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VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseases.

D. Huang, Y. Zhou, X. Yi, X. Fan, J. Wang, H. Yao, P. Sham, J. Hao, K. Chen, and M. Li. Nucleic Acids Res., 50 (D1): 1408-1416 (2022)

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Jun Li

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GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits.D. Huang, X. Yi, S. Zhang, Z. Zheng, P. Wang, C. Xuan, P. Sham, J. Wang, and M. Li. Nucleic Acids Res., 46 (Webserver-Issue): W114-W120 (2018)GWAS3D: detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications.M. Li, L. Wang, Z. Xia, P. Sham, and J. Wang. Nucleic Acids Res., 41 (Webserver-Issue): 150-158 (2013)QTLbase: an integrative resource for quantitative trait loci across multiple human molecular phenotypes.Z. Zheng, D. Huang, J. Wang, K. Zhao, Y. Zhou, Z. Guo, S. Zhai, H. Xu, H. Cui, H. Yao and 5 other author(s). Nucleic Acids Res., 48 (Database-Issue): D983-D991 (2020)vSampler: fast and annotation-based matched variant sampling tool.D. Huang, Z. Wang, Y. Zhou, Q. Liang, P. Sham, H. Yao, and M. Li. Bioinform., 37 (13): 1915-1917 (2021)Methods and resources to access mutation-dependent effects on cancer drug treatment.H. Yao, Q. Liang, X. Qian, J. Wang, P. Sham, and M. Li. Briefings Bioinform., 21 (6): 1886-1903 (2020)Predicting regulatory variants with composite statistic.M. Li, Z. Pan, Z. Liu, J. Wu, P. Wang, Y. Zhu, F. Xu, Z. Xia, P. Sham, J. Kocher and 3 other author(s). Bioinform., 32 (18): 2729-2736 (2016)ChIP-Array 2: integrating multiple omics data to construct gene regulatory networks.P. Wang, J. Qin, Y. Qin, Y. Zhu, L. Wang, M. Li, M. Zhang, and J. Wang. Nucleic Acids Res., 43 (Webserver-Issue): W264-W269 (2015)Exploring the function of genetic variants in the non-coding genomic regions: approaches for identifying human regulatory variants affecting gene expression.M. Li, B. Yan, P. Sham, and J. Wang. Briefings Bioinform., 16 (3): 393-412 (2015)VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseases.D. Huang, Y. Zhou, X. Yi, X. Fan, J. Wang, H. Yao, P. Sham, J. Hao, K. Chen, and M. Li. Nucleic Acids Res., 50 (D1): 1408-1416 (2022)webTWAS: a resource for disease candidate susceptibility genes identified by transcriptome-wide association study.C. Cao, J. Wang, D. Kwok, F. Cui, Z. Zhang, D. Zhao, M. Li, and Q. Zou. Nucleic Acids Res., 50 (D1): 1123-1130 (2022)

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Disambiguation of "Li, Mulin Jun"

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VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseases.

Please choose a person to relate this publication to

Jun Li

Jun Li

Jun Li

Jun Li

Jun Li

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Li, Mulin Jun"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseases.

Please choose a person to relate this publication to

Jun Li

Jun Li

Jun Li

Jun Li

Jun Li

Other publications of authors with the same name

Disambiguation

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VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseases.