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Alex H Wagner

Showing results (31-40 of 52) with videos related to

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Human Mutation|October 13, 2018
Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community-driven standardsArpad M Danos, Deborah I Ritter, Alex H Wagner, et al.
Advanced Genetics (Hoboken, N.J.)|March 13, 2023
GA4GH Phenopackets: A Practical IntroductionMarkus S Ladewig, Julius O B Jacobsen, Alex H Wagner, 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.
Genome Biology|June 25, 2025
Mapping MAVE data for use in human genomics applicationsJeremy A Arbesfeld, Estelle Y Da, James S Stevenson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 6, 2018
Standard operating procedure for somatic variant refinement of sequencing data with paired tumor and normal samplesErica K Barnell, Peter Ronning, Katie M Campbell, et al.
Genome Medicine|November 30, 2019
Standard operating procedure for curation and clinical interpretation of variants in cancerArpad M Danos, Kilannin Krysiak, Erica K Barnell, et al.
Cell Genomics|March 21, 2022
The GA4GH Variation Representation Specification: A computational framework for variation representation and federated identificationAlex H Wagner, Lawrence Babb, Gil Alterovitz, et al.
Nature Communications|September 19, 2018
Recurrent WNT pathway alterations are frequent in relapsed small cell lung cancerAlex H Wagner, Siddhartha Devarakonda, Zachary L Skidmore, et al.
Arxiv|January 7, 2025
GREGoR: Accelerating Genomics for Rare DiseasesMoez Dawood, Ben Heavner, Marsha M Wheeler, et al.
Nature Genetics|April 5, 2020
A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancerAlex H Wagner, Brian Walsh, Georgia Mayfield, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Human Mutation|October 13, 2018
Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community-driven standardsArpad M Danos, Deborah I Ritter, Alex H Wagner, et al.
Advanced Genetics (Hoboken, N.J.)|March 13, 2023
GA4GH Phenopackets: A Practical IntroductionMarkus S Ladewig, Julius O B Jacobsen, Alex H Wagner, 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.
Genome Biology|June 25, 2025
Mapping MAVE data for use in human genomics applicationsJeremy A Arbesfeld, Estelle Y Da, James S Stevenson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 6, 2018
Standard operating procedure for somatic variant refinement of sequencing data with paired tumor and normal samplesErica K Barnell, Peter Ronning, Katie M Campbell, et al.
Genome Medicine|November 30, 2019
Standard operating procedure for curation and clinical interpretation of variants in cancerArpad M Danos, Kilannin Krysiak, Erica K Barnell, et al.
Cell Genomics|March 21, 2022
The GA4GH Variation Representation Specification: A computational framework for variation representation and federated identificationAlex H Wagner, Lawrence Babb, Gil Alterovitz, et al.
Nature Communications|September 19, 2018
Recurrent WNT pathway alterations are frequent in relapsed small cell lung cancerAlex H Wagner, Siddhartha Devarakonda, Zachary L Skidmore, et al.
Arxiv|January 7, 2025
GREGoR: Accelerating Genomics for Rare DiseasesMoez Dawood, Ben Heavner, Marsha M Wheeler, et al.
Nature Genetics|April 5, 2020
A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancerAlex H Wagner, Brian Walsh, Georgia Mayfield, et al.
Pageof 6