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  • 蔣慶華

    蔣慶華(教授)

    蔣慶華,博士,教授,博士生導(dǎo)師。

    主要研究方向:生物信息學(xué)。2010年6月在哈工大計(jì)算機(jī)科學(xué)與技術(shù)學(xué)科獲得博士學(xué)位, 受國家留學(xué)基金委資助,2011年11月至2012年11月,公派至哈佛大學(xué)Dana-Farber癌癥研究所從事生物信息學(xué)研究工作,2012年入選“哈爾濱工業(yè)大學(xué)基礎(chǔ)研究杰出人才培育計(jì)劃III類”,2015年入選哈工大青年拔尖人才選聘計(jì)劃。

    主持國家自然科學(xué)面上項(xiàng)目、青年基金、中國博士后科學(xué)基金特別資助、中國博士后基金一等資助等科研項(xiàng)目7項(xiàng)。發(fā)表SCI論文35篇,EI論文2篇。 其中第一作者或通訊作者SCI論文19篇,單篇SCI最高影響因子9.9、單篇SCI最高他引522次(google scholar統(tǒng)計(jì)),2010年入選“中國百篇最具影響國際學(xué)術(shù)論文”,2011年獲“第十二屆黑龍江省自然科學(xué)技術(shù)學(xué)術(shù)成果一等獎(jiǎng)”。


    學(xué)術(shù)兼職

    《Nucleic Acids Research》、《Bioinformatics》、《Briefings in Bioinformatics》、《Scientific Reports》、 《Current Bioinformatics》、《Animal Genetics》、《International Journal of Data Mining and Bioinformatics (IJDMB)》等期刊審稿人《Austin Journal of Computational Biology and Bioinformatics》期刊編委 (2014-)《Austin Medical Sciences》期刊編委 (2015-)

    教育與工作經(jīng)歷

    教育經(jīng)歷

    1999.09-2003.07 吉林大學(xué) 計(jì)算數(shù)學(xué) 學(xué)士2003.09-2006.07吉林大學(xué)計(jì)算數(shù)學(xué) 碩士2007.03-2010.06哈爾濱工業(yè)大學(xué)計(jì)算機(jī)應(yīng)用技術(shù) 博士

    工作履歷

    2010.08-2012.12 哈爾濱工業(yè)大學(xué) 生物醫(yī)學(xué)工程研究中心 講師2011.11-2012.11 哈佛大學(xué) Dana Farber癌癥研究所 訪問學(xué)者2013.12-2015.12 哈爾濱工業(yè)大學(xué) 生物醫(yī)學(xué)工程研究中心 副教授2015.04-至今 哈爾濱工業(yè)大學(xué) 生命科學(xué)與技術(shù)學(xué)院 博士生導(dǎo)師2016.01-至今 哈爾濱工業(yè)大學(xué) 生物醫(yī)學(xué)工程研究中心 教授

    研究方向

    生物信息學(xué)、癌表觀基因組學(xué):發(fā)展信息學(xué)方法,對高通量組學(xué)及臨床數(shù)據(jù)進(jìn)行整合及分析,研究癌癥發(fā)生、發(fā)展過程中表觀及轉(zhuǎn)錄調(diào)控機(jī)制,計(jì)算預(yù)測、實(shí)驗(yàn)驗(yàn)證癌癥相關(guān)的非編碼基因(lncRNA、microRNA)。基于單核苷酸多態(tài)的阿爾斯海默。ˋD)遺傳標(biāo)記的識別與檢測:構(gòu)建中國或者亞洲人群AD遺傳標(biāo)記(SNP)知識庫系統(tǒng),研發(fā)疾病預(yù)測模型和算法,預(yù)測AD疾病風(fēng)險(xiǎn)。長鏈非編碼RNA(long non-coding RNA, lncRNA)綜合分析平臺:發(fā)展生物信息學(xué)方法,重點(diǎn)研究lncRNA轉(zhuǎn)錄調(diào)控、功能注釋及疾病lncRNA識別技術(shù),開發(fā)集數(shù)據(jù)中心、分析平臺、知識庫于一體的lncRNA分析系統(tǒng),推動在基因組范圍內(nèi)對lncRNA調(diào)控機(jī)制及功能的理解。腫瘤診斷與治療:基于腫瘤基因組數(shù)據(jù),發(fā)展腫瘤相關(guān)的遺傳變異識別及功能注釋方法, 基于變異與靶向藥物的關(guān)系信息,制定個(gè)體化用藥指導(dǎo)方案。健康管理:通過分析健康個(gè)體的基因組數(shù)據(jù),預(yù)測潛在的疾病風(fēng)險(xiǎn)、制定個(gè)體化用藥指導(dǎo)及健康生活方案。

