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Precision medicine entails access to genomic testing, including single gene assays and/or large next-generation sequencing (NGS) panels, in a given time point of the patient’s disease trajectory; data interpretation and reporting to physicians with acceptable turn-around times for straightforward decision making or case discussion; and access to drugs (preferably at the point-of-care) with approved therapies or clinical trial opportunities.
Abstract Background In order to facilitate implementation of precision medicine in clinical management of cancer, there is a need to harmonise and standardise the reporting and interpretation of clinically relevant genomics data.
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