five

Multi-ancestry maternal GWAS summary statistics from "Multi-ancestry, trans-generational GWAS meta-analysis of gestational diabetes and glycaemic traits during pregnancy reveals limited evidence of pregnancy-specific genetic effects"

收藏
DataCite Commons2025-08-18 更新2026-05-05 收录
下载链接:
https://espace.library.uq.edu.au/view/UQ:0aa6ba4
下载链接
链接失效反馈
官方服务:
资源简介:
Maternal henotypes analysed: 1-hour glucose post-OGTT (1h_Glucose), 2-hour glucose post-OGTT (2h_Glucose), fasting glucose (FG), gestational diabetes mellitus (GDM), and glycated haemoglobin (HbA1c). Quality control prior to the meta-analysis excluded SNVs with poor imputation quality (r² < 0.3 or info < 0.4), minor allele count < 10, and/or effect allele frequency < 0.1%; genetic data were lifted over to GRCh38 where required. Multi-ancestry maternal meta-analyses used MR-MEGA including three principal components; summary statistics are provided for all populations combined (FG n = 55,371; 1hG n = 38,439; 2hG n = 46,401; HbA1c n = 9,724; GDM n = 814,450 [38,305 cases]), filtered at MAF ≥ 0.01 with SNPs removed if absent from ≥ 50% of the sample. For further details on sample sizes, analytical pipelines, and cohort-specific QC procedures, see Supplementary Materials.

本研究分析的母亲表型包括:口服葡萄糖耐量试验(Oral Glucose Tolerance Test, OGTT)后1小时血糖(1h_Glucose)、OGTT后2小时血糖(2h_Glucose)、空腹血糖(fasting glucose, FG)、妊娠期糖尿病(gestational diabetes mellitus, GDM)以及糖化血红蛋白(glycated haemoglobin, HbA1c)。 荟萃分析前的质量控制步骤排除了填充质量不佳(r² < 0.3或信息得分<0.4)、次要等位基因计数<10以及/或效应等位基因频率<0.1%的单核苷酸变异(Single Nucleotide Variants, SNVs);若有需要,将遗传数据转换至人类参考基因组GRCh38版本。 多祖先母亲队列荟萃分析采用MR-MEGA方法,并纳入3个主成分;本研究提供了所有合并人群的汇总统计量(空腹血糖[FG]:n=55,371;1小时血糖[1hG]:n=38,439;2小时血糖[2hG]:n=46,401;糖化血红蛋白[HbA1c]:n=9,724;妊娠期糖尿病[GDM]:n=814,450,其中病例数为38,305),筛选标准为次要等位基因频率(Minor Allele Frequency, MAF)≥0.01%,并移除了在≥50%的样本中未检出的单核苷酸多态性(Single Nucleotide Polymorphisms, SNPs)。 关于样本量、分析流程以及队列特异性质量控制程序的更多细节,请参见补充材料。
提供机构:
The University of Queensland
创建时间:
2025-08-18
二维码
社区交流群
二维码
科研交流群
商业服务