Output from the Identify QIAseq Exome Causal Inherited Variants in Trio ready-to-use workflow
The Identify QIAseq Exome Causal Inherited Variants in Trio ready-to-use workflow produces the following outputs:
- A track list called Genome Browser View (
)
- A combined report (
) summarizing the results for the entire trio analysis
- A read mapping (
) for each family member
- A mapping report () for each family member
- A target region coverage report () and a target region coverage track (
) for each family member
- A variant track (
) for each family member containing annotated and filtered variants
- A variant track () showing de novo variants in the proband.
- A variant track () showing recessive variants in the proband.
- A gene list () with variants containing the identified putative compound heterozygous variants in the proband.
- A gene list () with variants containing the identified recessive variants in the proband.
- A gene list () with variants containing the identified de novo variants in the proband.
- An amino acid track (
) showing de novo mutations
- An amino acid track () showing the recessive variants