CLINICAL GENOMIC OPERATING SYSTEM
For Clinicians
StoreGene’s Clinical Genomic Operating System makes it faster, cheaper and easier to apply whole genome data into actionable clinical insights
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.
Rapid Turnaround Time
From sample extraction to analysis and finished report, our Whole Genome Sequencing process can be carried out in just 30 days. For reanalysis, this is reduced to just 7 days.
Increased Diagnostic Yield
Over a large number of studies, the diagnostic yield attained by WES ranges between 25 and 50%, while the WGS diagnostic yield is about 40–60%.
Medication management
99.7% of people have a genetic variation which alters how they metabolise common medications. By using pharmacogenomic data you can reduce adverse drug reactions by 30%.
Always Clinician-led
We believe that no individual should be presented with a genetic report without being provided with clinical guidance and context. Our reports are always shared with the clinician first, and released to the patient after consultation.
StoreGene provides virtual panels and bespoke genetic analysis services tailored to the needs of clinicians and their patients. We offer customisable genetic panels that allow you to select specific genes relevant to your patients’ conditions, ensuring a personalised and targeted approach to genetic testing. Our advanced analysis tools and expert support empower clinicians to make informed decisions, enhancing patient care with precision and accuracy
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
How it works
Register Patient
Simply and securely register a patient using either an NHS number, or Surname, Hospital number, DOB, and sex at birth. Existing patients can easily be reselected.
Upload Clinical Notes
Securely upload clinical notes, and we will use natural language processing to extract HPO terms and make recommendations for areas of analysis.
Choose Analysis
We give you complete control over your analysis. You can choose and combine panels, add individual genes, and request specific areas of interest. We use the most up-to-date clinical databases to surface pathogenic/likely pathogenic variants across all regions of the genome
Simple Consent Process
We aim to keep your patient informed every step of the way, to start the process we will collect a consent form to sequence and store their genome. We offer 100% transparency and give them the ability to manage their own consent and preferences at any time.
