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New version with GRCh38
Overdue by 1 year(s)•Due by March 31, 2024This milestone focuses on creating a new release of the project that incorporates a CNV (Copy Number Variation) version. The CNV version will introduce specific features and enhancements to support the analysis and interpretation of copy number variations in genetic data. This milestone aims to improve the project's capabilities by enabling the annotation, visualization, and analysis of CNVs, empowering clinicians in their genetic investigations.
Overdue by 1 year(s)•Due by December 24, 2023•0/2 issues closedThis milestone aims to create a new release of the project that includes a somatic version. The somatic version will introduce specific features and enhancements to support the interpretation of somatic mutations in genetic data. This milestone will focus on incorporating the necessary functionality to accurately analyze and interpret somatic variants, providing valuable insights for cancer research and personalized medicine applications.
Overdue by 1 year(s)•Due by October 31, 2023•0/3 issues closed