DNBSEQ-T1+
Rapid：PE150 < 24 Hours，127/Run,Q40 > 90%
Simple：Integrated DNB Make & Load Module，Reagent Kit One-step Operation,Integrated Sequencing and Cleaning
Flexible：Individually Addressable Lanes,Dual-Flow Cell,Dual-Configuration
| Maximum number of Flow Cells | Flow Cell Type | Lanes/Flow cell | Effective Reads*/Flow Cell | Read Lengths** | Data Output | Q30*** | Q40*** | Run Time**** |
|---|---|---|---|---|---|---|---|---|
| 2 | FCL | 4 | 2000 M | SE50/App-DSE50 | 100 Gb~200 Gb | >93% | >90% | ~7 h |
| SE100/App-DSE100 | 200 Gb~400 Gb | >93% | >90% | ~9.5 h | ||||
| PE150/App-D PE150 | 600 Gb~1,200 Gb | >93% | >90% | ~24 h | ||||
| FCM | 2 | 1000 M | App-DE100 | 100 Gb~200 Gb | >93% | >90% | ~8.5 h | |
| App-PE150 | 300 Gb~600 Gb | >93% | >90% | ~20 h | ||||
| FCS | 2 | 500 M | App-DE100 | 50 Gb~100 Gb | >93% | >90% | ~7.5 h | |
| App-PE150 | 150 Gb~300 Gb | >93% | >90% | ~19 h | ||||
| App-PE300 | 300 Gb~600 Gb | >85% | >75% | ~35 h | ||||
|
* The effective reads are based on the sequencing of an internal standard library. Actual output may vary depending on sample type and library preparation method. ** The instrument is equipped with SE50 and PE100 sequencing modes, and the existing reagent kits support SE50 and PE100 read length sequencing. *** The percentage of bases above Q30, Q40 and run time is the average of an internal standard library over the entire run. Actual performance is affected by factors such as sample type, library quality, and insert fragment length. **** Run time is calculated based on the dual-slide mode, referring to the statistical duration from ssCirDNA library to FastQ. FCM and FCS are theoretical estimates of duration. ***** FCS: Available in H2 2025. FCS PE300 and FCM: Available in H1 2026. |
||||||||
| Application Type | Recommended Data Size | Recommended Read Length | Max. Flow Cells/RUN: 2 | ||
|---|---|---|---|---|---|
| 1*FCS | 1*FCM | 1*FCL | |||
| 500 MM reads | 1000 MM reads | 2000 MM reads | |||
| NIPT/PGS | 10 M reads/sample | SE50/SE100 | 40 | 80 | 160 |
| RNA-Seq | 25 M reads/sample | SE50 | 16 | 32 | 64 |
| Metagenomics for pathogen detection | 20 M reads/sample | SE50/SE100 | 20 | 40 | 80 |
| Single cell RNA-Seq | 10K cells, 50K reads/cell, 500 M/sample | PE150 | 1 | 2 | 4 |
| Oncology panel | 10 Gb/sample (5000X ， 1Mb panel) | PE150 | 12 | 24 | 48 |
| Companion Diagnostic Onco panel | 1 Gb/sample | 120 | 240 | 480 | |
| Microbial WGS | 1 Gb/sample | 120 | 240 | 480 | |
| ATOPlex Panel | Respiratory tract panel/ COVID-19 panel：5M reads/sample | 80 | 160 | 320 | |
| Transcriptomics | 6 Gb/sample | 20 | 40 | 80 | |
| WES | 100X average sequencing depth 15 Gb/ sample | 8 | 16 | 32 | |
| WGS | 30X average sequencing depth 100 Gb/ sample | 1 | 2 | 4 | |
| WGBS | 30X average sequencing depth 120 Gb/sample | 1 | 2 | 4 | |
| Oncology targeted methylation panel | 5 Gb/sample (2000X, 0.5Mb panel) | 24 | 48 | 96 | |
| 16S | 0.1M reads/sample | 1152 (576/lane) | / | / | |
| Recommended data output and sample numbers are only for reference, actual application will require optimisation adjustments. | |||||
Key Highlights
the fastest T-level benchtop sequencers globally
DNBSEQ-T1+ is one of the fastest T-level benchtop sequencers globally, developed with MGI's core DNBSEQ™ sequencing technology. T1+
29
supports dual flow cell concurrent operation, generating up to 1.2 Tb of sequencing data within 24 hours (600 Gb per flow cell, totaling 1.2 Tb
for two flow cells). Additionally, T1+ offers an optional built-in bioinformatics module, enabling automated advanced analysis immediately
after the sequencing run.