The genes in CancerSELECT 125 were selected to aid in treatment decision-making based on their biological and functional relevance and clinical actionability. They include both likely and known regions associated with drug sensitivity and acquired drug resistance. CancerSELECT 125 identifies tumor-specific sequence mutations, amplifications, structural rearrangements and other alterations in tissue across multiple cancer types. CancerSELECT 125 also reports microsatellite instability status (MSI) to assess potential response to checkpoint inhibitor therapies--tumors with high MSI have been shown to have a much greater clinical response to these immunotherapies. CancerSELECT 125 additionally includes matched sequencing of normal patient tissue to accurately filter out germline variants and increase confidence that the identified alterations are truly somatic.
The exceptional accuracy afforded by CancerSELECT 125 reflects a number of PGDx's unique technologies and methods. These include the company's DNA extraction and proprietary sample preparation methods that accommodate low abundance DNA samples and its proprietary hybrid-capture processing in combination with high-coverage, next-generation sequencing. PGDx's proprietary PARE and Digital Karyotyping technologies, combined with its VariantDx™ computational algorithms, ensure that bona fide mutations are distinguished from sequencing artifacts and errors. All test results receive visual inspection by cancer genome experts and are accompanied by comprehensive clinical annotation of all the reported alterations, including FDA-approved therapies, clinical trials and published literature.
For more information on the CancerSELECT 125, click here.
PGDx offers a complete range of cancer genome analysis tools, including exome and targeted approaches for tissue specimens, targeted approaches for plasma samples, and a variety of custom tissue and plasma-based options designed to address the specific research needs of cancer researchers and drug developers. PGDx's service offerings for researchers and testing labs are complemented by the clinical services it provides through its CLIA-certified laboratory.
About Personal Genome Diagnostics
Personal Genome Diagnostics (PGDx) advances the frontiers of cancer medicine through innovative genomic technologies for oncology researchers, drug developers, clinicians and patients. The expert team at PGDx draws on a deep understanding of cancer biology, extensive experience in cancer genomics and clinical oncology, and the company's distinctive technologies. It was established in 2010 by researchers from Johns Hopkins University who are pioneers in cancer genome sequencing and liquid biopsy technologies. Under the leadership of founders Drs. Luis Diaz and Victor Velculescu, the company has achieved consistent growth by successfully commercializing novel clinical and investigational products and services. These novel technologies precisely identify and characterize unique genomic alterations in tumors. PGDx is working toward broad patient access to its genomic approaches, through a CLIA-certified facility providing comprehensive genomic services, as well as its PROGENEUS™ technology transfer solution and in vitro diagnostic products to enable other molecular laboratories to easily internalize genomic testing. For additional information, visit personalgenome.com.
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SOURCE Personal Genome Diagnostics Inc.