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Bingshan Li

Showing results (11-20 of 156) with videos related to

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Bioinformatics (Oxford, England)|November 1, 2016
Cancer driver gene discovery through an integrative genomics approach in a non-parametric Bayesian frameworkHai Yang, Qiang Wei, Xue Zhong, et al.
Bioinformatics (Oxford, England)|March 13, 2014
A gradient-boosting approach for filtering de novo mutations in parent-offspring triosYongzhuang Liu, Bingshan Li, Renjie Tan, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|June 4, 2008
Sequence variants in host cell factor C1 are associated with Ménière's diseaseJeffrey T Vrabec, Liqian Liu, Bingshan Li, et al.
Biomed Research International|August 28, 2014
Improved variant calling accuracy by merging replicates in whole-exome sequencing studiesYanfeng Zhang, Bingshan Li, Chun Li, et al.
Plos Genetics|June 30, 2022
Integration of multidimensional splicing data and GWAS summary statistics for risk gene discoveryYing Ji, Qiang Wei, Rui Chen, et al.
Bioinformatics (Oxford, England)|May 7, 2016
RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence dataXiaowei Zhan, Youna Hu, Bingshan Li, et al.
Frontiers in Pharmacology|September 25, 2023
Drug repurposing for Alzheimer's disease from 2012-2022-a 10-year literature reviewMonika E Grabowska, Annabelle Huang, Zhexing Wen, et al.
BMC Bioinformatics|April 23, 2022
A Bayesian framework to integrate multi-level genome-scale data for Autism risk gene prioritizationYing Ji, Rui Chen, Quan Wang, et al.
Genes|February 25, 2022
Leveraging Gene-Level Prediction as Informative Covariate in Hypothesis Weighting Improves Power for Rare Variant Association StudiesYing Ji, Rui Chen, Quan Wang, et al.
AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|June 12, 2018
Learning Opportunities for Drug Repositioning via GWAS and PheWAS FindingsWen Yin, Cheng Gao, Yaomin Xu, et al.
Pageof 16

Showing results (11-20 of 156) with videos related to

Sort By:
Pageof 16
Bioinformatics (Oxford, England)|November 1, 2016
Cancer driver gene discovery through an integrative genomics approach in a non-parametric Bayesian frameworkHai Yang, Qiang Wei, Xue Zhong, et al.
Bioinformatics (Oxford, England)|March 13, 2014
A gradient-boosting approach for filtering de novo mutations in parent-offspring triosYongzhuang Liu, Bingshan Li, Renjie Tan, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|June 4, 2008
Sequence variants in host cell factor C1 are associated with Ménière's diseaseJeffrey T Vrabec, Liqian Liu, Bingshan Li, et al.
Biomed Research International|August 28, 2014
Improved variant calling accuracy by merging replicates in whole-exome sequencing studiesYanfeng Zhang, Bingshan Li, Chun Li, et al.
Plos Genetics|June 30, 2022
Integration of multidimensional splicing data and GWAS summary statistics for risk gene discoveryYing Ji, Qiang Wei, Rui Chen, et al.
Bioinformatics (Oxford, England)|May 7, 2016
RVTESTS: an efficient and comprehensive tool for rare variant association analysis using sequence dataXiaowei Zhan, Youna Hu, Bingshan Li, et al.
Frontiers in Pharmacology|September 25, 2023
Drug repurposing for Alzheimer's disease from 2012-2022-a 10-year literature reviewMonika E Grabowska, Annabelle Huang, Zhexing Wen, et al.
BMC Bioinformatics|April 23, 2022
A Bayesian framework to integrate multi-level genome-scale data for Autism risk gene prioritizationYing Ji, Rui Chen, Quan Wang, et al.
Genes|February 25, 2022
Leveraging Gene-Level Prediction as Informative Covariate in Hypothesis Weighting Improves Power for Rare Variant Association StudiesYing Ji, Rui Chen, Quan Wang, et al.
AMIA Joint Summits on Translational Science Proceedings. AMIA Joint Summits on Translational Science|June 12, 2018
Learning Opportunities for Drug Repositioning via GWAS and PheWAS FindingsWen Yin, Cheng Gao, Yaomin Xu, et al.
Pageof 16