June 24th – 25th | Boston, MA | Booth 37A
Watchmaker Genomics offers high-performance sequencing solutions optimized for oncology applications, including FFPE and liquid biopsy samples. Our workflows deliver sensitive variant detection, high sequence accuracy, and streamlined library prep – enabling confident analysis from even the most challenging inputs.
Stop by booth 37A to meet the team and check out:
Tried-and-Tested NGS Solutions
- DNA Library Prep Solutions – achieve high conversion efficiency and improved sequence accuracy to improve rare variant detection
- RNA Library Prep Solutions – generate high-quality libraries in under 5 hours with integrated rRNA depletion or mRNA capture – ideal for FFPE samples and fusion detection
- Equinox® Library Amplification Kits – maximize fidelity and reduce PCR-induced errors (particularly C > T substitutions) by up to 40%
New: Better Blood-Based RNA-seq
- Ask us about our latest protocol designed to improve blood-based RNA-seq by combining globin depletion with mRNA capture to maximize informative transcript recovery while minimizing wasted reads
A Sneak Peek at What’s Next
- TAPS Methylation Sequencing – positive-readout methylation and variant detection from a single workflow
- NGS Library Normalization – effortless equimolar pooling without the need for quantification
Automation-Ready When You Are
- Our workflows are purpose-built for scalability and seamless integration with liquid handling systems, whether you’re processing hundreds or thousands of samples.
Let's Connect
Talk science, see new data, and get an exclusive first look at upcoming innovations designed to maximize your sequencing economy. Big ideas deserve even bigger data – and Watchmaker Genomics is ready to help you get there.
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Visit the Festival of Genomics 2025 Event Page for more information about the event.
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