HaloPlexHS Custom Kits
High-sensitivity, amplicon target capture enrichment for custom NGS, from 50 ng input DNA
- Superior on-target specificity, offering deeper coverage of targeted bases with minimal sequencing.
- Ultra high sensitivity is enabled by tagging every molecule with a unique molecular barcode, allowing deep sequencing for low allele frequency variants and capturing DNA from both strands.
- Confident detection of mutations present at below 1% allele frequency with molecular barcodes-enabled error correction and variant information from both strands in genetically heterogeneous samples.
- Accelerated workflow to complete target enriched next-generation sequencing (NGS) libraries in less than 6 hours from only 50 ng of gDNA.
- Intuitive and powerful data analysis capabilities supported by Agilent SureCall software
NGS SureSelect and HaloPlex Brochure 5991-5241EN