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    GenMineTOP Cancer Genome Profiling System utilizes next-generation sequencing to perform simultaneous analysis of DNA and RNA from paired tumor tissue specimen and non-tumor blood specimen to deliver broad detection of gene variants related to cancer. The comprehensive panel includes variant analysis of 737 cancer-related genes, including base substitutions, insertion/deletions and copy number aberrations, and RNA gene fusion detection in 455 genes, exon-skipping detection in 5 cancer-related genes, and expression profiling of 27 cancer-related genes.
    Cancer:
    Solid Tumor
    Method:
    Next-Generation Sequencing (NGS)