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DNBSEQ-T1+
Simple. Rapid. Flexible.
RUO
DNBSEQ-T1+, powered by DNBSEQ™ technology, is a highly efficient mid-throughput sequencer with Q40 accuracy, delivering 25Gb – 1.2Tb of data in under 24 hours. Its optimized performance and flexible sequencing options enable scientists to seamlessly explore genomics — from discovery to validation and production-scale sequencing — while maintaining cost-effectiveness.
Reads per Run
1.2 T/Run
Samples
4 WGS, 32 WES, 80 RNA-seq
Read Lengths
SE50, SE100, PE150, PE300* (*FCS: Available in H2 2025. FCS PE300 and FCM: Available in H1 2026)
Specifications
Explore the core capabilities and technical details.
Applications
Whole-Genome
Whole-Genome
Population Studies
Transcriptome
Methylation Analysis
Multiomics
Your Data Security is Our Top Priority
All our sequencing platforms can work as standalone systems from sample to result without any network connection, eliminating the risk of data breaches and ensuring complete data security.
The
DNBSEQ-T1+
Advantage
Possibilities
Unlock multi-omics potential with versatile, cost effective sequencing options
Speed
Unmatched performance, generating 1.2 Tb of data ~22.5 hours
Discovery
Enhance breackthroughs with Q40 accuracy and flexible read options
Possibilities
Unlock multi-omics potential with versatile, cost effective sequencing options
Speed
Unmatched performance, generating 1.2 Tb of data ~22.5 hours
Discovery
Enhance breackthroughs with Q40 accuracy and flexible read options
Possibilities
Unlock multi-omics potential with versatile, cost effective sequencing options
Speed
Unmatched performance, generating 1.2 Tb of data ~22.5 hours
Discovery
Enhance breackthroughs with Q40 accuracy and flexible read options
Possibilities
Unlock multi-omics potential with versatile, cost effective sequencing options
Speed
Unmatched performance, generating 1.2 Tb of data ~22.5 hours
Discovery
Enhance breackthroughs with Q40 accuracy and flexible read options
DNBSEQ-T1+
Simple. Rapid. Flexible.
RUO
DNBSEQ-T1+, powered by DNBSEQ™ technology, is a highly efficient mid-throughput sequencer with Q40 accuracy, delivering 25Gb – 1.2Tb of data in under 24 hours. Its optimized performance and flexible sequencing options enable scientists to seamlessly explore genomics — from discovery to validation and production-scale sequencing — while maintaining cost-effectiveness.
Reads per Run
1.2 T/Run
Samples
4 WGS, 32 WES, 80 RNA-seq
Read Lengths
SE50, SE100, PE150, PE300* (*FCS: Available in H2 2025. FCS PE300 and FCM: Available in H1 2026)
Specifications
Explore the core capabilities and technical details.
Applications
Whole-Genome
Whole-Genome
Population Studies
Transcriptome
Methylation Analysis
Multiomics
Your Data Security is Our Top Priority
All our sequencing platforms can work as standalone systems from sample to result without any network connection, eliminating the risk of data breaches and ensuring complete data security.
The
DNBSEQ-T1+
Advantage
Possibilities
Unlock multi-omics potential with versatile, cost effective sequencing options
Speed
Unmatched performance, generating 1.2 Tb of data ~22.5 hours
Discovery
Enhance breackthroughs with Q40 accuracy and flexible read options
Possibilities
Unlock multi-omics potential with versatile, cost effective sequencing options
Speed
Unmatched performance, generating 1.2 Tb of data ~22.5 hours
Discovery
Enhance breackthroughs with Q40 accuracy and flexible read options
Possibilities
Unlock multi-omics potential with versatile, cost effective sequencing options
Speed
Unmatched performance, generating 1.2 Tb of data ~22.5 hours
Discovery
Enhance breackthroughs with Q40 accuracy and flexible read options
Possibilities
Unlock multi-omics potential with versatile, cost effective sequencing options
Speed
Unmatched performance, generating 1.2 Tb of data ~22.5 hours
Discovery
Enhance breackthroughs with Q40 accuracy and flexible read options
DNBSEQ-T1+
Simple. Rapid. Flexible.
RUO
DNBSEQ-T1+, powered by DNBSEQ™ technology, is a highly efficient mid-throughput sequencer with Q40 accuracy, delivering 25Gb – 1.2Tb of data in under 24 hours. Its optimized performance and flexible sequencing options enable scientists to seamlessly explore genomics — from discovery to validation and production-scale sequencing — while maintaining cost-effectiveness.
Reads per Run
1.2 T/Run
Samples
4 WGS, 32 WES, 80 RNA-seq
Read Lengths
SE50, SE100, PE150, PE300* (*FCS: Available in H2 2025. FCS PE300 and FCM: Available in H1 2026)
Specifications
Explore the core capabilities and technical details.
Applications
Whole-Genome
Whole-Genome
Population Studies
Transcriptome
Methylation Analysis
Multiomics
Your Data Security is Our Top Priority
All our sequencing platforms can work as standalone systems from sample to result without any network connection, eliminating the risk of data breaches and ensuring complete data security.
The
DNBSEQ-T1+
Advantage
Possibilities
Unlock multi-omics potential with versatile, cost effective sequencing options
Speed
Unmatched performance, generating 1.2 Tb of data ~22.5 hours
Discovery
Enhance breackthroughs with Q40 accuracy and flexible read options
Possibilities
Unlock multi-omics potential with versatile, cost effective sequencing options
Speed
Unmatched performance, generating 1.2 Tb of data ~22.5 hours
Discovery
Enhance breackthroughs with Q40 accuracy and flexible read options
Possibilities
Unlock multi-omics potential with versatile, cost effective sequencing options
Speed
Unmatched performance, generating 1.2 Tb of data ~22.5 hours
Discovery
Enhance breackthroughs with Q40 accuracy and flexible read options
Possibilities
Unlock multi-omics potential with versatile, cost effective sequencing options
Speed
Unmatched performance, generating 1.2 Tb of data ~22.5 hours
Discovery
Enhance breackthroughs with Q40 accuracy and flexible read options
Resources
Product Brochure & Manuals
Resources
Product Brochure & Manuals
Resources
Product Brochure & Manuals
Product Brochure
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Join our newsletter to stay up to date on features and releases.
I have read and understood MGI’s Privacy Policy, and I consent to the collection and processing of my personal data for handling, responding to my contact, receiving your newsletter as well as promotion and marketing activities.
*For Research Use Only
Not for use in diagnostic procedures (except as specifically noted).
Join our newsletter to stay up to date on features and releases.
I have read and understood MGI’s Privacy Policy, and I consent to the collection and processing of my personal data for handling, responding to my contact, receiving your newsletter as well as promotion and marketing activities.
*For Research Use Only
Not for use in diagnostic procedures (except as specifically noted).