数据来自:复发性急性髓系白血病的基因组特征揭示新的潜在治疗靶点

包含73名复发或原发耐药急性髓系白血病患者的全基因组和全外显子测序数据,用于基因组特征分析和潜在治疗靶点研究。

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基因组Whole exome sequencing (WES)Whole Genome Sequencing dataAcute Myeloid LeukemiaCancerGenomics
Data from: Genomic characterization of relapsed acute myeloid leukemia reveals novel putative therapeutic targets

基本信息

模态
基因组
许可
Restricted Access
创建/更新时间
2026-10-07
版本
v1

资源简介

数据来自:复发性急性髓系白血病的基因组特征揭示新的潜在治疗靶点

【一句话概览】

本数据集是 figshare 公开的组学数据集,主题涵盖 Whole exome sequencing (WES)、Whole Genome Sequencing data、Acute Myeloid Leukemia、Cancer、Genomics,可用于生物标志物发现与分子分型研究,Restricted Access 许可开放获取。

【数据集背景】

本数据集源站标题为《Data from: Genomic characterization of relapsed acute myeloid leukemia reveals novel putative therapeutic targets》。配套论文《Genomic characterization of relapsed acute myeloid leukemia reveals novel putative therapeutic targets》发表于 Blood Advances(2021),DOI:10.1182/bloodadvances.2020003709。项目资助方:Knut and Alice Wallenberg Foundation (KAW 2013-0159)。源站首次发布:2021-02-11。

【数据内容】

源站原始描述:Data Set Description These data are collected from a total of 73 participants (48 adult; 25 pediatric), all of which had relapsed or primary resistant acute myeloid leukemia. The data, which here are separated into an adult and a pediatric dataset, were generated as part of a study by Stratmann et. al., 2021 ( Please note that separate applications are necessary for the adult and pediatric dataset, respectively. When applying for access, please indicate which of the datasets that the application…

【数据结构与技术规格】

数据集 DOI:10.17044/scilifelab.12292778.v1。

【主题与分类】

源站学科分类:Oncology and carcinogenesis not elsewhere classified、Genomics。主题标签:Whole exome sequencing (WES)、Whole Genome Sequencing data、Acute Myeloid Leukemia、Cancer、Genomics。

【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://figshare.scilifelab.se/articles/dataset/Data_from_Genomic_characterization_of_relapsed_acute_myeloid_leukemia_reveals_novel_putative_therapeutic_targets/12292778

使用许可:Restricted Access(https://www.scilifelab.se/data/restricted-access/)。

规范引用:Holmfeldt, Linda; Stratmann, Svea (2021). Data from: Genomic characterization of relapsed acute myeloid leukemia reveals novel putative therapeutic targets. Uppsala Universitet. Dataset

【使用注意】

· 源站最后修改于 2025-01-15,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。

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。

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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)

源站:https://figshare.com/articles/dataset/Data_from_Genomic_characterization_of_relapsed_acute_myeloid_leukemia_reveals_novel_putative_therapeutic_targets/12292778

按页面 Download 按钮获取。

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

Data Set Description

These data are collected from a total of 73 participants (48 adult; 25 pediatric), all of which had relapsed or primary resistant acute myeloid leukemia. The data, which here are separated into an adult and a pediatric dataset, were generated as part of a study by Stratmann et. al., 2021 (https://doi.org/10.1182/bloodadvances.2020003709).

Please note that separate applications are necessary for the adult and pediatric dataset, respectively. When applying for access, please indicate which of the datasets that the application applies for.

The adult dataset contains whole genome sequencing data from 62 diagnosis (D), relapse (R1/R2/R3) and/or primary resistant (PR) leukemia samples, and 37 normal (G) DNA samples from 37 patients, as well as whole exome sequencing data from 20 leukemia samples and one (1) normal DNA sample from 15 patients.

The pediatric dataset contains whole genome sequencing data from 49 diagnosis (D), relapse (R1/R2/R3), persistent relapse (R1/2-P) and/or primary resistant (PR) leukemia samples and 24 normal (G) DNA samples from 23 patients, as well as whole exome sequencing data from seven (7) leukemia samples from five (5) patients.

The leukemia samples originate from bone marrow or peripheral blood. The patient-matched normal DNA samples originate from either complete remission bone marrow or peripheral blood cells, or from normal bone marrow stromal cells cultivated from leukemia bone marrow. Further details regarding the samples are available in the Supplemental Information part of Stratmann et. al., 2021 (https://doi.org/10.1182/bloodadvances.2020003709).

Whole genome sequencing libraries and associated next-generation sequencing were carried out by the SNP&SEQ Technology platform, SciLifeLab, National Genomics Infrastructure Uppsala, Sweden. Libraries were prepared using the TruSeq PCR-free DNA sample preparation Kit, followed by paired-end 150bp read length sequencing on a HiSeqX (Illumina Inc.).

Whole exome sequencing libraries and associated next-generation sequencing were carried out by the Uppsala Genome Center, SciLifeLab, National Genomics Infrastructure Uppsala, Sweden. Libraries were performed using th

许可

Restricted Access

引用

学术使用请引用 DOI 10.17044/scilifelab.12292778.v1(source: https://figshare.scilifelab.se/articles/dataset/Data_from_Genomic_characterization_of_relapsed_acute_myeloid_leukemia_reveals_novel_putative_therapeutic_targets/12292778)。

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