精准心血管医学:人工智能和表观遗传学用于新生儿主动脉缩窄的发病机制和预测

基于新生儿血斑DNA甲基化数据,利用人工智能分析预测主动脉缩窄,并揭示表观遗传病因。

Taylor & FrancisTaylor & Francis
DataCite Commons
2022-01-24 更新
浏览 16
基因组Artificial intelligencecongenital heart defectdeep learningDNA methylationepigenetics
Precision cardiovascular medicine: artificial intelligence and epigenetics for the pathogenesis and prediction of coarctation in neonates

基本信息

模态
基因组
大小
0.0001535 GB
许可
CC BY 4.0
创建/更新时间
2022-01-24
版本
v1

资源简介

精准心血管医学:人工智能和表观遗传学用于新生儿主动脉缩窄的发病机制和预测

【一句话概览】

本数据集是 figshare 公开的组学数据集,收录 2 个文件、合计 153.50 KB,主题涵盖 Artificial intelligence、congenital heart defect、deep learning、DNA methylation、epigenetics,可用于生物标志物发现与分子分型研究,CC BY 4.0 许可开放获取。

【数据集背景】

本数据集源站标题为《Precision cardiovascular medicine: artificial intelligence and epigenetics for the pathogenesis and prediction of coarctation in neonates》。配套论文《Precision cardiovascular medicine: artificial intelligence and epigenetics for the pathogenesis and prediction of coarctation in neonates》发表于 The Journal of Maternal-Fetal & Neonatal Medicine(2020),DOI:10.1080/14767058.2020.1722995。源站首次发布:2020-02-05。

【数据内容】

源站原始描述:Advances in omics and computational Artificial Intelligence (AI) have been said to be key to meeting the objectives of precision cardiovascular medicine. The focus of precision medicine includes a better assessment of disease risk and understanding of disease mechanisms. Our objective was to determine whether significant epigenetic changes occur in isolated, non-syndromic CoA. Further, we evaluated the AI analysis of DNA methylation for the prediction of CoA. Genome-wide DNA methylation analysis…

【数据结构与技术规格】

文件数 2 个,合计 153.50 KB。ijmf_a_1722995_sm3189.docx:application/vnd.openxmlformats-officedocument.wordprocessingml.document,34.04 KB。ijmf_a_1722995_sm3188.docx:application/vnd.openxmlformats-officedocument.wordprocessingml.document,119.46 KB。数据集 DOI:10.6084/m9.figshare.11805795.v1。

【主题与分类】

源站学科分类:Medicine、Cell Biology、Genetics、Molecular Biology、Biotechnology、Environmental Sciences not elsewhere classified。主题标签:Artificial intelligence、congenital heart defect、deep learning、DNA methylation、epigenetics。

【适用方向】

组学数据适用于生物标志物发现与分子分型相关建模研究。

【获取与许可】

源站页面:https://tandf.figshare.com/articles/dataset/Precision_cardiovascular_medicine_artificial_intelligence_and_epigenetics_for_the_pathogenesis_and_prediction_of_coarctation_in_neonates/11805795

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

规范引用:Precision cardiovascular medicine: artificial intelligence and epigenetics for the pathogenesis and prediction of coarctation in neonates. Taylor & Francis. Bahado-Singh, Ray O.; Vishweswaraiah, Sangeetha; Aydas, Buket; Yilmaz, Ali; Saiyed, Nazia M.; Mishra, Nitish K.; et al

【使用注意】

· 源站最后修改于 2023-06-01,引用时请注意版本时效。

官方服务

专家保障全链路合规授权与标注交付

陕川双基地 × 超十家三甲医院直连

从合规授权、采集治理、专业标注到数据集交付,我们提供全链路闭环服务,让高质量临床数据即拿即用。

⚡️ 需要原始数据或标注支持?联系我们获取定制方案。

帮我联系

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。

暂未开放

公开下载

无需注册即可直接获取公开样本或文档,适合快速预览和评估数据集质量。

免登录

有偿下载

公开数据集受托下载与技术交付服务。

提供高速下载与技术交付服务(收技术服务费,非数据销售)

暂未开放

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 "ijmf_a_1722995_sm3189.docx" "https://ndownloader.figshare.com/files/21552924"
curl -L -o "ijmf_a_1722995_sm3188.docx" "https://ndownloader.figshare.com/files/21552927"

文件清单

  • ijmf_a_1722995_sm3189.docx(34.04 KB)
  • ijmf_a_1722995_sm3188.docx(119.46 KB)

文件总体积 153.50 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

Advances in omics and computational Artificial Intelligence (AI) have been said to be key to meeting the objectives of precision cardiovascular medicine. The focus of precision medicine includes a better assessment of disease risk and understanding of disease mechanisms. Our objective was to determine whether significant epigenetic changes occur in isolated, non-syndromic CoA. Further, we evaluated the AI analysis of DNA methylation for the prediction of CoA.
Genome-wide DNA methylation analysis of newborn blood DNA was performed in 24 isolated, non-syndromic CoA cases and 16 controls using the Illumina HumanMethylation450 BeadChip arrays. Cytosine nucleotide (CpG) methylation changes in CoA in each of 450,000 CpG loci were determined. Ingenuity pathway analysis (IPA) was performed to identify molecular and disease pathways that were epigenetically dysregulated. Using methylation data, six artificial intelligence (AI) platforms including deep learning (DL) was used for CoA detection.
We identified significant (FDR p-value ≤ .05) methylation changes in 65 different CpG sites located in 75 genes in CoA subjects. DL achieved an AUC (95% CI) = 0.97 (0.80–1) with 95% sensitivity and 98% specificity. Gene ontology (GO) analysis yielded epigenetic alterations in important cardiovascular developmental genes and biological processes: abnormal morphology of cardiovascular system, left ventricular dysfunction, heart conduction disorder, thrombus formation, and coronary artery disease.
In an exploratory study we report the use of AI and epigenomics to achieve important objectives of precision cardiovascular medicine. Accurate prediction of CoA was achieved using a newborn blood spot. Further, we provided evidence of a significant epigenetic etiology in isolated CoA development.

许可

CC BY 4.0

引用

学术使用请引用 DOI 10.6084/m9.figshare.11805795.v1(source: https://tandf.figshare.com/articles/dataset/Precision_cardiovascular_medicine_artificial_intelligence_and_epigenetics_for_the_pathogenesis_and_prediction_of_coarctation_in_neonates/11805795)。

数据缺失?

依托陕西、四川两大基地,我们与超过十家三甲医院建立直接合作关系,覆盖合规授权、采集治理、专业标注、数据交付的全流程,为AI医疗团队提供即拿即用的高质量临床数据。

⚡️ 需要数据支持或标注服务?立即联系我们获取专业方案。

获取专属数据定制方案