The Genomics CTU have 3 Illumina next generation sequencers; MiSeq personal sequencer, NextSeq 500, NovaSeq 600
The MiSeq is an integrated bench top sequencer. It features significantly faster cycle times allowing small projects to be completed quickly at a lower cost.
The MiSeq delivers high precision variant detection and is suitable for small-scale projects such as amplicon or small genome sequencing. It typically sequences more than 20 million inserts per lane from a sequencing run.
The NextSeq 550 allows researchers to perform many combinations of high- and mid-throughput sequencing applications. Researchers can carry out applications such as whole genome sequencing, exome sequencing, whole transcriptome sequencing, mRNA-Seq, and methylation sequencing, among others. It typically sequences more than 400 million inserts per lane from a sequencing run.
With The NovaSeq 6000 Sequencing System you can get scalable throughput and flexibility for virtually any sequencing method, genome, and scale of project. The NovaSeq 6000 System offers output up to 6 Tb and 20 B reads in < 2 days. Multiple flow cell types and read length combinations offer flexible output and run time configurations based on project needs (Table 1). NovaSeq S Prime (SP), S1, and S2 flow cells provide quick and powerful sequencing for most high-throughput applications. With fewer reads than a HiSeq 2500 or HiSeq 4000 flow cell and the flexibility of individual lane loading, the NovaSeq SP and S1 flow cells allows existing HiSeq System users to transition easily, without the need to batch additional samples per run. (Comparison reads for the HiSeq 2500 System based on specifications for the v4 high output flow cell.) The NovaSeq S4 flow cell enables high-throughput cost-effective sequencing across a range of applications, making in-house WGS or WES studies an attractive and affordable option for more labs.
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