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Polymerase specific error rates and profiles identified by single molecule sequencing.
Hestand, Matthew S; Van Houdt, Jeroen; Cristofoli, Francesca; Vermeesch, Joris R.
Affiliation
  • Hestand MS; Department of Human Genetics, KU Leuven, O&N I Herestraat 49-box 602, 3000 Leuven, Belgium.
  • Van Houdt J; Department of Human Genetics, KU Leuven, O&N I Herestraat 49-box 602, 3000 Leuven, Belgium.
  • Cristofoli F; Department of Human Genetics, KU Leuven, O&N I Herestraat 49-box 602, 3000 Leuven, Belgium.
  • Vermeesch JR; Department of Human Genetics, KU Leuven, O&N I Herestraat 49-box 602, 3000 Leuven, Belgium. Electronic address: joris.vermeesch@uzleuven.be.
Mutat Res ; 784-785: 39-45, 2016.
Article in En | MEDLINE | ID: mdl-26829216
DNA polymerases have an innate error rate which is polymerase and DNA context specific. Historically the mutational rate and profiles have been measured using a variety of methods, each with their own technical limitations. Here we used the unique properties of single molecule sequencing to evaluate the mutational rate and profiles of six DNA polymerases at the sequence level. In addition to accurately determining mutations in double strands, single molecule sequencing also captures direction specific transversions and transitions through the analysis of heteroduplexes. Not only did the error rates vary, but also the direction specific transitions differed among polymerases.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polymerase Chain Reaction / DNA-Directed DNA Polymerase Type of study: Prognostic_studies Language: En Journal: Mutat Res Year: 2016 Document type: Article Affiliation country: Belgium Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polymerase Chain Reaction / DNA-Directed DNA Polymerase Type of study: Prognostic_studies Language: En Journal: Mutat Res Year: 2016 Document type: Article Affiliation country: Belgium Country of publication: Netherlands