Evidence map›Paper›PMID 41126021›Full record

ArticleBMC genomics2025

Imputef: imputation of polyploid genotype classes and allele frequencies.

Jefferson Paril, Noel O I Cogan, M Michelle Malmberg

Abstract read
In one paragraph

Article in BMC genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

3 authors.

Jefferson ParilAgriculture Victoria, AgriBio, Centre for AgriBioscience, 5 Ring Rd, Bundoora, VIC, Australia, Bundoora. jeff.paril@agriculture.vic.gov.au.
Noel O I CoganAgriculture Victoria, AgriBio, Centre for AgriBioscience, 5 Ring Rd, Bundoora, VIC, Australia, Bundoora.
M Michelle MalmbergAgriculture Victoria, AgriBio, Centre for AgriBioscience, 5 Ring Rd, Bundoora, VIC, Australia, Bundoora.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is a lack of genotype imputation software tailored specifically for polyploids and pooled samples without phased haplotype information and reference panel of genotypes. Numerous important crops are polyploids, while pool sequencing is an emerging cost-effective approach for the genomic characterisation of breeding populations, families, and other segregating lines. The scarcity of imputation tools for these datasets results in the reliance on diploid-specific software, potentially leading to suboptimal outcomes. This necessitates the development of allele frequency imputation tools which accommodate the unique computational challenges presented by polyploid genomes and pooled sequencing data.

resultsWe developed imputef, an allele frequency imputation tool for polyploid individuals and pooled samples lacking the rich genomic information typically available to model species. Missing allele frequencies are imputed using the genetic distance-weighted mean of non-missing allele frequencies from k-nearest neighbours. Genetic distance is estimated as the mean absolute difference in allele frequencies across linked loci, with linkage estimated as Pearson's correlation between loci. The minimum loci correlation and maximum genetic distance thresholds can be optimised per locus to minimise imputation error. Imputef using the default parameters (minimum loci correlation, maximum genetic distance, minimum number of linked loci, and minimum number of nearest neighbours set to 0.9, 0.1, 20, and 5, respectively), generally outperformed mean value imputation and performed well across the range of sparsity levels (1% to 90% simulated missing data, and 6% to 50% empirical sparsity levels), and minor allele frequencies (1% and 5%). Imputation accuracy was further enhanced using the built-in per-locus optimisation. The maximum computation time ranged from 41 h (380 tetraploids; 233,627 loci) without optimisation to 6 days (275 polyploids; 1,526,917 loci) with per locus optimisation using 32 compute cores at 3.7 GHz and 60 to 320 GB of memory. Additionally, practical imputation approaches for large datasets with unordered loci were demonstrated using imputef.

conclusionImputef is an accurate allele frequency imputation tool for polyploid individuals and pooled samples lacking rich genomic information. This tool is expected to improve the statistical power of genomic analyses involving polyploids and pools, and enhance the adoption of pool-based methods in crop breeding and ecological genomics.

Indexed as

Gene FrequencyPolyploidySoftwareGenomicsGenotypeAllele frequencyImputationPolyploidPool sequencingUnphased genotypes

Identifiers

PMID41126021
PMCPMC12542404

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.