GS FLX+ System
Now delivering sequencing reads up to 1,000 bp in length! The GS FLX+ System features the unique combination of long reads, exceptional accuracy and high-throughput, making the system well suited for larger genomic projects. The GS FLX System has been at the heart of key breakthrough genomic discoveries and over 1,000 peer-reviewed publications to date.Advancements in sequencing chemistry, instrumentation and software offer t…
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Amplicon Multiplexed Sequencing
This product allowed me to get exon-intron spanning reads of 150 to 600 bp products of different 56 gene amplicons coded with specific primers, while being grouped together by taxa and taxon barcodes being loaded onto the A Adapter. I then could identify possible SNPs between the Taxa and go back to design primers around those SNP/SNV and INDELs. I really was happy since there was no reference sequence to compare to originally.
Review Date: 31 Jan 2012 | Roche
Now delivering sequencing reads up to 1,000 bp in length!
The GS FLX+ System features the unique combination of long reads, exceptional accuracy and high-throughput, making the system well suited for larger genomic projects. The GS FLX System has been at the heart of key breakthrough genomic discoveries and over 1,000 peer-reviewed publications to date.
Advancements in sequencing chemistry, instrumentation and software offer the latest improvements in GS FLX System performance, with read lengths up to 1 kb. Available as an on-site instrument upgrade or new instrument, the GS FLX+ System is designed for use with both the new long-read Sequencing Kit XL+ and existing Sequencing Kit XLR70.
GS FLX+ System Features:
- True capillary sequencing-like read lengths: Continuous development of the GS FLX Titanium chemistry now offers read lengths up to 1 kb
- Flexible sequencing formats: Broad selection of gaskets and Multiplex Identifiers (MIDs) enables efficient use of sequencing runs
- Point-and-click data analysis: Included GS Data Analysis Software for de novo assembly, reference mapping and amplicon variant analysis.
Applications:
- Whole Genome Sequencing: De novo sequencing of large, complex organisms or multiple bacterial genomes in a single run
- Transcriptome Sequencing: Full-length de novo sequencing and assembly of complex organisms
- Amplicon Sequencing: High-throughput sequencing of 100s to 1,000s of samples and loci
- Sequence Capture: Targeted resequencing of whole exomes or large capture regions
- Metagenomics: Characterization of complex environmental samples; pathogen discovery
Explore Next Generation Sequencing Possibilities with The GS Junior
This informative video from Roche introduces the conveniently sized bench top GS Junior DNA sequencing machine. This new technology provides an end to end next generation DNA sequencing system, enabling research labs to integrate NGS into everyday lab systems. Long reads of 400 – 500 bp can be obtained with a single run of up to 10 hours generating 35 million high quality bases.
