Increase RNA-seq efficiency and maximize unique reads with a new rRNA removal method

 
Join our webinar and discover how adopting a more effective rRNA removal strategy can positively impact on your RNA-seq results

Increasing the generation of unique reads in RNA-seq correlates with the efficacy of your rRNA removal strategy. Join our webinar, where we will present QIAseq FastSelect. This superior alternative to traditional rRNA removal methods for bacterial, mammalian and mixed RNA-seq samples works by neutralizing rRNA during the reverse transcription reaction as opposed to hybridization-capture or hybridization-enzymatic digestion. We will discuss the successful use of this innovative technology with fragmented and high-quality RNA for both short and long-read RNA-seq analysis. Discover how this fast and efficient method ensures greater rRNA removal from mammalian, bacterial and mixed samples in just a few pipetting steps and a 14-minute incubation.
• Title: QIAseq FastSelect rRNA removal as a new alternative to Ribo-Zero and RiboErase for bacterial and mammalian RNA-seq samples
• Date: Tuesday, November 19, 2019
• Time: 9:00 a.m. and 4:00 p.m. EDT Check your time zone
• Speakers: Samuel Rulli, Ph.D., Senior Global Product Manager, Genomics, QIAGEN
 
 
Call us during our office hours (Monday to Friday):
800-426-8157
 
For up-to-date licensing information and product-specific disclaimers, see the respective QIAGEN kit handbook or user manual. QIAGEN kit handbooks and user manuals are available at www.qiagen.com or can be requested from QIAGEN Technical Services or your local distributor.
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