性别差异研究衍生数据集

该数据集提供泛癌水平按性别分类的基因组突变数据,用于分析不同性别的突变模式差异。

Park, Seung-JinPark, Seung-Jin
Figshare
2023-08-16 更新
浏览 24
基因组分类TCGApan-cancer genomicsSex difference
Derived datasets on 'sexdiff research'

基本信息

模态
基因组
大小
2.814650816 GB
任务类型
分类
许可
CC BY 4.0
创建/更新时间
2023-08-16
版本
v1

资源简介

性别差异研究衍生数据集

【数据集背景】

本数据集源站标题为《Derived datasets on ''sexdiff research''》。源站首次发布:2023-08-16。

【数据内容】

源站原始描述:To treat cancer in this age of precision medicine, identifying effective patient groups or understanding the variations among patients is essential. Several recent reports have revealed that even the same treatment for the same disease has different effects depending on the sex. However, a detailed understanding of genomic differences according sex, including mutational differences, oncogenic signaling pathways, and co-occurrence or exclusivity networks, at the pan-cancer level remains elusive.…

主表 ACC_Clinical.txt 含 37 列、样本前 93 行结构完整。

主表 ACC_CNV.txt 含 89 列、样本前 2000 行结构完整。

【数据结构与技术规格】

文件数 75 个,合计 2.81 GB。ACC_Clinical.txt:text/plain,25.82 KB。ACC_CNV.txt:text/plain,5.03 MB。数据集 DOI:10.6084/m9.figshare.23961336.v1。

【主题与分类】

源站学科分类:Sequence analysis、Bioinformatics and computational biology not elsewhere classified。主题标签:TCGA、pan-cancer genomics、Sex difference。

【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。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。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://figshare.com/articles/dataset/Derived_datasets_on_sexdiff_research_/23961336

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

规范引用:Park, Seung-Jin (2023). Derived datasets on ''sexdiff research''. figshare. Dataset

官方服务

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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。

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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。

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 "ACC_Clinical.txt" "https://ndownloader.figshare.com/files/42014346"
curl -L -o "ACC_CNV.txt" "https://ndownloader.figshare.com/files/42014349"
curl -L -o "ACC_Mutation.txt" "https://ndownloader.figshare.com/files/42014352"
curl -L -o "BLCA_Clinical.txt" "https://ndownloader.figshare.com/files/42014355"
curl -L -o "BLCA_CNV.txt" "https://ndownloader.figshare.com/files/42014358"
curl -L -o "BLCA_Mutation.txt" "https://ndownloader.figshare.com/files/42014361"
curl -L -o "CHOL_Clinical.txt" "https://ndownloader.figshare.com/files/42014364"
curl -L -o "CHOL_CNV.txt" "https://ndownloader.figshare.com/files/42014367"

文件清单

  • ACC_Clinical.txt(25.82 KB)
  • ACC_CNV.txt(5.03 MB)
  • ACC_Mutation.txt(12.15 MB)
  • BLCA_Clinical.txt(120.23 KB)
  • BLCA_CNV.txt(23.15 MB)
  • BLCA_Mutation.txt(166.15 MB)
  • CHOL_Clinical.txt(11.26 KB)
  • CHOL_CNV.txt(2.17 MB)
  • CHOL_Mutation.txt(4.69 MB)
  • COADREAD_Clinical.txt(167.38 KB)
  • COADREAD_CNV.txt(61.95 MB)
  • COADREAD_Mutation.txt(356.37 MB)
  • DLBC_Clinical.txt(14.00 KB)
  • DLBC_CNV.txt(2.66 MB)
  • DLBC_Mutation.txt(8.03 MB)
  • ESCA_Clinical.txt(52.51 KB)
  • ESCA_CNV.txt(10.59 MB)
  • ESCA_Mutation.txt(49.42 MB)
  • GBM_Clinical.txt(112.24 KB)
  • GBM_CNV.txt(31.11 MB)

文件总体积 2.81 GB(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

To treat cancer in this age of precision medicine, identifying effective patient groups or understanding the variations among patients is essential. Several recent reports have revealed that even the same treatment for the same disease has different effects depending on the sex. However, a detailed understanding of genomic differences according sex, including mutational differences, oncogenic signaling pathways, and co-occurrence or exclusivity networks, at the pan-cancer level remains elusive. There were sex-biased mutation and tumor type dependent mutations such as significantly female-enriched EGFR mutation or male-enriched TP53 mutations. In addition, HUWE1 mutations and PHKA2 mutations showed female-specific prognostic effect in overall survival. Oncogenic signaling pathways and co-occurring networks also showed diverse differences across tumor types. Finally, we discovered associations male-enriched the chemotherapy signature and female-enriched several mutational signatures. Our findings identified genomic mutational landscape caused by different sex and confirmed that sex is an important biological variable for understanding tumor biology. Finally, our findings will offer new findings and conclusions from abundant but unfound public data.

许可

CC BY 4.0

引用

学术使用请引用 DOI 10.6084/m9.figshare.23961336.v1(source: https://figshare.com/articles/dataset/Derived_datasets_on_sexdiff_research_/23961336)。

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