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SOLiD® Next-Generation Sequencing Systems & Accessories
The 5500 W Series Genetic Analysis Systems - scalable and accurate next generation sequencing.
The 5500 W Series Genetic Analysis Systems support a wide range of applications on a per-lane basis with independently addressable and configurable lanes on either one or two FlowChips. The Exact Call Chemistry (ECC) module boosts the already industry leading accuracy of this ligation-based sequencing.
5500 W Series Genetic Analyzer V1.0 Specifications
System and Features | 5500 W System | 5500xl W System | |
|---|---|---|---|
| Pay-Per-Lane Sequencing | 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. | ||
| Multiplexing | 96 barcodes for both RNA and DNA applications. | ||
| Instrument Throughput1 1 x 50 | ~ 80 Gb | ~ 160 Gb | |
| Exomes/run2 | Up to 18 | Up to 36 | |
| Transcriptomes/run3 | Up to 12 | Up to 24 | |
| Small RNA/run4 | Up to 144 | Up to 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.
5500 W Series Genetic Analyzer V1.0 Specifications
System and Features | 5500 W System | 5500xl W System | |
|---|---|---|---|
| Pay-Per-Lane Sequencing | 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. | ||
| Multiplexing | 96 barcodes for both RNA and DNA applications. | ||
| Instrument Throughput1 1 x 50 | ~ 80 Gb | ~ 160 Gb | |
| Exomes/run2 | Up to 18 | Up to 36 | |
| Transcriptomes/run3 | Up to 12 | Up to 24 | |
| Small RNA/run4 | Up to 144 | Up to 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.
Product information
Connect with Sequencing Groups
For Research Use Only. Not for use in diagnostic procedures.