Bioinformatics Advance Access published online on June 29, 2006
Bioinformatics, doi:10.1093/bioinformatics/btl329
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1 Division of Biostatistics, Department of Medicine, Indiana University School of Medicine, Indianapolis, IN 47405
* To whom correspondence should be addressed.
Motivation: To detect and select patterns of transcription factor binding sites (TFBSs) which distinguish genes directly regulated by estrogen receptor- Results: Biologically, our proposed new algorithm clearly suggests that TFBSs are not randomly distributed within ER Availability: The software is available on request from the authors.
Received April 13, 2006
Revised May 24, 2006
Accepted June 9, 2006
Article
A mixture model based discriminate analysis for identifying ordered transcription factor binding site pairs in gene promoters directly regulated by estrogen receptor-
Lang Li 1 *,
Alfred S. L. Cheng 2,
Victor X. Jin 2,
Henry H. Paik 3,
Meiyun Fan 3,
Xiaoman Li 1,
Wei Zhang 1,
Jason Robarge 1,
Curtis Balch 3,
Ramana V. Davuluri 2,
Sun Kim 3,
Tim H.-M. Huang 2,
and
Kenneth P. Nephew 3
2 Division of Human Cancer Genetics, Department of Molecular Virology, Immunology, and Medical Genetics, Comprehensive Cancer Center, Ohio State University, Columbus, OH 43210
3 Medical Sciences, Indiana University School of Medicine, Bloomington, IN 47405
Lang Li, E-mail: lali{at}iupui.edu
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Abstract
(ER
), we developed an innovative mixture model-based discriminate analysis for identifying ordered TFBS pairs.
target promoters (p-value < 0.001). The up-regulated targets significantly (p-value < 0.01) possess TFBS pairs, (DBP, MYC), (DBP, MYC/MAX heterodimer), (DBP, USF2), and (DBP, MYOGENIN); and down-regulated ER
target genes significantly (p-value < 0.01) possess TFBS pairs, such as (DBP, c-ETS1-68), (DBP, USF2), and (DBP, MYOGENIN). Statistically, our proposed mixture model based-discriminate analysis can simultaneously perform TFBS pattern recognition, TFBS pattern selection, and target class prediction; such integrative power cannot be achieved by current methods.
Associate Editor: Martin Bishop
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