The Genome Sequencer FLX System, powered by 454 Sequencing, enables ground-breaking discoveries in de novo sequencing, resequencing of whole genomes and target DNA regions, metagenomics, and RNA analysis. Featuring a unique combination of long reads, exceptional accuracy, and ultra-high throughput, the Genome Sequencer FLX System delivers the most comprehensive result at a low total cost, giving it the best overall value of any next-generation sequencing platform.
.Get the complete picture with…
Read lengths averaging 200 to 300 bases per read
Throughput of more than 400,000 reads per run
High single-read accuracy of greater than 99.5% over 200 bases
Consensus-read accuracy of greater than 99.99%
Benefit from complete software packages included with the Genome Sequencer
FLX System, featuring easy-to-use graphical user interfaces (GUI) for
mapping, assembly, and amplicon variant analysis.
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