Learn how to generate duplex sequencing libraries in 3 hours at ABRF 2018

ABRF Annual Meeting 2018 | 04.22.2018 – 04.25.2018 | Myrtle Beach, SC

Paragon Genomics | Booth #218

Power your cancer research with CleanPlex® technology with molecular barcoding for confident detection of somatic mutations

Scientists at Paragon Genomics have been working hard to bring you technologies that will help you advance your translation research. At the 2018 ABRF Annual Meeting, we will be presenting our latest invention CleanPlex® technology with molecular barcoding, which will enable detection of ultralow-frequency somatic mutations in cell-free DNA via duplex sequencing. The new technology enjoys the same benefits as our classic CleanPlex technology, allowing cancer researchers to discover more from less.

Discover more with CleanPlex NGS Panels

  • Up to 20,000 amplicons per pool
  • High coverage uniformity
  • High on-target rate
  • High target design rate

Use less with CleanPlex NGS Panels

  • Inputs as low as 100 pg*
  • Fast 2.5-hour protocol
  • Simple single-tube workflow
  • Efficient use of NGS reads
*Higher input amounts may be required for detection of low-frequency variants

Talk to our Experts – Booth #218

Visit us at booth #218 to speak with our scientists about our new CleanPlex technology with molecular barcoding. Sign up below to schedule a one-on-one meeting with our experts to discuss your cell-free DNA research projects.

Visit our Posters – Poster #119 & Poster #108

Our scientists will be presenting our new CleanPlex technology with molecular barcoding at the poster session. Posters will be available for general viewing throughout the conference. Come to our booth if you miss the chance to speak with our scientists. Sign up below to receive copies of the posters if you can’t make it to the conference or the poster session.

Poster #119 – Detecting Low Allele Frequency Somatic Mutations using Targeted Amplicon Sequencing and a Novel Double Strand Molecular Barcoding Scheme

Date and Time: Monday, April 23, 6:30 PM – 7:30 PM
Location: Poster area in the Exhibit Hall


Poster #108 – 
CleanPlex’s Simple Workflow Produces NGS Libraries with Low Background and High Variant Detection Accuracy

Date and Time: Monday, April 23, 5:30 PM – 6:30 PM
Location: Poster area in the Exhibit Hall

Share your Challenges

What are your research and assay development challenges?

Stop by our booth #218 to share your challenges and needs in targeted sequencing and enter to win an Echo Dot by Amazon.

Download Posters

Download our ABRF posters here.

Request Poster/Schedule a Meeting

Sign up here to schedule a one-on-one session with our scientists to discuss your cell-free DNA research projects or to receive PDF copies of our posters after the conference.

2018-05-22T16:38:18+00:00 April 9th, 2018|Events|Comments Off on Learn how to generate duplex sequencing libraries in 3 hours at ABRF 2018
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