![]() iSeq 100 |
![]() MiniSeq |
![]() MiSeq Series |
![]() NextSeq 550 Series |
![]() NextSeq 1000 & 2000 |
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Popular Applications & Methods |
Key Application | Key Application | Key Application | Key Application | Key Application |
Large Whole-Genome Sequencing (human, plant, animal) | |||||
Small Whole-Genome Sequencing (microbe, virus) | |||||
Exome & Large Panel Sequencing (enrichment-based) | |||||
Targeted Gene Sequencing (amplicon-based, gene panel) | |||||
Single-Cell Profiling (scRNA-Seq, scDNA-Seq, oligo tagging assays) | |||||
Transcriptome Sequencing (total RNA-Seq, mRNA-Seq, gene expression profiling) | |||||
Targeted Gene Expression Profiling | |||||
miRNA & Small RNA Analysis | |||||
DNA-Protein Interaction Analysis (ChIP-Seq) | |||||
Methylation Sequencing | |||||
16S Metagenomic Sequencing | |||||
Metagenomic Profiling (shotgun metagenomics, metatranscriptomics) | |||||
Cell-Free Sequencing & Liquid Biopsy Analysis | |||||
Benchtop Sequencer Sheds Light on Ebola OutbreakLocal scientists use the iSeq 100 Sequencing System to analyze transmission patterns and trace the origin of an Ebola outbreak in the Democratic Republic of the Congo. Read Article |
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Run Time | 9.5–19 hrs | 4–24 hours | 4–55 hours | 12–30 hours | 11-48 hours |
Maximum Output | 1.2 Gb | 7.5 Gb | 15 Gb | 120 Gb | 360 Gb* |
Maximum Reads Per Run | 4 million | 25 million | 25 million † | 400 million | 1.2 billion* |
Maximum Read Length | 2 × 150 bp | 2 × 150 bp | 2 × 300 bp | 2 × 150 bp | 2 × 150 bp |
Order | Order | Request Pricing | Request Pricing | Request Pricing |
![]() NextSeq 550 Series |
![]() NextSeq 1000 & 2000 |
![]() NovaSeq 6000 |
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---|---|---|---|---|---|
Popular Applications & Methods |
Key Application | Key Application | Key Application | ||
Large Whole-Genome Sequencing (human, plant, animal) | |||||
Small Whole-Genome Sequencing (microbe, virus) | |||||
Exome & Large Panel Sequencing (enrichment-based) | |||||
Targeted Gene Sequencing (amplicon-based, gene panel) | |||||
Single-Cell Profiling (scRNA-Seq, scDNA-Seq, oligo tagging assays) | |||||
Transcriptome Sequencing (total RNA-Seq, mRNA-Seq, gene expression profiling) | |||||
Chromatin Analysis (ATAC-Seq, ChIP-Seq) | |||||
Methylation Sequencing | |||||
Metagenomic Profiling (shotgun metagenomics, metatranscriptomics) | |||||
Cell-Free Sequencing & Liquid Biopsy Analysis | |||||
Optimized NGS Sample Tracking and WorkflowsSee how a Laboratory Information Management System (LIMS) enabled this large genomics lab to standardize lab procedures and cope with increasing sample volumes from diverse clients. Read Case Study |
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Run Time | 12–30 hours | 11-48 hours | ~13 - 38 hours (dual SP flow cells) ~13–25 hours (dual S1 flow cells) ~16–36 hours (dual S2 flow cells) ~44 hours (dual S4 flow cells) |
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Maximum Output | 120 Gb | 360 Gb* | 6000 Gb | ||
Maximum Reads Per Run | 400 million | 1.2 billion* | 20 billion | ||
Maximum Read Length | 2 × 150 bp | 2 × 150 bp | 2 x 250** | ||
Request Pricing | Request Pricing | Request Pricing |
* Specifications based on Illumina PhiX control library at supported cluster densities.
** Specification based on dual flow cell run of SP flow cells.
† For MiSeq V3 kits only.
When determining the best sequencing platform for your lab, you’ll want to ask the right questions to evaluate your needs. These include:
Use this checklist as a framework. For detailed insight on the factors to consider in each area, download the full NGS System Buyer’s Guide.
Download Buyer’s GuideIllumina NGS instruments have been adopted by leading institutions around the globe, both big and small, and are the production platform for many genome centers. More than 90% of the world’s sequencing data is generated using Illumina instruments.*
Each sequencing platform delivers exceptional data quality and performance, with flexible throughput and simple, streamlined workflows—for every kind of researcher, for every scale of study.
*Data calculations on file, Illumina, Inc. 2017.
Illumina has pioneered major advances in sequencing simplicity, flexibility, and platform performance. Sequencing output has grown over a thousand-fold, from less than 1 gigabase to 6 terabases per run, while the number of reads has increased from millions to billions. Experiments that once required complex workflows now use simple push-button sequencing.
Learn More About NGSUse our interactive comparison tool to identify the best sequencing instrument for your lab and applications. This tool will help you compare next-generation sequencing systems and find the one that's right for your lab or application. You can email the results or request a consultation.
Launch Comparison Tool