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{{Unreferenced|date=October 2017}}
The '''selector technique''' allows multiplex amplification of arbitrary sets of genomic sequences. Genomic [[DNA]] is digested with restriction enzymes, circularized by [[hybridisation (molecular biology)|hybridisation]] to selectors and subsequenct [[ligation]]. The procedure results in circular [[DNA]] [[molecules]] with an included general primer pair motif that can be used for amplification by [[PCR]] or [[RCA]].▼
The '''selector technique''' is a method to [[polymerase chain reaction|amplify]] and [[Multiplexing|multiplex]] genomic DNA.
== Process ==
====The selector construct====▼
▲
A selector consists of two oligonucleotides, one '''Vector''' oligonucletide and one '''Selector probe'''. Together they form one '''Selector''' with target specific ends on each side of a general primer motif.▼
▲A selector consists of two oligonucleotides, one '''Vector'''
====Selection mechanisms====▼
* (I) A selector probe hybridizes with both ends of the selected target.▼
* (II) A selector probe hybridizes with one end to the 3’ end of the target and the other end to an internal sequence of the target. The protruding 5' end is cleaved off using [[Taq polymerase]].▼
====Publications====▼
▲
*[http://nar.oxfordjournals.org/cgi/content/full/33/8/e71 Demonstration of the selector method]▼
*[https://web.archive.org/web/20051127101236/http://nar.oxfordjournals.org/cgi/content/full/33/8/
▲*[https://archive.today/20130415163620/http://nar.oxfordjournals.org/cgi/content/full/33/8/
{{DEFAULTSORT:Selector-Technique}}
[[Category:DNA]]
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