DNBSEQ-T20X2 is a sequencer released by Complete Genomics in February 2023.
It is based
on DNA Nanoball Sequencing.
Image of DNBSEQ-T20X2: https://en.mgi-tech.com/products/instruments_info/33/ by MGI
Specifications
Manufacturer |
Complete Genomics |
Technology |
DNA Nanoball Sequencing |
Release date |
February 2023 |
Price [2] |
|
Type |
Industrial |
Weight |
3700 Kg |
Supports real-time analysis |
No |
Demultiplexing support |
Yes |
File format |
FASTQ |
Read length |
Complete Genomics DNBSEQ-T20X2: 2x100bp to 2x150bp
|
Run time |
Complete Genomics DNBSEQ-T20X2: 60 to 80 hours
|
Reagent cost per Gb [1] |
Complete Genomics DNBSEQ-T20X2: Unavailable
|
Data quality [3] |
Complete Genomics DNBSEQ-T20X2: ≥ 85% bases above Q30 for PE100
|
Maximum output per run (Gb)[4] |
Complete Genomics DNBSEQ-T20X2: 72000.00
|
Primary error type [5] |
Substitutions |
Notes about the specifications
More about the DNBSEQ-T20x2
The DNBSEQ-T20x2 from Complete Genomics, a subsidiary of MGI, is an ultra-high throughput next-generation sequencing (NGS) instrument positioned for large-scale, production-level genomic projects. It builds upon the same core technology as its predecessors in the DNBSEQ lineup, offering significant improvements in throughput and cost efficiency. If your research involves large population genome studies, building extensive genomic databases, or requires very high sequencing output, the DNBSEQ-T20x2 warrants serious consideration.
Key Innovations
The DNBSEQ-T20x2's key advancements center around significantly increased throughput and reduced sequencing costs:
- Robotic Automation: The DNBSEQ-T20x2 incorporates a sophisticated robotic system that automates various steps throughout the sequencing process, including library loading, reagent handling, and slide washing. This extensive automation minimizes hands-on time by lab personnel, reducing the risk of human error and improving overall workflow consistency. Additionally, automation helps to ensure standardized processing conditions across all samples, leading to more reliable and reproducible sequencing results.
- Increased Slide Capacity: The DNBSEQ-T20x2 can process up to six slides per run, a higher number than the previous models in the DNBSEQ lineup. The ability to process more slides per run translates to a significant boost in sequencing output. Researchers can sequence more samples per run, reducing total run time and costs required to achieve a desired level of coverage.
- Dip-Immersion Technology: DNBSEQ-T20x2 utilizes a novel dip-immersion flow cell design that reduces reagent consumption. In traditional flow cell sequencing, reagents flow over the surface of the slide. In dip-immersion technology, the slide is submerged in a trough containing the sequencing reagents. This reduces the amount of reagent required per sample, as the reagents are constantly replenished during the sequencing run. The T20x2’s dip-immersion system precisely controls the volume of reagent used and minimizes reagent waste. This technology contributes to significant cost savings, particularly for high-throughput sequencing projects.
Features and Technologies
- DNBseq Sequencing: Complete Genomics’s core sequencing technology uses DNA nanoballs (DNBs) for template generation, combined with combinatorial probe anchor synthesis (cPAS) sequencing chemistry. This technology offers high accuracy and flexibility.
- Ultra-High Throughput: The DNBSEQ-T20x2 can produce up to 72 Tb of data per run, enabling sequencing of around 50,000 whole human genomes (30x coverage) annually.
- Suitable Read Lengths: Supports read lengths that are the most common configuration for whole-genome sequencing, PE100 and PE150.
Intended Uses and Specific Applications
- Whole-Genome Sequencing (WGS): Ideal for large-scale population studies, disease association research, and the discovery of novel genetic variants. Compatible with standard third-party WGS library prep kits if using Complete Genomics library conversion kits.
- Exome Sequencing: Suitable for targeted sequencing of protein-coding regions. Compatible with standard third-party WES library prep kits if using Complete Genomics library conversion kits.
- Transcriptome Sequencing (RNA-seq): Can be used for gene expression profiling, transcript discovery, and differential expression analysis. Compatible with standard third-party RNA-Seq library prep kits if using Complete Genomics library conversion kits.
Comparison with Competing Instruments
- Complete Genomics DNBSEQ-T7: The T7 offers high-output but certainly not to the extent of the T20x2. However, the T7 run times are much faster and may be more affordable for most labs.
- Illumina NovaSeq X: The NovaSeq X offers high output, although again not to the level of the DNBSEQ-T20x2, and the NovaSeq X is also slightly more accurate with faster run times, especially with the 1.5B and 10B flow cells.
Special Considerations
The DNBSEQ-T20x2 is best suited for research projects that require ultra-high throughput sequencing and have a high sample volume to justify the instrument's capacity. Examples include large population genomics studies, large-scale cancer genomics studies, and functional genomics projects requiring deep whole-genome sequencing of many samples.
Need sequencing done on a Complete Genomics DNBSEQ-T20X2 or a specific instrument? Tell us about your project here, and we'll connect you with a qualified provider.
This information on this page is up-to-date as of April 15, 2024 and based on the spec
sheets published by the manufacturer.