Evidence map›Paper›PMID 38863802›Full record

ArticleJournal of applied statistics2024

Combining phenotypic and genomic data to improve prediction of binary traits.

D Jarquin, A Roy, B Clarke, S Ghosal

Abstract read
In one paragraph

Article in Journal of applied statistics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

4 authors.

D JarquinAgronomy, University of Florida, Gainesville, FL, USA.ORCID https://orcid.org/0000-0002-5098-2060
A RoyBiostatistics Department, University of Florida, Gainesville, FL, USA.
B ClarkeStatistics, University of Nebraska-Lincoln, Lincoln, NE, USA.
S GhosalStatistics, North Carolina State University, Raleigh, NC, USA.ORCID https://orcid.org/0000-0002-1710-9761

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plant breeders want to develop cultivars that outperform existing genotypes. Some characteristics (here 'main traits') of these cultivars are categorical and difficult to measure directly. It is important to predict the main trait of newly developed genotypes accurately. In addition to marker data, breeding programs often have information on secondary traits (or 'phenotypes') that are easy to measure. Our goal is to improve prediction of main traits with interpretable relations by combining the two data types using variable selection techniques. However, the genomic characteristics can overwhelm the set of secondary traits, so a standard technique may fail to select any phenotypic variables. We develop a new statistical technique that ensures appropriate representation from both the secondary traits and the genotypic variables for optimal prediction. When two data types (markers and secondary traits) are available, we achieve improved prediction of a binary trait by two steps that are designed to ensure that a significant intrinsic effect of a phenotype is incorporated in the relation before accounting for extra effects of genotypes. First, we sparsely regress the secondary traits on the markers and replace the secondary traits by their residuals to obtain the effects of phenotypic variables as adjusted by the genotypic variables. Then, we develop a sparse logistic classifier using the markers and residuals so that the adjusted phenotypes may be selected first to avoid being overwhelmed by the genotypic variables due to their numerical advantage. This classifier uses forward selection aided by a penalty term and can be computed effectively by a technique called the one-pass method. It compares favorably with other classifiers on simulated and real data.

Indexed as

62J0262J0762J12Classificationgenotypemultitype dataphenotypesparsity

Identifiers

PMID38863802
PMCPMC11164039

What OpenQuestion holds

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Registered trials

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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.