
NovaSeq 6000 Sequencing System
Vendor: Illumina
SKU: 20012850
In stock
The NovaSeq 6000 Sequencing System is an integrated ultrahigh throughput system performing onboard cluster generation and sequencing. This system includes installation and training and 12 months warranty (including parts and labor).
NovaSeq 6000 System expands sequencing capabilities by combining throughput, flexibility, and simplicity for virtually any method, genome, and scale.
Tried and true performance
System specifications
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Output range80–6000 Gb
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Single reads per run650M–20B
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Max read length2 × 250 bp
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Run time13–44 hr
A flexible workflow designed to help you accelerate your research and maximize results
Manage workflow
Manage your workflow seamlessly with Clarity LIMS software or your existing LIMS system.
Prepare libraries
Prepare libraries with a broad range of high-performance library preparation kits.
Sequence
Generate sequences with ready-to-use reagents featuring proven Illumina sequencing by synthesis chemistry.
Analyze data
Leverage Illumina DRAGEN software or BaseSpace Sequence Hub for accurate, rapid secondary analysis.
Interpret results
Gain insights and drive discovery with variant analysis and interpretation software.
Advanced applications. Impactful discoveries.
The NovaSeq 6000 System offers deep, broad coverage through advanced applications for a comprehensive view of the genome. Unlock a full spectrum of genetic variation and biological function with high-throughput sequencing.
Specifications
Output per flow cell for various read lengths
| Read length | SP | S1 | S2 | S4 |
|---|---|---|---|---|
| 1 × 35 bp | N/A | N/A | N/A | 280–350 Gb |
| 2 × 50 bp | 65–80 Gb | 134–167 Gb | 333–417 Gb | N/A |
| 2 × 100 bp | 134–167 Gb | 266–333 Gb | 667–833 Gb | 1600–2000 Gb |
| 2 × 150 bp | 200–250 Gb | 400–500 Gb | 1000–1250 Gb | 2400–3000 Gb |
| 2 × 250 bpb | 325-400 Gb | N/A | N/A | N/A |
Estimated sample throughput for key applications
| Application | SP | S1 | S2 | S4 |
|---|---|---|---|---|
| Human genomes per run | ~4 | ~8 | ~20 | ~48 |
| Exomes per run | ~40 | ~80 | ~200 | ~500 |
| Transcriptomes per run | ~32 | ~64 | ~164 | ~400 |
Reads passing filter per flow cell
| Read type | SP | S1 | S2 | S4 |
|---|---|---|---|---|
| Single-end reads | 650–800M | 1.3–1.6B | 3.3–4.1B | 8–10B |
| Paired-end reads | 1.3–1.6B | 2.6–3.2B | 6.6–8.2B | 16–20B |
Quality scores
| Read length | SP | S1 | S2 | S4 |
|---|---|---|---|---|
| 1 × 35 bp | N/A | N/A | N/A | ≥ 90% of bases higher than Q30 |
| 2 × 50 bp | ≥ 90% of bases higher than Q30 | N/A | ||
| 2 × 100 bp | ≥ 85% of bases higher than Q30 | |||
| 2 × 150 bp | ≥ 85% of bases higher than Q30 | |||
| 2 × 250 bp | ≥ 75% of bases higher than Q30 | N/A | N/A | N/A |
Run time
| Read length | SP | S1 | S2 | S4 |
|---|---|---|---|---|
| 1 × 35 bp | N/A | N/A | N/A | ~14 hr |
| 2 × 50 bp | ~13 hr | ~13 hr | ~16 hr | N/A |
| 2 × 100 bp | ~19 hr | ~19 hr | ~25 hr | ~36 hr |
| 2 × 150 bp | ~25 hr | ~25 hr | ~36 hr | ~44 hr |
| 2 × 250 bp | ~38 hr | N/A | N/A | N/A |
Documents
- Human Whole-Genome Sequencing with the NovaSeq 6000 Sequencing System
- NovaSeq 6000 System Quality Scores and RTA3 Software
- The NovaSeq Xp workflow provides flexibility and control without sacrificing data quality or yield
- High-performance whole-genome sequencing with Illumina DNA PCR-Free Prep, Tagmentation
- Illumina Proactive Service connectivity guide - NovaSeq 6000
Support Documentation
- NovaSeq 6000 Sequencing System Guide Documentation
- NovaSeq 6000 Sequencing System Site Prep Guide Documentation
- NovaSeq 6000 Sequencing System Safety and Compliance Guide Documentation
- NovaSeq Series Custom Primers Guide Documentation
- NovaSeq Xp Workflow Checklist Documentation
- All NovaSeq 6000 System Support
Specifications
- Sub category Sequencers
links and documants
- Source url Click here
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NovaSeq 6000 Sequencing System
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