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.
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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.
