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An implementation science approach to evaluating pathogen whole genome sequencing in public health



Pathogen whole genome sequencing (WGS) is being incorporated into public health surveillance and disease control systems worldwide and has the potential to make significant contributions to infectious disease surveillance, outbreak investigation and infection prevention and control. However, to date, there are limited data regarding (i) the optimal models for integration of genomic data into epidemiological investigations and (ii) how to quantify and evaluate public health impacts resulting from genomic epidemiological investigations.


We developed the Pathogen Genomics in Public HeAlth Surveillance Evaluation (PG-PHASE) Framework to guide examination of the use of WGS in public health surveillance and disease control. We illustrate the use of this framework with three pathogens as case studies: Listeria monocytogenes, Mycobacterium tuberculosis and SARS-CoV-2.


The framework utilises an adaptable whole-of-system approach towards understanding how interconnected elements in the public health application of pathogen genomics contribute to public health processes and outcomes. The three phases of the PG-PHASE Framework are designed to support understanding of WGS laboratory processes, analysis, reporting and data sharing, and how genomic data are utilised in public health practice across all stages, from the decision to send an isolate or sample for sequencing to the use of sequence data in public health surveillance, investigation and decision-making. Importantly, the phases can be used separately or in conjunction, depending on the need of the evaluator. Subsequent to conducting evaluation underpinned by the framework, avenues may be developed for strategic investment or interventions to improve utilisation of whole genome sequencing.


Comprehensive evaluation is critical to support health departments, public health laboratories and other stakeholders to successfully incorporate microbial genomics into public health practice. The PG-PHASE Framework aims to assist public health laboratories, health departments and authorities who are either considering transitioning to whole genome sequencing or intending to assess the integration of WGS in public health practice, including the capacity to detect and respond to outbreaks and associated costs, challenges and facilitators in the utilisation of microbial genomics and public health impacts.


Whole genome sequencing (WGS) is being incorporated into public health surveillance and disease control systems worldwide. The USA and the UK have both implemented national WGS services [1, 2], and in 2016, 26 European countries reported the use of WGS in routine public health practice [3]. The reduction in cost and advancement of portable sequencing technologies has continued to increase accessibility for low-resource settings and low- and middle-income countries [4,5,6].

Two major applications of pathogen WGS in disease control are (i) identifying and investigating outbreaks and (ii) genomic surveillance of pathogens of public health importance. WGS has higher discriminatory power than other genotyping methods and can divide clusters identified through other methods into more detailed groupings [7,8,9] and aid in mapping patterns of microbial relatedness across different human, animal and environmental samples [10]. A key advantage of WGS is the transferability of sequence data, which allows for rapid and interoperable national, international and cross-sectoral data sharing. This enhances the capacity of surveillance systems to quickly detect related cases where epidemiological links are difficult to identify. For example, epidemiological links may be difficult to identify in the case of geographically dispersed clusters, such as for food-borne illnesses caused by wide food dispersion, or temporally dispersed clusters, caused by pathogens with long incubation periods [11,12,13,14].

For laboratories, the direct costs of transitioning to WGS may include (i) the purchase of equipment and consumables; (ii) changes in laboratory workflows and methods, safety and training needs; and (iii) workforce remodelling [1]. In addition, the generation, analysis, visualisation and storage of genomic data require appropriate bioinformatics and data management infrastructure. Different analyses and reports may be produced based on the needs of diverse end users, and the reporting needs of end users may change according to circumstance, such as during an outbreak investigation. At present, standardised guidelines for the reporting of genomic data are limited [15,16,17], and end users may find it difficult to interpret the data being provided to them. Moreover, there may be end user variability in understanding the uses of genomics for public health, further impacting the utility of pathogen genomic data. Community expectations, including anticipated benefits and ethical concerns around privacy and stigma, also have implications for how pathogen genomic data are used, and the level of support and advocacy for its incorporation into public health systems [18,19,20].

To date, much of the literature on public health pathogen genomics comes from a research perspective. As such, it is often retrospective, illustrating ‘proof of concept’, and does not account for public health practice or outcomes [21,22,23]. Where there have been studies exploring the implications of public health utilisation of microbial genomics in relation to specific pathogens, the examination of public health practice has been undertaken in isolation from earlier steps such as sequencing and reporting practices, which have a profound impact on the utility of sequence data [24]. Further, the processes of workflow management, analysis and reporting have often been examined separately from the incorporation of genomic data into public health practice [1, 15]. To our knowledge, there are no whole-of-system evaluations of WGS in public health, nor any formal evaluation or implementation frameworks in this area. Yet, such an evaluation is critical for continued improvement of current genomic implementations, and to add to the evidence base available for other labs and jurisdictions currently embarking on this undertaking (Table 1). For these reasons, we developed the Pathogen Genomics in Public HeAlth Surveillance Evaluation (PG-PHASE) Framework, underpinned by the principles of implementation science, to examine the impact of WGS on public health. To illustrate application of the PG-PHASE Framework, we use three pathogens as case studies: Listeria monocytogenes, Mycobacterium tuberculosis and SARS-CoV-2.

Table 1 Potential benefits of evaluating WGS implementation in public health surveillance


Approach to designing the framework

The key objective of this study was to develop a framework for the evaluation of WGS implementation in public health. The framework development process consisted of three key stages: (i) a review of existing literature, (ii) a series of key stakeholder interviews with developers and end-users of pathogen genomic data and (iii) synthesis of information and design of the framework programme logic.

