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A general model of error-prone PCR
Authors:Pritchard Leighton  Corne Dave  Kell Douglas  Rowland Jem  Winson Mike
Affiliation:Institute of Biological Sciences, University of Wales, Aberystwyth, Ceredigion, SY23 3DD, Wales, UK. l.pritchard@scri.sari.ac.uk
Abstract:In this paper, we generalize a previously-described model of the error-prone polymerase chain reaction (PCR) reaction to conditions of arbitrarily variable amplification efficiency and initial population size. Generalisation of the model to these conditions improves the correspondence to observed and expected behaviours of PCR, and restricts the extent to which the model may explore sequence space for a prescribed set of parameters. Error-prone PCR in realistic reaction conditions is predicted to be less effective at generating grossly divergent sequences than the original model. The estimate of mutation rate per cycle by sampling sequences from an in vitro PCR experiment is correspondingly affected by the choice of model and parameters.
Keywords:The following abbreviations are used in this paper: PCR—polymerase chain reaction   DNA—deoxyribose nucleic acid   MDM—mutation data matrix   MMo—Moore and Maranas’ original model of error-prone PCR   MMc—Moore and Maranas’ model generalised to an arbitrary number of template sequences, but with constant amplification efficiency   MMv—Moore and Maranas’ model generalised to an arbitrary number of template sequences, with variable amplification efficiency.
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