Description:
Enhance the Variant-Linker tool to support Copy Number Variants (CNVs). This will allow users to analyze and annotate CNVs along with other types of genetic variants.
Acceptance Criteria:
Implement functionality to detect and process CNV inputs.
Integrate CNV-specific annotations from relevant sources.
Ensure that the tool can handle CNV-specific data fields and formats.
Update the documentation to describe how to use the tool for CNV analysis.
Description: Enhance the Variant-Linker tool to support Copy Number Variants (CNVs). This will allow users to analyze and annotate CNVs along with other types of genetic variants.
Acceptance Criteria:
Labels: enhancement, feature