Review of existing literature

A literature review was undertaken to identify studies incorporating (i) theorised advantages of WGS over traditional typing methods, (ii) experiences in transitioning to and utilising WGS in public health systems, (iii) evaluations of WGS utilisation in public health settings and (iv) frameworks for evaluation of surveillance systems. Specific search terms used are provided in Additional File 1, and a list of included studies are available in Additional File 2.

Key stakeholder interviews

A series of interviews was undertaken with seventeen individuals involved in generating and using pathogen genomic data. Interviewees were selected in order to encompass a wide variety of roles related to the generation and utilisation of pathogen genomic data. Individuals included laboratory scientists, bioinformaticians, genomic epidemiologists, field epidemiologists, infectious diseases clinicians, clinical microbiologists and decision-makers involved in funding pathogen genomic implementation. Major themes covered in the interviews were:

  • The transition to WGS and how practice differed before and after transition

  • The analysis of genomic data

  • Challenges in the transition to WGS and use of genomic data

  • Differences in how WGS was used in relation to specific pathogens

  • Anticipated and realised benefits of the transition to WGS (and who would accrue these benefits)

  • What individuals thought was important for an evaluation framework to cover

Interviews were an iterative process; initial interviews were undertaken to draft the framework, which was then fed back to interviewees and refined again. Multiple interviews were undertaken with some interviewees. Data collection ended when there was sufficient understanding to construct the framework, and this understanding was confirmed through the iterative nature of the interview process.

Designing and implementing the evaluation framework

Information from the literature review and stakeholder interviews was synthesised and used to design the framework. Two major approaches were used to underpin our framework: (i) the ‘Framework for evaluating public health surveillance systems for early detection of outbreaks: Recommendations from the CDC Working Group’ (the ‘CDC framework’) [25] and (ii) the ‘Process evaluation of complex interventions: Medical Research Council guidance’ (the ‘MRC framework’) [26]. The CDC framework outlines four categories to support evaluation of public health surveillance systems: system description, outbreak detection, experience, and conclusions and recommendations [25]. These four categories were used as the basis for conceptualising how the contribution of WGS to public health surveillance systems could be evaluated. The PG-PHASE Framework uses interviews with stakeholders, operational data and reports to develop a comprehensive description of how WGS data is produced and used, including system processes and understanding the perceived benefits from the perspective of both producers and users of data. The use of WGS data in outbreak detection is examined in the framework, focusing both on the sharing of genomic data to contribute to epidemiological investigations and on the perceived utility of the data shared. Ultimately, the framework is designed to identify strengths and weaknesses in WGS implementation and utilisation, and to subsequently produce recommendations to improve effectiveness and impact.

Where the CDC framework provides guidance on elements to be included for evaluations specific to surveillance systems, the MRC framework is focused more broadly on how to appropriately capture and assess the interdependencies and relationships inherent in complex interventions. The MRC framework was used to develop a framework that is sensitive to contextual factors while assessing not only impacts but elements of implementation and processes that generated impacts. Examination of laboratory processes, reporting mechanisms and the use of WGS data is situated within the needs of end users and the public health situation relative to the existing context. Processes and mechanisms are a key focus throughout, with an emphasis on why and how data is produced, shared and utilised—or not.

Finally, the phases for the framework were directly informed by the three phases of the total testing process in clinical laboratories (the pre-analytical, analytical and post-analytical phases). The final framework includes a range of data indicators and concepts (Additional File 3). The methods for development of the framework are illustrated in Fig. 1.

Fig. 1

Development of the Pathogen Genomics in Public HeAlth Surveillance Evaluation (PG-PHASE) Framework

The evaluation framework can be broadly applied to many pathogens; however, components of the evaluation are likely to vary according to the specific pathogen and/or disease. We investigated preliminary ‘proof-of-concept’ of the framework by applying it theoretically to the evaluation of two major public health pathogens, namely M. tuberculosis and L. monocytogenes. Subsequently, to demonstrate ‘real-world’ utility of the framework, we applied the framework to contemporaneous implementation of SARS-CoV-2 sequencing in our setting.


The final evaluation framework is comprised of three phases, namely (i) the pre-analysis and analysis phase; (ii) the reporting and communication phase and (iii) the implementation phase. The associated outputs, outcomes and indicators for each phase are provided in Additional File 3 and are described further below.

Phase 1: Pre-analysis and analysis

Given the relatively limited control the laboratory has regarding the pre-analytical phase (largely encompassing specimen selection, collection and transport), the pre-analytical and analytical phases are combined. This first phase focuses primarily on laboratory workflow in transitioning and undertaking WGS for the relevant pathogens. Initial ‘first-level’ data analysis is performed on individual sequences at this stage, including quality control, speciation, extraction of basic typing information and identifying the presence or absence of relevant loci/genes such as antimicrobial resistance (AMR) and virulence genes. Assessment encompasses (i) changes to workflow processes as ‘legacy’ laboratory methods are retired and pathogen characterisation is transitioned to WGS, (ii) the number of samples processed and analysed in a defined time period (efficiency) and (iii) costings, including costs for staff, instrumentation (including robotics) and reagents/consumables, and costs of data processing and storage. Decisions regarding which samples are selected for sequencing and sample processing and analysis times are also assessed as part of this phase of the evaluation. Elements of ‘future-proofing’ practices to ensure the future usability of isolates and sequence data, including adequate documentation of sample selection and how particular isolates are isolated, cultured and maintained, may also be explored [27]. Laboratory data, such as numbers of samples analysed, and purchasing data, such as reagent costs, may provide additional information. Interviews with laboratory staff may be useful to understand the impacts of workflow and other changes, such as change management, training staff in new processes and the adequacy of transition plans, as well as issues regarding sample transport and preparation. Interviews with both laboratory staff and end users may help define which isolates were selected for sequencing, why, and the role of laboratory and public health personnel in developing the sequencing strategy.

