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Gao T Wang

Showing results (1-10 of 21) with videos related to

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American Journal of Human Genetics|May 6, 2014
Variant association tools for quality control and analysis of large-scale sequence and genotyping array dataGao T Wang, Bo Peng, Suzanne M Leal
Bioinformatics (Oxford, England)|July 17, 2015
Generation of sequence-based data for pedigree-segregating Mendelian or Complex traitsBiao Li, Gao T Wang, Suzanne M Leal
BMC Genomics|March 6, 2025
The case-only design is a powerful approach to detect interactions but should be used with cautionRui Dong, Gao T Wang, Andrew T DeWan, et al.
European Journal of Human Genetics : EJHG|April 16, 2015
Collapsed haplotype pattern method for linkage analysis of next-generation sequence dataGao T Wang, Di Zhang, Biao Li, et al.
Biorxiv : the Preprint Server for Biology|June 5, 2026
Leveraging <i>cis-</i> and <i>trans-</i> variants to improve protein expression level prediction for proteome-wide association studiesRui Dong, Derek Lamb, Gao T Wang, et al.
Bioinformatics (Oxford, England)|April 30, 2014
Power analysis and sample size estimation for sequence-based association studiesGao T Wang, Biao Li, Regie P Lyn Santos-Cortez, et al.
American Journal of Human Genetics|July 4, 2017
SEQSpark: A Complete Analysis Tool for Large-Scale Rare Variant Association Studies Using Whole-Genome and Exome Sequence DataDi Zhang, Linhai Zhao, Biao Li, et al.
Frontiers in Genetics|March 10, 2023
The genetic contribution of the X chromosome in age-related hearing lossElnaz Naderi, Diana M Cornejo-Sanchez, Guangyou Li, et al.
European Journal of Human Genetics : EJHG|March 7, 2025
Mendelian non-syndromic and syndromic hearing loss genes contribute to presbycusisDiana M Cornejo-Sanchez, Thashi Bharadwaj, Rui Dong, et al.
American Journal of Human Genetics|February 4, 2017
Erratum: The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS DataZongxiao He, Di Zhang, Alan E Renton, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
American Journal of Human Genetics|May 6, 2014
Variant association tools for quality control and analysis of large-scale sequence and genotyping array dataGao T Wang, Bo Peng, Suzanne M Leal
Bioinformatics (Oxford, England)|July 17, 2015
Generation of sequence-based data for pedigree-segregating Mendelian or Complex traitsBiao Li, Gao T Wang, Suzanne M Leal
BMC Genomics|March 6, 2025
The case-only design is a powerful approach to detect interactions but should be used with cautionRui Dong, Gao T Wang, Andrew T DeWan, et al.
European Journal of Human Genetics : EJHG|April 16, 2015
Collapsed haplotype pattern method for linkage analysis of next-generation sequence dataGao T Wang, Di Zhang, Biao Li, et al.
Biorxiv : the Preprint Server for Biology|June 5, 2026
Leveraging <i>cis-</i> and <i>trans-</i> variants to improve protein expression level prediction for proteome-wide association studiesRui Dong, Derek Lamb, Gao T Wang, et al.
Bioinformatics (Oxford, England)|April 30, 2014
Power analysis and sample size estimation for sequence-based association studiesGao T Wang, Biao Li, Regie P Lyn Santos-Cortez, et al.
American Journal of Human Genetics|July 4, 2017
SEQSpark: A Complete Analysis Tool for Large-Scale Rare Variant Association Studies Using Whole-Genome and Exome Sequence DataDi Zhang, Linhai Zhao, Biao Li, et al.
Frontiers in Genetics|March 10, 2023
The genetic contribution of the X chromosome in age-related hearing lossElnaz Naderi, Diana M Cornejo-Sanchez, Guangyou Li, et al.
European Journal of Human Genetics : EJHG|March 7, 2025
Mendelian non-syndromic and syndromic hearing loss genes contribute to presbycusisDiana M Cornejo-Sanchez, Thashi Bharadwaj, Rui Dong, et al.
American Journal of Human Genetics|February 4, 2017
Erratum: The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS DataZongxiao He, Di Zhang, Alan E Renton, et al.
Pageof 3