SIRIUS™ is a cloud-based software tool that enables researchers to quickly and intuitively analyze whole genome (WGS), whole exome (WES) and gene panel sequencing data when exploring rare diseases.

CHANGING THE WAY YOU ANALYZE YOUR SEQUENCING DATA

 


Users can easily manage their projects thanks to SIRIUS’ unique interface which enables user to filter variants via a single click, annotate them, and save all analysis parameters. SIRIUS assists researchers to easily and quickly manage projects and save data in a safe manner.

TRANSFORMING SEQUENCING DATA INTO KNOWLEDGE

KEY FEATURES

 

Family transmissions are pre-set to enable researchers to identify a list of variants of interest in a family with just one click. All analysis parameters are modifiable, including impact of the variants and database thresholds. Analysis parameters can also be saved as “favorites” for future use.

 

 

 

SIRIUS enables the visualization of variants and provides users with access to full annotations for genes and variants. Users can also save lists of their favorite genes and variants, as well as genes and variants to exclude from analyses. These lists can be shared between the different users within the same account.

 

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For research use only. Not for use in diagnostic procedures.