Phase 2: Reporting and communication

Phase two examines reporting and communication processes from the dual perspectives of the laboratory and end-users. During this phase, ‘second-level’ analysis is undertaken, which relates first-level findings to additional metadata and extends analysis to a group of sequences (as distinct from an individual sequence) within the context of the request for analysis. Assessment in this phase encompasses the timeliness and utility of genomic data presented, and the structures in place to determine the most appropriate reporting formats and mechanisms, according to need. Reporting processes may vary and should be assessed according to (i) context and (ii) end user (e.g. epidemiologist, clinician). Evaluation of reporting processes may include the frequency of reports, level and type of information presented, visualisation of information, and adherence to information design principles [15, 28]. Included in this phase is an examination of the extent to which reporting mechanisms contribute to shared decision-making regarding sample selection, sequencing and analysis strategies between laboratory and public health personnel. Interviews with end users may include examination of intended use of genomic data and questions posed to inform analysis, satisfaction with communication and reporting processes, information retention, perceived utility of the information presented and level of understanding of information provided. Interviews with bioinformaticians and genomic epidemiologists can provide insight into the various ways sequence data is being used in addition to routine reporting (e.g. sequence data may be contributed to international databases, utilised in phylodynamic modelling or shared between public health agencies). Interviews may explore processes of data sharing, including data governance structures and legal or logistical barriers and facilitators. Through these interviews, areas for two-way learning may be identified, where end users are able to strengthen their understanding of the data provided, and bioinformaticians and genomic epidemiologists are better informed about what information is expected by end users and how it is intended to be used. Further, based on these interactions between those generating and those using genomic data, the format and contents of reports may be changed so that reports are better ‘fit for purpose.’

Phase 3: Implementation in public health practice

This phase consists of two parts. The first is a qualitative examination of how WGS data is integrated into public health practice and used to complement or inform epidemiological investigations. Key informant interviews can assess the perspectives of stakeholders regarding the acceptability, usefulness and sustainability of pathogen genomics in public health. Key informants may include medical professionals such as physicians, microbiologists and epidemiologists, representatives of public health departments and hospital infection control units and other stakeholders (e.g. regulatory agencies, industry, community members). Interviews may explore possible applications and perceived utility or risks of pathogen genomics in infectious disease prevention and control, including the benefits and risks associated with WGS data storage and the ability to rapidly ‘mine’ large repositories of genomic data. Data may be collected on how the transition to WGS has affected public health decision-making, including confidence in making decisions based on the information provided, time to action and the types of decision-making enabled by genomic data. In addition to interviews, data collected may include documented changes to public health policy or the development of guidelines regarding the use of pathogen genomics in public health practice.

The second part of this evaluation phase is a quantitative examination of public health outcomes following implementation of pathogen genomics, with traditional laboratory processes (e.g. legacy typing methods) as a comparator. Relevant indicators may include epidemiological measures such as the number of identified cases; size, duration and number of identified clusters; the proportion of cases linked to clusters; and the proportion of cases/clusters traced to a contamination source. Although challenging to collect economic data, additional indicators may relate to financial costs such as resource allocation for epidemiological investigations and infection control investigations and actions [24, 29]; direct health care costs [30]; financial losses relating to food-borne disease outbreaks (e.g. food recalls); clean-up costs in relation to water and environmental outbreaks [29, 31, 32]; and costs associated with sick leave, both for employers in the form of reduced productivity and for employees as loss of income [30]. Data collection and analyses may vary significantly depending on the epidemiology of the pathogen under consideration, the type of data available and the context (i.e. routine surveillance or outbreak investigation). Indicators and data collection methods across the three phases of the evaluation framework are outlined in Additional File 4: Table S1.

Evaluation case studies: Listeria monocytogenes and Mycobacterium tuberculosis

Listeriosis is a notifiable disease in many countries, including Australia and the USA [33,34,35,36]. WGS has emerged as a valuable tool for investigation of listeriosis outbreaks and is now routinely used for genomic surveillance in several countries [37, 38]. Previous research has shown that the higher discriminatory power of WGS can identify distinct nested clusters within groups of L. monocytogenes isolates that were otherwise indistinguishable using other typing methods [39] and has demonstrated utility in identifying contamination sources [40]. When there is data available from prior to the introduction of WGS, a pre/post study design can be used to examine data in defined time periods before (based on previously used typing methods) and after transitioning to WGS. Relevant variables to assess are detailed in Additional File 5: Table S2 and may include the number, size and geographical spread of identified clusters; the percent of isolates linked to a cluster; numbers of isolates/clusters traced to a common source; number of ‘solved’ isolates/clusters; and the time taken to identify and resolve outbreaks. Several of these outcomes have been assessed in genomic studies of other foodborne pathogens such as Shiga toxin-producing Escherichia coli [41, 42]. Jackson et al. examined listeriosis surveillance prior to and following integration of WGS, finding an increased number of clusters; identification of previously defined clusters that contained isolates that were not highly related; and the ability to link ‘unsolved’ cases to contamination sources [43]. Changes in costs relating to epidemiological investigation could also be analysed, given the utility of WGS in ruling out transmission links. The evaluation could additionally examine trends in food recalls due to L. monocytogenes, including the frequency and magnitude of recalls. A recent review identifies the application of WGS, including in industry, as key in increasing food safety and facilitating regulatory action to address listeria [44]. This approach allows for a comprehensive understanding of how the use of pathogen genomic data has affected the identification and characterisation of clusters across the surveillance system, as well as resulting effects on public health outcomes and use of public health resources.

