Outputs from QIAseq Fastq to Annotated Somatic Variants
The QIAseq Fastq to Annotated Somatic Variants template workflow produces the following outputs:
- Somatic Variants The variant track (
) with the annotated variants.
- LightSpeed Report A report (
) summarizing details of each analysis step performed by the LightSpeed Fastq to Somatic Variants tool.
- Inversions An annotation track (
) providing the called inversions.
- Ignored Regions An annotation track () providing regions where it was not possible to detect variants due to high complexity among the initial variants being tested.
- Mapped UMI Reads A read mapping track (
) with the mapped UMI reads.
- Amino Acid Track A track (
) providing a graphical representation of identified amino acid changes.
- Genome Browser View A track list (
) containing the Variants, the Inversions, the Ignored regions, the Amino Acid Track, the Mapped UMI Reads, the Target Region Statistics Track, the Gene-level CNV Track, the Target regions as well as the Reference sequence and the Genes, mRNA and CDS tracks.
- Sample Report A report () containing essential information from all reports produced by the workflow. For further details, see https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=Create_Sample_Report.html.
- Target Region Statistics Track A track () providing coverage information per target region.
- Coverage Report A report () summarizing coverage.
- Gene Coverage Track An annotation track () providing coverage informtion at the gene level.
- Target-level CNV Track An annotation track () providing CNV results per target.
- Region-level CNV Track An annotation track () providing CNV results per region, where regions are formed from adjacent targets with similar CNV states.
- Gene-level CNV Track An annotation track () providing CNV results per gene.
- CNV Results Report A report () providing an overview of identified CNVs.