HaloPlexHS Custom Kits
RUO
HaloPlexHS Custom Kits offer amplicon capture-based target enrichment with ultra-high sensitivity. By tagging every molecule with an unique molecular barcode, and capturing DNA from both strands, HaloPlexHS enables confident detection of rare variants with significantly improved base calling accuracy.
These kits utilize a fast workflow of as little as under 6 hours for flexible custom NGS panels of up to 5 MB, starting with only 50 ng of DNA. Data analysis of HaloPlex custom kits is seamlessly supported by Agilent SureCall software.
These kits utilize a fast workflow of as little as under 6 hours for flexible custom NGS panels of up to 5 MB, starting with only 50 ng of DNA. Data analysis of HaloPlex custom kits is seamlessly supported by Agilent SureCall software.
For Research Use Only. Not for use in diagnostic procedures.
- DNA-Seq Reagents
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This product is not available for purchase by the general public.
Product Details
Features
- 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.
Specifications
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How It Works
Literature
- Brochures
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HaloPlex Target Enrichment System
Flyer on the HaloPlexHS Target Enrichment product. HaloPlexHS uniquely tags each DNA library fragment with molecular barcodes, allowing the tracking of molecules through the library preparation process & deduplication of reads
- Brochures
- English
- 20 Dec 2022
- 1.31 MB
- Data Sheets
- Flyers
Support
- User Manuals
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HaloPlex HS Automated Target Enrichment System for Illumina Sequencing
Automation protocol for HaloPlex HS Target Enrichment System for Illumina on the NGS Bravo
- User Manuals
- English
- 16 Dec 2016
- 1.78 MB
HaloPlex HS Target Enrichment System for Illumina Sequencing
Optimized protocol for the HaloPlex HS Target Enrichment System to prepare target-enriched samples for sequencing on Illumina platforms.
- User Manuals
- English
- 16 Dec 2016
- 1.17 MB
Videos
Training & Events
Error-Corrected Sequencing to Detect Measurable Residual Disease in Post-Transplant MDS Cases
This is a webinar by Dr. Eric Duncavage from Washington University School of Medicine in St. Louis and Dr. Tracy Liu from Agilent on Error-Corrected Sequencing to Detect Measurable Residual Disease in Post-Transplant MDS Cases.
Webinar/Training
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