What's the best NGS way to go (if even possible) to produce a precise sequencing report from a sample containing ONLY sequence repeats; various lengths of 3-nucl repeats (e.g. 90, 150, 270 bases etc) so all lengths are in multiples of 3. The goal is to get the distribution of each length in the assay. Is this a case for techs like Hellicos and PacBio, which use single molecule sequencing ? Or can Illumina tech help also?
Thanks.
Thanks.
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