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Almac validated Illumina TruSight™ Tumor 170 cancer mutation panel. The assay is CLIA compliant for prospective clinical trial use, including Europe and the US

Almac Clinical Trial Assay

Almac Diagnostic Services has invested in the validation of this CLIA compliant assay and the full validation report is available on request.

Read the Validation Performance Specification

This Almac Diagnostic Services clinical trial assay will provide Pharmaceutical and Biotech companies with a new option in the marketplace to support their clinical trials and CDx development. The assay, based on the Illumina TruSight™ Tumor 170 chemistry and NextSeq platform, allows multiple biomarkers to be evaluated from one sample, thereby reducing the quantity of precious tissue sample necessary and offering a highly cost effective solution that will ultimately be kit-able further downstream.

Almac Diagnostic Services offer clients powerful reporting for the assay through our own bioinformatics pipeline and software solution providing enhanced variant call reproducibility, accuracy and QC.

Contact us today to discuss your requirements for future clinical trial enrichment.

Almac RUO Assay

Almac Diagnostic Services also offer Illumina TruSight™ Tumor 170 panel as a research use only (RUO) assay. Should clients need further RUO interpretation of detected variants, Almac can offer ‘IBM – Watson for Genomics’ reporting for processed samples.

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