Where others see data
We see answers
At the end of sequencing, there is more than data. Sometime there is doctor waiting for patient's result or sometimes a researcher is looking for answers. No matter what the use case maybe, our mission is make this journey easy for you.
Automated data upload directly from the sequencer
Dedicated data connection for blazing upload speed
Secure browser-based data upload
Upload data from multiple sequencers remotely
Analyze somatic or germline mutation
Whole exome, genome and panel
Custome proprietary pipeline integration
Integration of major clinical databases
Automated variant classification
Schedule analysis for convenience and cost optimization
Automated ACMG guidelines based classification
API based modular integration with LIMS, EMR, EPIC etc.
Visualization tool for easy interpretation
Medical database for literature search
Therapy recommendation based on variant classification
Your Data. Your Insights. Your Story!