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James D Fife

Showing results (1-10 of 9) with videos related to

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American Journal of Human Genetics|May 26, 2023
Estimating clinical risk in gene regions from population sequencing cohort dataJames D Fife, Christopher A Cassa
Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Estimating clinical risk in gene regions from population sequencing cohort dataJames D Fife, Christopher A Cassa
Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Joint estimation and imputation of variant functional effects using high throughput assay dataTian Yu, James D Fife, Ivan Adzhubey, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 28, 2022
Informing variant assessment using structured evidence from prior classifications (PS1, PM5, and PVS1 sequence variant interpretation criteria)Vineel Bhat, Ivan A Adzhubei, James D Fife, et al.
Cell Genomics|October 10, 2024
FUSE: Improving the estimation and imputation of variant impacts in functional screeningTian Yu, James D Fife, Vineel Bhat, et al.
Nature Communications|June 18, 2022
Peptide fusion improves prime editing efficiencyMinja Velimirovic, Larissa C Zanetti, Max W Shen, et al.
Cell Genomics|May 25, 2023
Systematic elucidation of genetic mechanisms underlying cholesterol uptakeMarisa C Hamilton, James D Fife, Ersin Akinci, et al.
Biorxiv : the Preprint Server for Biology|January 30, 2023
Systematic elucidation of genetic mechanisms underlying cholesterol uptakeMarisa C Hamilton, James D Fife, Ersin Akinci, et al.
Biorxiv : the Preprint Server for Biology|September 2, 2020
Elucidation of remdesivir cytotoxicity pathways through genome-wide CRISPR-Cas9 screening and transcriptomicsErsin Akinci, Minsun Cha, Lin Lin, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
American Journal of Human Genetics|May 26, 2023
Estimating clinical risk in gene regions from population sequencing cohort dataJames D Fife, Christopher A Cassa
Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Estimating clinical risk in gene regions from population sequencing cohort dataJames D Fife, Christopher A Cassa
Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Joint estimation and imputation of variant functional effects using high throughput assay dataTian Yu, James D Fife, Ivan Adzhubey, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 28, 2022
Informing variant assessment using structured evidence from prior classifications (PS1, PM5, and PVS1 sequence variant interpretation criteria)Vineel Bhat, Ivan A Adzhubei, James D Fife, et al.
Cell Genomics|October 10, 2024
FUSE: Improving the estimation and imputation of variant impacts in functional screeningTian Yu, James D Fife, Vineel Bhat, et al.
Nature Communications|June 18, 2022
Peptide fusion improves prime editing efficiencyMinja Velimirovic, Larissa C Zanetti, Max W Shen, et al.
Cell Genomics|May 25, 2023
Systematic elucidation of genetic mechanisms underlying cholesterol uptakeMarisa C Hamilton, James D Fife, Ersin Akinci, et al.
Biorxiv : the Preprint Server for Biology|January 30, 2023
Systematic elucidation of genetic mechanisms underlying cholesterol uptakeMarisa C Hamilton, James D Fife, Ersin Akinci, et al.
Biorxiv : the Preprint Server for Biology|September 2, 2020
Elucidation of remdesivir cytotoxicity pathways through genome-wide CRISPR-Cas9 screening and transcriptomicsErsin Akinci, Minsun Cha, Lin Lin, et al.
Pageof 1