Tuberculosis (TB) is the leading cause of death from a single infectious agent, with drug-resistant tuberculosis identified as a global health crisis [45]. The long incubation period and relatively high rates of asymptomatic and undiagnosed infection mean that it can be difficult to confirm transmission through epidemiological links alone. WGS has been shown to provide superior discrimination compared to other typing methods and may be more cost-effective [46, 47]. The use of WGS may therefore support more efficient and effective contact tracing, earlier and more appropriate treatment and the initiation of focused public health interventions [48, 49]. Suggested elements to include in an evaluation of TB WGS implementation are provided in Additional File 6: Table S3. Retrospective sequence data in combination with epidemiological data can be used to determine which TB cases may have been identified earlier, allowing for interventions to disrupt further transmissions. Estimates can then be made regarding the number of possible cases averted along with attendant costs to the health care system, including costs relating to epidemiological investigations that may not have been needed. Given the retrospective nature of this approach, it would be important to incorporate a strong understanding of how public health practice is informed by the use of pathogen genomic data, supported by phases 2 and 3 of the evaluation framework. As TB is a stigmatised illness, ethical considerations regarding the use of WGS, including issues around privacy; trust between individuals and communities affected by TB and public health agents and authorities; and community perception of the risks of WGS may also be explored as part of the evaluation [20]. Undertaking the evaluation in this way utilises a whole-of-system approach to draw links between how TB genomic data is used and eventual public health outcomes, enabling further refinement of pathogen genomics-informed public health practice.

Evaluating the implementation of SARS-CoV-2 genomics

From the first instance of genomic sequencing of SARS-CoV-2 [50], WGS has been integrated into the global public health response to COVID-19 [13, 51,52,53]. To investigate the applicability of our framework, we applied it to the initial public health implementation of SARS-CoV-2 sequencing in Victoria, Australia. Additional file 7: Table S4 outlines the PG-PHASE Framework as applied to SARS-CoV-2 sequencing, with Table 2 outlining the data collection undertaken according to each phase of the evaluation.

Table 2 Data collection in application of the PG-PHASE Framework to SARS-CoV-2 sequencing

Phase 1: Pre-analytical and analytical evaluation of SARS-CoV-2 sequencing

The Microbiological Diagnostic Unit Public Health Laboratory (MDU PHL) located in Melbourne, Victoria, began routine sequencing of SARS-CoV-2 in January 2020. For phase 1, we collected both quantitative and qualitative data. Quantitative data were collected on the number of samples received and sequenced, turnaround times and quality control data. These data were analysed to enable understanding of sequencing efficiency and how this changed over the course of the pandemic. Qualitative data were used to contextualise this performance data. Seven laboratory staff and two staff involved in specimen transport and processing were interviewed. Semi-structured interviews were tailored to individuals’ roles and explored the processes of implementing WGS for an emerging pathogen, including changes to workflows, development of new analytical procedures and change management. These interviews provided a clearer understanding of factors that enabled the laboratory to respond effectively to an emerging pathogen and the issues involved in doing so. Interviews were undertaken at various stages throughout the pandemic. Later interviews were useful in understanding how earlier challenges were subsequently resolved.

Phase 2: Reporting and communication of SARS-CoV-2 genomic data

Interviews with laboratory personnel also explored reporting processes, including how bioinformaticians and genomic epidemiologists understood the data as being used in the public health response, possible or perceived deficiencies in how genomic data were understood by end users and the perceived appropriateness of data or analyses requested by end users. Interviews with bioinformaticians and genomic epidemiologists also covered mechanisms, facilitators and challenges in sharing SARS-CoV-2 sequence data, particularly across national and international boundaries. To complement interviews with laboratory personnel, eleven interviews were undertaken with end users of genomic data (Additional file 7: Table S4). Interviewees were asked how they received SARS-CoV-2 genomic data, what data were being requested and why, whether the data was provided in an appropriate and timely manner, whether reporting processes were responsive and appropriate to the intended use and to what extent they believed bioinformaticians and genomic epidemiologists understood the data needs of end users. Interviews explored perceived risks and challenges around data sharing and the use of genomic data in public health practice, including privacy issues. Throughout the pandemic response, the evaluator attended weekly reporting meetings that were held between the public health laboratory, Department of Health and others involved in the use of genomic data to inform the public health response. Where possible, regular and ad hoc reports were also collected, as well as emails requesting ad hoc analyses of SARS-CoV-2 genomic data. Data also included the number of sequences uploaded to public databases, which provides an indication of data sharing. The observation of the weekly reporting meeting and review of reports and ad hoc requests provided triangulation of the interview data for a complete picture of what genomic data was being requested and presented, and how producers and users of data worked together and communicated throughout the pandemic response. Collectively, these data were useful to identify possible misalignments between the perceptions of those generating and analysing genomic data and those who utilise the data to inform public health implementation.

Phase 3: Utilising SARS-CoV-2 genomic data in public health practice

Interviews with end users explored how genomic data was used in operationalising the public health response, both in community and hospital settings, and perceived barriers to its utilisation. Data in the public domain were used to understand how genomic data were involved in public health decision-making, including press releases from government officials referencing genomic data in explaining the rationale behind specific public health interventions (Additional file 7: Table S4). Within Victoria, genomic data played a key role in identifying the source of the second wave of infection as a breach in the state hotel quarantine system. In this case, evaluation data included the transcripts and final recommendations of a judicial enquiry into the Victorian hotel quarantine scheme [54]. Collectively, these data are valuable in identifying facilitators to the application of WGS in public health, addressing barriers to the utilisation of genomic data and refining appropriate public health decision-making practices informed by genomic data.

