Cover all your bases with RNA-Seq Services


´╗┐Beckman Coulter Genomics RNA-Seq services ensure all your bases are covered providing an end-to-end solution including expert project design, automated Illumina* TruSeq* library construction, sequencing on the Illumina HiSeq* platforms and comprehensive data analysis.´╗┐

´╗┐Applications
RNA-SeqRNA-Seq is a powerful tool for studying the effect of the transcriptome on phenotype such as disease susceptibility, cancer progression and response to pharmaceuticals. Multiple applications are supported including:

  • Differential gene expression
  • Splice variant analysis
  • Gene fusion identification
  • Rare transcript identification

RNA-Seq Service Offering
The new fully automated sample preparation pipeline delivers consistent results run after run reducing user variability and bias and allowing processing of large amounts of samples with reduced turnaround time.

  • Project design consultation
  • Only 500 ng of total RNA required
  • Automated polyA capture, cDNA synthesis and library construction
  • Sequencing on Illumina HiSeq 2000/2500
  • Multiplexing up to 24 samples per lane
  • Range of data analysis options
  • Turnaround times from 4 weeks
  • Entire project overseen by expert study managers

RNA-Seq vs Microarray
The deep sequencing capabilities of RNA-Seq have opened up the transcriptome proposing many benefits over microarrays:

  • Profiling of the entire transcript
  • Detection of splice variants, novel isoforms and gene fusions
  • More sensitive detection of genes, transcripts and differential expression
  • Increased dynamic range
  • Reanalyzable data

 

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Beckman Coulter and the stylized logo are registered trademarks of Beckman Coulter, Inc.



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