SureCall
- As of December 31st, 2023, Agilent will cease to issue new licenses for SureCall, and all licenses will end June 30th, 2024, or earlier.
- SureCall is a research desktop application combining both novel and widely accepted opensource algorithms for end-to-end NGS data analysis from alignment to categorization and annotation of mutations, supporting Agilent Target Enrichment applications.
- SureCall provides four different types of analysis: Single, Pair, Trio, and OneSeq CNV and Mutation analysis. The SNPPET SNP caller is an Agilent algorithm, which is optimal for detecting low-frequency variants with high sensitivity and specificity.
- From alignment of raw data to categorization and annotation of mutations in three simple steps
- Supports four different types of analysis: Single Sample, Tumor-Normal, Trio and OneSeq CNV and Mutation Analysis
- Supports variant annotation from many public sources, including NCBI, COSMIC, PubMed, ClinVar and custom annotation
- Utilize single/duplex molecular barcodes (MBC) to remove false positives and accurately detect variants down to ≤1% variant allele frequency
- Addresses the needs of clinical researchers from analysis to reporting out of their target enrichment NGS data, eliminating data analysis as a bottleneck