Evidence map›Paper›PMID 36304259›Full record

ArticleFrontiers in bioinformatics2022

Sparse bayesian learning for genomic selection in yeast.

Maryam Ayat, Mike Domaratzki

Abstract read
In one paragraph

Article in Frontiers in bioinformatics, 2022. 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

2 authors.

Maryam AyatLactanet, Sainte-Anne-deBellevue, QC, Canada.
Mike DomaratzkiDepartment of Computer Science, University of Western Ontario, London, ON, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genomic selection, which predicts phenotypes such as yield and drought resistance in crops from high-density markers positioned throughout the genome of the varieties, is moving towards machine learning techniques to make predictions on complex traits that are controlled by several genes. In this paper, we consider sparse Bayesian learning and ensemble learning as a technique for genomic selection and ranking markers based on their relevance to a trait. We define and explore two different forms of the sparse Bayesian learning for predicting phenotypes and identifying the most influential markers of a trait, respectively. We apply our methods on a

Indexed as

bayesian learningexplainable artificial intelligencegenomic selectionkernel learningmachine learningmarker assisted selectionrelevance vector machine

Identifiers

PMID36304259
PMCPMC9580947

What OpenQuestion holds

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LicenceCC BY
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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.