Paper Details

Paper Title

Somatic cancer variant curation and harmonization through consensus minimum variant level data.

Paper Journal Title

Genome Med

Paper Citation Count

Paper Publication Year

2016

Bio Mention

ClinVar, MVLD, allele, cancer, cancer sequence variants, cancer variants, multiple cancer

Mesh Descriptor

Author Name	Affiliation
Deborah I Ritter	Baylor College of Medicine and Texas Children's Hospital
Angshumoy Roy	Baylor College of Medicine and Texas Children's Hospital
Shruti Rao	Innovation Center for Biomedical Informatics and Lombardi Comprehensive Cancer Center, Georgetown University Medical Center
Shruti Rao	Innovation Center for Biomedical Informatics and Lombardi Comprehensive Cancer Center, Georgetown University Medical Center
Melissa J Landrum	National Center for Biotechnology Information
Dmitriy Sonkin	National Cancer Institute
Dmitriy Sonkin	National Cancer Institute
Reece K Hart
Christine M Micheel	Vanderbilt University School of Medicine
Eliezer M Van Allen	Dana-Farber Cancer Institute
Eliezer M Van Allen	Dana-Farber Cancer Institute
Donald W Parsons	Baylor College of Medicine and Texas Children's Hospital
Donald W Parsons	Baylor College of Medicine and Texas Children's Hospital
Howard L McLeod	Moffitt Cancer Center
Howard L McLeod	Moffitt Cancer Center
Sharon E Plon	Baylor College of Medicine and Texas Children's Hospital
Shashikant Kulkarni	Baylor College of Medicine and Texas Children's Hospital
Subha Madhavan	Innovation Center for Biomedical Informatics and Lombardi Comprehensive Cancer Center, Georgetown University Medical Center
Subha Madhavan	Innovation Center for Biomedical Informatics and Lombardi Comprehensive Cancer Center, Georgetown University Medical Center

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

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