Evidence map›Paper›PMID 38970328›Full record

ArticleMolecular ecology resources2025

Missing genotype imputation in non-model species using self-organizing maps.

Fernando Mora-Márquez, Juan Carlos Nuño, Álvaro Soto, Unai López de Heredia

Abstract read
In one paragraph

Article in Molecular ecology resources, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
  2. Editorial 2026.Molecular ecology resources · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. EGGS: Empirical Genotype Generalizer for Samples.bioRxiv : the preprint server for biology · 2025
    Article
  7. 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.

Fernando Mora-MárquezGI en Especies Leñosas (WooSp), Dpto. Sistemas y Recursos Naturales, ETSI Montes, Forestal y del Medio Natural, Universidad Politécnica de Madrid, Ciudad Universitaria, Madrid, Spain.ORCID https://orcid.org/0000-0001-9007-6444
Juan Carlos NuñoGI en Especies Leñosas (WooSp), Dpto. Matemática Aplicada, ETSI Montes, Forestal y del Medio Natural, Universidad Politécnica de Madrid, Ciudad Universitaria, Madrid, Spain.ORCID https://orcid.org/0000-0003-4708-980X
Álvaro SotoGI en Especies Leñosas (WooSp), Dpto. Sistemas y Recursos Naturales, ETSI Montes, Forestal y del Medio Natural, Universidad Politécnica de Madrid, Ciudad Universitaria, Madrid, Spain.ORCID https://orcid.org/0000-0002-0144-1399
Unai López de HerediaGI en Especies Leñosas (WooSp), Dpto. Sistemas y Recursos Naturales, ETSI Montes, Forestal y del Medio Natural, Universidad Politécnica de Madrid, Ciudad Universitaria, Madrid, Spain.ORCID https://orcid.org/0000-0002-4705-9443

Funding

Ministerio de Ciencia e Innovación PID2019-110330GB-C22
6 · The paper itself

Abstract

Current methodologies of genome-wide single-nucleotide polymorphism (SNP) genotyping produce large amounts of missing data that may affect statistical inference and bias the outcome of experiments. Genotype imputation is routinely used in well-studied species to buffer the impact in downstream analysis, and several algorithms are available to fill in missing genotypes. The lack of reference haplotype panels precludes the use of these methods in genomic studies on non-model organisms. As an alternative, machine learning algorithms are employed to explore the genotype data and to estimate the missing genotypes. Here, we propose an imputation method based on self-organizing maps (SOM), a widely used neural networks formed by spatially distributed neurons that cluster similar inputs into close neurons. The method explores genotype datasets to select SNP loci to build binary vectors from the genotypes, and initializes and trains neural networks for each query missing SNP genotype. The SOM-derived clustering is then used to impute the best genotype. To automate the imputation process, we have implemented gtImputation, an open-source application programmed in Python3 and with a user-friendly GUI to facilitate the whole process. The method performance was validated by comparing its accuracy, precision and sensitivity on several benchmark genotype datasets with other available imputation algorithms. Our approach produced highly accurate and precise genotype imputations even for SNPs with alleles at low frequency and outperformed other algorithms, especially for datasets from mixed populations with unrelated individuals.

Indexed as

Computational BiologyGenotypeGenotyping TechniquesPolymorphism, Single NucleotideAlgorithmsNeural Networks, Computerimputationmachine learningmissing dataSNP genotypingSOM

Identifiers

PMID38970328
PMCPMC11887599

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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.