MiSeq is the only benchtop sequencer that can produce 2 x 300 paired-end reads and up to 15 Gb of data in a single run. This allows assembly of small genomes or detection of target variants with unmatched accuracy, especially within homopolymer regions. Now, even more samples can be processed in less time while generating more reads per run than any previous versions. All of this can be achieved using the shortest sample-to-data workflow benchtop sequencer.
With MiSeq, You Can: