A roadmap for the generation of benchmarking resources for antimicrobial resistance detection using next generation sequencing

Author:

Petrillo MauroORCID,Fabbri Marco,Kagkli Dafni Maria,Querci MaddalenaORCID,Van den Eede Guy,Alm Erik,Aytan-Aktug Derya,Capella-Gutierrez SalvadorORCID,Carrillo CatherineORCID,Cestaro Alessandro,Chan Kok-GanORCID,Coque Teresa,Endrullat ChristophORCID,Gut Ivo,Hammer Paul,Kay Gemma L.ORCID,Madec Jean-Yves,Mather Alison E.,McHardy Alice Carolyn,Naas Thierry,Paracchini Valentina,Peter Silke,Pightling Arthur,Raffael Barbara,Rossen JohnORCID,Ruppé Etienne,Schlaberg Robert,Vanneste Kevin,Weber Lukas M.ORCID,Westh Henrik,Angers-Loustau AlexandreORCID

Abstract

Next Generation Sequencing technologies significantly impact the field of Antimicrobial Resistance (AMR) detection and monitoring, with immediate uses in diagnosis and risk assessment. For this application and in general, considerable challenges remain in demonstrating sufficient trust to act upon the meaningful information produced from raw data, partly because of the reliance on bioinformatics pipelines, which can produce different results and therefore lead to different interpretations. With the constant evolution of the field, it is difficult to identify, harmonise and recommend specific methods for large-scale implementations over time. In this article, we propose to address this challenge through establishing a transparent, performance-based, evaluation approach to provide flexibility in the bioinformatics tools of choice, while demonstrating proficiency in meeting common performance standards. The approach is two-fold: first, a community-driven effort to establish and maintain “live” (dynamic) benchmarking platforms to provide relevant performance metrics, based on different use-cases, that would evolve together with the AMR field; second, agreed and defined datasets to allow the pipelines’ implementation, validation, and quality-control over time. Following previous discussions on the main challenges linked to this approach, we provide concrete recommendations and future steps, related to different aspects of the design of benchmarks, such as the selection and the characteristics of the datasets (quality, choice of pathogens and resistances, etc.), the evaluation criteria of the pipelines, and the way these resources should be deployed in the community.

Funder

European Commission

Biotechnology and Biological Sciences Research Counci

Publisher

F1000 Research Ltd

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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