Mulin Jun Li

According to our database, Mulin Jun Li authored at least 22 papers between 2010 and 2024.

Collaborative distances:

• Dijkstra number of four.
• Erdős number of four.

2024

SingleQ: a comprehensive database of single-cell expression quantitative trait loci (sc-eQTLs) cross human tissues.

Zhiwei Zhou, Jingyi Du, Jianhua Wang, Liangyi Liu, M. Gracie Gordon, Chun Jimmie Ye, Joseph E. Powell, Mulin Jun Li, Shuquan Rao

Database J. Biol. Databases Curation, January, 2024

2023

Inferring CTCF-binding patterns and anchored loops across human tissues and cell types.

Hang Xu, Xianfu Yi, Xutong Fan, Chengyue Wu, Wei Wang, Xinlei Chu, Shijie Zhang, Xiaobao Dong, Zhao Wang, Jianhua Wang, Yao Zhou, Ke Zhao, Hongcheng Yao, Nan Zheng, Junwen Wang, Yupeng Chen, Dariusz Plewczynski, Pak Chung Sham, Kexin Chen, Dandan Huang, Mulin Jun Li

Patterns, August, 2023

QTLbase2: an enhanced catalog of human quantitative trait loci on extensive molecular phenotypes.

Dandan Huang, Xiangling Feng, Hongxi Yang, Jianhua Wang, Wenwen Zhang, Xutong Fan, Xiaobao Dong, Kexin Chen, Ying Yu, Xin Ma, Xianfu Yi, Mulin Jun Li

Nucleic Acids Res., January, 2023

2022

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

Dandan Huang, Yao Zhou, Xianfu Yi, Xutong Fan, Jianhua Wang, Hongcheng Yao, Pak Chung Sham, Jihui Hao, Kexin Chen, Mulin Jun Li

Nucleic Acids Res., 2022

webTWAS: a resource for disease candidate susceptibility genes identified by transcriptome-wide association study.

Chen Cao, Jianhua Wang, Devin Kwok, Feifei Cui, Zilong Zhang, Da Zhao, Mulin Jun Li, Quan Zou

Nucleic Acids Res., 2022

2021

vSampler: fast and annotation-based matched variant sampling tool.

Dandan Huang, Zhao Wang, Yao Zhou, Qian Liang, Pak Chung Sham, Hongcheng Yao, Mulin Jun Li

Bioinform., 2021

2020

QTLbase: an integrative resource for quantitative trait loci across multiple human molecular phenotypes.

Zhanye Zheng, Dandan Huang, Jianhua Wang, Ke Zhao, Yao Zhou, Zhenyang Guo, Sinan Zhai, Hang Xu, Hui Cui, Hongcheng Yao, Zhao Wang, Xianfu Yi, Shijie Zhang, Pak Chung Sham, Mulin Jun Li

Nucleic Acids Res., 2020

CAUSALdb: a database for disease/trait causal variants identified using summary statistics of genome-wide association studies.

Jianhua Wang, Dandan Huang, Yao Zhou, Hongcheng Yao, Huanhuan Liu, Sinan Zhai, Chengwei Wu, Zhanye Zheng, Ke Zhao, Zhao Wang, Xianfu Yi, Shijie Zhang, Xiaorong Liu, Zipeng Liu, Kexin Chen, Ying Yu, Pak Chung Sham, Mulin Jun Li

Nucleic Acids Res., 2020

Methods and resources to access mutation-dependent effects on cancer drug treatment.

Hongcheng Yao, Qian Liang, Xinyi Qian, Junwen Wang, Pak Chung Sham, Mulin Jun Li

Briefings Bioinform., 2020

2018

GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traits.

Dandan Huang, Xianfu Yi, Shijie Zhang, Zhanye Zheng, Panwen Wang, Chenghao Xuan, Pak Chung Sham, Junwen Wang, Mulin Jun Li

Nucleic Acids Res., 2018

A powerful approach reveals numerous expression quantitative trait haplotypes in multiple tissues.

Dingge Ying, Mulin Jun Li, Pak Chung Sham, Miao-Xin Li

Bioinform., 2018

2017

mTCTScan: a comprehensive platform for annotation and prioritization of mutations affecting drug sensitivity in cancers.

Mulin Jun Li, Hongcheng Yao, Dandan Huang, Huanhuan Liu, Zipeng Liu, Hang Xu, Yiming Qin, Jeanette Prinz, Weiyi Xia, Panwen Wang, Bin Yan, Nhan L. Tran, Jean-Pierre A. Kocher, Pak Chung Sham, Junwen Wang

Nucleic Acids Res., 2017

2016

GWASdb v2: an update database for human genetic variants identified by genome-wide association studies.

Mulin Jun Li, Zipeng Liu, Panwen Wang, Maria P. Wong, Matthew R. Nelson, Jean-Pierre A. Kocher, Meredith Yeager, Pak Chung Sham, Stephen J. Chanock, Zhengyuan Xia, Junwen Wang

Nucleic Acids Res., 2016

Predicting regulatory variants with composite statistic.

Mulin Jun Li, Zhicheng Pan, Zipeng Liu, Jiexing Wu, Panwen Wang, Yun Zhu, Feng Xu, Zhengyuan Xia, Pak Chung Sham, Jean-Pierre A. Kocher, Miao-Xin Li, Jun S. Liu, Junwen Wang

Bioinform., 2016

2015

ChIP-Array 2: integrating multiple omics data to construct gene regulatory networks.

Panwen Wang, Jing Qin, Yiming Qin, Yun Zhu, Lily Yan Wang, Mulin Jun Li, Michael Q. Zhang, Junwen Wang

Nucleic Acids Res., 2015

Exploring the function of genetic variants in the non-coding genomic regions: approaches for identifying human regulatory variants affecting gene expression.

Mulin Jun Li, Bin Yan, Pak Chung Sham, Junwen Wang

Briefings Bioinform., 2015

2014

dbPSHP: a database of recent positive selection across human populations.

Mulin Jun Li, Lily Yan Wang, Zhengyuan Xia, Maria P. Wong, Pak Chung Sham, Junwen Wang

Nucleic Acids Res., 2014

DDGni: Dynamic delay gene-network inference from high-temporal data using gapped local alignment.

Hari Krishna Yalamanchili, Bin Yan, Mulin Jun Li, Jing Qin, Zhongying Zhao, Francis Y. L. Chin, Junwen Wang

Bioinform., 2014

2013

GWAS3D: detecting human regulatory variants by integrative analysis of genome-wide associations, chromosome interactions and histone modifications.

Mulin Jun Li, Lily Yan Wang, Zhengyuan Xia, Pak Chung Sham, Junwen Wang

Nucleic Acids Res., 2013

2012

GWASdb: a database for human genetic variants identified by genome-wide association studies.

Mulin Jun Li, Panwen Wang, Xiaorong Liu, Ee Lyn Lim, Zhangyong Wang, Meredith Yeager, Maria P. Wong, Pak Chung Sham, Stephen J. Chanock, Junwen Wang

Nucleic Acids Res., 2012

2011

ChIP-Array: combinatory analysis of ChIP-seq/chip and microarray gene expression data to discover direct/indirect targets of a transcription factor.

Jing Qin, Mulin Jun Li, Panwen Wang, Michael Q. Zhang, Junwen Wang

Nucleic Acids Res., 2011

2010

FastPval: a fast and memory efficient program to calculate very low <i>P</i>-values from empirical distribution.

Mulin Jun Li, Pak Chung Sham, Junwen Wang

Bioinform., 2010