Design a study for free and send it out to thousands of people.
Phenotype first, then you can decide to genotype or genome sequence later at a fraction of the cost. £25 per person for a genotype array, £250 for an exome, or £400 for a whole genome. Variant calling and quality control included.
How is it possible? The power of sharing. By phenotyping first and sequencing later, different researchers can include the same individual in different studies, sharing the cost. All of our studies run on a dynamic consent model, allowing you to collect more data or run follow-up studies with ease.