Bring the power of NGS to your lab with easy-to-use platforms
Benchtop sequencers give users the power of next-generation sequencing (NGS) in a flexible and accessible design. Built with operational simplicity including preconfigured analysis workflows, these systems enable novice and experienced NGS users to bring NGS in-house and perform targeted sequencing across a range of applications.
A benchtop sequencer can provide a cost-efficient solution for low and mid-throughput applications and for library quality control (QC) prior to large-scale studies.
For users that are outsourcing their sequencing projects, investing in a benchtop sequencer to bring NGS in house can offer several advantages:
Depending on your needs, benchtop sequencing systems feature low- or mid-throughput configurations to support a broad range of applications while delivering exceptional data quality and accuracy.
Output: 144 megabases (Mb) to 30 gigabases (Gb)
Single-end reads per run: 1 million to 100 million
Output: 10 Gb to 540 Gb
Single-end reads per run: 75 million to 1.8 billion
Benchtop sequencers support a broad range of applications and throughputs. Explore a step-by-step guide to aid you in choosing which NGS system best meets the needs of your lab.
Key factors to consider when looking to purchase a benchtop sequencing system include what applications your lab will use most and how you will analyze the data you generate.
Your methods and applications help determine if you need a low- or mid-throughput benchtop sequencer. If you’re primarily interested in small whole-genome, microbial metagenomics, and targeted gene sequencing, a low-throughput benchtop sequencer would be a good fit. For methods like whole-exome and single-cell sequencing, consider a mid-throughput benchtop sequencer.
Your goals for analysis are an important consideration when choosing a sequencing platform. Novice users may benefit from user-friendly, preconfigured analysis pipelines available on-instrument or in the cloud. For experienced users, you can take advantage of instrument compatibility with broader informatics pipelines or build your own.
Whether your lab is acquiring its first NGS sequencer, or is ready to scale up, Illumina offers proven benchtop sequencing systems with simplified operation, flexible and scalable sequencing, and intuitive data analysis. Straightforward, thoughtful design that includes onboard cluster generation and minimal maintenance sets these sequencers apart.
The MiSeq i100 Series makes it easy for novice and experienced users to access NGS with its easy operations and integrated data analysis. With run times as fast as four hours, receive same-day results to drive your discoveries faster than ever before.
The NextSeq 1000 and NextSeq 2000 Sequencing Systems are flexible and scalable, empowering scientists to explore applications like single cell, whole-exome, and RNA sequencing. With more than 2150 systems shipped globally, they feature simplified run setup, minimal touchpoints, and flexible informatics solutions, including onboard DRAGEN software.
Illumina benchtop sequencing systems are making NGS technology more accessible to laboratories worldwide. Learn how these systems provide the speed, power, and flexibility to make breakthroughs in microbiology, cancer research, and more. The MiSeq i100 Series or NextSeq 1000 and NextSeq 2000 Systems can help make your NGS research goals within reach.
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When determining the best benchtop sequencer for your lab, it is important to select a vendor with a record of excellence. At Illumina, we continue our pursuit of innovation to inspire scientists to join our growing genomics community, and our proven performance has contributed to Illumina being cited more than any other sequencing company.
In these videos and articles, hear from others about their experience with Illumina benchtop sequencing systems.
In this video, learn about the robustness of the NextSeq 2000 System and how it was able to support Dr Tomas Szemes’ team from Comenius University Science Park, in Slovakia, to double their previous sequencing efforts.
Hear from researchers who have used the NextSeq 1000 and NextSeq 2000 Systems for genomic surveillance, CRISPR screening, single-cell RNA-Seq, and more, in this introductory video.
In this article, Dr Philip Supply explains how he uses the MiSeq System to evaluate patterns of extensive resistance, transmission, and evolution to identify multidrug-resistant tuberculosis strains responsible for silent outbreaks.
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