Agilent Technologies, Inc. software

Agilent SureCall software allows clinical researchers who use NGS panels for inherited diseases and cancer, to analyze, visualize, and contextualize NGS data using a single application. SureCall is a key component of Agilent`s NGS Target Enrichment solution which includes SureDesign, Agilent`s custom design tool and HaloPlex or SureSelect Target Enrichment panels. Download SureCall free-of-charge from our website.

The SureSelect Focused Exome is a highly targeted design that enables analysis of only the disease-associated targets providing deep coverage even on a benchtop sequencer. This design provides 20 or more reads for 95% of targets at 1.5Gb (100x) of sequencing and 98% of targets with 3Gb (200x) of sequencing enabling superior coverage of disease-associated regions even when sequenced on benchtop sequencers, facilitating highly sensitive and accurate variant calling greatly reducing time to answers. Coupled with SureSelectQXT, the fastest target enrichment workflow that enables 3.5x faster sample to sequencing compared to other competing solutions, and SureCall, a raw data to variant analysis software, this combined solution enables an efficient workflow providing reduced turn-around time from raw data to mutation report.

Agilent`s GeneSpring provides powerful, accessible statistical tools for intuitive data analysis and visualization. Designed specifically for the needs of biologists, GeneSpring offers an interactive environment that promotes investigation and enables understanding of Transcriptomics, Metabolomics, Proteomics and NGS data within a biological context. GeneSpring allows you to quickly and reliably identify targets of interest that are both statistically and biologically meaningful.