返回 SOLiD 5500测序系统(... 返回 SOLiD 5500测序系统(... 
我要纠错
5500 W Series Genetic Analyzer V1.0 Specifications
| System and Features | 5500 W System (1 FlowChip) | 5500xl W System (2 FlowChips) | |
|---|---|---|---|
| 按每条泳道收费测序 | Reagent consumption engineered independently for each lane; users pay only for the consumables in the active lanes when performing a partial run. | ||
| Application-Per-Lane Sequencing | Independent FlowChip lanes allow users to configure read length of chemistry for each lane enabling multiple applications in a single run. | ||
| 多重 | 96 barcodes for both RNA and DNA applications. | ||
|
Instrument Throughput1 1 x 50 1 x 75 2 x 50 MP |
~ 80 Gb ~ 120 Gb ~ 160 Gb |
~ 160 Gb ~ 240 Gb ~ 320 Gb | |
| Exomes/run2 | 高达 18% | 高达 36% | |
| Transcriptomes/run3 | 高达 12% | 高达 24% | |
| Small RNA/run4 | 高达 144% | 高达 288% | |
| Maximum Read Lengths5 | 1 x 75 Frag, 2 x 50 MP | ||
Instrument throughput is estimated using typical runs at a density of 700,000/panel, 65%-70% passing filter. Actual throughput will depend on the samples being run. Throughput uses the quality reads from the instrument that pass the primary analysis filter.
~50 Mb exome, >100x average coverage using fragment chemistry, 1 x 75 bp run.
Transcriptome assumes > 100 million reads/sample using fragment chemistry, 1x 50 bp run.
~8 million reads/sample for each small-RNA sample and utilizing barcodes (48).
New Wildfire paired-end (wPE) 50 bp x 50 bp early access to start by the end of 2012.