RTG Software

Real Time Genomics offers sequence data analysis software based on patented search technology for the rapid production of high quality genomic sequence data. RTG software supports read mapping and protein search with gapped alignment, SNP and Indel calling, coverage depth and copy number variation statistics reporting, contaminant filtering and all-by-all coverage mapping. Licensed software is delivered as a single customer-installed executable with a consistent command line interface (CLI) for easy integration of functions into existing pipeline scripts.

RTG gapped alignment commands for read mapping and protein search are highly tolerant of sequence mismatches and gaps introduced by machine error and underlying genome mutation. More information and less noise in the underlying gapped alignments to a reference (sequence template or protein database) can lead to more accurate sequence data analysis results.

RTG software reduces CPU processing load in the data center and increases productivity in the bioinformatics department.  The ability to produce alignments with high sensitivity and accuracy comes with no compromise in speed.  This means an existing data center can deliver on scientists' desired depth of analysis with cycles to spare for additional projects and analysis.

Additionally, a comprehensive line of easy-to-integrate sequence data analysis functions allows rapid development of genomic sequence production pipelines for variant detection and metagenomics.  Scarce bioinformatics talent can then focus on novel computational analysis problems unique to each advanced research organization.

Running natively in either Linux (Java) or Windows (.NET) environments, and supported with extensive documentation, reliable and flexible RTG software satisfies the operational requirements of large-scale data center environments. Contact Real Time Genomics now for an initial consultation.