描述
Oncology
Solid Tumor Testing Solutions
Sequanta provides comprehensive genomic profiling solutions for solid tumor biomarker testing, covering tissue testing, liquid biopsy, and MRD dynamic monitoring.
描述
FoundationOne CDx Series -
Exclusive Authorization, Supporting Global Multi-Center Clinical Trials
Foundationone CDx (F1CDx) and Foundationone Liquid CDx (F1 Liquid CDx) are FDA-approved tumor NGS large-panel companion diagnostic products. They detect 324 genes along with immunotherapy biomarkers such as MSl-H/dMMR and TMB, and have become the standard testing methods for international multi-center clinical trials.
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TSO500 Series
TSO500 (TruSight Oncology 500) is a pan-cancer NGS testing product launchedby Illumina. Through a single test, it can simultaneously analyze 523 DNA genes and 55 RNA genes, detecting variants such as SNVs, Indels, CNVs, and genefusions, while calculating TMB, MSI, and HRD biomarkers. This provides acomprehensive genomic analysis solution for the precision diagnosis andtreatment of solid tumors.
1. The first clinical trial partner for Illumina TSO 500 in China.
2. Passed CAP NGSST, NGSHM (Hematological Malignancies), RNA,and other proficiency testing (PT) with perfect scores.
3. Supports 523-gene comprehensive genomic profiling.
4. The full series of products has been validated and launched.
描述
  • 25+
    Conducted 25+ Global Multi-Center Clinical Trials
  • 5000+
    Tested over 5,000 Global Samples
OncoCODE769 Series
Based on the NGS platform, this panel includes 769 critical pathway genes related to tumor occurrence, development, and treatment,. It conducts detections for Single Nucleotide Variants (SNV), Insertions/Deletions (INDEL), Fusions (FUSION), Copy Number Variations (CNV), Tumor Mutational  Burden (TMB), Microsatellite Instability (MSI), and Human Leukocyte Antigen  (HLA) Class mInolecule genotyping.
It covers all common solid tumors. it is applicable for targeted, immumem and chemotherapy drugs, supports genetic susceptibility risk assessment, and simultaneously facilitates the exploration of tumor occurrence and development mechanisms, providing references for prognosis and diagnosis.
描述
  • 70000+
    Tissue Test
  • 50000+
    Plasma ctDNA Tests

Core Applications Profiled
1. TMB/MSI Related.
2. HLA/MED score.
3. Chemotherapy toxicity and efficacy related
4. Diagnosis and subtyping related.
5. Prognosis related biomarkers
Solid Tumor MRD
Detecting circulating tumor DNA (ctDNA) for Molecular Residual Disease (MRD) after surgery or the completion of standard systemic therapy can indicate poor prognosis and screen for high-risk recurence populations. Incorporating ctDNA endpoints into prospective randomized clinical trials is essentlal for furthergenerating evidence to support the regulatory and clinical application of ctDNA.
Sequanta provides two solid tumor MRD solutions: a fixed panel (plasma -informed) and personalized panel customization (tumorinformed).
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  • 40000+
    MRD/Liquic Samples Processed
  • 3000+
    Custumized Profiles Cpmpleted