Report types supported
Reports generated by the following tools in CLC Genomics Workbench 20.0 can be combined using the Combined Reports tool. In addition to these, reports generated by some tools delivered by plugins are also supported.
- Copy Number Variant Detection (CNVs)
- Create Variant Track Statistics Report
- Indels and Structural Variants
- Map Reads to Reference
- QC for Read Mapping
- QC for Sequencing Reads
- QC for Targeted Sequencing
- RNA-Seq Analysis
- Remove Duplicate Mapped Reads
- Trim Reads
- Whole Genome Coverage Analysis
- Demultiplex Reads