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Christopher A Cassa

Showing results (21-30 of 50) with videos related to

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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.
Plos Genetics|August 29, 2015
Dominance of Deleterious Alleles Controls the Response to a Population BottleneckDaniel J Balick, Ron Do, Christopher A Cassa, 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.
American Journal of Human Genetics|July 10, 2025
Extracting and calibrating evidence of variant pathogenicity from population biobank dataVineel Bhat, Tian Yu, Lara Brown, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2025
Extracting and calibrating evidence of variant pathogenicity from population biobank dataVineel Bhat, Tian Yu, Lara Brown, et al.
Cell|June 14, 2020
Determinants of Base Editing Outcomes from Target Library Analysis and Machine LearningMandana Arbab, Max W Shen, Beverly Mok, et al.
Genome Research|December 8, 2011
Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibilityChristopher A Cassa, Sarah K Savage, Patrick L Taylor, et al.
Plos Computational Biology|January 8, 2021
Machine learning based CRISPR gRNA design for therapeutic exon skippingWilson Louie, Max W Shen, Zakir Tahiry, et al.
Elife|December 14, 2022
The missing link between genetic association and regulatory functionNoah J Connally, Sumaiya Nazeen, Daniel Lee, et al.
Pageof 5

Showing results (21-30 of 50) with videos related to

Sort By:
Pageof 5
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.
Plos Genetics|August 29, 2015
Dominance of Deleterious Alleles Controls the Response to a Population BottleneckDaniel J Balick, Ron Do, Christopher A Cassa, 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.
American Journal of Human Genetics|July 10, 2025
Extracting and calibrating evidence of variant pathogenicity from population biobank dataVineel Bhat, Tian Yu, Lara Brown, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2025
Extracting and calibrating evidence of variant pathogenicity from population biobank dataVineel Bhat, Tian Yu, Lara Brown, et al.
Cell|June 14, 2020
Determinants of Base Editing Outcomes from Target Library Analysis and Machine LearningMandana Arbab, Max W Shen, Beverly Mok, et al.
Genome Research|December 8, 2011
Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibilityChristopher A Cassa, Sarah K Savage, Patrick L Taylor, et al.
Plos Computational Biology|January 8, 2021
Machine learning based CRISPR gRNA design for therapeutic exon skippingWilson Louie, Max W Shen, Zakir Tahiry, et al.
Elife|December 14, 2022
The missing link between genetic association and regulatory functionNoah J Connally, Sumaiya Nazeen, Daniel Lee, et al.
Pageof 5