Life Science/

Next Generation Sequencing

StarSEQ offers all types of Next Generation Sequencing applications on three Illumina platforms: the NextSeq 2000, the MiSeq and the NovaSeq 6000 (full flow cells only)

The NextSeq 2000™ system:


The NextSeq 2000 desktop sequencing system is the newest development from Illumina and redesigned from ground up. It provides tunable output and industry-leading data quality. The NextSeq 2000 will give flexible read lengths (1×50 nt, 2×50 nt, 1×100 nt, 2×100 nt, 2×150 nt,  2×300 nt) with 40 Gb to 330 Gb output that is perfect for applications like whole genome sequencing (WGS), whole exome sequencing (WES), transcriptome sequencing, single cell gene expression, highly multiplexed sequencing, amplicon sequencing, ChIP-Seq, small RNA sequencing and targeted resequencing.

The MiSeq system:


The MiSeq is the only desktop sequencer that can produce 2 x 300 nt paired-end reads. The MiSeq is capable of producing true paired-end reads. The system enables a broad range of applications: targeted gene sequencing, targeted resequencing, amplicon sequencing, metagenomics, hybrid capture, clone checking, small genome sequencing, small RNA sequencing, microbial RNA-Seq, ChIP-Seq and Library QC. The MiSeq provides flexible read lengths: 1x 50 nt, 1x 150 nt, 2x 75 nt, 2×150 nt, 2×250 nt and 2×300 nt with outputs of 850 Mb to 15 Gb.

The NovaSeq system:


The NovaSeq 6000 System provides tremendous scalability and flexibility to accommodate diverse applications and project sizes, while achieving maximum operational efficiency. Users can run 1 or 2 flow cells at a time and choose between 3 flow cell types, easily adjusting output for each sequencing run. With highly tunable data output you can run virtually any genome, sequencing method, and scale of project.

The NovaSeq 6000 System is compatible with a broad range of Illumina library preparation kits, from transcriptome sequencing to whole-genome sequencing and everything in between. High-quality, high-coverage sequencing offers a comprehensive view of the genome to detect variants accurately, characterize isoforms, and more. With increased throughput and reduced price per sample, the NovaSeq 6000 System is ideal for data-intensive applications.

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