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NEW YORK (GenomeWeb) – PreludeDx said today that the State of New York Clinical Laboratory Evaluation Program (CLEP) has approved its DCISionRT test, which assesses recurrence risk and can predict radiation therapy benefit in patients diagnosed with non-invasive breast cancers known as ductal carcinoma in situ (DCIS).

PreludeDx's laboratory is also accredited by the College of American Pathology and has CLIA certification, so with CLEP approval, DCISionRT is now available in all 50 US states, the company said.

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