Redefining the price of discovery
Researchers are shifting to NGS to expand the scale and discovery power of their genomics studies. With the simplicity and cost efficiencies of benchtop sequencing systems, NGS equipment is now accessible to laboratories of all sizes.
Many laboratories are choosing to bring NGS in-house to increase lab efficiency, save time, and tighten control over data privacy and NGS projects. Some perceive NGS to be too expensive vs. other methods, but the reality is that NGS can be a very cost-effective method to complement or replace other molecular methods. NGS can add substantial value and utility in an individual lab, with no expertise required.
Key questions to consider
As you begin the decision process, start with evaluating your research goals, budget, and laboratory needs. Consider these key questions before purchasing your NGS system:
- What methods and applications will I use most?
- What are the best instrumentation options for my methods and scale of study?
- How do I ensure quality in data, instrumentation, and workflow?
- What are the ongoing costs beyond the initial purchase?
- How will I analyze and store NGS data?
- How will I collaborate with other researchers?
- What level of product support will I receive?
Evaluate NGS costs and plan your budget
A holistic view
When purchasing an NGS platform, lots of factors need to be considered, not just the instrument price or the cost/Gb—these factors alone can be quite misleading. Total cost of ownership needs to be evaluated closely, which includes everything from set up to ancillary equipment, ease of use, level of support/instrument uptime, company reputation/longevity, training, and much more.
Instrument
The best type of sequencing instrument for your lab is mainly determined by the throughput and data intensity of the NGS applications you wish to perform. Remember to consider your needs now and in the future. Most researchers start with a benchtop sequencer.
Running expenses
- Cost per experiment
- Cost per sample (eg, DNA isolation, library prep, and sequencing reagents)
- For higher-output applications, economies of scale can help reduce cost
Laboratory space and ancillary equipment
- Consider your laboratory space and facility systems
- Nucleic acid quantitation instrument
- Nucleic acid quality analyzer
- Separate cluster generation instrument
- Thermocycler
- Ultrasonicator (used in some library prep methods)
- Centrifuge
- Common lab supplies (eg, pipettors, 96-well plates, centrifuge tubes)
- Additional specialized equipment
Data quality, analysis, and storage
- Data quality (Q scores) to prevent repeat operations
- Software licenses
- Storing data/servers (often part of the licensing cost)
- Running data analysis apps (also known as the compute cost)
- Security and compliance requirements
- Analysis pipelines scalability
- Data compression and archiving solutions
Instrument support
- Onboarding and staff training
- Opportunity cost of troubleshooting equipment
- Preventive maintenance via proactive instrument monitoring
- Hands-on time: efficiency and workflow simplicity to free up lab tech time
- Turnaround time can be costly when outsourcing (opportunity cost, fewer experiments)
Choosing an NGS system: A step-by-step guide
This comprehensive guide will walk you through the entire decision process by helping you evaluate your research goals and laboratory needs.
- Key questions to ask before purchasing your NGS system
- Key considerations for sequencing and data analysis platforms
- NGS buyer’s checklist
A complete sequencing ecosystem
As next-generation sequencing costs continue to decline, Illumina is leading the way in making NGS more affordable and accessible through continuous innovation. There has been a 96% decrease in the average cost-per-genome since 20131,2. We strive to help labs of all sizes access the potential of this powerful technology.
When you purchase an Illumina sequencer, you benefit from:
A complete and connected portfolio ecosystem for a streamlined workflow
Innovations that deliver operational simplicity and fast, easy onboarding
Comprehensive product support with 96% customer satisfaction, <1 day mean repair time, 24/5 technical support, and more
Instrument service plans with highly-qualified service teams of engineers, technical application scientists, bioinformaticians, and IT experts
A community of leading researchers sharing best practices and approaches
Powerful, yet easy-to-use data analysis and storage solutions
"The cost barrier has gone way down. That's probably one of the things that kept people out. But Illumina has made great strides in making sequencing technologies more accessible for a lower cost. The expertise is there."
Kristen Jepsen, PhD, Director of IGM Genomics Center
NGS cost FAQ
Designed for the iSeq 100 System, this grant writing assistance document can help you justify funding in your grant applications.
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With multiplex sequencing, you can pool multiple libraries together and sequence them simultaneously. Multiplexing exponentially increases the number of samples analyzed in a single run, without drastically increasing cost or time.
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We have an equipment trade-in program, leasing options, and bundles to help you get started with NGS. Explore different buying options to find which best fits your needs.
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Financing and leasing options
Illumina Financial Services offers fast, easy, and affordable financing and leasing programs. With our Illumina-backed solutions and our network of leasing partners, we are able to offer options that can fit your needs, so you can preserve valuable lines of credit or overcome capital budget constraints while still keeping pace with advancing technology.
View our financing optionsRequest an NGS cost consultation
Have questions about how next-generation sequencing fits into your budget? Connect with an Illumina Sales Specialist today.
References
- National Human Genome Research Institute. DNA Sequencing Costs: Data. genome.gov/about-genomics/fact-sheets/DNA-Sequencing-Costs-Data. Accessed April 10, 2023.
- 3billion. Whole Genome Sequencing cost 2023. 3billion.io/blog/whole-genome-sequencing-cost-2023. Accessed April 10, 2023