The MiSeqDx NGS Sequencer is manufactured by Illumina. The MiSeqDx instrument is the first Food and Drug Administration-cleared in vitro diagnostic & next-generation sequencing (NGS) system. Illumina also received Food and Drug Administration premarket clearance for the MiSeqDx Cystic Fibrosis 139-Variant Assay, MiSeqDx Cystic Fibrosis Clinical Sequencing Assay, and MiSeqDx Universal Kit.
Specification
Condition: Certified pre-owned Maximum Read Length: Up to 2 × 300 bp Output (2 x 150 bp run): ≥ 5 Gb Reads passing filters (2 x 150 bp run): ≥ 15 million Accuracy-Germline: >99.9% Overall Percent Agreement to Reference Results Accuracy-Somatic: 100% Overall Percent Agreement to Reference Results Reproducibility-Germline: 99.88% Overall Percent Agreement to Reference Results Reproducibility-Somatic: 99.6% Percent Expected Call for mutant samples Q30 score (at read length of 2 × 150 bp): ≥ 80% Power Requirements: 100–240V AC at 50/60Hz, 10A, 400W RFID Radio Frequency: 13.56 MHz RFID Power: 100 mW Samples per Run: Depending on assay LED: 520, 660 nm Warranty: 90-day warranty (US and Canada ONLY)
Features
Food and Drug Administration-Regulated and CE-IVD-Marked NGS System A Growing IVD Menu Simple NGS Workflow User-Friendly, Intuitive Software