For life science research only. Not for use in diagnostic procedures.
NIMBLEGEN and SEQCAP are trademarks of Roche. © 2016 Roche PP-US-05018-0716
Why waste RNA Seq reads on high expressors that have no relevance to the genes you're studying?
Before sequencing, use the SeqCap RNA Enrichment System to enrich the transcripts for any
number of genes that truly matter to you.
• Sequence less—without sacrifi ce
Maintain transcript abundance, and detect more transcripts from much less sequencing (Figure 1).
• Start with ≥10 ng RNA
Analyze samples with limited starting material.
• Quantify and discover novel transcripts
Move beyond expression profi ling to discover fusion transcripts and other isoforms that purely
quantitative methods can't detect.
• Analyze more samples for less
Pre-capture multiplex to cost-effectively sequence more samples, and eliminate the expense of
rRNA depletion.
Design your own RNA target enrichment today.
Visit www.nimblegen.com/SeqCapRNA for more information, or visit
design.nimblegen.com to create your own human or mouse panel.
SIGNIFICANTLY IMPROVE YOUR ODDS
IN RNA SEQUENCING
Figure 1. Preserve transcript abundance and
sensitivity with 1/50th of the sequencing, as
demonstrated with ERCC Controls.
RNA Seq with rRNA depletion,
142.8 million reads
Sample captured with SeqCap
RNA Enrichment System,
2.8 million reads