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DOI 10.1093/jamia/ocy153

Медицинская библиотека · Journal of the American Medical Informatics Association : JAMIA · 2019

Development and user evaluation of a rare disease gene prioritization workflow based on cognitive ergonomics.

Lee Jessica J Y, van Karnebeek Clara D M, Wasserman Wyeth W

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

OBJECTIVE

The clinical diagnosis of genetic disorders is undergoing transformation, driven by whole exome sequencing and whole genome sequencing (WES/WGS). However, such nucleotide-level resolution technologies create an interpretive challenge. Prior literature suggests that clinicians may employ characteristic cognitive processes during WES/WGS investigations to identify disruptions in genes causal for the observed disease. Based on cognitive ergonomics, we designed and evaluated a gene prioritization workflow that supported these cognitive processes.

MATERIALS AND

METHODS

We designed a novel workflow in which clinicians recalled known genetic diseases with similarity to patient phenotypes to inform WES/WGS data interpretation. This prototype-based workflow was evaluated against the common computational approach based on physician-specified sets of individual patient phenotypes. The evaluation was conducted as a web-based user study, in which 18 clinicians analyzed 2 simulated patient scenarios using a randomly assigned workflow. Data analysis compared the 2 workflows with respect to accuracy and efficiency in diagnostic interpretation, efficacy in collecting detailed phenotypic information, and user satisfaction.

RESULTS

Participants interpreted genetic diagnoses faster using prototype-based workflows. The 2 workflows did not differ in other evaluated aspects.

DISCUSSION: The user study findings indicate that prototype-based approaches, which are designed to model experts' cognitive processes, can expedite gene prioritization and provide utility in synergy with common phenotype-driven variant/gene prioritization approaches. However, further research of the extent of this effect across diverse genetic diseases is required.

CONCLUSION

The findings demonstrate potential for prototype-based phenotype description to accelerate computer-assisted variant/gene prioritization through complementation of skills and knowledge of clinical experts via human-computer interaction.

Для цитирования: Lee Jessica J Y, van Karnebeek Clara D M, Wasserman Wyeth W. Development and user evaluation of a rare disease gene prioritization workflow based on cognitive ergonomics.. Journal of the American Medical Informatics Association : JAMIA. 2019. DOI: 10.1093/jamia/ocy153.

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