Evidence map›Paper›PMID 36974068›Full record

ReviewBioinformatics advances2023

Inferring the heritability of bacterial traits in the era of machine learning.

T Tien Mai, John A Lees, Rebecca A Gladstone, Jukka Corander

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In one paragraph

Review in Bioinformatics advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

4 authors.

T Tien MaiDepartment of Mathematical Sciences, Norwegian University of Science and Technology, Trondheim 7034, Norway.ORCID https://orcid.org/0000-0002-3514-9636
John A LeesEuropean Molecular Biology Laboratory, European Bioinformatics Institute EMBL-EBI, Hinxton CB10 1SD, UK.ORCID https://orcid.org/0000-0001-5360-1254
Rebecca A GladstoneDepartment of Biostatistics, University of Oslo, Oslo 0372, Norway.ORCID https://orcid.org/0000-0002-7993-3051
Jukka CoranderDepartment of Biostatistics, University of Oslo, Oslo 0372, Norway.ORCID https://orcid.org/0000-0002-7752-1942

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Quantification of heritability is a fundamental desideratum in genetics, which allows an assessment of the contribution of additive genetic variation to the variability of a trait of interest. The traditional computational approaches for assessing the heritability of a trait have been developed in the field of quantitative genetics. However, the rise of modern population genomics with large sample sizes has led to the development of several new machine learning-based approaches to inferring heritability. In this article, we systematically summarize recent advances in machine learning which can be used to infer heritability. We focus on an application of these methods to bacterial genomes, where heritability plays a key role in understanding phenotypes such as antibiotic resistance and virulence, which are particularly important due to the rising frequency of antimicrobial resistance. By designing a heritability model incorporating realistic patterns of genome-wide linkage disequilibrium for a frequently recombining bacterial pathogen, we test the performance of a wide spectrum of different inference methods, including also GCTA. In addition to the synthetic data benchmark, we present a comparison of the methods for antibiotic resistance traits for multiple bacterial pathogens. Insights from the benchmarking and real data analyses indicate a highly variable performance of the different methods and suggest that heritability inference would likely benefit from tailoring of the methods to the specific genetic architecture of the target organism. Availability and implementation: The R codes and data used in the numerical experiments are available at: https://github.com/tienmt/her_MLs.

Identifiers

PMID36974068
PMCPMC10039732

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