Using ClinVar as a Resource to Support Variant Interpretations

समान संसाधन

• ClinVar Is a Critical Resource to Advance Variant Interpretation
  द्वारा: Rehm, Heidi L., और अन्य
  प्रकाशित: (2017)
• Points to consider for sharing variant-level information from clinical genetic testing with ClinVar
  द्वारा: Azzariti, Danielle R., और अन्य
  प्रकाशित: (2018)
• ClinVar Miner: Demonstrating Utility of a Web-Based Tool for Viewing and Filtering ClinVar Data
  द्वारा: Henrie, Alex, और अन्य
  प्रकाशित: (2018)
• Clinical Laboratories Collaborate to Resolve Differences in Variant Interpretations Submitted to ClinVar
  द्वारा: Harrison, Steven M., और अन्य
  प्रकाशित: (2017)
• Is ‘likely pathogenic’ really 90% likely? Reclassification data in ClinVar
  द्वारा: Harrison, Steven M., और अन्य
  प्रकाशित: (2019)