ArticleMathematical biosciences2025
Hybrid analysis with phylogeny and population modeling to estimate the recent founding date of a population: A case study in the origins of COVID-19 illustrates how a branching process approximation can simplify a hybrid analysis.
Article in Mathematical biosciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
1 author.
Funding
Abstract
The exact date of the primary infection in COVID-19 remains unknown. One influential article (Pekar et al. (2021)) estimated the date with a hybrid analysis combining epidemiological and phylogenetic methods. The phylogenetic methods analyzed 583 SARS-COV-2 complete genomes to estimate the sample tMRCA (time of the most recent common ancestor). Before igniting as an epidemic, however, COVID-19 may have had several population bottlenecks with only a single infected person, so the MRCA merely represents the last such bottleneck. Pekar et al. (2021) therefore used epidemiological methods to estimate the time from the primary infection to the sample MRCA. The hybrid method involved several arbitrary decisions, however, reflecting the fact that the epidemiological and phylogenetic analyses overlap at the sample MRCA and are generally probabilistically dependent. Towards removing the dependence, note that the start of an epidemic has a branching process approximation. Let the branching process have a single ancestor. If the branching process does not go extinct, define skeleton particles (individuals) to be particles whose lineages do not go extinct, and define the long-time MRCA as the earliest skeleton particle with at least two skeleton offspring. A linear phylogeny of skeleton particles therefore separates the ancestor from the long-time MRCA. Probabilistically, the linear phylogeny is a defective renewal process of skeleton particles, making the generation count geometrically distributed. Moreover, the terminology "long-time MRCA" is apt, because as time becomes arbitrarily large, the MRCA of the corresponding extant population approaches the long-time MRCA. Effectively, the focus on the long-time MRCA makes the forward epidemiological and backward phylogenetic analyses probabilistically independent. The present article can therefore confirm most of the epidemiological conclusions of the hybrid analysis of Pekar et al. (2021). Its use of branching process approximations also points the way to noticeable simplifications in the hybrid method.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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 OpenQuestion graph.