Advanta Solid Tumor NGS Library Prep Assay
Confidently analyze multiple somatic variants with a flexible, automated NGS workflow
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To advance our understanding of cancer and make strides toward improved patient care, researchers have a growing need to interrogate somatic mutations, often from limited quantities of available samples. Adding to the challenge, translational and clinical researchers in academia and industry face increasing pressure to maximize laboratory efficiency and productivity by controlling costs and implementing automation to reduce hands-on and turnaround time, while ensuring consistent performance and high-quality results.
The Advanta™ Solid Tumor NGS Library Prep Assay with the automated Juno™ system produces targeted amplicon-based barcoded libraries for subsequent analysis on Illumina® NGS platforms. The Advanta Solid Tumor panel is optimized to interrogate a comprehensive selection of high-value, low-variant-frequency somatic mutations within oncology-relevant genes and requires as little as 12.5 ng of DNA starting material per sample.
Powerful content
Confidently interrogate SNVs, indels and CNVs with a comprehensive panel of 53 high-value genes to analyze FFPE and fresh-frozen tissue from multiple solid tumor cancers.
High efficiency
Maximize laboratory resources by minimizing hands-on time and costly reagent consumption with nanoliter-scale walkaway automation leveraging Standard BioTools™ microfluidic technology.
Flexible workflow
Streamline NGS library preparation of up to 6 unique assay panels generating actionable insights from both DNA and RNA variants in a single run on the Juno system.
