GeneRead QIAact Custom Panels
For targeted sequencing of the variants most relevant to your research
- Select the genomic regions of most relevance to your medical research
- All mutation types: SNVs, InDels, CNVs and fusions
- For use with FFPE and liquid biopsy samples
- Uniform sequence coverage enabled by UMI technology
- Integrated as part of a complete Sample to Insight NGS workflow including full bioinformatics analysis and interpretation
