Evidence map›Paper›PMID 34758743›Full record

ArticleBMC bioinformatics2021

Employing phylogenetic tree shape statistics to resolve the underlying host population structure.

Hassan W Kayondo, Alfred Ssekagiri, Grace Nabakooza, Nicholas Bbosa, Deogratius Ssemwanga, Pontiano Kaleebu, Samuel Mwalili, John M Mango, Andrew J Leigh Brown, Roberto A Saenz and 2 more

Abstract read
In one paragraph

Article in BMC bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

12 authors.

Hassan W KayondoInstitute of Basic Sciences, Technology and Innovation (PAUSTI), Pan African University, Nairobi, Kenya. whkayondo@gmail.com.ORCID http://orcid.org/0000-0001-8607-6636
Alfred SsekagiriUganda Virus Research Institute (UVRI), Entebbe, Uganda.
Grace NabakoozaDepartment of Immunology and Molecular Biology, Makerere University, Kampala, Uganda.
Nicholas BbosaMedical Research Council (MRC)/Uganda Virus Research Institute (UVRI) and London School of Hygiene and Tropical Medicine (LSHTM) Uganda Research Unit, Entebbe, Uganda.
Deogratius SsemwangaUganda Virus Research Institute (UVRI), Entebbe, Uganda.
Pontiano KaleebuUganda Virus Research Institute (UVRI), Entebbe, Uganda.
Samuel MwaliliDepartment of Statistics and Actuarial Sciences, Jomo Kenyatta University of Agriculture and Technology, Nairobi, Kenya.
John M MangoDepartment of Mathematics, Makerere University, Kampala, Uganda.
Andrew J Leigh BrownInstitute of Evolutionary Biology, University of Edinburg, Edinburg, UK.
Roberto A SaenzFacultad de Ciencias, Universidad de Colima, Colima, Mexico.
Ronald GaliwangoCentre for Computational Biology, Uganda Christian University, Mukono, Uganda.
John M KitayimbwaCentre for Computational Biology, Uganda Christian University, Mukono, Uganda.

Funding

Medical Research Council MC_UU_00027/1
6 · The paper itself

Abstract

backgroundHost population structure is a key determinant of pathogen and infectious disease transmission patterns. Pathogen phylogenetic trees are useful tools to reveal the population structure underlying an epidemic. Determining whether a population is structured or not is useful in informing the type of phylogenetic methods to be used in a given study. We employ tree statistics derived from phylogenetic trees and machine learning classification techniques to reveal an underlying population structure.

resultsIn this paper, we simulate phylogenetic trees from both structured and non-structured host populations. We compute eight statistics for the simulated trees, which are: the number of cherries; Sackin, Colless and total cophenetic indices; ladder length; maximum depth; maximum width, and width-to-depth ratio. Based on the estimated tree statistics, we classify the simulated trees as from either a non-structured or a structured population using the decision tree (DT), K-nearest neighbor (KNN) and support vector machine (SVM). We incorporate the basic reproductive number ([Formula: see text]) in our tree simulation procedure. Sensitivity analysis is done to investigate whether the classifiers are robust to different choice of model parameters and to size of trees. Cross-validated results for area under the curve (AUC) for receiver operating characteristic (ROC) curves yield mean values of over 0.9 for most of the classification models.

conclusionsOur classification procedure distinguishes well between trees from structured and non-structured populations using the classifiers, the two-sample Kolmogorov-Smirnov, Cucconi and Podgor-Gastwirth tests and the box plots. SVM models were more robust to changes in model parameters and tree size compared to KNN and DT classifiers. Our classification procedure was applied to real -world data and the structured population was revealed with high accuracy of [Formula: see text] using SVM-polynomial classifier.

Indexed as

Machine LearningSupport Vector MachineAlgorithmsPhylogenyROC CurveClassificationHost populationnon-structuredPhylogenetic treeSimulationStructuredTree statistics

Identifiers

PMID34758743
PMCPMC8579572

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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 OpenQuestion graph.