Remove variants tools

Comparison with known variants from variant databases is a key concept when working with resequencing data. The CLC Cancer Research Workbench provides two types of tools for facilitating this task: one for adding information to your experimental variants with information from known variants (e.g. adding information about phenotypes like cancer associated with a certain variant allele), and one for removing your experimental variants based on this information (e.g. for removing common variants).



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