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Error-correcting Barcoded Primers for Pyrosequencing Hundreds of Samples in Multiplex

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Journal Nat Methods
Date 2008 Feb 12
PMID 18264105
Citations 586
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Abstract

We constructed error-correcting DNA barcodes that allow one run of a massively parallel pyrosequencer to process up to 1,544 samples simultaneously. Using these barcodes we processed bacterial 16S rRNA gene sequences representing microbial communities in 286 environmental samples, corrected 92% of sample assignment errors, and thus characterized nearly as many 16S rRNA genes as have been sequenced to date by Sanger sequencing.

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