Literature DB >> 7937094

A simple procedure for optimising the polymerase chain reaction (PCR) using modified Taguchi methods.

B D Cobb1, J M Clarkson.   

Abstract

Taguchi methods are used widely as the basis for development trials during industrial process design. Here, we describe their suitability for optimisation of the PCR. Unlike conventional strategies, these arrays revealed the effects and interactions of specific reaction components simultaneously using just a few reactions, negating the need for extensive experimental investigation. Reaction components which effected product yield were easily determined. In addition, this technique was applied to the qualitative investigation of RAPD-PCR profiles, where optimisation of the size and distribution of a number of products was determined.

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Year:  1994        PMID: 7937094      PMCID: PMC308365          DOI: 10.1093/nar/22.18.3801

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  14 in total

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Journal:  Annu Rev Genet       Date:  1992       Impact factor: 16.830

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Review 4.  Direct sequencing of polymerase chain reaction-amplified DNA.

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6.  Rapid identification of markers linked to a Pseudomonas resistance gene in tomato by using random primers and near-isogenic lines.

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10.  Extension of base mispairs by Taq DNA polymerase: implications for single nucleotide discrimination in PCR.

Authors:  M M Huang; N Arnheim; M F Goodman
Journal:  Nucleic Acids Res       Date:  1992-09-11       Impact factor: 16.971

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  54 in total

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9.  Using the Taguchi method for rapid quantitative PCR optimization with SYBR Green I.

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10.  Genetic diversity analysis of Sclerotinia sclerotiorum causing stem rot in chickpea using RAPD, ITS-RFLP, ITS sequencing and mycelial compatibility grouping.

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