GQ-Dx
GQ-Dx provides comprehensive genomic information capabilities for whole-genome diagnostics at clinical-scale, including:

Sequence Processing

• Automated transfer of raw data from sequencing machines
• Alignment of the reads against reference genomes
• Variant detection and annotation

Diagnostic Reporting

• Mapping and documentation of variants against known inherited and somatic mutations
• Integration with other clinical data systems such as Electronic Health Records and therapy protocols to create a comprehensive patient diagnostic record
• Customized reporting

Diagnostic Research

• Comparison against other datasets and patient populations studies
• Interactive querying of reads, variants, and comparison results
• Access to research workflows such as RNA-Seq, Whole Genome Analysis, ChIP-Seq, and Bacterial/Viral Detection
• A “learning system” to capture, manage, and reapply new findings