IRVING, Texas, May 31, 2013 /PRNewswire/ -- Caris Life Sciences™, a leading biosciences company focused on fulfilling the promise of personalized medicine, today announced it intends to expand its Next-Generation Sequencing (NGS) capabilities to include whole exome and transcriptome sequencing. The offering will provide physicians with an in-depth report focusing on the 452 well-documented somatic alterations present across all cancer types.
Once launched, this expanded mutational analysis will be available for order as a standalone panel or in combination with other molecular tests. This 450-plus gene profile will include all relevant genomic alterations, including translocations, rearrangements, copy number alterations, base substitutions, insertions and deletions. The expanded profile utilizes the COSMIC database to identify and include every gene that has been shown to contain alterations in any type of cancer. As new genes important to the understanding of cancer are identified, they can quickly be included in the report prepared for physicians, ensuring that patients receive the most comprehensive and up-to-date information available. Increasing the breadth of genes profiled will provide the next level of biomarker analysis, and will complement the company's flagship molecular profiling offering, which already equips oncologists with the most clinically actionable biomarker data and drug correlations available today.
"Our molecular profiling service, Caris Molecular Intelligence™, utilizes the most relevant technologies to interrogate proteins, RNA and DNA," said David D. Halbert , Chairman and Chief Executive Officer of Caris Life Sciences. "We've found that many of our customers were curious to see more genetic mutations, so as the leading service provider in the molecular profiling space, we wanted to be responsive and further develop our DNA and RNA mutational
|SOURCE Caris Life Sciences|
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