Supplemental Material for Vandenplas, Calus, and Gorjanc, 2018
This study presents a method for genomic prediction that uses individual-level data and summary statistics from multiple populations. Genome-wide markers are nowadays widely used to predict complex traits, and genomic prediction using multi-population data are an appealing approach to achieve higher prediction accuracies. However, sharing of individual-level data across populations is not always possible. We present a method that enables integration of summary statistics from separate analyses with the available individual-level data. The data can either consist of individuals with single or multiple (weighted) phenotype records per individual. We developed a method based on a hypothetical joint analysis model and absorption of population-specific information. We show that population-specific information is fully captured by estimated allele substitution effects and the accuracy of those estimates, i.e., the summary statistics. The method gives identical result as the joint analysis of all individual-level data when complete summary statistics are available. We provide a series of easy-to-use approximations that can be used when complete summary statistics are not available or impractical to share. Simulations show that approximations enable integration of different sources of information across a wide range of settings, yielding accurate predictions. The method can be readily extended to multiple-traits. In summary, the developed method enables integration of genome-wide data in the individual-level or summary statistics from multiple populations to obtain more accurate estimates of allele substitution effects and genomic predictions.
Main Authors: | , , |
---|---|
Format: | Dataset biblioteca |
Published: |
Wageningen University & Research
|
Subjects: | genomic prediction, meta-analysis, multi-population, quantitative trait, statistical method, summary statistics, |
Online Access: | https://research.wur.nl/en/datasets/supplemental-material-for-vandenplas-calus-and-gorjanc-2018 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
id |
dig-wur-nl-wurpubs-561553 |
---|---|
record_format |
koha |
spelling |
dig-wur-nl-wurpubs-5615532024-12-23 Vandenplas, Jeremie Calus, Mario Gorjanc, Gregor Dataset Supplemental Material for Vandenplas, Calus, and Gorjanc, 2018 2018 This study presents a method for genomic prediction that uses individual-level data and summary statistics from multiple populations. Genome-wide markers are nowadays widely used to predict complex traits, and genomic prediction using multi-population data are an appealing approach to achieve higher prediction accuracies. However, sharing of individual-level data across populations is not always possible. We present a method that enables integration of summary statistics from separate analyses with the available individual-level data. The data can either consist of individuals with single or multiple (weighted) phenotype records per individual. We developed a method based on a hypothetical joint analysis model and absorption of population-specific information. We show that population-specific information is fully captured by estimated allele substitution effects and the accuracy of those estimates, i.e., the summary statistics. The method gives identical result as the joint analysis of all individual-level data when complete summary statistics are available. We provide a series of easy-to-use approximations that can be used when complete summary statistics are not available or impractical to share. Simulations show that approximations enable integration of different sources of information across a wide range of settings, yielding accurate predictions. The method can be readily extended to multiple-traits. In summary, the developed method enables integration of genome-wide data in the individual-level or summary statistics from multiple populations to obtain more accurate estimates of allele substitution effects and genomic predictions. Wageningen University & Research text/html https://research.wur.nl/en/datasets/supplemental-material-for-vandenplas-calus-and-gorjanc-2018 10.25386/genetics.6216533 https://edepot.wur.nl/515410 genomic prediction meta-analysis multi-population quantitative trait statistical method summary statistics Wageningen University & Research |
institution |
WUR NL |
collection |
DSpace |
country |
Países bajos |
countrycode |
NL |
component |
Bibliográfico |
access |
En linea |
databasecode |
dig-wur-nl |
tag |
biblioteca |
region |
Europa del Oeste |
libraryname |
WUR Library Netherlands |
topic |
genomic prediction meta-analysis multi-population quantitative trait statistical method summary statistics genomic prediction meta-analysis multi-population quantitative trait statistical method summary statistics |
spellingShingle |
genomic prediction meta-analysis multi-population quantitative trait statistical method summary statistics genomic prediction meta-analysis multi-population quantitative trait statistical method summary statistics Vandenplas, Jeremie Calus, Mario Gorjanc, Gregor Supplemental Material for Vandenplas, Calus, and Gorjanc, 2018 |
description |
This study presents a method for genomic prediction that uses individual-level data and summary statistics from multiple populations. Genome-wide markers are nowadays widely used to predict complex traits, and genomic prediction using multi-population data are an appealing approach to achieve higher prediction accuracies. However, sharing of individual-level data across populations is not always possible. We present a method that enables integration of summary statistics from separate analyses with the available individual-level data. The data can either consist of individuals with single or multiple (weighted) phenotype records per individual. We developed a method based on a hypothetical joint analysis model and absorption of population-specific information. We show that population-specific information is fully captured by estimated allele substitution effects and the accuracy of those estimates, i.e., the summary statistics. The method gives identical result as the joint analysis of all individual-level data when complete summary statistics are available. We provide a series of easy-to-use approximations that can be used when complete summary statistics are not available or impractical to share. Simulations show that approximations enable integration of different sources of information across a wide range of settings, yielding accurate predictions. The method can be readily extended to multiple-traits. In summary, the developed method enables integration of genome-wide data in the individual-level or summary statistics from multiple populations to obtain more accurate estimates of allele substitution effects and genomic predictions. |
format |
Dataset |
topic_facet |
genomic prediction meta-analysis multi-population quantitative trait statistical method summary statistics |
author |
Vandenplas, Jeremie Calus, Mario Gorjanc, Gregor |
author_facet |
Vandenplas, Jeremie Calus, Mario Gorjanc, Gregor |
author_sort |
Vandenplas, Jeremie |
title |
Supplemental Material for Vandenplas, Calus, and Gorjanc, 2018 |
title_short |
Supplemental Material for Vandenplas, Calus, and Gorjanc, 2018 |
title_full |
Supplemental Material for Vandenplas, Calus, and Gorjanc, 2018 |
title_fullStr |
Supplemental Material for Vandenplas, Calus, and Gorjanc, 2018 |
title_full_unstemmed |
Supplemental Material for Vandenplas, Calus, and Gorjanc, 2018 |
title_sort |
supplemental material for vandenplas, calus, and gorjanc, 2018 |
publisher |
Wageningen University & Research |
url |
https://research.wur.nl/en/datasets/supplemental-material-for-vandenplas-calus-and-gorjanc-2018 |
work_keys_str_mv |
AT vandenplasjeremie supplementalmaterialforvandenplascalusandgorjanc2018 AT calusmario supplementalmaterialforvandenplascalusandgorjanc2018 AT gorjancgregor supplementalmaterialforvandenplascalusandgorjanc2018 |
_version_ |
1822268891826487296 |