    項(xiàng)目與獲獎(jiǎng)

    主持的科研項(xiàng)目

    2016.1-2019.12,國家自然科學(xué)基金面上項(xiàng)目2016.1-2019.12,哈工大青年拔尖人才選聘計(jì)劃項(xiàng)目2016.1-2017.12, 黑龍江省自然科學(xué)基金面上項(xiàng)目2016.1-2016.12,黑龍江省留學(xué)人員擇優(yōu)資助項(xiàng)目2012.7-2015.06,哈工大基礎(chǔ)研究杰出人才培育計(jì)劃III2012.1-2014.12,國家自然科學(xué)青年基金2012.9-2014.12,中國博士后第五批特別資助基金2011.7-2013.12,中國博士后科學(xué)基金(一等資助)2011.1-2012.12,哈工大科研創(chuàng)新基金2012.1-2013.12,黑龍江省博士后基金

    參與的科研項(xiàng)目

    2010.01-2012.12,國家自然科學(xué)基金, 排名:9/22014.01-2017.12,國家自然科學(xué)基金, 排名:8/22012.01-2015.12,國家863項(xiàng)目, 排名:17/112015.01-2017.12,國家863重大項(xiàng)目,排名18/69

    榮譽(yù)稱號

    2010年 獲“中國百篇最具影響國際學(xué)術(shù)論文”2011年 獲”第十二屆黑龍江省自然科學(xué)技術(shù)學(xué)術(shù)成果一等獎(jiǎng)"2012年 入選“哈爾濱工業(yè)大學(xué)基礎(chǔ)研究杰出人才培育計(jì)劃III”2015年 入選“哈爾濱工業(yè)大學(xué)青年拔尖人才選聘計(jì)劃”

    代表性學(xué)術(shù)論文

    2016

      Guiyou Liu,Qinghua Jiang*. Alzheimer’s disease CD33 rs3865444 variant does not contribute to congnitive performance. 2016. PNAS. DOI: 10.1073/pnas.1600852113 (SCI IF: 9.674) (*通訊作者)Guiyou Liu,Qinghua Jiang, Yongshuai Jiang, Keshen Li. Junwei Hao*. Ischaemic stroke variants from genome-wide association studies and Alzheimeru2019s disease susceptibility. Annals of Neurology. 2016. (SCI IF: 9.977) (Accepted)Qinghua Jiang, Guiyou Liu*. Lack of association between MC1R variants and Parkinsonu2019s disease in European descent. 2016. Annals of Neurology. DOI: 10.1002/ana.24627 (SCI IF: 9.977)Qinghua Jiang, Guiyou Liu*. REST rs3796529 variant does not influence human subcortical brain structures. Annals of Neurology. 2016 Feb;79(2):334-5. (SCI IF: 9.977)Qinghua Jiang#, Shuilin Jin#, Yongshuai Jiang, Mingzhi Liao, Rennan Feng,Liangcai Zhang, Guiyou Liu*, Junwei Hao*. Alzheimer’s disease variants with the genome-wide significance are significantly enriched in immune pathways and active in immune cells. 2016. doi:10.1007/s12035-015-9670-8. Molecular Neurobiology. (SCI, IF: 5.137)Guiyou Liu#, Yining Xu#, Yongshuai Jiang, Mingzhi Liao, Rennan Feng,Qinghua Jiang*. PICALM rs3851179 variant confers susceptibility to Alzheimer’s disease in Chinese population. 2016. Molecular Neurobiology. (SCI, IF: 5.137) (Accepted) (*通訊作者)Yining Xu,Qinghua Jiang, Guiyou Liu*. PICALM rs3851179 variant and Alzheimer’s disease in Asian population. 2016. NeuroMolecular Medicine. (SCI, IF: 3.678) (Accepted)Weiyang Bai, Wen Yang, Wenjing Wang, Yang Wang, Can Liu,Qinghua Jiang, Jinlian Hua, Mingzhi Liao*. GED: a manually curated comprehensive resource for epigenetic modification of gametogenesis. Briefings in Bioinformatics. 2016 Feb 5. pii: bbw007. (SCI, IF: 9.617)

