Explore Watchmaker’s Library Prep Solutions at ESHG 2024

June 1st – 4th | Berlin, Germany | Booth 656

Visit us at booth 656 to learn about our rapid and sensitive RNA and DNA library prep solutions that improve sequence data quality and accuracy with challenging sample types, including FFPE and cfDNA from liquid biopsies:

• DNA library prep kits that improve coverage of low-input samples and reduce sequence artifacts by up to 90%
• RNA library prep kits that generate sequencing-ready libraries in under 5 hours, including rRNA depletion or mRNA capture, and improve sensitivity with challenging samples
• Library amplification kits which reduce misincorporation rates by up to 40% and enable methyl sequencing applications

Sunday, 02 June at 8:30 CEST | New York 2

Part 1: Advancing DNA and RNA NGS library prep solutions to overcome data quality bottlenecks in clinically relevant sequencing applications

Presented by Jen Pavlica, Watchmaker Genomics

Part 2: Customizing Watchmaker DNA PCR-Free Library Prep Kit for Improved NovaSeq X Performance

Presented by Anna Lyander, PhD, Clinical Genomics Stockholm, Science for Life Laboratory, Karolinska Institutet and KTH Royal Institute of Technology

Part 3: Non-Invasive Prenatal Testing: Embracing Low Input Methodologies

Presented by Gabriel Minárik, RNDr., PhD, TrisomyTest Ltd.

ET-Assisted Pyridine-Borane Sequencing version 1.0 – A rapid, scalable, and non-destructive sequencing approach to methylation profiling

Poster Number: P21.004.C
Monday, 3rd June, 13:00:00 – 14:00:00 CEST

Surveying the RNA-seq landscape: A multi-workflow comparison for mRNA and whole transcriptome sequencing applications

Poster Number: P21.005.D
Monday, 3rd June, 15:45:00 – 16:45:00 CEST

We’d love to learn about your projects! Stop by Booth 656 or schedule a meeting to talk about our new products and early access programs.

Please provide your selection and contact information below.

Visit the ESHG 2024 Meeting Page for more information about the event.