囊性纤维化肺病严重程度预测性表观遗传生物标志物识别
该数据集来自 clinicaltrials.gov,聚焦囊性纤维化(CF)患者肺病严重程度的预测性表观遗传生物标志物识别

基本信息
资源简介
囊性纤维化肺病严重程度预测性表观遗传生物标志物识别
该数据集来自 clinicaltrials.gov,聚焦囊性纤维化(CF)患者肺病严重程度的预测性表观遗传生物标志物识别。CF 由 CFTR 基因突变引起,肺病是患者发病和死亡的主要原因,且严重程度在相同基因型患者间也存在差异。这种临床变异性取决于遗传因素(CFTR 复杂等位基因和修饰基因)与环境因素,遗传因素已被广泛探索并发现多个修饰基因,而环境因素仍知之甚少,已知环境因素通过作用于表观遗传标记来修饰表型。数据可用于探索表观遗传标志物与肺病严重程度的关联,支持预测性生物标志物研究(来源 clinicaltrials.gov)。
【数据内容】
源站描述(机器翻译,仅供参考):病症:囊性纤维化。囊性纤维化(CF)是一种常染色体隐性遗传病,由 CFTR 基因突变引起。CFTR 编码一种氯离子通道,主要表达于上皮细胞顶膜。CFTR 功能障碍导致黏液增稠,引起呼吸道、消化道和生殖道的多种疾病。在 CF 患者中,肺病是发病和死亡的主要原因,其严重程度在 CF 患者之间可变,即使在具有相同基因型的患者之间也是如此。这种临床变异性取决于两个因素:遗传因素(CFTR 基因的复杂等位基因和修饰基因)和环境因素。遗传因素已被广泛探索,并已鉴定出多个修饰基因。相比之下,环境因素仍鲜为人知。已充分证实,环境因素通过作用于表观遗传标记来修饰表型(即
【主题与分类】
主题标签:Cystic Fibrosis。本站分类:呼吸系统疾病。
【获取与许可】
源站页面:https://clinicaltrials.gov/study/NCT02976714
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
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免登录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
源站:https://clinicaltrials.gov/study/NCT02976714
标准获取流程:
- 访问源站链接,注册/登录账号;
- 进入数据集详情页,按页面指引申请权限或直接下载;
- 部分平台提供 SDK,例如:
- OpenDataLab:
pip install openxlab后openxlab.dataset.get(...) - ModelScope:
pip install modelscope后modelscope download - 天池: 登录后页面提供直链下载
以源站「数据下载/使用文档」页面为准。
- OpenDataLab:
数据说明
Conditions: Cystic Fibrosis. Cystic Fibrosis (CF) is an autosomal recessive disease resulting from mutations in the CFTR gene. CFTR encodes a chloride channel, mainly expressed at the apical membrane of epithelial cells. CFTR dysfunction induces mucus thickening, causing multiple disorders in respiratory, digestive and reproductive tracts. In CF patients, lung disease is the main cause of morbidity and mortality, and its severity is variable among CF patients, even among those with the same genotype. This clinical variability depends on two factors: genetic (complex alleles of CFTR gene and modifier genes) and environmental factors. Genetic factors have been largely explored, and several modifier genes have been identified. By contrast, environmental factors are still poorly known. It is well established that environmental factors modify the phenotype by acting on epigenetic marks (i.e. DNA methylation, histone modification) present in the genome. Epigenetic modifications regulate and modulate gene expression. In a previous we profiled DNA methylation genome-wide in nasal epithelial cell samples from 32 CF patients and 24 healthy controls. CF patients homozygous for the p.Phe508del mutation and >18-years-old were stratified according to the lung disease severity. Through this study, we identified 187 genomic regions (CpG dinucleotides) differentially methylated between CF patients with mild lung disease and CF patients with severe lung disease. The present project aims at identifying predictive epigenetic biomarkers of lung disease severity, among these 187 regions. While the previous study was carried out on genomic DNA extracted from nasal epithelial cells, in the present project we will use a non-invasive model: spontaneous sputum. Hypothesis: some differentially methylated genomic regions between mild and severe CF patients can be used as predictive epigenetic biomarkers of lung disease severity in cystic fibrosis. Objectives: (i) to identify predictive epigenetic biomarkers of lung disease
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。
需要用于商业化训练或医疗器械注册(NMPA/FDA)?
公开数据往往缺乏完整的病理回证与专家标注。千方医数集依托陕川双基地与超十家三甲医院直连,提供完全合规、去标识化、支持注册级质控的专病数据集交易服务。




