師資
個人簡介：
2009 年畢業(yè)于北京大學醫(yī)學部醫(yī)學實驗專業(yè)，取得學士學位，2012年在英國曼徹斯特大學生命科學系取得博士學位。博士期間以研究蛋白-DNA 結(jié)合特異性以及細胞周期 G2/M 期的調(diào)控為主題，發(fā)現(xiàn)并且闡明了一個促癌轉(zhuǎn)錄因子FOXM1調(diào)控G2/M期的特殊機制。在完成博士研究之后，于2013年來到歐洲生物信息研究所(European Bioinformatics Institute)從事博士后工作，進行表觀遺傳學、生物信息學，以及單細胞測序方面的研究。2016年加入維康桑格研究所(Wellcome Sanger Institute)成為高級研究員。2019年加入南方科技大學生物系，任助理教授。
研究領域：
(1) 單細胞表觀遺傳以及轉(zhuǎn)錄組測序技術(shù)開發(fā)
(2) 基因組學數(shù)據(jù)的挖掘以及生物信息分析
(3) 以T細胞和干細胞為模型，研究轉(zhuǎn)錄因子以及染色質(zhì)復合物在控制細胞命運決定以及記憶中的作用和機制
工作經(jīng)歷：
2019 至 今 南方科技大學生物系 助理教授
2016 至 2019 維康桑格研究所 高級研究員
2013 至 2016 歐洲生物信息研究所 博士后
2012 至 2013 曼徹斯特大學生命科學系 研究助理
學習經(jīng)歷：
2009 至 2012 曼徹斯特大學生命科學系 博士
2005 至 2009 北京大學醫(yī)學部醫(yī)學實驗專業(yè) 本科
代表文章： (*共同一作)
學術(shù)文章：
1. Henriksson, J.*, Chen, X.*, Gomes, T., Ullah, U., and Meyer, K.B. (2019). Genome-wide CRISPR screens in T helper cells reveal pervasive cross-talk between activation and differentiation. Cell 176, 1–15.
2.Zhang, W.*, Chronis, C.*, Chen, X.*, Zhang, H., Spalinskas, R., Pardo, M., Chen, L., Wu, G., Zhu, Z., Yu, Y., et al. (2019). The BAF and PRC2 Complex Subunits Dpf2 and Eed Antagonistically Converge on Tbx3 to Control ESC Differentiation. Cell Stem Cell 24, 138–152.e8.
3.Chen, X., Miragaia, R.J., Natarajan, K.N., and Teichmann, S.A. (2018). A rapid and robust method for single cell chromatin accessibility profiling. Nat. Commun. 9, 5345.
4.Jia, G.*, Preussner, J.*, Chen, X.*, Guenther, S., Yuan, X., Yekelchyk, M., Kuenne, C., Looso, M., Zhou, Y., Teichmann, S., et al. (2018). Single cell RNA-seq and ATAC-seq analysis of cardiac progenitor cell transition states and lineage settlement. Nat. Commun. 9, 4877.
5.Hagai, T., Chen, X., Miragaia, R.J., Rostom, R., Gomes, T., Kunowska, N., Henriksson, J., Park, J.-E., Proserpio, V., Donati, G., et al. (2018). Gene expression variability across cells and species shapes innate immunity. Nature 563, 197–202.
6.Pramanik, J., Chen, X., Kar, G., Henriksson, J., Gomes, T., Park, J.-E., Natarajan, K., Meyer, K.B., Miao, Z., McKenzie, A.N.J., et al. (2018). Genome-wide analyses reveal the IRE1a-XBP1 pathway promotes T helper cell differentiation by resolving secretory stress and accelerating proliferation. Genome Med. 10, 76.
7.Chen, X., Ji, Z., Webber, A., and Sharrocks, A.D. (2016). Genome-wide binding studies reveal DNA binding specificity mechanisms and functional interplay amongst Forkhead transcription factors. Nucleic Acids Res. 44, 1566–1578.
8.Yu, Y., Tsang, J.C.H., Wang, C., Clare, S., Wang, J., Chen, X., Brandt, C., Kane, L., Campos, L.S., Lu, L., et al. (2016). Single-cell RNA-seq identifies a PD-1hi ILC progenitor and defines its development pathway. Nature 539, 102–106.
9.Aguilar-Martinez, E., Chen, X., Webber, A., Paul Mould, A., Seifert, A., Hay, R.T., and Sharrocks, A.D. (2015). Screen for multi-SUMO–binding proteins reveals a multi-SIM–binding mechanism for recruitment of the transcriptional regulator ZMYM2 to chromatin. Proc. Natl. Acad. Sci. U. S. A. 112, E4854–E4863.
10.Wiseman, E.F., Chen, X., Han, N., Webber, A., Ji, Z., Sharrocks, A.D., and Ang, Y.S. (2015). Deregulation of the FOXM1 target gene network and its coregulatory partners in oesophageal adenocarcinoma. Mol. Cancer 14, 69.
11.Chen, X., Müller, G.A., Quaas, M., Fischer, M., Han, N., Stutchbury, B., Sharrocks, A.D., and Engeland, K. (2013). The forkhead transcription factor FOXM1 controls cell cycle-dependent gene expression through an atypical chromatin binding mechanism. Mol. Cell. Biol. 33, 227–236.
評論與綜述：
1.Chen, X., Teichmann, S.A., and Meyer, K.B. (2018). From Tissues to Cell Types and Back: Single-Cell Gene Expression Analysis of Tissue Architecture. Annu. Rev. Biomed. Data Sci. 1, 29-51.
2.Chen, X., Love, J.C., Navin, N.E., Pachter, L., Stubbington, M.J.T., Svensson, V., Sweedler, J.V., and Teichmann, S.A. (2016). Single-cell analysis at the threshold. Nat. Biotechnol. 34, 1111–1118.
3.Vieira Braga, F.A.*, Teichmann, S.A., and Chen, X.* (2016). Genetics and immunity in the era of single-cell genomics. Hum. Mol. Genet. 25, R141–R148.
圖書章節(jié)：
1.Kunowska, N.*, Chen, X*. (2019). ChIPmentation for Low-Input Profiling of In Vivo Protein-DNA Interactions. Methods Mol Biol. 1979: 269-282.