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资源简介：
T helper cell type 2 ChIP-seq
应用场景：
创建时间：
2017-12-06
相关数据集
Comprehensive identification and characterization of the binding sites in Th2 cells
Comprehensive identification and characterization of the binding sites of Th2 cells. We used ChIP-Seq method, in which next gene sequencing technology and chromatin-immunopreci
NIAID Data Ecosystem80
Comprehensive identification and characterization of the binding sites in Th2 cells
Comprehensive identification and characterization of the binding sites of Th2 cells. We used ChIP-Seq method, in which next gene sequencing technology and chromatin-immunopreci
NIAID Data Ecosystem50
Patterns of heterochromatin distribution alterations linked to transcriptional changes at Plasmodium falciparum clonally variant gene loci [ChIP-seq]
The survival of malaria parasites in the changing human blood environment largely depends on their ability to alter gene expression by epigenetic mechanisms. The active state of Plasmodium falciparum
NIAID Data Ecosystem40
T helper cell type 2 ATAC-seq time-course. T helper cell type 2 ATAC-seq time-course
CD4+ T cells were extracted from mouse and human. They were activated in vitro with CD3/28 and cultured with Il4. ATAC-seq was then performed at different time points
NIAID Data Ecosystem70
Genome-wide mapping of hnRNPA2B1 binding in human adipose derived stem cells isolated from gluteofemoral (GF) subcutaneous adipose tissue
NOT PROVIDED; REQUESTED Human adipose serived stem cells (ASC) isolated from GF adipose tissue obtained from premenopausal women were used to perform assess hnRNPA2B1 binding by ChIP-seq
NIAID Data Ecosystem40
