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Mulin Jun Li

Showing results (31-40 of 107) with videos related to

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Human Mutation|February 14, 2015
wKGGSeq: A Comprehensive Strategy-Based and Disease-Targeted Online Framework to Facilitate Exome Sequencing Studies of Inherited DisordersMulin Jun Li, Jiaen Deng, Panwen Wang, et al.
Scientific Data|July 23, 2025
A highly annotated drug combination resource for catalyzing precision combinatorial therapyTianyi You, Lili Wang, Jianhua Wang, et al.
Nucleic Acids Research|April 29, 2015
ChIP-Array 2: integrating multiple omics data to construct gene regulatory networksPanwen Wang, Jing Qin, Yiming Qin, et al.
Communications Biology|January 12, 2020
Diversity spectrum analysis identifies mutation-specific effects of cancer driver genesXiaobao Dong, Dandan Huang, Xianfu Yi, et al.
Nucleic Acids Research|May 18, 2018
GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traitsDandan Huang, Xianfu Yi, Shijie Zhang, et al.
Oncogene|February 9, 2023
Retrograde regulation of mitochondrial fission and epithelial to mesenchymal transition in hepatocellular carcinoma by GCN5L1Linmeng Han, Chunyu Zhang, Danni Wang, et al.
Brain : a Journal of Neurology|November 17, 2018
Neurobiological substrates underlying the effect of genomic risk for depression on the conversion of amnestic mild cognitive impairmentJiayuan Xu, Qiaojun Li, Wen Qin, et al.
Parasites & Vectors|July 10, 2025
Clonorchis sinensis infection remodels chromatin accessibility in hepatocellular carcinomaWeilong Yang, Caibiao Wei, Junxian Chen, et al.
Nucleic Acids Research|September 27, 2021
VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseasesDandan Huang, Yao Zhou, Xianfu Yi, et al.
Database : the Journal of Biological Databases and Curation|March 9, 2024
SingleQ: a comprehensive database of single-cell expression quantitative trait loci (sc-eQTLs) cross human tissuesZhiwei Zhou, Jingyi Du, Jianhua Wang, et al.
Pageof 11

Showing results (31-40 of 107) with videos related to

Sort By:
Pageof 11
Human Mutation|February 14, 2015
wKGGSeq: A Comprehensive Strategy-Based and Disease-Targeted Online Framework to Facilitate Exome Sequencing Studies of Inherited DisordersMulin Jun Li, Jiaen Deng, Panwen Wang, et al.
Scientific Data|July 23, 2025
A highly annotated drug combination resource for catalyzing precision combinatorial therapyTianyi You, Lili Wang, Jianhua Wang, et al.
Nucleic Acids Research|April 29, 2015
ChIP-Array 2: integrating multiple omics data to construct gene regulatory networksPanwen Wang, Jing Qin, Yiming Qin, et al.
Communications Biology|January 12, 2020
Diversity spectrum analysis identifies mutation-specific effects of cancer driver genesXiaobao Dong, Dandan Huang, Xianfu Yi, et al.
Nucleic Acids Research|May 18, 2018
GWAS4D: multidimensional analysis of context-specific regulatory variant for human complex diseases and traitsDandan Huang, Xianfu Yi, Shijie Zhang, et al.
Oncogene|February 9, 2023
Retrograde regulation of mitochondrial fission and epithelial to mesenchymal transition in hepatocellular carcinoma by GCN5L1Linmeng Han, Chunyu Zhang, Danni Wang, et al.
Brain : a Journal of Neurology|November 17, 2018
Neurobiological substrates underlying the effect of genomic risk for depression on the conversion of amnestic mild cognitive impairmentJiayuan Xu, Qiaojun Li, Wen Qin, et al.
Parasites & Vectors|July 10, 2025
Clonorchis sinensis infection remodels chromatin accessibility in hepatocellular carcinomaWeilong Yang, Caibiao Wei, Junxian Chen, et al.
Nucleic Acids Research|September 27, 2021
VannoPortal: multiscale functional annotation of human genetic variants for interrogating molecular mechanism of traits and diseasesDandan Huang, Yao Zhou, Xianfu Yi, et al.
Database : the Journal of Biological Databases and Curation|March 9, 2024
SingleQ: a comprehensive database of single-cell expression quantitative trait loci (sc-eQTLs) cross human tissuesZhiwei Zhou, Jingyi Du, Jianhua Wang, et al.
Pageof 11