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Performing whole blood RNA-Seq studies? Join Dr. Andrew Brooks for an exclusive webinar!

Tips for RNA-Seq studies using whole blood

In RNA-Seq studies using whole blood, the number of sequencing reads derived from globin and rRNA transcripts can represent more than 80% of the data, meaning wasted sequencing resources.

In this new webinar, Dr. Andrew Brooks describes a novel method for integrating state-of-the-art blood collection and high-quality RNA extraction with strand-specific RNA-Seq library construction.

The focus will be on

  • Effective removal of specific transcripts from RNA-Seq libraries without impacting non-targeted transcripts
  • Validation of an end-to-end workflow for RNA-Seq analysis from human whole blood
     
Webinar details

Speaker: Dr. Andrew Brooks

Dr. Brooks is the Chief Operating Officer of RUCDR Infinite Biologics and Director of the Bionomics Research and Technology Center at Rutgers University. He is also one of the founding members of the Bioprocessing Solutions Alliance.

Date: June 22

Place: Online

Time: 1 p.m. EDT

Duration: 1 hour

Scheduling conflict? Don’t worry! Register and you’ll receive a link to view an on-demand recording after the event.

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