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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 subsequently attached to a vector sequence by [[DNA ligase|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 construct==
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