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DINGO:提高母胎全基因组关联研究中围产儿特征的定位发现能力。

DINGO: increasing the power of locus discovery in maternal and fetal genome-wide association studies of perinatal traits.

机构信息

Institute for Molecular Bioscience, The University of Queensland, St Lucia, Australia.

Gilead Sciences, Inc, Foster City, CA, USA.

出版信息

Nat Commun. 2024 Oct 26;15(1):9255. doi: 10.1038/s41467-024-53495-9.

DOI:10.1038/s41467-024-53495-9
PMID:39461952
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11513127/
Abstract

Perinatal traits are influenced by fetal and maternal genomes. We investigate the performance of three strategies to detect loci in maternal and fetal genome-wide association studies (GWASs) of the same quantitative trait: (i) the traditional strategy of analysing maternal and fetal GWASs separately; (ii) a two-degree-of-freedom test which combines information from maternal and fetal GWASs; and (iii) a one-degree-of-freedom test where signals from maternal and fetal GWASs are meta-analysed together conditional on estimated sample overlap. We demonstrate that the optimal strategy depends on the extent of sample overlap, correlation between phenotypes, whether loci exhibit fetal and/or maternal effects, and whether these effects are directionally concordant. We apply our methods to summary statistics from a recent GWAS meta-analysis of birth weight. Both the two-degree-of-freedom and meta-analytic approaches increase the number of genetic loci for birth weight relative to separately analysing the scans. Our best strategy identifies an additional 62 loci compared to the most recently published meta-analysis of birth weight. We conclude that whilst the two-degree-of-freedom test may be useful for the analysis of certain perinatal phenotypes, for most phenotypes, a simple meta-analytic strategy is likely to perform best, particularly in situations where maternal and fetal GWASs only partially overlap.

摘要

围产特征受胎儿和母体基因组的影响。我们研究了三种策略在检测母体和胎儿全基因组关联研究(GWAS)中相同定量性状的基因座的性能:(i)分别分析母体和胎儿 GWAS 的传统策略;(ii)一种两自由度检验,它结合了母体和胎儿 GWAS 的信息;(iii)一种自由度检验,其中母体和胎儿 GWAS 的信号在估计的样本重叠条件下一起进行荟萃分析。我们证明,最优策略取决于样本重叠的程度、表型之间的相关性、基因座是否表现出胎儿和/或母体效应以及这些效应是否方向一致。我们将我们的方法应用于最近对出生体重进行的 GWAS 荟萃分析的汇总统计数据。与分别分析扫描相比,两自由度和荟萃分析方法都增加了与出生体重相关的遗传基因座的数量。与最近发表的出生体重荟萃分析相比,我们的最佳策略确定了另外 62 个与出生体重相关的基因座。我们得出的结论是,虽然两自由度检验可能对某些围产特征的分析有用,但对于大多数特征,简单的荟萃分析策略可能表现最佳,尤其是在母体和胎儿 GWAS 仅部分重叠的情况下。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1995/11513127/161a06948c90/41467_2024_53495_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1995/11513127/853a9084cf5c/41467_2024_53495_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1995/11513127/486e8b47221a/41467_2024_53495_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1995/11513127/ab1679314fba/41467_2024_53495_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1995/11513127/2794b07fca6c/41467_2024_53495_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1995/11513127/69ed032984a5/41467_2024_53495_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1995/11513127/161a06948c90/41467_2024_53495_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1995/11513127/853a9084cf5c/41467_2024_53495_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1995/11513127/486e8b47221a/41467_2024_53495_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1995/11513127/ab1679314fba/41467_2024_53495_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1995/11513127/2794b07fca6c/41467_2024_53495_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1995/11513127/69ed032984a5/41467_2024_53495_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1995/11513127/161a06948c90/41467_2024_53495_Fig6_HTML.jpg

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Genetic effects on the timing of parturition and links to fetal birth weight.遗传对分娩时间的影响及其与胎儿出生体重的关系。
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FinnGen provides genetic insights from a well-phenotyped isolated population.
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