truCOVER® Total RNA Library Prep Kit Trial

 

Test truCOVER® Total RNA Library Prep on your most challenging samples.

 

 

Assess truCOVER Total RNA Library Prep performance on degraded or low-input RNA in your existing RNA-Seq workflow. See for yourself how controlled Adaptive Focused Acoustics® (AFA®) fragmentation and our streamlined, automatable library preparation workflow improves usable reads and lowers sequencing costs.

 

With truCOVER Total RNA Library Prep, you can:

 

  • Detect gene fusions with confidence across standard RNA-seq analysis workflows

  • Generate superior, strand specific RNA sequencing libraries with uniform whole transcriptome coverage and minimal duplication
  • Harness AFA Technology for RNA library preparation with precise, reproducible fragmentation and controlled insert size
  • Recover more from less: Optimized for 10–500 ng input and degraded RNA (DV200 ≥30%), including FFPE and low-input applications
  • Reduce hands on time by up to 40% with a streamlined, automation ready RNA-seq workflow
  • Capture high proportion of exonic reads (~40%), giving high value data for differential gene expression
  • Drive rRNA down to <1% of reads, maximizing usable sequencing data and lowering cost per sample
 

Let’s Optimize Your RNA-seq Workflow

Request your trial kit today.

 

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Simplified workflow reduces turnaround time by up to 40%.
 
By utilizing a single-enzyme, single-incubation step for cDNA synthesis and optimizing magnetic bead clean-ups, the protocol reduces workflow time to approximately 4 hours.
 
Confident gene fusion detection.
 
Qubit/qPCR Conversion Rate Chart
truCOVER detected all gene fusions and alternatively spliced RNAs in the Seraseq® FFPE Tumor Fusion RNA Reference Material, at a depth of only 25 reads (typical kits require 50M+ reads).