TY - JOUR
T1 - GeSICA
T2 - Genome segmentation from intra-chromosomal associations
AU - Liu, Lin
AU - Zhang, Yiqian
AU - Feng, Jianxing
AU - Zheng, Ning
AU - Yin, Junfeng
AU - Zhang, Yong
N1 - Funding Information:
We would like to thank X. Shirley Liu, Kai Fu and Qian Zhao and two anonymous reviewers for their advices on our method and the insightful suggestions on the accomplishment of this paper. This study was supported by funds from National Natural Science Foundation of China (31071114), the National Basic Research Program of China (973 Program; No. 2010CB944904, and 2011CB965104), the Shanghai Rising-Star Program (10QA1407300), the New Century Excellent Talents in the University of China (NCET-11-0389) and the Innovative Research Team Program Ministry of Education of China (IRT1168).
PY - 2012/5/4
Y1 - 2012/5/4
N2 - Background: Various aspects of genome organization have been explored based on data from distinct technologies, including histone modification ChIP-Seq, 3C, and its derivatives. Recently developed Hi-C techniques enable the genome wide mapping of DNA interactomes, thereby providing the opportunity to study genome organization in detail, but these methods also pose challenges in methodology development.Results: We developed Genome Segmentation from Intra Chromosomal Associations, or GeSICA, to explore genome organization and applied the method to Hi-C data in human GM06990 and K562 cells. GeSICA calculates a simple logged ratio to efficiently segment the human genome into regions with two distinct states that correspond to rich and poor functional element states. Inside the rich regions, Markov Clustering was subsequently applied to segregate the regions into more detailed clusters. The binding sites of the insulator, cohesion, and transcription complexes are enriched in the boundaries between neighboring clusters, indicating that inferred clusters may have fine organizational features.Conclusions: Our study presents a novel analysis method, known as GeSICA, which gives insight into genome organization based on Hi-C data. GeSICA is open source and freely available at: http://web.tongji.edu.cn/~zhanglab/GeSICA/.
AB - Background: Various aspects of genome organization have been explored based on data from distinct technologies, including histone modification ChIP-Seq, 3C, and its derivatives. Recently developed Hi-C techniques enable the genome wide mapping of DNA interactomes, thereby providing the opportunity to study genome organization in detail, but these methods also pose challenges in methodology development.Results: We developed Genome Segmentation from Intra Chromosomal Associations, or GeSICA, to explore genome organization and applied the method to Hi-C data in human GM06990 and K562 cells. GeSICA calculates a simple logged ratio to efficiently segment the human genome into regions with two distinct states that correspond to rich and poor functional element states. Inside the rich regions, Markov Clustering was subsequently applied to segregate the regions into more detailed clusters. The binding sites of the insulator, cohesion, and transcription complexes are enriched in the boundaries between neighboring clusters, indicating that inferred clusters may have fine organizational features.Conclusions: Our study presents a novel analysis method, known as GeSICA, which gives insight into genome organization based on Hi-C data. GeSICA is open source and freely available at: http://web.tongji.edu.cn/~zhanglab/GeSICA/.
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U2 - 10.1186/1471-2164-13-164
DO - 10.1186/1471-2164-13-164
M3 - Article
C2 - 22559164
AN - SCOPUS:84860525165
SN - 1471-2164
VL - 13
JO - BMC Genomics
JF - BMC Genomics
IS - 1
M1 - 164
ER -