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Alan F Rubin

Showing results (41-50 of 54) with videos related to

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Genome Biology|April 15, 2025
Guidelines for releasing a variant effect predictorBenjamin J Livesey, Mihaly Badonyi, Mafalda Dias, et al.
Arxiv|May 3, 2024
Guidelines for releasing a variant effect predictorBenjamin J Livesey, Mihaly Badonyi, Mafalda Dias, et al.
Medrxiv : the Preprint Server for Health Sciences|April 22, 2024
Defining and Reducing Variant Classification DisparitiesMoez Dawood, Shawn Fayer, Sriram Pendyala, et al.
Genome Medicine|December 4, 2024
Using multiplexed functional data to reduce variant classification inequities in underrepresented populationsMoez Dawood, Shawn Fayer, Sriram Pendyala, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2024
Mapping MAVE data for use in human genomics applicationsJeremy A Arbesfeld, Estelle Y Da, James S Stevenson, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
Image-based, pooled phenotyping reveals multidimensional, disease-specific variant effectsSriram Pendyala, Katie Partington, Nicholas Bradley, et al.
Genetics|September 25, 2024
Deep mutational scanning of CYP2C19 in human cells reveals a substrate specificity-abundance tradeoffGabriel E Boyle, Katherine A Sitko, Jared G Galloway, et al.
Genome Biology|June 25, 2025
Mapping MAVE data for use in human genomics applicationsJeremy A Arbesfeld, Estelle Y Da, James S Stevenson, et al.
Cell|May 13, 2026
Image-based, pooled phenotyping reveals multidimensional, disease-specific variant effectsSriram Pendyala, Katie Partington, Nicholas Bradley, et al.
Cell Genomics|April 9, 2026
ClinGen API platform for classification of human genetic variantsNeethu Shah, Tierra Farris, Arturo Alejandro Zuniga, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Genome Biology|April 15, 2025
Guidelines for releasing a variant effect predictorBenjamin J Livesey, Mihaly Badonyi, Mafalda Dias, et al.
Arxiv|May 3, 2024
Guidelines for releasing a variant effect predictorBenjamin J Livesey, Mihaly Badonyi, Mafalda Dias, et al.
Medrxiv : the Preprint Server for Health Sciences|April 22, 2024
Defining and Reducing Variant Classification DisparitiesMoez Dawood, Shawn Fayer, Sriram Pendyala, et al.
Genome Medicine|December 4, 2024
Using multiplexed functional data to reduce variant classification inequities in underrepresented populationsMoez Dawood, Shawn Fayer, Sriram Pendyala, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2024
Mapping MAVE data for use in human genomics applicationsJeremy A Arbesfeld, Estelle Y Da, James S Stevenson, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
Image-based, pooled phenotyping reveals multidimensional, disease-specific variant effectsSriram Pendyala, Katie Partington, Nicholas Bradley, et al.
Genetics|September 25, 2024
Deep mutational scanning of CYP2C19 in human cells reveals a substrate specificity-abundance tradeoffGabriel E Boyle, Katherine A Sitko, Jared G Galloway, et al.
Genome Biology|June 25, 2025
Mapping MAVE data for use in human genomics applicationsJeremy A Arbesfeld, Estelle Y Da, James S Stevenson, et al.
Cell|May 13, 2026
Image-based, pooled phenotyping reveals multidimensional, disease-specific variant effectsSriram Pendyala, Katie Partington, Nicholas Bradley, et al.
Cell Genomics|April 9, 2026
ClinGen API platform for classification of human genetic variantsNeethu Shah, Tierra Farris, Arturo Alejandro Zuniga, et al.
Pageof 6