OncoCDx Panel is a pan-solid tumor panel product independently developed by MEDx Translational Medicine. This assay uses Probe-Based Hybridization Capture and Next Generation Sequencing (NGS) technology for the detection of gene mutations, such as point mutations, insertion/ Deletion, copy number variation, fusion/rearrangement, and other mutation types. To meet clinical needs, MEDx provides patients with a cost-effective genetic testing in order to direct clinicians to select right medicine for a right patient, called personalized medicine involving targeted therapy, immunotherapy, and chemotherapy for the cancers.
The detection area and function of this assay are shown in Figure 1
【Certification】Refer to NCCN, CSCO, and other institutional guidelines and unified consensus, including all the drug genes with clear clinical significance.
【Precise】The industry's highest sequencing depth, and low-frequency loci not missed.
【Cost-effective】Gene detection can be performed at the initial diagnosis, postoperation, relapse and drug resistance stages of cancers, and real-time gene mutation results can be obtained.
【Assure】Has an exclusive genetic counseling team to provide each customer with personalized genetic testing report with interpretation.
【comprehensive】Full-featured: One-time detection can be used to guide targeted therapy, chemotherapy, and immunotherapy for cancers, as well as to analyze hereditary tumors.
Comprehensive sites: detection of 191 tumor-related genes with all-exon regions, rare targets are not missed.
【high quality】The best raw materials: imported raw materials are used for testing to ensure the quality of testing from the primary cancers.
Strict quality control: HE staining and white blood cell control detection, to fully guarantee the quality of the test.
If you have any of the following needs, feel free to contact us or email us at inquiry@MEDxTMC.net . We will reply within 24 hours.
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