Abstract

BackgroundMultiple laboratories now offer clinical whole genome sequencing (WGS). We anticipate WGS becoming routinely used in research and clinical practice. Many institutions are exploring how best to educate geneticists and other professionals about WGS. Providing students in WGS courses with the option to analyze their own genome sequence is one strategy that might enhance students’ engagement and motivation to learn about personal genomics. However, if this option is presented to students, it is vital they make informed decisions, do not feel pressured into analyzing their own genomes by their course directors or peers, and feel free to analyze a third-party genome if they prefer. We therefore developed a 26-hour introductory genomics course in part to help students make informed decisions about whether to receive personal WGS data in a subsequent advanced genomics course. In the advanced course, they had the option to receive their own personal genome data, or an anonymous genome, at no financial cost to them. Our primary aims were to examine whether students made informed decisions regarding analyzing their personal genomes, and whether there was evidence that the introductory course enabled the students to make a more informed decision.MethodsThis was a longitudinal cohort study in which students (N = 19) completed questionnaires assessing their intentions, informed decision-making, attitudes and knowledge before (T1) and after (T2) the introductory course, and before the advanced course (T3). Informed decision-making was assessed using the Decisional Conflict Scale.ResultsAt the start of the introductory course (T1), most (17/19) students intended to receive their personal WGS data in the subsequent course, but many expressed conflict around this decision. Decisional conflict decreased after the introductory course (T2) indicating there was an increase in informed decision-making, and did not change before the advanced course (T3). This suggests that it was the introductory course content rather than simply time passing that had the effect. In the advanced course, all (19/19) students opted to receive their personal WGS data. No changes in technical knowledge of genomics were observed. Overall attitudes towards WGS were broadly positive.ConclusionsProviding students with intensive introductory education about WGS may help them make informed decisions about whether or not to work with their personal WGS data in an educational setting.

Highlights

  • Multiple laboratories offer clinical whole genome sequencing (WGS)

  • We report the results from analyses in which we assessed whether the students made informed decisions, and whether their decisions appeared to be more informed as a consequence of having engaged in the introductory course

  • Aim 1: To assess key whole genome sequencing decision-related attitudes and knowledge at the start of an introductory genomics course (T1) Interest and decision At baseline, 17 of the 19 students selected ‘Option 1: I would like to analyze my own genome as part of an advanced WGS course’, while the remaining two students selected ‘Option 2: I would not like to analyze my own genome as part of an advanced WGS course, and would rather analyze an anonymous donated genome’

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Summary

Introduction

Multiple laboratories offer clinical whole genome sequencing (WGS). We anticipate WGS becoming routinely used in research and clinical practice. Providing students in WGS courses with the option to analyze their own genome sequence is one strategy that might enhance students’ engagement and motivation to learn about personal genomics. If this option is presented to students, it is vital they make informed decisions, do not feel pressured into analyzing their own genomes by their course directors or peers, and feel free to analyze a third-party genome if they prefer. We developed a 26-hour introductory genomics course in part to help students make informed decisions about whether to receive personal WGS data in a subsequent advanced genomics course. Medical professionals will need to keep pace with these developments in personal genomics [1], whether the personal genomic information is obtained inside or outside of a clinical setting

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