    2015

      Jiang QH, Wang JX, Wu XL, Ma R, Jin SL, Han ZJ, Tan RJ, Peng JJ, Liu GY, Li Y, Wang YD*. LncRNA2Target: a database for differentially expressed genes after lncRNA knockdown or overexpression. 2015. Nucleic Acids Research. DOI 10.1093/nar/gku1173 (SCI, IF: 9.112)Jiang QH, Ma R, Wang JX, Wu XL, Jin SL, Peng JJ, Tan RJ, Zhang TJ, Li Y, Wang YD*. LncRNA2Function: a comprehensive resource for functional investigation of human lncRNAs based on RNA-seq data. 2015. BMC genomics. 16(s3):s2. (SCI, IF: 3.986)Han ZJ,Jiang QH*, Zhang TJ, Wu XL, Ma R, Wang JX, Bai Y, Wang RJ, Tan RJ, Wang YD*. Analyzing large-scale samples confirms the association between the rs1051730 polymorphism and lung cancer susceptibility. 2015. Scientific Reports. (Accepted) (SCI, IF: 5.578) (*通訊作者)Zhang SY, Li X, Ma G, Jiang YS, Liao MZ, Feng RN, Zhang LC, Liu JF, Wang GY, Zhao B,Jiang QH*, Li KS*, Liu GY*. CLU rs9331888 Polymorphism Contributes to Alzheimer’s Disease Susceptibility in Caucasian But Not East Asian Populations. 2015. Molecular Neurobiology, 53(3), 1446-1451. (*通訊作者) (SCI, IF: 5.137)Li YN, Song DJ, Jiang YS, Wang J, Feng R, Zhang LC, Wang GY, Chen ZG, Wang RZ*,Jiang QH*, Liu GY*. CR1 rs3818361 Polymorphism Contributes to Alzheimer’s Disease Susceptibility in Chinese Population. Molecular Neurobiology. 2015 July 21. [Epub ahead of print]. (*通訊作者) (SCI, IF: 5.137)Li KS,Jiang QH, Xu AD, Liu GY. REST rs3796529 variant does not confer susceptibility to Alzheimer’s disease. Annals of Neurology. 2015 Aug 18. doi: 10.1002/ana.24503. [Epub ahead of print] (SCI IF: 9.977)Guiyou Liu, Yongquan Liu,Qinghua Jiang, Yongshuai Jiang, Rennan Feng, Liangcai Zhang, Zugen Chen, Keshen Li , Jiafeng Liu. Convergent Genetic and Expression Datasets Highlight TREM2 in Parkinsonu2019s Disease Susceptibility. Molecular Neurobiology. 2015. DOI 10.1007/s12035-015-9416-7. (SCI, IF: 5.137)Bai Y, Ji SF,Jiang QH, Wang YD. Identification exon skipping events from high-throughput RNA sequencing data. IEEE Transactions on NanoBioscience. 2015 Jul;14(5):562-9 (SCI IF: 2.309)Xinjie Bao, Gengfeng Chen, Yongshuai Jiang,Qinghua Jiang, Mingzhi Liao, Rennan Feng, LiangcaiZhang, Guoda Ma, Shuyan Zhang, Zugen Chen, Bin Zhao, Renzhi Wang*, Keshen Li*, Guiyou Liu*. Cell adhesion molecules pathways genes are regulated by cis-regulatory SNPs and show significantly altered expression in Alzheimeru2019s disease brains. Neurobiol Aging. 2015 Jun 12 (SCI, IF: 5.013)Xiao Zhu, Henry C.M. Leung, Rongjie Wang, Francis Y.L. Chin, Siu Ming Yiu, Guangri Quan, Yajie Li, Rui Zhang,Qinghua Jiang, Bo Liu, Yucui Dong, Guohui Zhou, Yadong Wang. misFinder: Identify mis-assemblies in an unbiased manner using reference and paired-end reads. BMC Bioinformatics. 2015 (Accepted) (SCI IF: 2.44)Peng JJ, Li HX, Liu YZ, Juan LR,Jiang QH, Wang YD*. InteGO2: a web tool for measuring and visualizing gene semantic similarities using Gene Ontology. BMC Bioinformatics. 2015 (Accepted) (SCI, IF: 2.576)Zhu X, Leung HC, Wang R, Chin FY, Yiu SM, Quan G, Li Y, Zhang R,Jiang Q, Liu B, Dong Y, Zhou G, Wang Y. misFinder: identify mis-assemblies in an unbiased manner using reference and paired-end reads. BMC Bioinformatics. 2015 Nov 16;16(1):386 (SCI, IF: 2.576)

