• 题目:CGM 第148期: Systematic inference and comparison of multi-scale chromatin sub-compartments connects spatial organization to cell phenotypes
  • 时间:欧洲中部时间 2021年4月8日(星期四)08PM(美国中部时间 4月8日 12PM,北京时间 4月9日 02AM)
  • 主讲人:刘远龙(Yuanlong LIU),2010-2013:中国科学技术大学,概率论与数理统计,理学硕士;2013-2017:法国国家医学健康研究院(巴黎七大),计算基因组学 PhD,导师 Prof. Florence Dememais;2018-至今:计算基因组学 Postdoc, 导师 Prof. Giovanni Ciriello (瑞士洛桑大学), Prof. Elisa Oricchio (瑞士洛桑联邦理工学院)

摘要

Chromatin compartmentalization reflects biological activity. However, inference of chromatin sub-compartments and compartment domains from chromosome conformation capture (Hi-C) experiments is limited by data resolution. As a result, these have been characterized only in a few cell types and systematic comparisons across multiple tissues and conditions are missing. Here, we present Calder, an algorithmic approach that enables the identification of multi-scale sub-compartments at variable data resolution. Calder allows to infer and compare chromatin sub-compartments and compartment domains in >100 cell lines. Our results reveal sub-compartments enriched for poised chromatin states and undergoing spatial repositioning during lineage differentiation and oncogenic transformation.

参考文献

Rao, S. S., Huntley, M. H., Durand, N. C., Stamenova, E. K., Bochkov, I. D., Robinson, J. T., … & Aiden, E. L. (2014). A 3D map of the human genome at kilobase resolution reveals principles of chromatin looping. Cell, 159(7), 1665-1680.

Xiong, K., & Ma, J. (2019). Revealing Hi-C subcompartments by imputing inter-chromosomal chromatin interactions. Nature communications, 10(1), 1-12.

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