Professor | 帅世民 | 数字化转型顾问

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Name	帅世民
Contact Information	shuaism@sustech.edu.cn
Language ability	英语, 汉语
Province	广东省

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Name

帅世民

Contact Information

shuaism@sustech.edu.cn

Language ability

英语, 汉语

Province

广东省

University/Lab Affiliation and Title	南方科技大学
Faculty	Medical School
Academic Background & Achievements	2014-2019: 多伦多大学，计算生物学，博士，加拿大 2010-2014: 浙江大学，生物科学，本科，中国
Work Experience	2022.6-至今: 南方科技大学，医学院，人类细胞生物和遗传学系，副教授，中国 2021.9-2022.5: 南方科技大学，医学院，人类细胞生物和遗传学系，助理教授，中国 2020.10-2021.8: 欧洲生物信息学研究所（EMBL-EBI），联合博士后，英国 2020.1-2021.8: 欧洲分子生物学实验室（EMBL），EIPOD4博士后（玛丽·居里学者联合资助），德国 2015.1-2019.11: 安大略省癌症研究所（OICR），计算生物学项目，博士生研究员，加拿大
Awards	2021: 深圳市高层次人才（国家级领军人才） 2020: EMBL跨学科博士后奖学金（EIPOD4），由玛丽·居里行动共同资助 2019: 加拿大癌症协会旅行奖

University/Lab Affiliation and Title

南方科技大学

Faculty

Medical School

Academic Background & Achievements

2014-2019: 多伦多大学，计算生物学，博士，加拿大
2010-2014: 浙江大学，生物科学，本科，中国

Work Experience

2022.6-至今: 南方科技大学，医学院，人类细胞生物和遗传学系，副教授，中国
2021.9-2022.5: 南方科技大学，医学院，人类细胞生物和遗传学系，助理教授，中国
2020.10-2021.8: 欧洲生物信息学研究所（EMBL-EBI），联合博士后，英国
2020.1-2021.8: 欧洲分子生物学实验室（EMBL），EIPOD4博士后（玛丽·居里学者联合资助），德国
2015.1-2019.11: 安大略省癌症研究所（OICR），计算生物学项目，博士生研究员，加拿大

Awards

2021: 深圳市高层次人才（国家级领军人才）
2020: EMBL跨学科博士后奖学金（EIPOD4），由玛丽·居里行动共同资助
2019: 加拿大癌症协会旅行奖

Areas of Focus	生物信息学和计算生物学全尺度遗传变异与人类疾病的关联 RNA异常剪接与人类疾病的关联疾病生态系统研究多组学数据分析与新型组学数据分析工具研发
Publications	Combined burden and functional impact tests for cancer driver discovery using DriverPower, 帅世民, PCAWG Drivers and Functional Interpretation Working Group, Gallinger S, Stein LD & PCAWG Consortium, 2020 The U1 spliceosomal RNA is recurrently mutated in multiple cancers, 帅世民, Suzuki H, Diaz-Navarro A, Nadeu F, Kumar SA, Gutierrez-Fernandez A, Delgado J, Pinyol M, López-Otín C, Puente XS, Taylor MD, Campo E & Stein LD, 2019 Analyses of non-coding somatic drivers in 2,658 cancer whole genomes, Rheinbay E, Nielsen MM, Abascal F, Wala JA, Shapira O, Tiao G, Hornshøj H, Hess JM, Juul RI, Lin Z, Feuerbach L, Sabarinathan R, Madsen T, Kim J, Mularoni L, 帅世民, Lanzós A, Herrmann C, Maruvka YE, Shen C, et al, 2020 Candidate Cancer Driver Mutations in Distal Regulatory Elements and Long-Range Chromatin Interaction Networks, Zhu H, Uusküla-Reimand L, Isaev K, Wadi L, Alizada A, 帅世民, Huang V, Aduluso-Nwaobasi D, Paczkowska M, Abd-Rabbo D, Ocsenas O, Liang M, Thompson JD, Li Y, Ruan L, Krassowski M, Dzneladze I, Simpson JT, Lupien M, Stein LD, et al, 2020 Recurrent noncoding U1 snRNA mutations drive cryptic splicing in SHH medulloblastoma, Suzuki H, Kumar SA, 帅世民, Diaz-Navarro A, Gutierrez-Fernandez A, De Antonellis P, Cavalli FMG, Juraschka K, Farooq H, Shibahara I, Vladoiu MC, Zhang J, Abeysundara N, Przelicki D, Skowron P, Gauer N, Luu B, Daniels C, Wu X, Forget A, et al, 2019 Recurrent noncoding regulatory mutations in pancreatic ductal adenocarcinoma, Feigin ME, Garvin T, Bailey P, Waddell N, Chang DK, Kelley DR, 帅世民, Gallinger S, McPherson JD, Grimmond SM, Khurana E, Stein LD, Biankin AV, Schatz MC & Tuveson DA, 2017 Pan-cancer analysis of whole genomes, ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium [including 帅世民], 2020 Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis, Carlevaro-Fita J, Lanzós A, Feuerbach L, Hong C, Mas-Ponte D, Pedersen JS, PCAWG Drivers and Functional Interpretation Group [including 帅世民], Johnson R & PCAWG Consortium, 2020 Integrative pathway enrichment analysis of multivariate omics data, Paczkowska M, Barenboim J, Sintupisut N, Fox NS, Zhu H, Abd-Rabbo D, Mee MW, Boutros PC, PCAWG Drivers and Functional Interpretation Working Group [including 帅世民], Reimand J & PCAWG Consortium, 2020 Pathway and network analysis of more than 2500 whole cancer genomes, Reyna MA, Haan D, Paczkowska M, Verbeke LPC, Vazquez M, Kahraman A, Pulido-Tamayo S, Barenboim J, Wadi L, Dh

