SureCall

RUO

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.

For Research Use Only. Not for use in diagnostic procedures.

NGS Data Analysis & Interpretation

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Features

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

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SureCall

Product Details

Alissa Reporter - Improving Secondary Data Analysis Tools

Agilent NGS Genomics Solutions Workflow Infographic

SureCall 4.2 Installation Guide