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Integrated routine workflow using next-generation sequencing and a fully-automated platform for the detection of KRAS, NRAS and BRAF mutations in formalin-fixed paraffin embedded samples with poor DNA quality in patients with colorectal carcinoma.

Claire FranczakLudovic DubouisPauline GilsonMarie HussonMarie RouyerJessica DemangeAgnès LerouxJean-Louis MerlinAlexandre Harlé
Published in: PloS one (2019)
Our study shows that an integrated workflow using NGS and Idylla platform allows the determination of KRAS, NRAS and BRAF mutational statuses of 651/669 (97.3%) samples and retrieve 49/67 (73.1%)samples that don't reach DNA quality requirements for NGS.
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