Genome Sequencer FLX System

Genome Sequencer FLX System
by Roche Applied Science - a member of the Roche Group
 3.1/5.0 (2 reviews)

The Roche 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, gi...read more

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Reviews

AVERAGE RATING: 3.1

2 scientists have reviewed this product

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

Nicola Cannata


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Member since 2011

Organization:
University Camerino
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RATING: 1.6

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




Review date: 19 Oct 2011

Genome Sequencer FLX System

"I found it hard to get this machine fully working. There were problems with the chemistry and problems with after sales assistance."

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Andrew Hollinger


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Member since 2008

Organization:
The Broad Institute of MIT & Harvard
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RATING: 4.6

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




Review date: 04 Apr 2008

Genome Sequencer FLX System

"Fantastic support and trouble shooting."

Description

 

The Roche 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.

Features of the Roche Genome Sequencer FLX System include:

• Obtain more comprehensive data.
Generate more than 1,000,000 individual reads with improved Q20 read length of 400 bases per 10-hour instrument run. 
Expand your project capabilities.
Harness the power of DNA sequencing for your complete genome project with one versatile system. Combine long single reads and Long-Tag Paired end reads to completely assemble genomes-often within a single run. 
Reduce your cost per result.
Ultra-high throughput delivers the data you need at an affordable price while longer reads reduce over-sampling requirements, keeping data requirements manageable. Benefit from flexible sample-loading options that support various throughput and experimental design needs, enabling efficient use of reagents and consumables. 
Increase your productivity.
Streamline library preparation of genomics samples and eliminate the laborious tasks of cloning and colony picking - genomic libraries are constructed in hours in a single tube. 
Drive results, not the accumulation of data files.
Perform data analysis without the need for enterprise scale IT solutions with the included easy-to-use software tools - GS De Novo Assembler, GS Reference Mapper, and GS Amplicon Variant Analyzer. Straightforward interpretation of data means faster discovery of biologically meaningful results.

Product Overview

Genome Sequencer FLX System by Roche Applied Science - a member of the Roche Group
Genome Sequencer FLX System




  • 3out of 5EASE OF USE
  • 3 out of 5AFTER SALES SERVICE
  • 3 out of 5VALUE FOR MONEY





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