9. Variant detection and reporting
- 9.1. Which steps should I follow to perform a resequencing analysis in the CLC Genomics Workbench?
- 9.2. How to add flanking sequence to variants in the CLC Genomics Workbench?
- 9.3. How can I get amino acid prediction information for the variants in my data?
- 9.4. How are the homozygous and heterozygous calls determined?