Targeted Panel Assays:
Plasma-Safe-SeqS (PSS) Technology
HNSCC-SEQ:
Reliable detection of clinically relevant mutations in HPV-negative HNSCC
AML-SEQ™ :
Ultra-sensitive detection of the most common Acute Myeloid Leukemia (AML) biomarkers with maximum efficiency.
AML-MRD-SEQ:
Reliable detection of AML-MRD relevant and promising mutations. AML-MRD-SEQ detects 68 mutations across 20 genes, including established AML markers, such as IDH1, IDH2, and NPM1, and it demonstrates a significant potential for use as an investigational tool for other markers with prognostic values that are not yet well established.
RAS-RAF-SEQ:
Detection of mutations in the five most relevant targets for cancers (e.g., colorectal, pancreatic, gallbladder, ovarian, and lung) impacted by the RAS-RAF and PI3K signaling pathways.
BC-SEQ:
BC-SEQ detects mutations in established and emerging predictive markers, resistance mutations, and frequently occurring genetic alterations in breast cancer.
Plasma-Safe-SeqS panel | Clinically relevant gene regions | Intended uses |
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RAS-RAF-SEQ RAS-RAF Pathway | BRAF, KRAS, NRAS, AKT1, PIK3CA | |
HPV-SEQ & HPV Pathway | HPV 16, HPV 18 | |
BC-SEQ & Breast Cancer | AKT1, ERBB2, ESR1, KRAS, PIK3CA, TP53 | |
AML-MRD-SEQ & AML MRD | FLT3, IDH1, IDH2, NPM1, BCOR, BRAF, CEBPA, GATA2, JAK2, KIT, KRAS, NRAS, PRPF8, PTPN11, SETBP1, SF3B1, SRSF2, TP53, U2AF1, ZRSR2 | |
HNSCC-SEQ & H&N HPV(-) cancers | CDKN2A, EGFR, ERBB2, FGFR3, HRAS, KRAS, NOTCH1, PIK3CA, PTEN, TP53 |
Plasma-Safe-SeqS technology platform general test specifications
Cell-free DNA analysis for solid tumors | Hematological malignancies | |
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Sample types accepted |
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Sample requirements |
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Turnaround time |
7 – 10 Business days | |
Performance |
Plasma-Safe-SeqS can detect between 5-7 mutant molecules (95% CI) irrespective of the amount of wildtype DNA present and/or the panel configuration. For 33 ng DNA input, this corresponds to 0.05-0.07% mutant allele frequency (MAF). |