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Genomics and epigenomics with automated sample prep workflows
Sample prep, including homogenization and nucleic acid extraction, automated library prep for research geneticists and epigeneticists
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Biomarker discovery and companion diagnostic research sample prep workflows
Sample prep, including homogenization and nucleic acid extraction, automated PCR and NGS prep for biomarker and companion diagnostic research
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Ex Vivo Functional Drug Testing of 3D Patient-Derived Cancer Cells Shows Promise for Personalized Medicine
Demonstrating how functional testing of 3D patient-derived cancer cells enables effective drug sensitivity testing.
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Quantum GX3 product note
High resolution, high speed, high performance preclinical microCT imaging with the Quantum GX3. Spatial resolution down to 5 microns, wide FOV from 8 - 86 mm for imaging ex vivo sample and larger species.
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End-to-end whole genome sequencing metagenomics solutions
This flyer describes Revvity and CosmosIDs solution for WGS for metagenomics.
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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).
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Transforming bottlenecks into breakthroughs: solutions for single-cell sequencing workflows
Discover how to transform your single-cell sequencing bottlenecks into breakthroughs with our guide.
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Get the answers you need with single-cell sequencing
Revvity's solutions for key steps of your single-cell sequencing journey.
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Elevate your single-cell sequencing: Beat the stats
Discover simple strategies to overcome single cell sequencing obstacles in our infographic.
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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.
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DepleteX™ Globin Depletion Kit
Remove contaminating globin fragments for RNA-Seq
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CRISPRclean® depletion technology: A new tool to better understand rare diseases
Enhanced RNA-Seq delivers double the genes detected with confidence
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