Evidence map›Paper›PMID 39554245›Full record

ArticleWellcome open research2024

Modelling transmission dynamics and genomic diversity in a recombining parasite population.

Dominic Kwiatkowski

Abstract read
In one paragraph

Article in Wellcome open research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Rare variation in malaria parasites biases population-genetic inference.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Review
  5. Pf8: an open dataset ofWellcome open research · 2025
    Article
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

1 author.

Dominic KwiatkowskiSt. John's College, University of Oxford, Oxford, UK.

Funding

Wellcome Trust
6 · The paper itself

Abstract

The genomic diversity of a parasite population is shaped by its transmission dynamics but superinfection, cotranmission and recombination make this relationship complex and hard to analyse. This paper aims to simplify the problem by introducing the concept of a genomic transmission graph with three basic parameters: the effective number of hosts, the quantum of transmission and the crossing rate of transmission chains. This enables rapid simulation of coalescence times in a recombining parasite population with superinfection and cotransmission, and it also provides a mathematical framework for analysis of within-host variation. Taking malaria as an example, we use this theoretical model to examine how transmission dynamics and migration affect parasite genomic diversity, including the effective recombination rate and haplotypic metrics of recent common ancestry. We show how key transmission parameters can be inferred from deep sequencing data and as a proof of concept we estimate the Plasmodium falciparum transmission bottleneck. Finally we discuss the potential applications of this novel inferential framework in genomic surveillance for malaria control and elimination. Online tools for exploring the genomic transmission graph are available at d-kwiat.github.io/gtg.

Indexed as

cotransmissionmalariamathematical modellingparasitepopulation geneticsrecombinationsuperinfectiontransmission dynamics

Identifiers

PMID39554245
PMCPMC11569386

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.