The next-generation sequencing (NGS)-based HTG EdgeSeq Precision Immuno-Oncology Panel is designed to measure the immune response both inside the tumor and the surrounding microenvironment. HTG’s quantitative nuclease protection assay does not require nucleic acid extraction and is automated using the HTG EdgeSeq processor. By leveraging the high sensitivity and dynamic range of NGS instrumentation, this powerful tool interrogates 1,392 genes from a single section of formalin-fixed, paraffin-embedded (FFPE) tissue, extracted RNA, or PAXgene samples.
The breadth of the immune response in a tumor can be measured using the HTG EdgeSeq Precision Immuno-Oncology Panel. Relatively higher levels of IFNG (interferon γ), a key pro-inflammation cytokine, are measured in non-small cell lung cancer samples 3 and 5. IFNG production stimulates the production of T-cell attractant chemokines CXCL9, CXCL10, and CCL5, with a subsequent increase in production of cytolytic molecules such as perforin and granzymes.
Immune loads of NSCLC tumors were assessed using T cell (CD3, CD4, and CD8) markers as well as CD68 (macrophages, myeloid cells). A range of expression was obtained indicating variable loads of immune cells.
Genes associated with WNT (WNT5A) and EMT drivers (ZEB1, TWIST1) are more highly expressed in tumors with lower immune loads. NK cells (NCAM1) are seen at higher levels in tumors with WNT and/or EMT activity, consistent with the literature report.
HTG EdgeSeq Reveal is a powerful software product that streamlines analysis of biomarker data from samples analyzed with the
HTG EdgeSeq Precision Immuno-Oncology Panel on the HTG EdgeSeq system. HTG EdgeSeq Reveal enables characterization and visualization of immune response in the tumor environment which continues to be an important step in developing biomarker strategies to understand the body’s immune response in relation to cancer biology and potential response to mono- and combination therapies. The HTG EdgeSeq Reveal was designed to be a scalable, flexible data analysis product that will expand with new applications to support HTG’s growing translational research product portfolio.
HTG’s new product, when coupled with the HTG EdgeSeq Precision Immuno-Oncology Panel, enables applications such as:
Together with the HTG EdgeSeq system, customers using the new HTG EdgeSeq Reveal product will have the ability to conduct molecular profiling using a wide variety of sample types, potentially enabling them to accelerate discovery, support translational applications, and determine potential biomarkers for development of companion diagnostics.
For more information and a product demonstration, contact your HTG representative.
When placing an order, please specify the catalog number. The HTG EdgeSeq Precision Immuno-Oncology Panel is compatible with Illumina sequencers .
916-011-208 HTG EdgeSeq Precision I/O Panel (2X8)
916-011-008 HTG EdgeSeq Precision I/O Panel (4X8)
916-011-224 HTG EdgeSeq Precision I/O Panel (1X24)
916-011-024 HTG EdgeSeq Precision I/O Panel (4X24)
916-011-096 HTG EdgeSeq Precision I/O Panel (1X96)
916-011-308 HTG EdgeSeq Precision I/O Panel (2x8)
916-011-108 HTG EdgeSeq Precision I/O Panel (4x8)
916-011-324 HTG EdgeSeq Precision I/O Panel (1x24)
916-011-124 HTG EdgeSeq Precision I/O Panel (4x24)
916-011-196 HTG EdgeSeq Precision I/O Panel (1x96)
Learn more about the HTG EdgeSeq Precision Immuno-Oncology Panel
Tech Note: Immunophenotyping Lymphocytes in Tumors
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Tech Note: Measuring Immune Checkpoint Genes from FFPE Tissue
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Tech Note: Assessing Tumor Inflammation
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Tech Note: Epithelial Mesenchymal Transition in Immuno-Oncology
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HTG EdgeSeq Precision Immuno-Oncology Panel Product Sheet
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Annotated Gene List HTG EdgeSeq Precision Immuno-Oncology Panel
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HTG EdgeSeq Precision Immuno-Oncology Panel Gene List
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Tislelizumab plus chemotherapy as first-line treatment for recurrent or metastatic nasopharyngeal cancer: A multicenter phase 3 trial (RATIONALE-309)
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Phase II trial of neoadjuvant sitravatinib plus nivolumab in patients undergoing nephrectomy for locally advanced clear cell renal cell carcinoma
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Tumor Microenvironment and Its Clinicopathologic and Prognostic Association in Cutaneous and Noncutaneous Angiosarcomas
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Co-enrichment of CD8-positive T cells and macrophages is associated with clinical benefit of tislelizumab in solid tumors
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Understanding the immune microenvironment of pancreatic ductal adenocarcinoma patients. A transcriptomic study.
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25P - Prognostic classification of endometrial cancer according to transcriptomic-based immunophenotype
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Tumor Microenvironment and Its Clinicopathologic and Prognostic Association in Cutaneous and Noncutaneous Angiosarcomas
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Understanding the immune microenvironment of pancreatic ductal adenocarcinoma patients. A transcriptomic study.
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Prognostic classification of endometrial cancer
according to transcriptomic based immunophenotype
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SABCS 2022: P3-05-09: vLAG3+ Tumor Infiltrating Lymphocytes Predict Outcome in Treatment Naïve Triple Negative Breast Carcinoma
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Gene Expression Profiling of CD23+ T(14;18)-negative follicular lymphoma demonstrates activation of the IL4/JAK/STAT6 pathway and a role in its pathogenesis
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Nivolumab in patients with relapsed or refractory peripheral T-cell lymphoma: modest activity and cases of hyperprogression
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Evaluation of the EdgeSeq Precision Immuno-Oncology Panel for Gene Expression Profiling From Clinical Formalin-Fixed Paraffin-Embedded Tumor Specimens
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CD8 T cells and macrophage abundances associated with clinical benefit of tislelizumab in various tumor types
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The combination of hyper-amplification and tumor mutational burden as a pan-cancer biomarker in patients treated with tislelizumab
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Genetic and phenotypic attributes of splenic marginal zone lymphoma
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360 Tumor-immune signatures associated with response or resistance to tislelizumab in patients with previously treated advanced hepatocellular carcinoma (HCC)
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High-dimensional and single-cell transcriptome analysis of tumor microenvironment in angioimmunoblastic T cell lymphoma AITL)
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CD73 expression defines immune, molecular, and clinicopathological subgroups of lung adenocarcinoma
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HTG EdgeSeq technology offers a competitive alternative to RNA-Seq with equivalent performance and distinct advantages.
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Sarcomatoid Renal Cell Carcinoma Demonstrates an Immunosuppressive Tumor Microenvironment - Implication for Therapeutic Benefit in the Immunotherapy Era
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Next Generation Sequencing and Functional Pathway Analysis to Understand the Mechanism of Action of Copper-Tolfenamic Acid Against Pancreatic Cancer.
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Neutrophil content predicts lymphocyte depletion and anti-PD1 treatment failure in NSCLC
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Genetic associations of T cell cancer immune response with tumor aggressiveness in localized prostate cancer patients and disease reclassification in an active surveillance cohort.
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Pazopanib for treatment of advanced malignant and dedifferentiated solitary fibrous tumour: a multicentre, single-arm, phase 2 trial
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Dynamic change of immune-related gene expression status during chemoradiotherapy in locally advanced esophageal cancer
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For further information about the HTG EdgeSeq Precision Immuno-Oncology Panel, please fill out the registration form below or call us at (877) 507-3259.
Page last updated June 29, 2022