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Chad Huff

Showing results (11-20 of 54) with videos related to

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Nature Communications|November 28, 2025
Benchmarking DNA foundation models for genomic and genetic tasksHaonan Feng, Lang Wu, Bingxin Zhao, et al.
Cell Reports|June 2, 2021
Inhibiting an RBM39/MLL1 epigenomic regulatory complex with dominant-negative peptides disrupts cancer cell transcription and proliferationPavan Kumar Puvvula, Yao Yu, Kaelan Renaldo Sullivan, et al.
Current Protocols in Human Genetics|April 26, 2014
Using VAAST to Identify Disease-Associated Variants in Next-Generation Sequencing DataBrett Kennedy, Zev Kronenberg, Hao Hu, et al.
BMC Genetics|May 22, 2012
Genetic analysis of ancestry, admixture and selection in Bolivian and Totonac populations of the New WorldW Scott Watkins, Jinchuan Xing, Chad Huff, et al.
G3 (Bethesda, Md.)|September 1, 2018
Targeted Gene Sequencing in Children with Crohn's Disease and Their Parents: Implications for Missing HeritabilityJiun-Sheng Chen, Fulan Hu, Subra Kugathasan, et al.
BMC Bioinformatics|February 22, 2018
The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization toolSteven Flygare, Edgar Javier Hernandez, Lon Phan, et al.
Haematologica|February 14, 2013
The phenotype of polycythemia due to Croatian homozygous VHL (571C>G:H191D) mutation is different from that of Chuvash polycythemia (VHL 598C>T:R200W)Nikica Ljubas Tomasic, Lucie Piterkova, Chad Huff, et al.
Plos One|November 17, 2015
Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, TexasEric L Brown, Jennifer E Below, Rebecca S B Fischer, et al.
Fertility and Sterility|May 10, 2015
Whole-exome sequencing identifies novel homozygous mutation in NPAS2 in family with nonobstructive azoospermiaRanjith Ramasamy, M Emre Bakırcıoğlu, Cenk Cengiz, et al.
Scientific Reports|November 3, 2016
Personalized Risk Assessment in Never, Light, and Heavy Smokers in a prospective cohort in TaiwanXifeng Wu, Chi Pang Wen, Yuanqing Ye, et al.
Pageof 6

Showing results (11-20 of 54) with videos related to

Sort By:
Pageof 6
Nature Communications|November 28, 2025
Benchmarking DNA foundation models for genomic and genetic tasksHaonan Feng, Lang Wu, Bingxin Zhao, et al.
Cell Reports|June 2, 2021
Inhibiting an RBM39/MLL1 epigenomic regulatory complex with dominant-negative peptides disrupts cancer cell transcription and proliferationPavan Kumar Puvvula, Yao Yu, Kaelan Renaldo Sullivan, et al.
Current Protocols in Human Genetics|April 26, 2014
Using VAAST to Identify Disease-Associated Variants in Next-Generation Sequencing DataBrett Kennedy, Zev Kronenberg, Hao Hu, et al.
BMC Genetics|May 22, 2012
Genetic analysis of ancestry, admixture and selection in Bolivian and Totonac populations of the New WorldW Scott Watkins, Jinchuan Xing, Chad Huff, et al.
G3 (Bethesda, Md.)|September 1, 2018
Targeted Gene Sequencing in Children with Crohn's Disease and Their Parents: Implications for Missing HeritabilityJiun-Sheng Chen, Fulan Hu, Subra Kugathasan, et al.
BMC Bioinformatics|February 22, 2018
The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization toolSteven Flygare, Edgar Javier Hernandez, Lon Phan, et al.
Haematologica|February 14, 2013
The phenotype of polycythemia due to Croatian homozygous VHL (571C>G:H191D) mutation is different from that of Chuvash polycythemia (VHL 598C>T:R200W)Nikica Ljubas Tomasic, Lucie Piterkova, Chad Huff, et al.
Plos One|November 17, 2015
Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, TexasEric L Brown, Jennifer E Below, Rebecca S B Fischer, et al.
Fertility and Sterility|May 10, 2015
Whole-exome sequencing identifies novel homozygous mutation in NPAS2 in family with nonobstructive azoospermiaRanjith Ramasamy, M Emre Bakırcıoğlu, Cenk Cengiz, et al.
Scientific Reports|November 3, 2016
Personalized Risk Assessment in Never, Light, and Heavy Smokers in a prospective cohort in TaiwanXifeng Wu, Chi Pang Wen, Yuanqing Ye, et al.
Pageof 6