TY - GEN
T1 - Higher-order partial least squares for predicting gene expression levels from chromatin states
AU - Sun, Shiquan
AU - Sun, Xifang
AU - Zheng, Yan
N1 - Publisher Copyright:
© 2017 IEEE.
PY - 2017/12/15
Y1 - 2017/12/15
N2 - Multiple publications have indicated that gene expression levels are strongly affected by chromatin mark combinations via at least two mechanisms, i.e., activation or repression. But their combinatorial patterns remain unresolved. To further understand the relationship between histone modifications and gene expression levels, here in this paper, we introduce a purely geometric higher-order representation, tensor (also called multidimensional array), which might contain more hidden information from chromatin states to predicting gene expression levels. The prediction models were learned from regions around upstream 10k base pairs and downstream 10k base pairs of the transcriptional start sites (TSSs) over three species (i.e., Human, Rhesus Macaque, and Chimpanzee) with five histone modifications (i.e., H3K4me1, H3K4me3, H3K27ac, H3K27me3, and Pol II). Experimental results demonstrate that the proposed method is more powerful for predicting gene expression levels than several commonly used methods. Specifically, our method improves the performance on both criteria, R and RMSE as high as 1.7% and 11%, respectively.
AB - Multiple publications have indicated that gene expression levels are strongly affected by chromatin mark combinations via at least two mechanisms, i.e., activation or repression. But their combinatorial patterns remain unresolved. To further understand the relationship between histone modifications and gene expression levels, here in this paper, we introduce a purely geometric higher-order representation, tensor (also called multidimensional array), which might contain more hidden information from chromatin states to predicting gene expression levels. The prediction models were learned from regions around upstream 10k base pairs and downstream 10k base pairs of the transcriptional start sites (TSSs) over three species (i.e., Human, Rhesus Macaque, and Chimpanzee) with five histone modifications (i.e., H3K4me1, H3K4me3, H3K27ac, H3K27me3, and Pol II). Experimental results demonstrate that the proposed method is more powerful for predicting gene expression levels than several commonly used methods. Specifically, our method improves the performance on both criteria, R and RMSE as high as 1.7% and 11%, respectively.
KW - Higher-order partial least squares
KW - chromatin states
KW - gene expression levels
KW - tensor decomposition
UR - https://www.scopus.com/pages/publications/85045972559
U2 - 10.1109/BIBM.2017.8217912
DO - 10.1109/BIBM.2017.8217912
M3 - 会议稿件
AN - SCOPUS:85045972559
T3 - Proceedings - 2017 IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2017
SP - 1678
EP - 1683
BT - Proceedings - 2017 IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2017
A2 - Yoo, Illhoi
A2 - Zheng, Jane Huiru
A2 - Gong, Yang
A2 - Hu, Xiaohua Tony
A2 - Shyu, Chi-Ren
A2 - Bromberg, Yana
A2 - Gao, Jean
A2 - Korkin, Dmitry
PB - Institute of Electrical and Electronics Engineers Inc.
T2 - 2017 IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2017
Y2 - 13 November 2017 through 16 November 2017
ER -