While these qualitative aspects of evaluation are essential, quantifying the impact of genomic sequencing is challenging for SARS-CoV-2 and other emerging pathogens, as there is no ‘counterfactual’ where WGS has not been used. Because of this, it is difficult to definitively attribute public health outcomes to the use of WGS, in comparison to an alternative situation where WGS is not available or utilised. Public health data from similar contexts where WGS has not been used, in conjunction with existing epidemiological data from the setting under consideration, could form the basis of mathematical models to estimate differences in case numbers and characterised outbreaks. While confounders would need to be accounted for in such a model, the aim would not be to arrive at absolute numbers, but rather relative results, such as the proportion of unidentified cases or the probability of being able to detect outbreaks of a certain size with and without the use of genomics [55]. In the absence of suitable comparative data, available epidemiological data may be examined to determine where identification of transmission events would have been uncertain, or where distinct transmission networks may have been merged without the use of genomic data.


Given the large investments that many laboratories and public health agencies have made in applying WGS to public health pathogen genomics [1, 56], it is essential to have a clear framework for evaluating the clinical, public health and economic impact (positive and negative) of WGS implementation and to derive the best value for money. Here, we present a framework for evaluating the use of WGS in public health surveillance and disease control across all stages, from the decision to send an isolate for sequencing, to the use of sequence data in public health surveillance, investigation and responses.

The benefits arising from transition to WGS and its subsequent use in public health surveillance are highly context dependent and rely on each part of the system working in conjunction with the others. Ideally, analysis, reporting and translation into practice work together as interconnected parts of an iterative process. Decisions regarding the selection and identification of isolates for sequencing may be informed by previously provided public health information, and WGS approaches need to be rapidly adaptable in order to respond to new and emerging pathogens and AMR. Analysis and reporting are dependent on the various needs of end users, which in turn are also influenced by the wider context. For this reason, a whole-of-system approach is necessary to understand how each step in the process of data generation, analysis and use are interconnected. The introduction of pathogen genomics into surveillance and disease control systems has had considerable impact on how laboratory and public health systems operate, with attendant uncertainty about the best approaches to: (i) facilitate the integration of genomic data into epidemiological investigations, (ii) define the necessary investment for pathogen genomics and (iii) evaluate public health impacts. The evaluation of public health programmes and interventions, including surveillance systems, is crucial to inform appropriate resource allocation, improve system responsiveness and ensure that programme goals are being met [57, 58]. The three phases of our evaluation framework are designed to support understanding of WGS laboratory processes, analysis, reporting and data sharing, and how genomic data are utilised in public health practice. Importantly, the phases can be used separately or in conjunction, depending on the need of the evaluator.

To test our framework, we applied it to SARS-CoV-2 sequencing in our setting and assessed the feasibility of collecting specific indicators that would enable a comprehensive evaluation. Phase 1 of the evaluation highlighted elements established before the pandemic that contributed to the laboratory being able to rapidly develop and implement protocols for sequencing and analysis of a new pathogen. Interviews with end users and documentation regarding public health decision-making provided an understanding of how genomic data informed (and continues to inform) public health practice. Data collection for this evaluation is ongoing, and the evidence arising from the final evaluation will provide guidance on appropriate investment for future pandemic preparedness planning, particularly for emerging pathogens. Moreover, the evaluation will help to develop a better understanding of the processes by which genomic data is effectively utilised in public health practice, thereby improving the impact of WGS and strengthening the use of genomics in public health surveillance systems.


WGS is now a major part of public health surveillance and the control of infectious diseases, yet there are no defined ways of measuring the overall utility of this approach. This is a ‘first-in-field’ framework for the evaluation of whole genome sequencing (WGS) implementation in public health surveillance and outbreak investigation. The current evaluation framework is presented as a conceptual model, through a whole-of-system lens, to identify barriers and facilitators to the acceptable utilisation of WGS in public health throughout the process. Rigorous evaluation is critical for continued improvement in public health implementation of pathogen genomics and will increase clarity among stakeholders regarding expected outcomes and whether the aims of the programme are being achieved. This framework responds to a global increase in pathogen WGS in surveillance systems and a growing need for rigorous evaluation to support effective and efficient integration of pathogen WGS in public health. Ultimately, it is our hope and expectation that utilisation of the evaluation framework will support more effective and efficient integration of pathogen WGS in public health, leading to improved resource allocation, strengthened and more responsive surveillance systems and improved public health outcomes.

Availability of data and materials

Not applicable.


  1. 1.

    Grant K, Jenkins C, Arnold C, Green J, Zambon M. Implementing pathogen genomics: a case study. London: Public Health England; 2018.

  2. 2.

    Food and Drug Administration. WGS and GenomeTrakr Q&A. White Oak: FDA; 2018.

  3. 3.

    Revez J, Espinosa L, Albiger B, et al. Survey on the Use of Whole-Genome Sequencing for Infectious Diseases Surveillance: Rapid Expansion of European National Capacities, 2015–2016. Front Public Health. 2017;5(347).

  4. 4.

    Hendriksen RS, Lukjancenko O, Munk P, et al. Pathogen surveillance in the informal settlement, Kibera, Kenya, using a metagenomics approach. Plos One. 2019;14(10):15.

    Article  Google Scholar 

  5. 5.

