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![]() Classify cancer specimens across 30 cancer genes in real time to provide a complete pharmacogenomic profile.
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MolecularMD PGx Profiler™ Service offers rapid, sensitive detection of up to 380 known somatic mutations across 30 genes involved in cell growth signaling (see Tables for complete listing). Using as little as 500 nanograms of DNA per sample, a complete oncogenic profile can be generated across hundreds of specimens in days instead of months. Two separate panels are offered tailored to somatic mutations in either solid or hematologic tumors.
This powerful service is ideal for screening and cataloging specimens for predictive mutations linked to response or resistance to targeted cancer therapies. Entire libraries of tumor specimen subtypes can be profiled to support biomarker assay development efforts and early phase clinical research programs.
Panel Profiles **

* This service is intended for investigational use only. Not for use in clinical diagnostic procedures.
** Specific mutations provided upon request.
The mass spectroscopy-based sequencing approach has a sensitivity of 10% mutant allele (twice as sensitive as standard sequencing). Mass spec profiles of all positive results are provided with the final analysis report.
The MolecularMD PGx Profiler Service is offered in collaboration with the Laboratory of Dr. Christopher Corless, Oregon Health & Science University. Dr. Corless is co-director of the Pathology Translational Research Laboratory and a leader in the development and performance of mass spectrometry-based multiplex molecular diagnostics.
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Literature References
THOMAS, R. K., ET AL. High-throughput oncogene mutation profiling in human cancer. Nat Genet 39(3): 347-51.
MACCONAILL LE, CAMPBELL CD, KEHOE SM, BASS AJ, HATTON C, ET AL. (2009) Profiling Critical Cancer Gene Mutations in Clinical Tumor Samples. PLoS ONE 4(11): e7887. doi:10.1371/journal.pone.0007887
Refer to the PGx Profiler.pdf for description and test specifications.