Highly sensitive, non-invasive detection of colorectal cancer mutations using single molecule, third generation sequencing.

Appl Transl Genom · 2015 · PMC4803778 · PMID 27054083

Europe PMC DOI

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extremely significantP = 2.72e-26actually significant

This codon is the eighth most frequently mutated codon in CRC and this mutation is extremely significant in our stool sample (P = 2.72e-26, P Bonf = 9.35e-24).

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