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Matt W Wright

Showing results (1-10 of 13) with videos related to

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Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 10, 2021
An Investigation of the Knowledge Overlap between Pharmacogenomics and Disease GeneticsBinglan Li, Michelle Whirl-Carrillo, Matt W Wright, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 27, 2021
Evaluating the impact of in silico predictors on clinical variant classificationEmma H Wilcox, Mahdi Sarmady, Bryan Wulf, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 5, 2019
LitGen: Genetic Literature Recommendation Guided by Human ExplanationsAllen Nie, Arturo L Pineda, Matt W Wright, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 21, 2022
Accessing clinical-grade genomic classification data through the ClinGen Data PlatformKaren P Dalton, Heidi L Rehm, Matt W Wright, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 3, 2026
ClinGen Variant Curation Interface Workshops: Training Variant Scientists on an International PlatformDeborah I Ritter, Mark Mandell, Christine Preston, et al.
Human Mutation|October 13, 2018
ClinGen Allele Registry links information about genetic variantsPiotr Pawliczek, Ronak Y Patel, Lillian R Ashmore, et al.
Genome Medicine|January 2, 2020
Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation frameworkSarah E Brnich, Ahmad N Abou Tayoun, Fergus J Couch, et al.
American Journal of Human Genetics|June 7, 2020
Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity MeasuresAlice B Popejoy, Kristy R Crooks, Stephanie M Fullerton, et al.
Human Mutation|October 13, 2018
Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase GeneDiane B Zastrow, Heather Baudet, Wei Shen, 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 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 10, 2021
An Investigation of the Knowledge Overlap between Pharmacogenomics and Disease GeneticsBinglan Li, Michelle Whirl-Carrillo, Matt W Wright, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 27, 2021
Evaluating the impact of in silico predictors on clinical variant classificationEmma H Wilcox, Mahdi Sarmady, Bryan Wulf, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 5, 2019
LitGen: Genetic Literature Recommendation Guided by Human ExplanationsAllen Nie, Arturo L Pineda, Matt W Wright, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 21, 2022
Accessing clinical-grade genomic classification data through the ClinGen Data PlatformKaren P Dalton, Heidi L Rehm, Matt W Wright, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 3, 2026
ClinGen Variant Curation Interface Workshops: Training Variant Scientists on an International PlatformDeborah I Ritter, Mark Mandell, Christine Preston, et al.
Human Mutation|October 13, 2018
ClinGen Allele Registry links information about genetic variantsPiotr Pawliczek, Ronak Y Patel, Lillian R Ashmore, et al.
Genome Medicine|January 2, 2020
Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation frameworkSarah E Brnich, Ahmad N Abou Tayoun, Fergus J Couch, et al.
American Journal of Human Genetics|June 7, 2020
Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity MeasuresAlice B Popejoy, Kristy R Crooks, Stephanie M Fullerton, et al.
Human Mutation|October 13, 2018
Unique aspects of sequence variant interpretation for inborn errors of metabolism (IEM): The ClinGen IEM Working Group and the Phenylalanine Hydroxylase GeneDiane B Zastrow, Heather Baudet, Wei Shen, 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 2