Areas of Focus

生物信息学和计算生物学
全尺度遗传变异与人类疾病的关联
RNA异常剪接与人类疾病的关联
疾病生态系统研究
多组学数据分析与新型组学数据分析工具研发

Publications

Combined burden and functional impact tests for cancer driver discovery using DriverPower, 帅世民*, PCAWG Drivers and Functional Interpretation Working Group, Gallinger S, Stein LD* & PCAWG Consortium, 2020
The U1 spliceosomal RNA is recurrently mutated in multiple cancers, 帅世民, Suzuki H, Diaz-Navarro A, Nadeu F, Kumar SA, Gutierrez-Fernandez A, Delgado J, Pinyol M, López-Otín C, Puente XS, Taylor MD, Campo E & Stein LD, 2019
Analyses of non-coding somatic drivers in 2,658 cancer whole genomes, Rheinbay E, Nielsen MM, Abascal F, Wala JA, Shapira O, Tiao G, Hornshøj H, Hess JM, Juul RI, Lin Z, Feuerbach L, Sabarinathan R, Madsen T, Kim J, Mularoni L, 帅世民, Lanzós A, Herrmann C, Maruvka YE, Shen C, et al, 2020
Candidate Cancer Driver Mutations in Distal Regulatory Elements and Long-Range Chromatin Interaction Networks, Zhu H, Uusküla-Reimand L, Isaev K, Wadi L, Alizada A, 帅世民, Huang V, Aduluso-Nwaobasi D, Paczkowska M, Abd-Rabbo D, Ocsenas O, Liang M, Thompson JD, Li Y, Ruan L, Krassowski M, Dzneladze I, Simpson JT, Lupien M, Stein LD, et al, 2020
Recurrent noncoding U1 snRNA mutations drive cryptic splicing in SHH medulloblastoma, Suzuki H, Kumar SA, 帅世民, Diaz-Navarro A, Gutierrez-Fernandez A, De Antonellis P, Cavalli FMG, Juraschka K, Farooq H, Shibahara I, Vladoiu MC, Zhang J, Abeysundara N, Przelicki D, Skowron P, Gauer N, Luu B, Daniels C, Wu X, Forget A, et al, 2019
Recurrent noncoding regulatory mutations in pancreatic ductal adenocarcinoma, Feigin ME, Garvin T, Bailey P, Waddell N, Chang DK, Kelley DR, 帅世民, Gallinger S, McPherson JD, Grimmond SM, Khurana E, Stein LD, Biankin AV, Schatz MC & Tuveson DA, 2017
Pan-cancer analysis of whole genomes, ICGC/TCGA Pan-Cancer Analysis of Whole Genomes Consortium [including 帅世民], 2020
Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis, Carlevaro-Fita J, Lanzós A, Feuerbach L, Hong C, Mas-Ponte D, Pedersen JS, PCAWG Drivers and Functional Interpretation Group [including 帅世民], Johnson R & PCAWG Consortium, 2020
Integrative pathway enrichment analysis of multivariate omics data, Paczkowska M, Barenboim J, Sintupisut N, Fox NS, Zhu H, Abd-Rabbo D, Mee MW, Boutros PC, PCAWG Drivers and Functional Interpretation Working Group [including 帅世民], Reimand J & PCAWG Consortium, 2020
Pathway and network analysis of more than 2500 whole cancer genomes, Reyna MA, Haan D, Paczkowska M, Verbeke LPC, Vazquez M, Kahraman A, Pulido-Tamayo S, Barenboim J, Wadi L, Dh

生物信息学计算生物学遗传变异人类疾病 Rna剪接疾病生态系统多组学数据分析组学工具研究

曹丽伟 - 南方科技大学

Area of Focus
蛋白质组学 | 方法开发 | 技术创新 | 生物问题 | 人类疾病 | 治疗 | 应用 | 研究 | 科学 | 医学

郭锋彪 - 武汉大学

胡汉昆 - 武汉大学

Area of Focus
药学 | 临床 | 研究 | 教学 | 药物开发 | 中药 | 器官芯片 | 质谱 | 多组学 | 生物样本

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