    Marquez S, Prado-Vivar B, Guadalupe JJ, et al. Genome sequencing of the first SARS-CoV-2 reported from patients with COVID-19 in Ecuador. medRxiv 2020: 2020.06.11.20128330.

  6. 6.

    Gardy JL, Loman NJ. Towards a genomics-informed, real-time, global pathogen surveillance system. Nat Rev Genet. 2018;19(1):9–20.

    CAS  Article  PubMed  Google Scholar 

  7. 7.

    Jajou R, de Neeling A, Rasmussen EM, et al. A predominant variable-number tandem-repeat cluster of Mycobacterium tuberculosis isolates among asylum seekers in the Netherlands and Denmark, deciphered by whole-genome sequencing. J Clin Microbiol. 2018;56(2):e01100–17.

    PubMed  PubMed Central  Google Scholar 

  8. 8.

    Ford L, Wang QN, Stafford R, Ressler KA, Norton S, Shadbolt C, et al. Seven Salmonella Typhimurium outbreaks in Australia linked by trace-back and whole genome sequencing. Foodborne Pathogens Dis. 2018;15(5):285–92.

    CAS  Article  Google Scholar 

  9. 9.

    Rumore J, Tschetter L, Kearney A, Kandar R, McCormick R, Walker M, et al. Evaluation of whole-genome sequencing for outbreak detection of Verotoxigenic Escherichia coli O157:H7 from the Canadian perspective. BMC Genomics. 2018;19(1):870.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  10. 10.

    Pightling AW, Pettengill JB, Luo Y, Baugher JD, Rand H, Strain E. Interpreting whole-genome sequence analyses of foodborne bacteria for regulatory applications and outbreak investigations. Front Microbiol. 2018;9:1482.

    Article  Google Scholar 

  11. 11.

    World Health Organization. Whole genome sequencing for foodborne disease surveillance: Landscape paper. Geneva: WHO; 2018.

    Google Scholar 

  12. 12.

    Inns T, Lane C, Peters T, Dallman T, Chatt C, McFarland N, Crook P, Bishop T, Edge J, Hawker J, Elson R, Neal K, Adak GK, Cleary P, Outbreak Control Team. A multi-country Salmonella Enteritidis phage type 14b outbreak associated with eggs from a German producer: 'near real-time' application of whole genome sequencing and food chain investigations, United Kingdom, May to September 2014. Euro Surveill. 2015;20(16):21098.

  13. 13.

    Seemann T, Lane CR, Sherry NL, Duchene S, Gonçalves da Silva A, Caly L, Sait M, Ballard SA, Horan K, Schultz MB, Hoang T, Easton M, Dougall S, Stinear TP, Druce J, Catton M, Sutton B, van Diemen A, Alpren C, Williamson DA, Howden BP. Tracking the COVID-19 pandemic in Australia using genomics. Nat Commun. 2020;11(1):4376.

  14. 14.

    Rockett RJ, Arnott A, Lam C, Sadsad R, Timms V, Gray KA, et al. Revealing COVID-19 transmission in Australia by SARS-CoV-2 genome sequencing and agent-based modeling. Nat Med. 2020;26(9):1398–404.

    CAS  Article  PubMed  Google Scholar 

  15. 15.

    Crisan A, McKee G, Munzner T, Gardy JL. Evidence-based design and evaluation of a whole genome sequencing clinical report for the reference microbiology laboratory. PeerJ. 2018;6:25.

    Article  Google Scholar 

  16. 16.

    Griffiths EJ, Timme RE, Page AJ, et al. The PHA4GE SARS-CoV-2 contextual data specification for open genomic epidemiology. Preprints. 2020.

  17. 17.

    Tornheim JA, Starks AM, Rodwell TC, Gardy JL, Walker TM, Cirillo DM, et al. Building the framework for standardized clinical laboratory reporting of next-generation sequencing data for resistance-associated mutations in Mycobacterium tuberculosis Complex. Clin Infect Dis. 2019;69(9):1631–3.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  18. 18.

    Johnson SB, Parker M. The ethics of sequencing infectious disease pathogens for clinical and public health. Nat Rev Genet. 2019;20(6):313–5.

    CAS  Article  PubMed  Google Scholar 

  19. 19.

    Degeling C, Carter SM, van Oijen AM, et al. Community perspectives on the benefits and risks of technologically enhanced communicable disease surveillance systems: a report on four community juries. BMC Med Ethics. 2020;21(1):14.

    Article  Google Scholar 

  20. 20.

    Jackson C, Gardy JL, Shadiloo HC, Silva DS. Trust and the ethical challenges in the use of whole genome sequencing for tuberculosis surveillance: a qualitative study of stakeholder perspectives. BMC Med Ethics. 2019;20(1):43.

    Article  PubMed  PubMed Central  Google Scholar 

  21. 21.

    McDonnell J, Dallman T, Atkin S, et al. Retrospective analysis of whole genome sequencing compared to prospective typing data in further informing the epidemiological investigation of an outbreak of Shigella sonnei in the UK. Epidemiol Infect. 2013;141(12):2568–75.

    CAS  Article  PubMed  Google Scholar 

  22. 22.

    Whaley MJ, Joseph SJ, Retchless AC, et al. Whole genome sequencing for investigations of meningococcal outbreaks in the United States: a retrospective analysis. Sci Rep. 2018;8:13.

    Article  Google Scholar 

  23. 23.

    Leekitcharoenphon P, Nielsen EM, Kaas RS, Lund O, Aarestrup FM. Evaluation of whole genome sequencing for outbreak detection of Salmonella enterica. Plos One. 2014;9(2):11.

