MiSeq is the only desktop sequencer that can produce 2 x 300 paired-end reads in a single run. This allows small genome sequencing and assembly, and enables 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 targeted gene and small genome sequencer with the shortest sample-to-data workflow.

With MiSeq, you can
• Access the world's most widely-published and accurate sequencing chemistry, backed by > 4,800 peer-reviewed publications
• Multiplex up to 96 samples per run for greater efficiency
• Get accurate bi-directional amplicon sequencing
• Generate more complete de novo assemblies

• Broadest applications base
MiSeq facilitates your research with a wide range of sequencing applications. It is capable of automated paired-end reads and up to 15 Gb per run, delivering over 600 bases of sequence data per read. The library prep kits that it uses are optimized for a variety of applications, whether targeted DNA or RNA resequencing, small-genome sequencing, or RNA sequencing.