
SureSelectXT HS Reagent Kits
The SureSelectXT HS Reagent Kits incorporate molecular barcodes to detect variants allele frequency down to 1% or less. They are optimized for FFPE samples with as little as 10 ng of input DNA and offer an 8-hour workflow. Samples are indexed prior to capture, eliminating the concern of cross contamination.
- DNA-Seq Reagents
Product Details
- Generate libraries from as little as 10 ng of input from intact or highly fragmented FFPE DNA
- Use molecular barcodes (MBC) to remove false positives and accurately detect variant allele frequency down to 1% or less
- Increase positive predictive value (PPV) by creating consensus reads for more accurate variant calling
- Generate higher complexity libraries with higher percentage reads in targeted regions
- Streamline your workflow with a 90-minute hybridization and master-mixed reagents
- Transform samples into sequencing-ready libraries in 8 hours for a faster, more efficient workflow
- Use with SureSelect exomes, or catalog panels or easily create custom panels with the SureDesign software application
- Optional enzymatic fragmentation module for more flexibility
- Key Literature
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SureSelectXT HS Target Enrichment
Brochure for the SureSelectXT HS product
- Brochures
- English
- 11 Sep 2018
- 1.01 MB
Ultra-sensitive Cancer Liquid Biopsy Analysis with the Agilent SureSelectXT HS Target Enrichment Workflow
Low input cfDNA sequencing and molecular barcode error correction with Agilent SureSelectXT HS technology
- Application Notes
- English
- 03 Nov 2017
- 1.00 MB
Comparisons among Six Different Library Preparation Kits using FFPE Samples for Exome
Comparisons among Six Different Library Preparation Kits using FFPE Samples for Exome Enrichment Applications
- Application Notes
- English
- 24 Apr 2018
- 286.69 KB
- Application Notes
- Data Sheets
- Support
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SureSelect Enzymatic Fragmentation Kit
Protocol for enzymatic fragmentation of gDNA for NGS library prep using compatible SureSelect Reagent Kits.
- User Manuals
- English
- 05 Oct 2022
- 397.31 KB
- User Manuals
Videos
Combined Mutation Detection and Copy Number Profiling by Error-Corrected ctDNA Sequencing
Combined Mutation Detection and Copy Number Profiling by Error-Corrected ctDNA Sequencing
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