    Article  Google Scholar 

  24. 24.

    Mook P, Gardiner D, Verlander NQ, McCormick J, Usdin M, Crook P, et al. Operational burden of implementing Salmonella Enteritidis and Typhimurium cluster detection using whole genome sequencing surveillance data in England: a retrospective assessment. Epidemiol Infect. 2018;146(11):1452–60.

    CAS  Article  PubMed  Google Scholar 

  25. 25.

    Buehler JW, Hopkins RS, Overhage JM, Sosin DM, Tong V. Framework for evaluating public health surveillance systems for early detection of outbreaks: Recommendations from the CDC Working Group. Atlanta: Centers for Disease Control and Prevention; 2004.

  26. 26.

    Moore GF, Audrey S, Barker M, Bond L, Bonell C, Hardeman W, et al. Process evaluation of complex interventions: Medical Research Council guidance. BMJ. 2015;350(mar19 6):h1258.

    Article  PubMed  PubMed Central  Google Scholar 

  27. 27.

    Baltrus DA, Cuomo CA, Dennehy JJ, et al. Future-proofing your Microbiology Resource Announcements genome assembly for reproducibility and clarity. Microbiol Resour Ann. 2019;8(36):e00954–19.

    Google Scholar 

  28. 28.

    Valenstein PN. Formatting patholgy reports: Applying four design principles to improve communication and patient safety. Arch Pathol Lab Med. 2008;132(1):84–94.

    Article  PubMed  Google Scholar 

  29. 29.

    Van Goethem N, Struelens MJ, De Keersmaecker SCJ, et al. Perceived utility and feasibility of pathogen genomics for public health practice: a survey among public health professionals working in the field of infectious diseases, Belgium, 2019. BMC Public Health. 2020;20(1):18.

    Article  Google Scholar 

  30. 30.

    Luheshi L, Raza S, Moorthie S, et al. Pathogen genomics into practice. Cambridge: PHG Foundation; 2015.

  31. 31.

    Armstrong GL, MacCannell DR, Taylor J, et al. Pathogen genomics in public health. N Engl J Med. 2019;381(26):2569–80.

    Article  PubMed  PubMed Central  Google Scholar 

  32. 32.

    Van Goethem N, Descamps T, Devleesschauwer B, et al. Status and potential of bacterial genomics for public health practice: a scoping review. Implement Sci. 2019;14(1):79.

    Article  PubMed  PubMed Central  Google Scholar 

  33. 33.

    Australian Department of Health. Listeriosis case definition. Available at: Accessed 14 Sept 2020.

  34. 34.

    Centres for Disease Control and Prevention. The Listeria initiative. Available at: Accessed 14 Sept 2020.

  35. 35.

    Public Health England. Notifiable diseases and causative organisms: How to report Available at: Accessed 14 Sept 2020.

  36. 36.

    Desai AN, Anyoha A, Madoff LC, Lassmann B. Changing epidemiology of Listeria monocytogenes outbreaks, sporadic cases, and recalls globally: a review of ProMED reports from 1996 to 2018. Int J Infect Dis. 2019;84:48–53.

    Article  PubMed  PubMed Central  Google Scholar 

  37. 37.

    Department of Health. Canberra: National Microbial Genomics Framework 2019 – 2022 Australian Government; 2019.

  38. 38.

    Brown E, Dessai U, McGarry S, Gerner-Smidt P. Use of whole-genome sequencing for food safety and public health in the United States. Foodborne Pathogens Dis. 2019;16(7):441–50.

    Article  Google Scholar 

  39. 39.

    Kwong JC, Mercoulia K, Tomita T, Easton M, Li HY, Bulach DM, et al. Prospective whole-genome sequencing enhances national surveillance of Listeria monocytogenes. J Clin Microbiol. 2016;54(2):333–42.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  40. 40.

    Thomas J, Govender N, McCarthy KM, et al. Outbreak of listeriosis in South Africa associated with processed meat. N Engl J Med. 2020;382(7):632–43.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  41. 41.

    Berenger BM, Berry C, Peterson T, Fach P, Delannoy S, Li V, Tschetter L, Nadon C, Honish L, Louie M, Chui L. The utility of multiple molecular methods including whole genome sequencing as tools to differentiate Escherichia coli O157:H7 outbreaks. Euro Surveill. 2015;20(47).

  42. 42.

    Dallman TJ, Byrne L, Ashton PM, Cowley LA, Perry NT, Adak G, et al. Whole-genome sequencing for national surveillance of Shiga toxin–producing Escherichia coli O157. Clin Infect Dis. 2015;61(3):305–12.

    Article  PubMed  PubMed Central  Google Scholar 

  43. 43.

    Jackson BR, Tarr C, Strain E, Jackson KA, Conrad A, Carleton H, et al. Implementation of nationwide real-time whole-genome sequencing to enhance listeriosis outbreak detection and investigation. Clin Infect Dis. 2016;63(3):380–6.

    Article  PubMed  PubMed Central  Google Scholar 

  44. 44.

    Jagadeesan B, Gerner-Smidt P, Allard MW, Leuillet S, Winkler A, Xiao Y, et al. The use of next generation sequencing for improving food safety: Translation into practice. Food Microbiol. 2019;79:96–115.

    CAS  Article  PubMed  Google Scholar 

  45. 45.

    World Health Organization. Global tuberculosis report 2018. Geneva: WHO; 2018.

    Google Scholar 

  46. 46.

