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Alex H Wagner

Showing results (41-50 of 52) with videos related to

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Nature|November 12, 2025
GREGoR: accelerating genomics for rare diseasesMoez Dawood, Ben Heavner, Marsha M Wheeler, et al.
BMC Genomics|December 5, 2021
Discovery of clinically relevant fusions in pediatric cancerStephanie LaHaye, James R Fitch, Kyle J Voytovich, et al.
Experimental Hematology|May 17, 2016
Comprehensive genomic analysis reveals FLT3 activation and a therapeutic strategy for a patient with relapsed adult B-lymphoblastic leukemiaMalachi Griffith, Obi L Griffith, Kilannin Krysiak, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 1, 2022
Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)Peter Horak, Malachi Griffith, Arpad M Danos, et al.
Database : the Journal of Biological Databases and Curation|May 26, 2022
A Simple Standard for Sharing Ontological Mappings (SSSOM)Nicolas Matentzoglu, James P Balhoff, Susan M Bello, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 5, 2022
Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)Peter Horak, Malachi Griffith, Arpad M Danos, et al.
Nature Genetics|February 1, 2017
CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancerMalachi Griffith, Nicholas C Spies, Kilannin Krysiak, et al.
Nature Biotechnology|June 15, 2022
The GA4GH Phenopacket schema defines a computable representation of clinical dataJulius O B Jacobsen, Michael Baudis, Gareth S Baynam, et al.
Nature Cancer|May 27, 2022
A community approach to the cancer-variant-interpretation bottleneckKilannin Krysiak, Arpad M Danos, Susanna Kiwala, et al.
Nucleic Acids Research|November 14, 2022
CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebaseKilannin Krysiak, Arpad M Danos, Jason Saliba, et al.
Pageof 6

Showing results (41-50 of 52) with videos related to

Sort By:
Pageof 6
Nature|November 12, 2025
GREGoR: accelerating genomics for rare diseasesMoez Dawood, Ben Heavner, Marsha M Wheeler, et al.
BMC Genomics|December 5, 2021
Discovery of clinically relevant fusions in pediatric cancerStephanie LaHaye, James R Fitch, Kyle J Voytovich, et al.
Experimental Hematology|May 17, 2016
Comprehensive genomic analysis reveals FLT3 activation and a therapeutic strategy for a patient with relapsed adult B-lymphoblastic leukemiaMalachi Griffith, Obi L Griffith, Kilannin Krysiak, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 1, 2022
Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)Peter Horak, Malachi Griffith, Arpad M Danos, et al.
Database : the Journal of Biological Databases and Curation|May 26, 2022
A Simple Standard for Sharing Ontological Mappings (SSSOM)Nicolas Matentzoglu, James P Balhoff, Susan M Bello, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 5, 2022
Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC)Peter Horak, Malachi Griffith, Arpad M Danos, et al.
Nature Genetics|February 1, 2017
CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancerMalachi Griffith, Nicholas C Spies, Kilannin Krysiak, et al.
Nature Biotechnology|June 15, 2022
The GA4GH Phenopacket schema defines a computable representation of clinical dataJulius O B Jacobsen, Michael Baudis, Gareth S Baynam, et al.
Nature Cancer|May 27, 2022
A community approach to the cancer-variant-interpretation bottleneckKilannin Krysiak, Arpad M Danos, Susanna Kiwala, et al.
Nucleic Acids Research|November 14, 2022
CIViCdb 2022: evolution of an open-access cancer variant interpretation knowledgebaseKilannin Krysiak, Arpad M Danos, Jason Saliba, et al.
Pageof 6