SureCall Software

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.

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
• Reduces time-to-results from days to hours without complex IT infrastructure or special hardware
• Addresses the needs of clinical researchers from analysis to reporting out of their target enrichment NGS data, eliminating data analysis as a bottleneck

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