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Novel multi-cluster workflow system to support real-time HPC-enabled epidemic science: Investigating the impact of vaccine acceptance on COVID-19 spread.

Authors :
Bhattacharya P
Machi D
Chen J
Hoops S
Lewis B
Mortveit H
Venkatramanan S
Wilson ML
Marathe A
Porebski P
Klahn B
Outten J
Vullikanti A
Xie D
Adiga A
Brown S
Barrett C
Marathe M
Source :
Journal of parallel and distributed computing [J Parallel Distrib Comput] 2024 Sep; Vol. 191. Date of Electronic Publication: 2024 May 04.
Publication Year :
2024

Abstract

We present MacKenzie, a HPC-driven multi-cluster workflow system that was used repeatedly to configure and execute fine-grained US national-scale epidemic simulation models during the COVID-19 pandemic. Mackenzie supported federal and Virginia policymakers, in real-time, for a large number of "what-if" scenarios during the COVID-19 pandemic, and continues to be used to answer related questions as COVID-19 transitions to the endemic stage of the disease. MacKenzie is a novel HPC meta-scheduler that can execute US-scale simulation models and associated workflows that typically present significant big data challenges. The meta-scheduler optimizes the total execution time of simulations in the workflow, and helps improve overall human productivity. As an exemplar of the kind of studies that can be conducted using Mackenzie, we present a modeling study to understand the impact of vaccine-acceptance in controlling the spread of COVID-19 in the US. We use a 288 million node synthetic social contact network (digital twin) spanning all 50 US states plus Washington DC, comprised of 3300 counties, with 12 billion daily interactions. The highly-resolved agent-based model used for the epidemic simulations uses realistic information about disease progression, vaccine uptake, production schedules, acceptance trends, prevalence, and social distancing guidelines. Computational experiments show that, for the simulation workload discussed above, MacKenzie is able to scale up well to 10K CPU cores. Our modeling results show that, when compared to faster and accelerating vaccinations, slower vaccination rates due to vaccine hesitancy cause averted infections to drop from 6.7M to 4.5M, and averted total deaths to drop from 39.4K to 28.2K across the US. This occurs despite the fact that the final vaccine coverage is the same in both scenarios. We also find that if vaccine acceptance could be increased by 10% in all states, averted infections could be increased from 4.5M to 4.7M (a 4.4% improvement) and total averted deaths could be increased from 28.2K to 29.9K (a 6% improvement) nationwide.<br />Competing Interests: Parantapa Bhattacharya reports financial support was provided by Centers for Disease Control and Prevention. Parantapa Bhattacharya reports financial support was provided by Virginia Department of Health. Parantapa Bhattacharya reports financial support was provided by National Science Foundation. Parantapa Bhattacharya reports financial support was provided by National Institutes of Health.

Details

Language :
English
ISSN :
0743-7315
Volume :
191
Database :
MEDLINE
Journal :
Journal of parallel and distributed computing
Publication Type :
Academic Journal
Accession number :
38774820
Full Text :
https://doi.org/10.1016/j.jpdc.2024.104899