Evidence map›Paper›PMID 30951095›Full record

ArticleThe plant genome2019

Machine Learning as an Effective Method for Identifying True Single Nucleotide Polymorphisms in Polyploid Plants.

Walid Korani, Josh P Clevenger, Ye Chu, Peggy Ozias-Akins

Open access · goldAbstract readEvaluation StudyValidation Study
In one paragraph

Article in The plant genome, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
11.6field-weighted citation impact, top 2% of its field
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

33 citing papers in PubMed, 85 citations in OpenAlex.

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  4. A single hybrid origin of cultivated peanut.The Plant journal : for cell and molecular biology · 2025
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  6. Surprisingly frequent chromosomal instability in cultivated peanut.The Plant journal : for cell and molecular biology · 2025
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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

4 authors at 1 institution in 1 country.

Walid Korani
Josh P Clevenger
Ye Chu
Peggy Ozias-Akins
University of Georgia · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single nucleotide polymorphisms (SNPs) have many advantages as molecular markers since they are ubiquitous and codominant. However, the discovery of true SNPs in polyploid species is difficult. Peanut ( L.) is an allopolyploid, which has a very low rate of true SNP calling. A large set of true and false SNPs identified from the Axiom_ 58k array was leveraged to train machine-learning models to enable identification of true SNPs directly from sequence data to reduce ascertainment bias. These models achieved accuracy rates above 80% using real peanut RNA sequencing (RNA-seq) and whole-genome shotgun (WGS) resequencing data, which is higher than previously reported for polyploids and at least a twofold improvement for peanut. A 48K SNP array, Axiom_2, was designed using this approach resulting in 75% accuracy of calling SNPs from different tetraploid peanut genotypes. Using the method to simulate SNP variation in several polyploids, models achieved >98% accuracy in selecting true SNPs. Additionally, models built with simulated genotypes were able to select true SNPs at >80% accuracy using real peanut data. This work accomplished the objective to create an effective approach for calling highly reliable SNPs from polyploids using machine learning. A novel tool was developed for predicting true SNPs from sequence data, designated as SNP machine learning (SNP-ML), using the described models. The SNP-ML additionally provides functionality to train new models not included in this study for customized use, designated SNP machine learner (SNP-MLer). The SNP-ML is publicly available.

Indexed as

Machine LearningPolymorphism, Single NucleotideArachisDatasets as TopicModels, GeneticPolyploidy

Identifiers

PMID30951095
PMCPMC12962348
OpenAlexW2921271640

What OpenQuestion holds

Textmetadata
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.