Completed Pregnancy, Children & Inherited Conditions Genetics & Molecular Biology

TwinsUK (2017-2019): An epidemiological and genomic resource

In plain English

AI plain-English summary

A registry of 13,000 twins, with over 300,000 biological samples collected over decades, is being kept running and open for any scientist to use. This matters because twin studies are one of the few ways to untangle the roles of genetics and environment in human health. By comparing identical and non-identical twins, researchers can identify which diseases have a strong heritable component and which are driven by lifestyle or exposure. The TwinsUK resource is uniquely detailed, with extensive “omics” data (genetic, protein, and metabolic profiles) linked to long-term health records. Without continued funding, this infrastructure would decay, and the longitudinal data—which becomes more valuable with each passing year—would be lost. If the resource is maintained, it will continue to serve as a shared platform for biomedical discovery. Over 700 data requests and 90,000 sample distributions in the last five years have already fed into studies on ageing, chronic disease, and drug response. The project also pilots linkage with NHS health records, which could make future studies faster and more powerful. This is primarily an infrastructure grant—it does not test a specific hypothesis, but it enables hundreds of other research projects that do.

View original technical description
Funding is requested to maintain TwinsUK resource, of 13,000 twins with over 300,000 longitudinal samples and the most detailed phenotypes and “omics” of any UK cohort. Continuing extensive data sharing (700 data requests and 90,000 samples to researchers in the last five years), the TwinsUK resource will make further contributions to biomedical science over the next decade. Key objectives are: Continue the TwinsUK Registry providing support for core staff (85% of budget) and facilitate data sharing with scientists (aim 120/year). Maintain and improve open access to the data and samples by improving data access systems (“Phenobase2” database to go live). Further upgrade the extensive biobank of biological samples adding new and longitudinal DNA samples to UKBiocentre’s robotic facility (8,000 samples). Replenish DNA stocks in 800 of our most valuable twins to ensure increased sample availability and long-term use. Digitise paper records for secure access and storage. Address attrition of valuable frail participants targeting 250 twins/year through a dedicated assistant for continuity of contact and home packs to enable data and DNA collections Pilot data linkage with NHS health data using a subset of twins with practices already registered with the national CPRD (Clinical Practice Research Datalink, http://www.cprd.com/intro.asp) and HSCIC.

View the original record at the funder ↗

Researchers

Tim Spector (EPMC Awardee)

Related Research

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Original classification

Biomedical Resources Grant

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