How to Use OpenCravat for Cancer Variant Annotation?
Using OpenCravat involves several steps:
Input Data: Upload your genomic variants data in a supported format (e.g., VCF). Select Annotation Tools: Choose from a variety of built-in annotation tools tailored for cancer research. Run Analysis: Execute the analysis pipeline, which annotates the variants and provides detailed reports. Interpret Results: Review the annotated data to identify significant mutations and potential therapeutic targets.
