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Paper Details

Adapting crowdsourced clinical cancer curation in CIViC to the ClinGen minimum variant level data community-driven standards.
Hum Mutat
11
2018
CIViC, ClinGen Allele Registry IDs, cancer
Databases, Genetic, Genetic Testing, Genetic Variation, Genome, Human, Genomics, High-Throughput Nucleotide Sequencing, Humans, Neoplasms, Software
Author NameAffiliation
Arpad M DanosMcDonnell Genome Institute, Washington University School of Medicine
Deborah I RitterBaylor College of Medicine
Alex H WagnerMcDonnell Genome Institute, Washington University School of Medicine
Kilannin KrysiakMcDonnell Genome Institute, Washington University School of Medicine
Dmitriy SonkinNational Cancer Institute
Dmitriy SonkinNational Cancer Institute
Christine M MicheelVanderbilt-Ingram Cancer Center
Matthew D McCoyGeorgetown Lombardi Comprehensive Cancer Center
Shruti RaoGeorgetown Lombardi Comprehensive Cancer Center
Shruti RaoGeorgetown Lombardi Comprehensive Cancer Center
Gordana RacaKeck School of Medicine, University of Southern California
Simina M BocaGeorgetown Lombardi Comprehensive Cancer Center
Simina M BocaGeorgetown Lombardi Comprehensive Cancer Center
Angshumoy RoyBaylor College of Medicine
Erica K BarnellMcDonnell Genome Institute, Washington University School of Medicine
Joshua F McMichaelMcDonnell Genome Institute, Washington University School of Medicine
Joshua F McMichaelMcDonnell Genome Institute, Washington University School of Medicine
Susanna KiwalaMcDonnell Genome Institute, Washington University School of Medicine
Adam C CoffmanMcDonnell Genome Institute, Washington University School of Medicine
Lynzey KujanMcDonnell Genome Institute, Washington University School of Medicine
Shashikant KulkarniBaylor College of Medicine
Shashikant Kulkarni
Shashikant KulkarniDan L. Duncan Cancer Center
Malachi GriffithMcDonnell Genome Institute, Washington University School of Medicine
Subha MadhavanGeorgetown Lombardi Comprehensive Cancer Center
Subha MadhavanGeorgetown Lombardi Comprehensive Cancer Center
Obi L GriffithMcDonnell Genome Institute, Washington University School of Medicine
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Datasets

ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink