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Circulating tumour DNA (ctDNA) is evolving as a promising, non-invasive, personalised tumour marker for different malignancies. By providing different laboratories the same samples for analysis of ctDNA, we show for the first time that there is a wide variability and lack of harmonisation regarding critical analytical issues that have to be addressed before this new diagnostic application is ready to be implemented into a routine set-up.

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This page is a summary of: Results of the first external quality assessment scheme (EQA) for isolation and analysis of circulating tumour DNA (ctDNA), Clinical Chemistry and Laboratory Medicine (CCLM), August 2017, De Gruyter,
DOI: 10.1515/cclm-2017-0283.
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