TruSight Tumor 26

TruSight Tumor 26 takes a deeper view of variation in solid tumors including lung, colon, melanoma, gastric and ovarian. This enables clinical researchers to identify low-frequency variation across 26 genes for a more comprehensive view of somatic variation.

• Highly accurate variant analysis at limit of detection below 5% variant allele frequency across 174 amplicons, with 1000x minimum coverage of each region
• Exceptional sample success rates with minimal DNA input for accurate base calling, even in degraded FFPE samples
• Coverage of complete exons for analysis of molecular heterogeneity in highly relevant content selected from CAP¹ and NCCN² guidelines, and late stage clinical trials³

This panel provides amplicon-based library preparation reagents, DNA QC, sample indexes, and oligos targeting identified regions of interest.

Genes in TruSight Tumor 26

See which solid tumor-related genes are represented in TruSight Tumor 26. View Gene List.

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