Library Quantification
Quantification of libraries for use in NGS is generally performed before the libraries are pooled for target enrichment or amplification to ensure equal representation of indexed libraries in multiplexed applications. Accurate and precise library quantification is a critical step in both Illumina and Ion Torren workflows, allowing for maximizing sequencing yields downstream. A reliable and accurate DNA quantification strategy will permit researchers to fully utilize sequencer capacity with reducing costs.
Our library quantitation kit, with a user-friendly workflow, enables accurate and reproducible quantitation of Illumina and Ion torrent libraries, with a user-friendly workflow.
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Customer Reviews
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Specificity:"The bead-based technology in the DNA Prep kit ensured high specificity, minimizing off-target effects and providing clean, reliable sequencing results."
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Sensitivity:"The DNA Library Prep Kit showed remarkable sensitivity. Even with minimal input DNA, it produced high-quality libraries, ensuring all significant variants were detected."
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Accuracy:"Using the DNA Library Prep Kit, we achieved highly accurate sequencing data. The results matched our expectations, confirming the reliability of the kit in various applications."
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Stability:"The DNA Library Prep Kit demonstrated exceptional stability, maintaining consistent performance across multiple runs and different sample types, including FFPE samples."
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Customer Support:"The customer support for the Seq Kit was outstanding. They provided prompt and comprehensive assistance, ensuring we could troubleshoot and optimize our experiments efficiently."
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Note: Our sequencing services are for Research Use Only. Not For Clinical Diagnosis.