Next Generation Sequencing with Roche 454 GS FLX+
The unique combination of long sequencing reads and exceptional
accuracy make the system well suited for the sequencing of genomes
that contain repetitive or unknown regions.
Limited time offer - Free genomic library prep with any
order*
Why choose the Roche 454 GS FLX+ for your
sequencing
- Long read lengths up to 700bp - ideal for
whole genome de novo sequencing, metagenomics and
transcriptome sequencing
- Increased data volumes - up to 1 million
high-quality reads per run
- Improved de novo assemblies -
generate more accurate assemblies with fewer gaps, longer scaffolds
and contigs and better asignment of repeat regions
- Easy to integrate data - into de novo
assemblies, reference mapping and amplicon variant analysis
- Multiplex - up to 132 samples per pool
Applications
- Whole genome sequencing (of small genomes)
- De novo transcriptome sequencing
- Amplicon sequencing
- Metagenomics
For more information complete your details below:
Alternatively please contact us on
sales@sourcebioscience.com
*valid until 31st March 2013. Excluding paired-end library
preps.
