Evidence map›Paper›PMID 37476534›Full record

ArticleBioinformatics advances2023

Network-augmented compartmental models to track asymptomatic disease spread.

Devavrat Vivek Dabke, Kritkorn Karntikoon, Chaitanya Aluru, Mona Singh, Bernard Chazelle

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In one paragraph

Article in Bioinformatics advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Devavrat Vivek DabkeThe Program in Applied and Computational Mathematics, Princeton University, Princeton, NJ 08544, USA.ORCID https://orcid.org/0000-0002-5073-135X
Kritkorn KarntikoonDepartment of Computer Science, Princeton University, Princeton, NJ 08544, USA.ORCID https://orcid.org/0000-0002-6398-3097
Chaitanya AluruDepartment of Computer Science, Princeton University, Princeton, NJ 08544, USA.ORCID https://orcid.org/0000-0002-8693-6410
Mona SinghDepartment of Computer Science, Princeton University, Princeton, NJ 08544, USA.ORCID https://orcid.org/0000-0001-8271-6026
Bernard ChazelleDepartment of Computer Science, Princeton University, Princeton, NJ 08544, USA.ORCID https://orcid.org/0000-0001-8542-0247

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Summary: A major challenge in understanding the spread of certain newly emerging viruses is the presence of asymptomatic cases. Their prevalence is hard to measure in the absence of testing tools, and yet the information is critical for tracking disease spread and shaping public health policies. Here, we introduce a framework that combines classic compartmental models with travel networks and we use it to estimate asymptomatic rates. Our platform, traSIR ("tracer"), is an augmented susceptible-infectious-recovered (SIR) model that incorporates multiple locations and the flow of people between them; it has a compartment model for each location and estimates of commuting traffic between compartments. TraSIR models both asymptomatic and symptomatic infections, as well as the dampening effect symptomatic infections have on traffic between locations. We derive analytical formulae to express the asymptomatic rate as a function of other key model parameters. Next, we use simulations to show that empirical data fitting yields excellent agreement with actual asymptomatic rates using only information about the number of symptomatic infections over time and compartments. Finally, we apply our model to COVID-19 data consisting of reported daily infections in the New York metropolitan area and estimate asymptomatic rates of COVID-19 to be ∼34%, which is within the 30-40% interval derived from widespread testing. Overall, our work demonstrates that traSIR is a powerful approach to express viral propagation dynamics over geographical networks and estimate key parameters relevant to virus transmission. Availability and implementation: No public repository.

Identifiers

PMID37476534
PMCPMC10354004

What Socratic holds

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LicenceCC BY
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.