    2014

      Jiang QH, Wang JX, Wu XL, Ma R, Jin SL, Han ZJ, Tan RJ, Peng JJ, Liu GY, Li Y, Wang YD. LncRNA2Target: a database for differentially expressed genes after lncRNA knockdown or overexpression. 2014.Nucleic Acids Research. DOI 10.1093/nar/gku1173 (SCI,IF: 8.808)Quan BK, Qi XS, Yu ZH, Jiang YS, Liao MZ, Wang GY, Feng RN, Zhang LC, Chen ZG,Jiang QH*, Liu GY*. Pathway analysis of genome-wide association study and transcriptome data highlights new biological pathways in colorectal cancer. 2014.Molecular Genetics and Genomics. DOI 10.1007/s00438-014-0945-y. (*通訊作者) (SCI,IF: 2.831)Liu GY, Bao XJ, Jiang Y,S Liao MZ,Jiang QH, Feng RN, Zhang LC, Ma GD, Chen ZG, Wang GY, Wang RZ, Zhao B, Li KS.Identifying the Association Between Alzheimer’s Disease and Parkinson’s Disease Using Genome-Wide Association Studies and Protein-Protein Interaction Network. 2014.Molecular Neurobiology. DOI 10.1007/s12035-014-8946-8 (SCI,IF=5.286)Li X, Shen N, Zhang SY, Liu JF,Jiang QH, Liao MZ, Feng RN, Zhang LC, Wang GY, Ma GD, Zhou HH, Chen ZG, Jiang YS*, Zhao B*, Li KS*, Liu GY* (2014) CD33 rs3865444 polymorphism contributes to Alzheimeru2019s disease susceptibility in European and North American but not Asian populations.Molecular Neurobiology. DOI 10.1007/s12035-014-8880-9 (SCI,IF=5.286)Xiang ZM, Xu ML, Liao MZ, Jiang YS,Jiang QH, Feng RN, Zhang LC, Ma GD, Wang GY, Chen ZG, Zhao B, Sun TS*, Li KS*, Liu GY* (2014) Integrating genome-wide association study and brain expression data highlights cell adhesion molecules and purine metabolism in Alzheimeru2019s disease.Molecular Neurobiology. DOI 10.1007/s12035-014-8884-5 (SCI,IF=5.286)Peng JJ, Li HX,Jiang QH, Wang YD, Chen J. TITLE: An Integrative Approach for Measuring Semantic Similarities using Gene Ontology.BMC systems biology. 2014, 8 (Suppl 5): S8 (SCI,IF: 2.853)Tan RJ, Wang YD, Kleinstein S, Liu YZ, Zhu XL,Jiang QH, Zhu MF. An Evaluation of Copy Number Variation Detection Tools from Whole-Exome Sequencing Data.Human mutation.2014 Mar 5. doi: 10.1002/humu.22537. [Epub 2014 May 1] (SCI,IF: 5.213)Jin SL, Tan RJ,Jiang QH, Xu L, Peng JJ, Wang Y, Wang YD. A generalized topological entropy for analyzing the complexity of DNA sequences.PLoS One. 2014 Feb 12;9(2):e88519 (SCI,IF: 3.73)Jiang QH, Wang JX, Wang YD, Ma R, Wu XL, Li Y. TF2LncRNA: Identifying common transcription factors for a list of lncRNA genes from ChIP-Seq data.BioMed Research International. vol. 2014, Article ID 317642, 5 pages, 2014. doi:10.1155/2014/317642 (SCI,IF: 2.706)

    2013

      Jiang QH, Wang GH, Li Y, Jin SL, Wang YD. Predicting Human microRNA-disease Associations Based on Support Vector Machine. International Journal of Data Mining and Bioinformatics. 2013.vol.8, No.3. 282-239

