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Showing papers by "Alun G. Williams published in 2015"


Journal ArticleDOI
TL;DR: In the current state of knowledge, no child or young athlete should be exposed to DTC genetic testing to define or alter training or for talent identification aimed at selecting gifted children or adolescents.
Abstract: The general consensus among sport and exercise genetics researchers is that genetic tests have no role to play in talent identification or the individualised prescription of training to maximise performance. Despite the lack of evidence, recent years have witnessed the rise of an emerging market of direct-to-consumer marketing (DTC) tests that claim to be able to identify children's athletic talents. Targeted consumers include mainly coaches and parents. There is concern among the scientific community that the current level of knowledge is being misrepresented for commercial purposes. There remains a lack of universally accepted guidelines and legislation for DTC testing in relation to all forms of genetic testing and not just for talent identification. There is concern over the lack of clarity of information over which specific genes or variants are being tested and the almost universal lack of appropriate genetic counselling for the interpretation of the genetic data to consumers. Furthermore independent studies have identified issues relating to quality control by DTC laboratories with different results being reported from samples from the same individual. Consequently, in the current state of knowledge, no child or young athlete should be exposed to DTC genetic testing to define or alter training or for talent identification aimed at selecting gifted children or adolescents. Large scale collaborative projects, may help to develop a stronger scientific foundation on these issues in the future.

106 citations


Journal ArticleDOI
TL;DR: The RugbyGene project is a multi-institutional research collaboration in rugby union that will perform molecular genetic analyses of varying complexity that could become useful tools for rugby practitioners in the future and provide complementary and additional information to that provided by the non-genetic tests currently used.
Abstract: This article introduces some aspects of sports genomics in a rugby union context, considers the rugby-specific genetic data in the published literature and outlines the next research steps required if the potential applications of genetic technology in rugby union, also identified here, are to become possible. A substantial proportion of the inter-individual variation for many traits related to rugby performance, including strength, short-term muscle power, VO2 max, injury susceptibility and the likelihood of being an elite athlete is inherited and can be investigated using molecular genetic techniques. In sports genomics, significant efforts have been made in recent years to develop large DNA biobanks of elite athletes for detailed exploration of the heritable bases of those traits. However, little effort has been devoted to the study of rugby athletes, and most of the little research that has focused on rugby was conducted with small cohorts of non-elite players. With steadily growing knowledge of the molecular mechanisms underpinning complex performance traits and the aetiology of injury, investigating sports genomics in the context of rugby is now a viable proposition and a worthwhile endeavour. The RugbyGene project we describe briefly in this article is a multi-institutional research collaboration in rugby union that will perform molecular genetic analyses of varying complexity. Genetic tests could become useful tools for rugby practitioners in the future and provide complementary and additional information to that provided by the non-genetic tests currently used.

31 citations


Book ChapterDOI
01 Jan 2015
TL;DR: The procedures included in this chapter focus on amplicon library preparation, DNA library quantitation options, next generation pyrosequencing with the 454 GS Junior system and data analysis.
Abstract: Gene differences predisposing to atherosclerosis disease are important to identify and allow us to understand cellular processes involved in the progression and development of atherosclerotic disease. This protocol describes the experimental procedure for multiplex amplicon sequencing using barcoded primers. The procedures included in this chapter focus on amplicon library preparation (including polymerase chain reaction (PCR) conditions), DNA library quantitation options, next generation pyrosequencing with the 454 GS Junior system and data analysis. The process from DNA to sequencing data can be completed within 5 days.