Our Mission:
Empower.
ClearSKY Genomics helps people understand, engage and make use of the information in their DNA. We work with clinicians to make it easier to find meaning in a patient’s genetic data, and we provide patients and their loved ones, individualised resources that helps them understand what their DNA means for them.
Our mission is to make understanding your patient’s genetic information as simple, and as easy as looking at an x-ray.
mychro
There is so much complexity in the genome that patients, their families and even some healthcare workers are unable to fully utilise this resource. To address this, we’ve developed Mychro (short for my chromosomes) as an interface between the clinical and the human sides of genomics.
Mychro the first genome browser designed for doctors and their patients. Currently it allows genetic specialists to easily contextualise large-scale, chromosomal changes from cytogenetic, microarray and NGS data sources, with high-quality peer-reviewed information. Mychro also dynamically generates resources for consults, tailored to each patient’s genome.
engaging patients
Mychro has been designed to make the genome accessible for patients, their loved ones, and for people who aren’t genetics specialists.
Built for the clinic
Genetic counsellors & clinical geneticists are essential to clinical genomics. This important work is slowed down by tools designed for researchers. We’ve built Mychro to support them.
Just the start
Mychro currently supports germline chromosomal anomalies - a main driver of genetic disease. We’re developing new features to support other forms of variation.
Supporters
I didn’t think i’d ever UNDERSTAND my mutation. I know it’s important; I live with it everyday. but when the doctors start talking, I can’t really follow what they say.
But this, this is amazing. It changes everything. I can see it now. YOU’VE MADE google maps but for my genes.
An individual with genetic abnormality.
How it works
STANDARD RESULTS
Mychro ingests the standard results from genetic tests. Simply enter a standard variant identified by a genetic pathologist into mychro and you’re ready to go.
QUICKLY REVIEW
It can be time consuming to verify these results. Mychro brings together high-quality, peer reviewed data in a simple portal to make the review process almost effortless.
SUPPORT
Helping patients & their loved ones understand their DNA can be challenging. Mychro dynamically generates personalised materials for each patient to support your consult.
GENETICS HAS SUCH AN IMPORTANT ROLE TO PLAY IN the future of medicine. But for most CLINICIANS, it’s been out of reach.
too hard. too risky. too many unknowns.
mychro has changed that. it gives more doctors the power to understand their patient’s dna with the context provided by their complete medical history.
A chief clinical information officer