P673: Batch ClinVar submission support in ClinGen’s Variant Curation Interface (VCI)

Lignende værker

• P673: Batch ClinVar submission support in ClinGen’s Variant Curation Interface (VCI)
  af: Matthew Wright, et al.
  Udgivet: (2023-01-01)
• P630: ClinGen curation of ClinVar: Improving a critical community resource*
  af: Heidi Rehm, et al.
  Udgivet: (2025-01-01)
• O56: The Clinical Genome Resource (ClinGen): Engaging the patient community in ClinGen’s work through Facebook Hereditary Cancer Groups
  af: Deborah Ritter, et al.
  Udgivet: (2023-01-01)
• P155: The ClinGen framework for naming monogenic diseases*
  af: Courtney Thaxton, et al.
  Udgivet: (2024-01-01)
• P826: Evaluating HLA allele-disease associations in ClinGen: Development of a new curation tool
  af: Ingrid Keseler, et al.
  Udgivet: (2024-01-01)