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archerdx fusionplex pan solid tumor v2 panel primers  (Danaher)

 
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    Danaher archerdx fusionplex pan solid tumor v2 panel primers
    Archerdx Fusionplex Pan Solid Tumor V2 Panel Primers, supplied by Danaher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fusionplex+pan+solid+tumor+v2+panel/pm39489385-68-10-17?v=Danaher
    Average 90 stars, based on 1 article reviews
    archerdx fusionplex pan solid tumor v2 panel primers - by Bioz Stars, 2026-07
    90/100 stars

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    Image Search Results


    Relevant parameters for the bioinformatic pipeline used for the analysis of the Archer FusionPlex Pan Solid Tumor v2 assay.

    Journal: CytoJournal

    Article Title: Precision medicine for patients with salivary gland neoplasms: Determining the feasibility of implementing a next-generation sequencing-based RNA assay in a hospital laboratory

    doi: 10.25259/Cytojournal_152_2024

    Figure Lengend Snippet: Relevant parameters for the bioinformatic pipeline used for the analysis of the Archer FusionPlex Pan Solid Tumor v2 assay.

    Article Snippet: Residual formalin-fixed paraffin-embedded salivary gland neoplasm specimens from a cohort of 17 patients were analyzed with the Archer FusionPlex Pan Solid Tumor v2 panel by NGS on an Illumina NextSeq550 platform.

    Techniques:

    Capabilities of selected NGS assays for detection of targetable alterations in NSCLC.

    Journal: Current Oncology

    Article Title: Consensus Recommendations to Optimize Testing for New Targetable Alterations in Non-Small Cell Lung Cancer

    doi: 10.3390/curroncol29070396

    Figure Lengend Snippet: Capabilities of selected NGS assays for detection of targetable alterations in NSCLC.

    Article Snippet: FusionPlex Pan Solid Tumor v2 Panel [ ] , RNA , Anchored Multiplex PCR , Illumina ® and Ion TorrentTM , can only detect MET ex14 skipping, SNVs in KRAS, ERBB2 , and BRAF, MET and NRG1 fusions , 137 gene targets; 17 SNV/indels, 137 fusions/splicing/exon skipping , SNVs, indels, fusions.

    Techniques: Variant Assay, Amplification, Gene Expression, Clinical Proteomics, Multiplex Assay