DNBSEQ-G50
10Gb ～ 150Gb per run
PE150 sequencing within only 40 hrs
support several read lengths including SE50, PE50, SE100, PE100, and PE150
support sequencing applications for research, clinic, agriculture, etc
| Item | Specification | |
|---|---|---|
| Module | DNBSEQ-G50 | |
| Power Type | 100 V~240 V ,50/60 Hz | |
| Rated Power | 900 VA | |
| Dimensions(L×W×H) | 654 mm×489 mm×545 mm | |
| Net Weight | 200 kg | |
| Flow Cell Type | FCS | FCL |
| No. of Lanes per Flow Cell | 1 lane | |
| fective Reads | 100 M | 500 M |
| Effective Reads | 100 M | 500 M |
| Read Length | SE100 PE100 PE150 | SE50 PE50 SE100 PE100 PE150 |
| * The maximum number of effective reads are based on the sequencing of an internal standard library. Actual output may vary with sample types and library preparation methods. | ||
| Performance | ||||
|---|---|---|---|---|
| Read Lengths | Reads | Data Output | Q30 * | Run Time** |
| SE50-FCL | 500 M | ~25 Gb | >85% | ~7 hrs |
| PE50-FCL | 500 M | ~50 Gb | >85% | ~15 hrs |
| SE100-FCL | 500 M | ~50 Gb | >85% | ~13 hrs |
| PE100-FCL | 500 M | ~100 Gb | >85% | ~26 hrs |
| PE150-FCL | 500 M | ~150 Gb | >80% | ~40 hrs |
| SE100-FCS | 100 M | ~10 Gb | >80% | ~10 hrs |
| PE100-FCS | 100 M | ~20 Gb | >85% | ~20 hrs |
| PE150-FCS | 100 M | ~30 Gb | >80% | ~28 hrs |
| * The percentage of base above Q30 is the average of an internal standard library over the entire run. The actual performance is affected by factors such as sample type, library quality, and insert fragment length. | ||||
| ** Run time is calculated over the entire run including sample loading, sequencing, base calling, and data processing. | ||||
Key Highlights
compact and flexible benchtop genetic sequencer
DNBSEQ-G50
(1) is a compact and flexible benchtop genetic sequencer. With the design of two
different Flow Cells, it empowers flexibility and creates an ideal balance between speed and
affordability. FCS (Flow Cell Small) allows short turnaround time for STAT samples. FCL (Flow Cell
Large) enables lower cost per sample. DNBSEQ-G50 offers 3~5 read length options for both FCS and
FCL, which support a wide range of researches and clinical applications such as low-pass whole
genome sequencing, targeted sequencing, small whole genome sequencing, RNA sequencing and
whole exome sequencing, etc.