GS FLX+ System

GS FLX+ System
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 3.6/5.0 (1 review)

Roche Applied Science - a member of the Roche Group

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...read more

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Reviews

Carla Young


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Member since 2009

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TAMU
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RATING: 3.6

  • 4 out of 5EASE OF USE
  • 2 out of 5AFTER SALES SERVICE
  • 5 out of 5VALUE FOR MONEY




Review date: 31 Jan 2012

Application Area: Amplicon Multiplexed Sequencing
GS FLX+ System

"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."

Description

 

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

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