Description:
Saluseq Nimbo Low Throughput Sequencer is a compact benchtop NGS sequencing platform designed for rapid and efficient low- to medium-throughput sequencing applications. The instrument uses semiconductor sequencing technology and enables laboratories to perform targeted sequencing workflows directly in their own facilities.
Saluseq Nimbo is designed for flexible use in molecular biology, clinical research, and other applications requiring rapid sequencing data generation. Its compact design and simplified workflow make it suitable for laboratories requiring an in-house NGS solution.
The system supports different sequencing chip configurations and provides scalable sequencing output depending on the selected run capacity.
Features:
- compact benchtop NGS sequencing system
- semiconductor sequencing technology
- suitable for targeted sequencing applications
- flexible sequencing capacity options
- rapid sequencing data generation
- simple operation and workflow
- suitable for research and diagnostic laboratories
- supports multiple sequencing applications
Instrument Specification:
| Parameter |
Specifications |
| Instrument type |
Low throughput NGS sequencer |
| Technology |
Semiconductor sequencing |
| Sequencing capacity |
25M / 60M / 100M reads per run |
| Data output |
1.25 Gb – 40 Gb |
| Run time |
Approximately 3.4 – 25 hours |
| Weight |
115 kg |
| Size |
619 mm(W) x 682 mm (D) x 738 mm (H) |
| Display |
13.3" touchscreen display |
| Display resolution |
1920 × 1080 |
| Processor |
12th Gen Intel® Core™ i9-12900 |
| Memory |
128 GB |
| Storage |
2 TB SSD |
| Operating system |
Windows 10 X64 |
| Power supply |
100–240 V AC |
| Frequency |
50/60 Hz |
| Power |
1000 VA |
| Operating temperature |
15–30 °C |
| Operating humidity |
20–80% RH (non-condensing) |
Applications:
- targeted NGS
- molecular diagnostics
- personalized medicine
- NIPT analysis
- forensic analysis
- environmental DNA (eDNA)
- genomic research
The table 1 shows the available read lengths (SE50–SE400 and PE150/PE300), data output per run ranging from 1.25 to 40 Gb, sequencing time from 3.4 to 25 hours, and data quality with Q30 values up to ≥ 90%.
The table 2 presents the recommended sequencing methods, typical applications, required data volume per sample, read length, and the estimated number of samples per run for the 25M, 60M, and 100M reagent kits.