RESOURCES

Why Whole Genome?

Whole genome analysis is currently the most comprehensive genetic test available. It sequences the vast majority of the genome, encompassing genes, non-coding regions, and regulatory elements. This ensures that no genetic information is missed and provides a dataset that can be reanalysed as academics complete the full picture.

Since it covers the entire genome, whole genome analysis is future-proof. As our understanding of genetics and the significance of specific genetic regions evolves, you won’t need to re-sequence to capture newly discovered variants or genes, it can be simply reanalysed

Whole genome analysis is not limited to a predefined set of genes or regions. It can identify genetic variants associated with a wide range of diseases, including rare and novel diseases that may not be part of a panel or exome test. This information can be used to identify individuals who are at higher risk of developing these conditions, leading to earlier diagnosis and treatment.

WGS can be used for population screening to identify individuals who are at higher risk of developing certain diseases. This can enable targeted prevention efforts, such as early screening and lifestyle interventions, to reduce the incidence of these conditions.

Most people assume that if a medication is prescribed, it will work the same way for everyone. 99.7% of us carry genetic variations that affect how we metabolise common drugs, meaning the same pill can work brilliantly for one person and cause serious side effects for another. Pharmacogenomic testing takes the guesswork out of prescribing. By understanding your genetic makeup, your doctor can make better, safer choices, reducing the risk of adverse drug reactions by up to 30%.
https://pubmed.ncbi.nlm.nih.gov/36739136/

WGS can help identify genetic mutations that can be passed down through families, allowing individuals and families to make informed decisions about family planning and reproductive options.

For some people, getting a diagnosis can take years. Tests come back inconclusive. Referrals lead nowhere. The search for answers, known as the diagnostic odyssey can be exhausting, emotionally and physically. Whole genome sequencing changes that. By capturing your complete genetic blueprint in a single test, we can look deep into regions of the genome that standard tests simply don’t reach; structural variants, copy number variants, short tandem repeats, and beyond. And because your whole genome is already sequenced, if nothing is found today, reanalysis is straightforward as science advances. No starting from scratch. No waiting years for the next test. Just answers, when the time is right.

Whole genome sequencing can help avoid the need for multiple, targeted genetic tests and diagnostic procedures. This can reduce the generation of medical waste, such as used test kits, disposable instruments, and biohazardous materials associated with traditional diagnostic methods. By providing comprehensive genetic information in a single test, WGS can help healthcare providers arrive at a more accurate and efficient diagnosis. This can lead to more targeted treatments, potentially reducing the need for extended hospital stays, additional tests, and associated energy consumption.

Our Mission

We know that the future application of genetics into clinical practice relies on Whole Genome data.  Everything we do at StoreGene is about facilitating that transition. We believe that to do this, we must focus on making genomics more:

Affordable

Keeping the cost of analysis down, so that WGS becomes a viable and cost-effective solution

Accessible

Available to as many people as possible and understandable, even for non-genetic specialists

Actionable

Providing real insights to inform decision-making around healthcare and treatment