OUR MISSION
Affordable, accessible & actionable genomics
As our understanding of genetics and the significance of non-coding regions evolves, there is no need to re-sequence to capture newly discovered variants or genes. A single sample today has the potential to provide insights throughout an individual’s entire lifetime.
OUR VISION
The power of reanalysis
In the last 3 years alone, researchers have identified over 70,000 new pathogenic variants. With approximately 60 new disease-causing variants being discovered daily, reanalysis is a vital part of clinical care. The beauty of StoreGene is that there is no need to order another test, and no additional sample is required. Simply specify your area of analysis and we’ll take care of the rest
OUR METHOD
Utilising the Whole Genome
At StoreGene, we analyse whole genome data. Our incredible bioinformatic pipelines allow you to surface variants from all regions of the genome, and our simple reanalysis process allows you to use the most up-to-date clinical research to inform your decision-making.
FOR CLINICIANS
Instant personalised insights for your patient
StoreGene’s Clinical Genomic Operating System (CGOS) enables you to tailor treatment for your patient. Our ever-expanding library of the most up-to-date genetic tests can be applied to your patient’s genomic data throughout their lifetime, and reanalysis is simple, fast and affordable.
FOR PATIENTS
Take control of your genome data
StoreGene’s Clinical Genomic Operating System (CGOS) enables you, with your clinician, to access personalised healthcare that is tailored specifically to you. Our ever-expanding library of the most up-to-date genetic tests can be applied to your genomic data throughout your lifetime.
OUR AFFILIATES
