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In the protocol we followed, 16S rRNA gene segments were amplified by PCR, then individually ligated...

In the protocol we followed, 16S rRNA gene segments were amplified by PCR, then individually ligated into a vector, transformed and propagated in bacteria, and 9 bacterial “clones” sequenced by the Sanger method. Each clone had a unique sequence we subsequently compared. If we had used an Illumina Next Generation Sequencing method, would the “cloning” of individual fragments have been necessary?

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