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Alan F Rubin

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

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Biorxiv : the Preprint Server for Biology|May 7, 2026
CountESS: a flexible, graphical pipeline tool for deep mutational scanning analysisNick Moore, Callum J Sargeant, Matthew J Wakefield, et al.
The Journal of Biological Chemistry|June 22, 2021
Human and viral membrane-associated E3 ubiquitin ligases MARCH1 and MIR2 recognize different features of CD86 to downregulate surface expressionRaphael Trenker, Xinyu Wu, Julie V Nguyen, et al.
Bioinformatics (Oxford, England)|March 28, 2021
MaveRegistry: a collaboration platform for multiplexed assays of variant effectDa Kuang, Jochen Weile, Nishka Kishore, et al.
Genome Biology|February 9, 2018
Correction to: A statistical framework for analyzing deep mutational scanning dataAlan F Rubin, Hannah Gelman, Nathan Lucas, et al.
Genome Biology|August 9, 2017
A statistical framework for analyzing deep mutational scanning dataAlan F Rubin, Hannah Gelman, Nathan Lucas, et al.
Genome Biology|November 5, 2019
MaveDB: an open-source platform to distribute and interpret data from multiplexed assays of variant effectDaniel Esposito, Jochen Weile, Jay Shendure, et al.
Genetics|March 4, 2016
Comprehensive Analysis of the SUL1 Promoter of Saccharomyces cerevisiaeMatthew S Rich, Celia Payen, Alan F Rubin, et al.
Nature Methods|September 18, 2024
Genomics 2 Proteins portal: a resource and discovery tool for linking genetic screening outputs to protein sequences and structuresSeulki Kwon, Jordan Safer, Duyen T Nguyen, et al.
Biorxiv : the Preprint Server for Biology|January 23, 2024
Genomics 2 Proteins portal: A resource and discovery tool for linking genetic screening outputs to protein sequences and structuresSeulki Kwon, Jordan Safer, Duyen T Nguyen, et al.
Biorxiv : the Preprint Server for Biology|July 14, 2025
Gene-based calibration of high-throughput functional assays for clinical variant classificationDaniel Zeiberg, Malvika Tejura, Abbye E McEwen, et al.
Pageof 6

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

Sort By:
Pageof 6
Biorxiv : the Preprint Server for Biology|May 7, 2026
CountESS: a flexible, graphical pipeline tool for deep mutational scanning analysisNick Moore, Callum J Sargeant, Matthew J Wakefield, et al.
The Journal of Biological Chemistry|June 22, 2021
Human and viral membrane-associated E3 ubiquitin ligases MARCH1 and MIR2 recognize different features of CD86 to downregulate surface expressionRaphael Trenker, Xinyu Wu, Julie V Nguyen, et al.
Bioinformatics (Oxford, England)|March 28, 2021
MaveRegistry: a collaboration platform for multiplexed assays of variant effectDa Kuang, Jochen Weile, Nishka Kishore, et al.
Genome Biology|February 9, 2018
Correction to: A statistical framework for analyzing deep mutational scanning dataAlan F Rubin, Hannah Gelman, Nathan Lucas, et al.
Genome Biology|August 9, 2017
A statistical framework for analyzing deep mutational scanning dataAlan F Rubin, Hannah Gelman, Nathan Lucas, et al.
Genome Biology|November 5, 2019
MaveDB: an open-source platform to distribute and interpret data from multiplexed assays of variant effectDaniel Esposito, Jochen Weile, Jay Shendure, et al.
Genetics|March 4, 2016
Comprehensive Analysis of the SUL1 Promoter of Saccharomyces cerevisiaeMatthew S Rich, Celia Payen, Alan F Rubin, et al.
Nature Methods|September 18, 2024
Genomics 2 Proteins portal: a resource and discovery tool for linking genetic screening outputs to protein sequences and structuresSeulki Kwon, Jordan Safer, Duyen T Nguyen, et al.
Biorxiv : the Preprint Server for Biology|January 23, 2024
Genomics 2 Proteins portal: A resource and discovery tool for linking genetic screening outputs to protein sequences and structuresSeulki Kwon, Jordan Safer, Duyen T Nguyen, et al.
Biorxiv : the Preprint Server for Biology|July 14, 2025
Gene-based calibration of high-throughput functional assays for clinical variant classificationDaniel Zeiberg, Malvika Tejura, Abbye E McEwen, et al.
Pageof 6