Flow Cell Type | 1.5B | 10B | 25B |
---|---|---|---|
2 × 50 bp | ~165 Gb | ~1 Tb | N/A |
2 × 100 bp | ~330 Gb | ~2 Tb | N/A |
2 × 150 bp | ~500 Gb | ~3 Tb | ~8 Tb |
* 10B flow cell available now. 1.5B and 25B flow cells available H2 2023. NovaSeq X Plus system available now. NovaSeq X system available later in 2023. Performance metrics subject to change.
† Specifications based on Illumina PhiX control library or a TruSeq DNA Library created with NA12878 at supported cluster densities.
Flow Cell Type‡ | 1.5B | 10B | 25B |
---|---|---|---|
2 × 50 bp | ~165-330 Gb | ~1-2 Tb | N/A |
2 × 100 bp | ~330-660 Gb | ~2-4 Tb | N/A |
2 × 150 bp | ~500-1000 Gb | ~3-6 Tb | ~8-16 Tb |
Flow Cell Type‡ | 1.5B | 10B | 25B |
---|---|---|---|
2 × 50 bp | ~165 Gb | ~1 Tb | N/A |
2 × 100 bp | ~330 Gb | ~2 Tb | N/A |
2 × 150 bp | ~500 Gb | ~3 Tb | ~8 Tb |
* Specifications based on Illumina PhiX control library or a TruSeq DNA Library created with NA12878 at supported cluster densities.
† NovaSeq X Plus system is capable of single flow cell runs or dual flow cell runs. NovaSeq X system is capable of single flow cell runs.
‡ 10B flow cell available now. 1.5B and 25B flow cells available H2 2023. NovaSeq X Plus system is available now. NovaSeq X system available later in 2023. Performance metrics subject to change.
Flow Cell Type | 1.5B | 10B | 25B |
---|---|---|---|
Human Genomes per Flow Cell | ~4 | ~24 | ~64 |
Exomes per Flow Cell | ~41 | ~250 | ~750 |
Transcriptomes per Flow Cell | ~30 | ~200 | ~520 |
*All sample throughputs are estimates per single flow cell run. Human genomes assumes > 120 Gb of data per sample to achieve 30× genome coverage. Exomes assumes ~8 Gb per sample to achieve 100x coverage. Transcriptomes assumes ≥ 50M reads. Throughput may vary based on library preparation kit used.
Flow Cell Type | 1.5B | 10B | 25B |
---|---|---|---|
Single-end Reads | 1.6 billion | 10 billion | 26 billion |
Paired-end Reads | 3.2 billion | 20 billion | 52 billion |
Flow Cell Type 10B Reagent Kits |
1.5B | 10B | 25B |
---|---|---|---|
Quality Scores | |||
2 × 50 bp | ≥ 90% of bases higher than Q30 | ||
2 × 100 bp | ≥ 85% of bases higher than Q30 | ||
2 × 150 bp | ≥ 85% of bases higher than Q30 | ||
Run Time | |||
2 × 50 bp | ~13 hr | ~18 hr | N/A |
2 × 100 bp | ~18 hr | ~22 hr | N/A |
2 × 150 bp | ~21 hr | ~24 hr | ~48 hr |
* A quality score (Q-score) is a prediction of the probability of an error in base calling. The percentage of bases > Q30 is averaged across the entire run. Quality scores are based on NovaSeq X series 10B reagents using an Illumina PhiX control library. Performance may vary based on library type and quality, insert size, loading concentration, and other experimental factors.
† Run time includes automated cluster generation, sequencing, automated post-run wash, and base calling. Run times are based on Illumina PhiX control library at supported cluster densities. Performance may vary based on library type and quality, insert size, loading concentration, and other experimental factors.
The NovaSeq X series is powered by XLEAP-SBS chemistry, our fastest, highest quality, and most robust sequencing by synthesis (SBS) chemistry to date. Built upon the proven foundation of standard Illumina SBS chemistry, XLEAP-SBS chemistry delivers improved reagent stability with two-fold faster incorporation times.
The NovaSeq X series incorporates patterned flow cell technology to generate an ultra-high level of throughput for a broad range of sequencing applications. NovaSeq X patterned flow cells contain tens of billions of nanowells at fixed locations, a design that provides even spacing of sequencing clusters. This delivers significant increases in sequencing reads and total output of the system.
The NovaSeq X and NovaSeq X Plus systems are integrated with the DRAGEN Bio-IT Platform for ultra-rapid, accurate genomic data analysis. Run multiple secondary analysis pipelines in parallel, onboard or in the cloud. Run up to four simultaneous applications per flow cell in a single run.
Integrated DRAGEN ORA (original read archive) can perform lossless compression to reduce FASTQ file sizes by up to five-fold. This optimized genomics data compression enables faster data transfers and easier data management. The smaller data footprint also reduces storage and energy consumption costs.
The NovaSeq X series was purpose-built for improved sustainability. Innovations include lyophilized reagents that arrive at room temperature and a ~90% reduction in packaging waste for reagents. Plastic mass is reduced by over 50% and the buffer cartridge is made with a plant-based biopolymer.
The NovaSeq X series achieves ultra-high-resolution imaging through higher numerical aperture, a custom CMOS sensor, and two-channel SBS with blue-green optics. The smaller wavelengths allow for tighter spacing between nanowells for up to 26 billion single reads on NovaSeq X series 25B flow cells.