Data in Brief (Jun 2018)

Detailed overview on the mutations detected by and the sensitivity of the GeneReader NGS sequencing platform

  • Jessica Lüsebrink,
  • Monika Pieper,
  • Ramona-Liza Tillmann,
  • Michael Brockmann,
  • Oliver Schildgen,
  • Verena Schildgen

Journal volume & issue
Vol. 18
pp. 1962 – 1966

Abstract

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This article presents additional next generation data from our pre-clinical validation study. In total 121 samples (clinical specimen and interlaboratory test samples) were tested successfully with next generation sequencing. 38 different mutations in six different genes were detected. Next to the detection of different mutations, the reproducibility of the NGS test was analyzed. Three samples were analyzed five times and the results were compared. Several mutations classified as non-pathogenic so far, have been detected repeatedly.