    Wyllie DH, Davidson JA, Grace Smith E, Rathod P, Crook DW, Peto TEA, et al. A quantitative evaluation of MIRU-VNTR typing against whole-genome sequencing for identifying Mycobacterium tuberculosis transmission: A Prospective observational cohort study. EBioMedicine. 2018;34:122–30.

    Article  PubMed  PubMed Central  Google Scholar 

  47. 47.

    Roetzer A, Diel R, Kohl TA, et al. Whole genome sequencing versus traditional genotyping for investigation of a Mycobacterium tuberculosis outbreak: a longitudinal molecular epidemiological study. Plos Med. 2013;10(2):e1001387-e.

    Article  Google Scholar 

  48. 48.

    Jajou R, de Neeling A, van Hunen R, et al. Epidemiological links between tuberculosis cases identified twice as efficiently by whole genome sequencing than conventional molecular typing: A population-based study. Plos One. 2018;13(4):e0195413.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  49. 49.

    Guthrie JL, Strudwick L, Roberts B, Allen M, McFadzen J, Roth D, et al. Comparison of routine field epidemiology and whole genome sequencing to identify tuberculosis transmission in a remote setting. Epidemiol Infect. 2020;148:e15.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  50. 50.

    Wu F, Zhao S, Yu B, Chen YM, Wang W, Song ZG, et al. A new coronavirus associated with human respiratory disease in China. Nature. 2020;579(7798):265–9.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  51. 51.

    Watson C. How countries are using genomics to help avoid a second coronavirus wave. Available at: Accessed 24 Aug 2020.

  52. 52.

    Meredith LW, Hamilton WL, Warne B, Houldcroft CJ, Hosmillo M, Jahun AS, Curran MD, Parmar S, Caller LG, Caddy SL, Khokhar FA, Yakovleva A, Hall G, Feltwell T, Forrest S, Sridhar S, Weekes MP, Baker S, Brown N, Moore E, Popay A, Roddick I, Reacher M, Gouliouris T, Peacock SJ, Dougan G, Török ME, Goodfellow I. Rapid implementation of SARS-CoV-2 sequencing to investigate cases of health-care associated COVID-19: a prospective genomic surveillance study. Lancet Infect Dis. 2020 Nov;20(11):1263–71. Epub 2020 Jul 14. Erratum in: Lancet Infect Dis. 2021;21(3):e36. Erratum in: Lancet Infect Dis. 2021;21(3):e36.

  53. 53.

    Geoghegan JL, Ren X, Storey M, Hadfield J, Jelley L, Jefferies S, Sherwood J, Paine S, Huang S, Douglas J, Mendes FK, Sporle A, Baker MG, Murdoch DR, French N, Simpson CR, Welch D, Drummond AJ, Holmes EC, Duchêne S, de Ligt J. Genomic epidemiology reveals transmission patterns and dynamics of SARS-CoV-2 in Aotearoa New Zealand. Nat Commun. 2020;11(1):6351.

  54. 54.

    COVID-19 hotel quarantine inquiry, final report and recommendations, 2020.

  55. 55.

    Gerber L, González-Suárez M. Population viability analysis: Origins and contributions. Na Educ Knowledge 2010;3(10).

  56. 56.

    Gwinn M, MacCannell D, Armstrong GL. Next-Generation Sequencing of Infectious Pathogens. JAMA. 2019;321(9):893–4.

  57. 57.

    Centers for Disease Control and Prevention. Framework for program evaluation in public health. Atlanta: US Department of Health and Human Services; 1999.

    Google Scholar 

  58. 58.

    Calba C, Goutard FL, Hoinville L, Hendrikx P, Lindberg A, Saegerman C, et al. Surveillance systems evaluation: a systematic review of the existing approaches. BMC Public Health. 2015;15(1):448.

    Article  PubMed  PubMed Central  Google Scholar 

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The authors would like to acknowledge and thank those individuals from the Communicable Diseases Section of the Victorian Department of Human Health and Services and the Microbiological Diagnostic Unit Public Health Laboratory who have contributed their time to support the understanding that underpinned this article.


This work was supported by a National Health and Medical Research Council (NHMRC), Australia Partnership Grant [APP1149991]. BPH is supported by an NHMRC Practitioner Fellowship [APP1105905]. DAW is supported by an NHMRC Investigator Grant [APP1174555].

Author information




ASF, MK, DAW and BPH conceived the study. ASF developed the evaluation framework with support from all authors. ASF and DAW wrote the manuscript in consultation with MK and BPH. All authors contributed to the conception of the framework and the final manuscript. All authors read and approved the final manuscript.

Corresponding authors

Correspondence to Angeline S. Ferdinand or Deborah A. Williamson.

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Supplementary Information

Additional file 1.

Literature review search terms and databases.

Additional file 2.

Studies and reports included in the literature review.

Additional file 3.

The evaluation framework: Key activities in utilising pathogen WGS in public health and associated outputs, outcomes and indicators.

Additional file 4: Table S1.

Indicators and data collection methods.

Additional file 5: Table S2.

Application of the evaluation framework for Listeria monocytogenes WGS.

Additional file 6: Table S3.

Application of the evaluation framework for Mycobacterium tuberculosis WGS.

Additional file 7: Table S4.

Application of the evaluation framework for SARS-CoV-2 WGS.

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Ferdinand, A.S., Kelaher, M., Lane, C.R. et al. An implementation science approach to evaluating pathogen whole genome sequencing in public health. Genome Med 13, 121 (2021).

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  • Pathogen genomics
  • Evaluation
  • SARS-CoV-2
  • Listeria
  • Tuberculosis