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, developed by Illumina, represents a cutting-edge advancement in desktop sequencing technology. Redesigned from the ground up, this system offers a host of features that make it a valuable asset in genomics research.


Key Features:

1. Tunable Output: The NextSeq 2000 is known for its remarkable flexibility in output. It can produce data ranging from 40 Gb to 330 Gb, allowing researchers to tailor their sequencing runs to specific project requirements.

2. Versatile Read Lengths: Researchers can choose from a range of read lengths, including 1×50 nt, 2×50 nt, 1×100 nt, 2×100 nt, 2×150 nt, and 2×300 nt, enabling the system to accommodate a wide variety of sequencing applications.

3. Industry-Leading Data Quality: The system is renowned for its exceptional data quality, ensuring that researchers can rely on accurate and reliable results for their experiments.



Whole Genome Sequencing (WGS): Ideal for comprehensive analysis of an organism’s entire genome.
Whole Exome Sequencing (WES): Targeted sequencing of exons for cost-effective genomics research.
Transcriptome Sequencing: Profiling gene expression at the RNA level.
Single Cell Gene Expression: Enabling single-cell analysis for a deeper understanding of biological processes.
Highly Multiplexed Sequencing: Efficiently process multiple samples in a single run.
Amplicon Sequencing: Targeted amplification for focused genetic analysis.
ChIP-Seq: Investigating protein-DNA interactions.
Small RNA Sequencing: Studying small RNA molecules.
Targeted Resequencing: Revisiting specific genomic regions for variant detection.


The NextSeq 2000™ system empowers researchers across various fields with its adaptability and high-quality performance, making it an indispensable tool in genomics research.

The MiSeq System: Empowering Your Sequencing Needs


The MiSeq is a cutting-edge desktop sequencer that redefines DNA sequencing capabilities. With its unique ability to produce 2 x 300 nt paired-end reads, it stands as the pinnacle of sequencing technology. Here’s what sets the MiSeq apart:


1. True Paired-End Reads: Unlike other desktop sequencers, the MiSeq excels in producing true paired-end reads, ensuring the highest data quality and accuracy.

2. Versatile Applications: The MiSeq opens up a world of possibilities in genomics research. It supports a wide array of applications, including:
– Targeted Gene Sequencing
– Targeted Resequencing
– Amplicon Sequencing
– Metagenomics
– Hybrid Capture
– Clone Checking
– Small Genome Sequencing
– Small RNA Sequencing
– Microbial RNA-Seq
– ChIP-Seq
– Library QC

3. Flexible Read Lengths: Adapt your sequencing to fit your research needs. The MiSeq offers flexible read lengths, ranging from 1x 50 nt to 2x 300 nt. This versatility ensures compatibility with various experimental designs.

4. Impressive Throughput: With outputs spanning from 850 Mb to a staggering 15 Gb, the MiSeq delivers the data you require, whether it’s a small-scale project or a comprehensive genomic study.


Incorporate the MiSeq into your research arsenal and experience unparalleled sequencing power. It’s more than a sequencer; it’s a scientific breakthrough. Unlock the potential of genomics with MiSeq.

The NovaSeq 6000 System: Revolutionizing Genomic Sequencing


Unleash the Power of NovaSeq


The NovaSeq 6000 System is a game-changer in the world of genomics, offering unmatched scalability and flexibility for a wide range of applications. Here’s why it’s the ultimate choice for your sequencing needs:


1. Scalability & Flexibility
– Accommodate projects of any size with ease. Whether it’s a small-scale study or a large-scale genome project, the NovaSeq 6000 adapts effortlessly, saving you time and resources.

2. Flow Cell Options
– Tailor your sequencing runs by choosing from three different flow cell types. This customization ensures optimal output for each project, enhancing cost-effectiveness and efficiency.

3. Versatile Sequencing
– NovaSeq 6000 offers highly tunable data output, making it compatible with virtually any genome, sequencing method, and project scale. Say goodbye to limitations and hello to endless possibilities.

4. Comprehensive Library Compatibility
– From transcriptome sequencing to whole-genome sequencing and everything in between, the NovaSeq 6000 seamlessly integrates with a broad range of Illumina library preparation kits.

5. High-Quality Results
– Experience high-quality, high-coverage sequencing that provides a deep dive into the genome. Detect variants with precision, characterize isoforms, and unlock insights like never before.

6. Cost Efficiency
– NovaSeq 6000 delivers increased throughput, reducing the price per sample. It’s the perfect choice for data-intensive applications, optimizing your budget without compromising on quality.

In summary, the NovaSeq 6000 System empowers researchers to push the boundaries of genomics. Its scalability, versatility, and cost-effectiveness make it an indispensable tool for advancing scientific discoveries.

  • This field is for validation purposes and should be left unchanged.