    2012

      Jin SL, Xu L,Jiang QH*, Duan GR. A Joint Spectral Characterization of C* Independence. Infinite Dimensional Analysis Quantum Probability and Related Topics. Vol. 15, No. 2 (2012) 1250013:1-5 ( *通訊作者)Jin SL, Jiang QH*, Wang YD*, Duan GR. On joint spectrum of infinite direct sums. Operators and Matrices. Vol. 6, No. 3 (2012), 529u2013533 ( *通訊作者)Jin SL, Xu L, Jiang QH* and L Li*. Conditions equivalent to C* independence, Studia Math. 2012,211, 191-197 ( *通訊作者)Jin SL, Xu L, Jiang QH. Joint Spectrum and Joint Distribution. Complex analysis and operator theory. 2012. DOI 10.1007/s11785-012-0258-2

    2011

      Zhu SJ, Jiang QH, Wang GH, Liu B, Teng MX, Wang YD. Chromatin structure characteristics of pre-miRNA genomic sequences. BMC genomics.2011. 12(1):329.

    2010

      Jiang QH, Hao YY, Wang GH, Juan LR, Zhang TJ, Teng MX, Liu YL, Wang YD. Prioritization of disease microRNAs through a human phenome-microRNAome network, Bmc Systems Biology, 2010, 4 Suppl 1, S2.Jiang QH, Hao YY, Wang GH, Zhang TJ, Wang YD. Weighted network-based inference of human microRNA-disease associations. The 5th International Conference on Frontier of Computer Science and Technology - Workshop on Bioinformatics and System Biology. 2010. 431-435Jiang QH, Wang GH, Wang YD. An approach for prioritizing disease-related microRNAs based on genomic data integration. The 3rd International Conference on BioMedical Engineering and Informatics. 2010. 2270-2274

    2009

      Jiang QH, Wang YD, Hao YY, Juan LR, Teng MX, Zhang XJ, Li MM, Wang GH, Liu YL. miR2Disease: a manually curated database for microRNA deregulation in human disease. Nucleic Acids Res.2009,37: D98-104

    現(xiàn)承擔(dān)課程

    生物信息學(xué)(授課對象:生命學(xué)院三年級本科生)生物信息技術(shù)(授課對象:生命學(xué)院碩士一年級)

    本課程主要介紹生物信息學(xué)基本概念及特點(diǎn)、常用生物數(shù)據(jù)庫、基因組瀏覽器、Linux系統(tǒng)常用命令、R語言編程、基因芯片原理及數(shù)據(jù)分析、新一代DNA測序技術(shù)原理及其數(shù)據(jù)分析、生物信息學(xué)熱點(diǎn)問題分析等內(nèi)容。通過本課程的講授,旨在使學(xué)生了解生命科學(xué)學(xué)術(shù)前沿技術(shù)及研究問題、培養(yǎng)學(xué)生運(yùn)用所學(xué)的數(shù)據(jù)分析技術(shù)解決生命科學(xué)中前沿問題的能力,為今后從事生命科學(xué)研究奠定基礎(chǔ)。

    研究生培養(yǎng)

    2017年招生:博士生2名,碩士生3名,歡迎計(jì)算機(jī)、數(shù)學(xué)、生物、生物信息學(xué)等相關(guān)專業(yè)的同學(xué)報(bào)考。

    蔣慶華教授歡迎所有喜歡閱讀頂級期刊論文,希望在哈工大生命學(xué)院攻讀碩士學(xué)位并以發(fā)表學(xué)術(shù)論文為樂趣的有志青年加入他的研究團(tuán)隊(duì),有意者可致信qhjiang at hit.edu.cn。

    對于沒有任何編程及信息技術(shù)基礎(chǔ)的學(xué)生,蔣慶華教授會用大約半年的時(shí)間與他們一起學(xué)習(xí)經(jīng)典實(shí)用的編程語言(R、Python等),指導(dǎo)學(xué)生掌握基本的統(tǒng)計(jì)與數(shù)據(jù)挖掘方法,發(fā)現(xiàn)并跟蹤最前沿的生命科學(xué)熱點(diǎn)問題,并用所學(xué)的編程技能及信息學(xué)方法解決這些問題。

    蔣慶華教授鼓勵(lì)他的學(xué)生將科研作為畢生的追求和事業(yè),支持他的學(xué)生在畢業(yè)后繼續(xù)攻讀博士學(xué)位(出國攻博或公派出國進(jìn)行二年的博士生聯(lián)合培養(yǎng))。

    蔣慶華

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