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Molecular detection of Borrelia burgdorferi sensu lato - An analytical comparison of real-time PCR protocols from five different Scandinavian laboratories.

Malin LagerMaximilian FallerPeter WilhelmssonVivian KjellandÅshild AndreassenRimtas DargisHanne QuarstenRam DessauVolker FingerleGabriele MargosSølvi NoraasKatharina OrnsteinAnn-Cathrine PeterssonAndreas MatussekPer-Eric LindgrenAnna J Henningsson
Published in: PloS one (2017)
The analytical sensitivities and the concordance between the eight protocols were in general high. The concordance was especially high between the protocols using 16S rRNA as the target gene, however, this concordance was mainly related to cDNA as the type of template. When comparing cDNA and DNA as the type of template the analytical sensitivity was in general higher for the protocols using DNA as template regardless of the use of target gene. The analytical specificity for all eight protocols was high. However, some protocols were not able to detect Borrelia spielmanii, Borrelia lusitaniae or Borrelia japonica.
Keyphrases
  • circulating tumor
  • liquid chromatography
  • genome wide
  • real time pcr
  • single molecule
  • molecularly imprinted
  • copy number
  • cell free
  • dna methylation
  • genome wide identification