Table_6_基于台湾电子病历的甲状腺功能亢进症全基因组关联研究

基于台湾电子病历的甲状腺功能亢进症GWAS数据集,包含35,009例患者的44个新风险位点和共病分析结果。

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表格genome-wide association study (GWAS)hyperthyroidismelectronic medical record (EMR)stroke
Table_6_Genome-wide association study of hyperthyroidism based on electronic medical record from Taiwan

基本信息

模态
表格
大小
0.000017593 GB
许可
CC BY 4.0
创建/更新时间
2026-10-08
版本
v1

资源简介

Table_6_基于台湾电子病历的甲状腺功能亢进症全基因组关联研究

【一句话概览】

该研究结合台湾35,009人队列的电子病历表型与基因型数据,开展甲状腺功能亢进症全基因组关联分析,通过诊断代码识别2,767例患者。GWAS在2、6、14号染色体10个位点发现44个新风险标记,包括CTLA4、HCP5、HLA-B等。共病分析显示甲状腺功能亢进伴甲状腺风暴与卒中强相关。结果提示常见遗传风险因素,且性别、BMI和甲状腺风暴与卒中风险升高相关(来源 figshare,CC BY 4.0 许可)。

【数据集背景】

本数据集源站标题为《Table_6_Genome-wide association study of hyperthyroidism based on electronic medical record from Taiwan.xlsx》。配套论文《PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses》发表于 The American Journal of Human Genetics(2007),DOI:10.1086/519795。源站首次发布:2022-07-27。

【数据内容】

源站原始描述:Excess thyroid hormones have complex metabolic effects, particularly hyperthyroidism, and are associated with various cardiovascular risk factors. Previous candidate gene studies have indicated that genetic variants may contribute to this variable response. Electronic medical record (EMR) biobanks containing clinical and genomic data on large numbers of individuals have great potential to inform the disease comorbidity development. In this study, we combined electronic medical record (EMR) -deri…

【数据结构与技术规格】

文件数 1 个,合计 17.59 KB。Table_6_Genome-wide association study of hyperthyroidism based on electronic medical record from Taiwan.xlsx:application/vnd.openxmlformats-officedocument.spreadsheetml.sheet,17.59 KB。数据集 DOI:10.3389/fmed.2022.830621.s007。

【主题与分类】

源站学科分类:Radiology and Organ Imaging、Foetal Development and Medicine、Obstetrics and Gynaecology、Primary Health Care、Medical and Health Sciences not elsewhere classified、Dermatology。主题标签:genome-wide association study (GWAS)、hyperthyroidism、electronic medical record (EMR)、stroke。

【适用方向】

结构化表格数据可直接用于统计建模、特征工程与队列分析。

【获取与许可】

源站页面:https://frontiersin.figshare.com/articles/dataset/Table_6_Genome-wide_association_study_of_hyperthyroidism_based_on_electronic_medical_record_from_Taiwan_xlsx/20380839

使用许可:CC BY 4.0(https://creativecommons.org/licenses/by/4.0/)。

规范引用:Liu, Ting-Yuan; Liao, Wen-Ling; Wang, Tzu-Yuan; Chan, Chia-Jung; Chang, Jan-Gowth; Chen, Yu-Chia; et al. (2022). Table_6_Genome-wide association study of hyperthyroidism based on electronic medical record from Taiwan.xlsx. Frontiers. Dataset

【使用注意】

· 源站最后修改于 2023-06-16,引用时请注意版本时效。

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下载信息

注册下载

需要注册 Kaggle 账号并登录后下载,适合需要跟踪下载记录和使用 API 的用户。

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公开下载

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当前数据集主要来源为 Kaggle 公开托管,完整影像包建议通过原始链接或 Kaggle API 获取。

使用方式

数据集获取(Figshare)

命令行下载

curl -L -o "Table_6_Genome-wide association study of hyperthyroidism based on electronic medical record from Taiwan.xlsx" "https://ndownloader.figshare.com/files/36427800"

文件清单

  • Table_6_Genome-wide association study of hyperthyroidism based on electronic medical record from Taiwan.xlsx(17.59 KB)

文件总体积 17.59 KB(源站 API 实测)。

数据加载示例(图像类)

from PIL import Image
import glob, os

files = (glob.glob(os.path.join(path, "**", "*.png"), recursive=True)
       + glob.glob(os.path.join(path, "**", "*.jpg"), recursive=True)
       + glob.glob(os.path.join(path, "**", "*.tif"), recursive=True))
print("图像文件数:", len(files))
img = Image.open(files[0]); print("尺寸/模式:", img.size, img.mode)

# torchvision Dataset 方式:
# from torchvision import datasets
# ds = datasets.ImageFolder(path)  # 要求 子目录=类别

目录组织与标注格式以源站说明和下载后实际文件为准。

数据说明

Excess thyroid hormones have complex metabolic effects, particularly hyperthyroidism, and are associated with various cardiovascular risk factors. Previous candidate gene studies have indicated that genetic variants may contribute to this variable response. Electronic medical record (EMR) biobanks containing clinical and genomic data on large numbers of individuals have great potential to inform the disease comorbidity development. In this study, we combined electronic medical record (EMR) -derived phenotypes and genotype information to conduct a genome-wide analysis of hyperthyroidism in a 35,009-patient cohort in Taiwan. Diagnostic codes were used to identify 2,767 patients with hyperthyroidism. Our genome-wide association study (GWAS) identified 44 novel genomic risk markers in 10 loci on chromosomes 2, 6, and 14 (P < 5 × 10–14), including CTLA4, HCP5, HLA-B, POU5F1, CCHCR1, HLA-DRA, HLA-DRB9, TSHR, RPL17P3, and CEP128. We further conducted a comorbidity analysis of our results, and the data revealed a strong correlation between hyperthyroidism patients with thyroid storm and stroke. In this study, we demonstrated application of the PheWAS using large EMR biobanks to inform the comorbidity development in hyperthyroidism patients. Our data suggest significant common genetic risk factors in patients with hyperthyroidism. Additionally, our results show that sex, body mass index (BMI), and thyroid storm are associated with an increased risk of stroke in subjects with hyperthyroidism.

许可

CC BY 4.0

引用

学术使用请引用 DOI 10.3389/fmed.2022.830621.s007(source: https://frontiersin.figshare.com/articles/dataset/Table_6_Genome-wide_association_study_of_hyperthyroidism_based_on_electronic_medical_record_from_Taiwan_xlsx/20380839)。

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