TruSight Tumor 26

TruSight Tumor 170

TruSight Tumor 170, a next-generation sequencing assay designed to cover 170 genes associated with common solid tumors, is an enrichment-based targeted panel that simultaneously analyzes DNA and RNA, covering a wide range of genes and variant types. The comprehensive nature provides laboratories with a deep view into the genetics of cancer.

Catalog ID(s)
OP-101-1003: TruSight Tumor 170 – Library Prep for 24 Samples and Sequencing Consumables for 3 NextSeq runs
OP-101-1004 (24 samples): TruSight Tumor 170 – Library Prep only for 24 Samples

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Project Recommendations*
Species compatibility Human
Recommended Illumina instrument NextSeq 500/550 HiSeq 2500 NovaSeq 6000 (Dual Flow Cell)
Recommended samples per run and chemistry version (eg, 24 on v3) 16 (8 DNA + 8 RNA)
10 if DNA only
16 is RNA only
12 (6 DNA + 6 RNA)
6 if DNA only
12 if RNA only
96 96 192
Run mode High Output Rapid run mode S1 S2 S4
Max recommended read length 2×101 bp 2×101 2×100 bp
Recommended secondary analysis (eg, MiSeq Reporter, Basespace) TruSight Tumor 170 App
Recommended down stream analysis (eg, VariantStudio) There are a number of third party solutions for analysis of variant calls produced by TruSight Tumor 170. Illumina is agnostic to which solution a customer would choose. Consult your Illumina sales representative for more information.

* Library prep is compatible with all Illumina instruments. Recommended instruments chosen based on typical output and analysis need for selected application.

† Limited by index combinations (HT).

‡ NovaSeq S1 Reagent Kits are not currently available.