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Assessment of patient-derived tumour xenografts (PDXs) as a discovery tool for cancer epigenomics

ChEBI2014-11-26 更新2026-07-21 收录

肿瘤异种移植模型评估

癌症表观基因组学

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-59352 数据链接链接失效反馈

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资源简介：

Assessment of patient-derived tumour xenografts (PDXs) as a discovery tool for cancer epigenomics

应用场景：

创建时间：

2014-11-26

癌症表观基因组学

转录调控ChIP-seq

Discovery of the genome-wide location of proteins using ChIP-Seq has allowed global mapping of the key transcription factors and chromatin regulators that control gene expression programs in various c

NIAID Data Ecosystem90

Genome-wide profiling of the functional DNA methylation landscape at base-pair resolution in human cancer types [BS-seq]

癌症表观基因组学

差异甲基化分析

Whole genome bisulphite sequencing of 13 human cancer samples and 9 normal controls. The main goal is to find the Diffrenetial methylated regions (DMR) at Genome wide level in different tissues and ca

NIAID Data Ecosystem80

TF ChIP-seq from HepG2 (ENCSR011INW)

转录因子结合位点分析

癌症表观基因组学

ChIP-Seq on HepG2 For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov/Pages/Research/ENCODE/ENCODE_Data_Use_Policy_for_External_Users_03-07-1

NIAID Data Ecosystem40

ChIP-seq analysis of HIF-1b binding in hypoxic cancer cell lines. ChIP-seq analysis of HIF-1b binding in hypoxic cancer cell lines

缺氧响应转录调控

癌症表观基因组学

Pan-genomic analysis of hypoxic HIF-1b binding by ChIP-seq in cancer cell lines Overall design: ChIP_seq analysi of HIF-1b binding in 4 cancer cell lines incubated in 0.5% hypoxia for 16 hours

NIAID Data Ecosystem80

Integrated epigenomic analyses of enhancer as well as promoter regions in gastric cancer. Homo sapiens

癌症表观基因组学

增强子启动子分析

To understand epigenetic changes in the distal regulatory as well as proximal regions, we performed RNA-seq, MBD-seq, and H3K27ac ChIP-seq on gastric tissues and cell lines. Overall design: mRNA seque

NIAID Data Ecosystem50

Assessment of patient-derived tumour xenografts (PDXs) as a discovery tool for cancer epigenomics

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