Methodology is provided for developing probes for identifying sequence differences between two related DNA populations, sets of DNA fragments or collections of restriction-endonuclease-cleaved DNA or CODA. The method employs an initial stage to obtain a representation of both DNA populations, namely using the PCR to produce relatively short fragments, referred to as amplicons. Tester amplicons containing target DNA, sequences of interest, are ligated to adaptors and mixed with excess driver amplicons under melting and annealing conditions, followed by PCR amplification. The process may be repeated so as to greatly enrich the target DNA. Optionally, the target DNA may then be cloned and the DNA used as probes
Methods using oligonucleotide probes are powerful tools for the analysis of nucleic acids. During re...
Background The technological development of DNA analysis has had tremendous developm...
A method is described for the absolute quantification by polymerase chain reaction (PCR) of nucleic ...
Methodology is provided for developing probes for identifying sequence differences between two relat...
Methodology is provided for developing probes for identifying sequence differences between two relat...
Methodology is provided for developing probes for identifying sequence differences between two relat...
Methodology is provided for developing probes for identifying sequence differences between two relat...
It is an object of the present invention to provide a solution to problems associated with the use o...
DNA amplification is a very powerful tool that can be used to replicate one molecule of DNA into mil...
A method for the amplification of a single DNA strand at Dow copy number is described. U is a wholly...
It is an object of the present invention to provide a solution to problems associated with the use o...
The NucleoLink surface is a physically modified, thermo-stable, optically clear resin. It allows the...
Detection and visualisation of nucleic acids is integral to genome analyses. Exponential amplificati...
International audienceA simple and efficient ligation-mediated PCR (LMPCR) is described for amplifyi...
Patent: WO/2006/094360. PCT/AU2006/00031. Published14.09.2006The present invention provides a method...
Methods using oligonucleotide probes are powerful tools for the analysis of nucleic acids. During re...
Background The technological development of DNA analysis has had tremendous developm...
A method is described for the absolute quantification by polymerase chain reaction (PCR) of nucleic ...
Methodology is provided for developing probes for identifying sequence differences between two relat...
Methodology is provided for developing probes for identifying sequence differences between two relat...
Methodology is provided for developing probes for identifying sequence differences between two relat...
Methodology is provided for developing probes for identifying sequence differences between two relat...
It is an object of the present invention to provide a solution to problems associated with the use o...
DNA amplification is a very powerful tool that can be used to replicate one molecule of DNA into mil...
A method for the amplification of a single DNA strand at Dow copy number is described. U is a wholly...
It is an object of the present invention to provide a solution to problems associated with the use o...
The NucleoLink surface is a physically modified, thermo-stable, optically clear resin. It allows the...
Detection and visualisation of nucleic acids is integral to genome analyses. Exponential amplificati...
International audienceA simple and efficient ligation-mediated PCR (LMPCR) is described for amplifyi...
Patent: WO/2006/094360. PCT/AU2006/00031. Published14.09.2006The present invention provides a method...
Methods using oligonucleotide probes are powerful tools for the analysis of nucleic acids. During re...
Background The technological development of DNA analysis has had tremendous developm...
A method is described for the absolute quantification by polymerase chain reaction (PCR) of nucleic ...