
Korbel, JO ;
Selzer, R ;
Richmond, T ;
Hacker, A ;
Popescu, GV ;
Clubells, JF ;
Green, R ;
Emanuel, BS ;
Gerstein, MB ;
Weissman, SM ;
Snyder, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (12) :4534-4539
[22]   Distribution, silencing potential and evolutionary impact of promoter DNA methylation in the human genome [J].
Weber, Michael ;
Hellmann, Ines ;
Stadler, Michael B. ;
Ramos, Liliana ;
Paabo, Svante ;
Rebhan, Michael ;
Schubeler, Dirk .
NATURE GENETICS, 2007, 39 (04) :457-466
[23]   A model-based background adjustment for oligonucleotide expression arrays [J].
Wu, ZJ ;
Irizarry, RA ;
Gentleman, R ;
Martinez-Murillo, F ;
Spencer, F .
JOURNAL OF THE AMERICAN STATISTICAL ASSOCIATION, 2004, 99 (468) :909-917
[24]   Genome-scale identification of nucleosome positions in S-cerevisiae [J].
Yuan, GC ;
Liu, YJ ;
Dion, MF ;
Slack, MD ;
Wu, LF ;
Altschuler, SJ ;
Rando, OJ .
SCIENCE, 2005, 309 (5734) :626-630
[25]   Genome-wide high-resolution mapping and functional analysis of DNA methylation in Arabidopsis [J].
Zhang, Xiaoyu ;
Yazaki, Junshi ;
Sundaresan, Ambika ;
Cokus, Shawn ;
Chan, Simon W. -L. ;
Chen, Huaming ;
Henderson, Ian R. ;
Shinn, Paul ;
Pellegrini, Matteo ;
Jacobsen, Steve E. ;
Ecker, Joseph R. .
CELL, 2006, 126 (06) :1189-1201
[26]   A gene expression bar code for microarray data [J].
Zilliox, Michael J. ;
Irizarry, Rafael A. .
NATURE METHODS, 2007, 4 (11) :911-913