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Automated integrity assessment of RNA samples.
Automated integrity assessment of RNA samples.

Transforming bottlenecks into breakthroughs: solutions for single-cell sequencing workflows
Discover how to transform your single-cell sequencing bottlenecks into breakthroughs with our guide.

Get the answers you need with single-cell sequencing
Revvity's solutions for key steps of your single-cell sequencing journey.

Solutions for precision medicine research
Our wide range of technologies can help you gain the knowledge you need to identify genomic vulnerabilities, screen functional responses, and evaluate how well a treatment is working.

BioQule DNA-Seq library prep: Samples to ready-to-use NGS libraries
Learn about the the BioQule DNA Library Prep Kit, which utilizes enzymatic fragmentation, and the BioQule NGS System for Whole Genome Sequencing (WGS).

Overcoming the technical and economic hurdles of single-cell sequencing
This white paper offers valuable insights from an expert panel discussion on navigating single-cell sequencing challenges to enhance your research outcomes.

Improving precision stratification using patient-derived model systems
Precision stratification using patient-derived model systems.

Genetically engineered PDX models as patient avatars in preclinical evaluation of acute leukemias
Identifying therapeutic targets using gene silencing techniques in PDX models

Gel-free small RNA library prep kit for Illumina sequencing
This flyer describes the benefits of the NEXTFLEX® Small RNA-Seq Kit v4 kit

Simplify Low-Input Small RNA-seq Library Prep and Improve Discovery Application Note
Simplify Low-Input Small RNA-seq Library Prep and Improve Discovery


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