Evidence map›Paper›PMID 26024866›Full record

ArticleG3 (Bethesda, Md.)2015

Using Bayesian Multilevel Whole Genome Regression Models for Partial Pooling of Training Sets in Genomic Prediction.

Frank Technow, L Radu Totir

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

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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

9 citing papers in PubMed.

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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

2 authors.

Frank TechnowDuPont Pioneer, Johnston, Iowa 50131 Frank.Technow@pioneer.com.
L Radu TotirDuPont Pioneer, Johnston, Iowa 50131.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Training set size is an important determinant of genomic prediction accuracy. Plant breeding programs are characterized by a high degree of structuring, particularly into populations. This hampers the establishment of large training sets for each population. Pooling populations increases training set size but ignores unique genetic characteristics of each. A possible solution is partial pooling with multilevel models, which allows estimating population-specific marker effects while still leveraging information across populations. We developed a Bayesian multilevel whole-genome regression model and compared its performance with that of the popular BayesA model applied to each population separately (no pooling) and to the joined data set (complete pooling). As an example, we analyzed a wide array of traits from the nested association mapping maize population. There we show that for small population sizes (e.g., <50), partial pooling increased prediction accuracy over no or complete pooling for populations represented in the training set. No pooling was superior; however, when populations were large. In another example data set of interconnected biparental maize populations either partial or complete pooling was superior, depending on the trait. A simulation showed that no pooling is superior when differences in genetic effects among populations are large and partial pooling when they are intermediate. With small differences, partial and complete pooling achieved equally high accuracy. For prediction of new populations, partial and complete pooling had very similar accuracy in all cases. We conclude that partial pooling with multilevel models can maximize the potential of pooling by making optimal use of information in pooled training sets.

Indexed as

Models, GeneticBayes TheoremGenome, PlantLinkage DisequilibriumQuantitative Trait LociSelection, GeneticZea maysBayesian whole-genome regressiondata poolinggenomic predictiongenomic selectionGenPredmultilevel modelsmultiple populationsshared data resource

Identifiers

PMID26024866
PMCPMC4528317

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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.