GeneRead QIAact BRCA 1/2 Panel
For breast and ovarian cancer insights from FFPE samples on the GeneReader NGS System
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Full coverage: all coding regions of BRCA 1 and 2 + 20 bp flanking intronic regions
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All mutations: germline or somatic, mutations or deletions
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Proven performance with automation on the GeneReader NGS System
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Integrated as part of a complete Sample to Insight workflow including bioinformatics analysis and interpretation
The GeneRead QIAact BRCA 1/2 panel comprises 253 pooled primer pairs custom designed to cover all coding regions of the BRCA 1 and 2 genes, including 20bp flanking regions in adjacent introns. Designed as an integrated part of the GeneReader NGS System, and incorporating QIAGEN’s pre-eminent QCI automated bioinformatics for analysis and interpretation, this panel enables clinical research insights into both breast and ovarian cancers from 40 ng of input material. Target enriched DNA with the GeneRead QIAact BRCA 1/2 panel is ready for fully automated library preparation on the QIAcube instrument in the next step of the workflow.
