Next Generation Sequencing with Roche 454 GS FLX+ System
The Source BioScience sequencing service now includes the GS
FLX+ System. 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.
Advancements in sequencing chemistry, instrumentation and
software mean we can offer the latest improvements in GS FLX System
performance.
Why choose the GS FLX+ System
- True capillary sequencing-like read lengths
- High-throughput: Generate 1 million high-quality reads per run;
~700 Mb throughput
- Flexible sequencing formats: Broad selection of gaskets and
Multiplex Identifiers (MIDs) enables efficient use of sequencing
runs
- Easy to integrate the data into de novo assemblies,
reference mapping and amplicon variant analysis
Combined Illumina HiSeq and 454 FLX+
Sequencing
The best of both worlds
- High-confidence backbone assemblies for de novo
sequencing projects
- Unprecedented coverage and gap closure rates utilising Illumina
paired-end reads
Our bioinformatics expertise is capable of integrating data from
both platforms to achieve the best possible results.
For more information on how we can help with your research,
please contact
us.
