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21 - 28 of 28
File
Intramural Genomic Data Sharing Plan - October 2020
… GEO ☐ dbVar dbSNP Sequence Read Archive (SRA) 1☐ GenBank ☐ ClinVar ☐ Model Organism Database (specify): ☐ Yes ☐No Are …
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Clinical Sequencing Exploratory Research Consortium.pdf
… Ancestry • Contribute to national databases of variants (ClinVar) • We will likely come across these again Rate of … by Ancestry Group 626 variant classifications deposited to ClinVar EVS 6503, Pathogenic Cancer Variants Amendola et al., …
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Clnical Sequencing Evidence-gathering Research (CSER 2).pdf
… sequence and variant interpretation data with dbGaP and ClinVar , it will also pilot the exchange of multiple data …
File
American College of Medical Genetics and Genomics Report.pdf
… their variant interpretations in the public domain through ClinVar, differences in variant interpretation will be … the genome with community-driven approaches and ClinVar activities. Finally, the Closing Plenary Session, …
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Report- NAM Report on Evidence Framework for Genetic Testing.pdf
… participate fully in evidence repositories (such as ClinVar) and work with partners to improve the clinical …
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2016 International Summit in Human Genetics and Genomics Meeting Agenda
… Section, NINDS 9.15 - 10.15 am Genetic Databases (ClinVar, dbGap, GTR) Dr. Wendy Rubinstein , Senior Scien …
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Integrating Genomic Sequencing into Clinical Care- CSER and Beyond.pdf
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2020 International Summit Annual Report
… (43), cancer (332), dementia (88); Reported a variant to ClinVar; Initiated registryfor breast -ovarian cancer, …