官方服务:
资源简介:
ChIP-seq analysis was performed in Jurkat cells (T-cell acute lymphoblastic leukemia cell line) ARID5B ChIP-seq
应用场景:
创建时间:
2019-05-15
相关数据集
ChIP-seq from K562 (ENCSR283ZNI)
ZBTB8A ChIP-seq on human K562 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_U
NIAID Data Ecosystem70
UV irradiation remodels the specificity landscape of transcription factors [84702_PhotoProduct_Antibody]. UV irradiation remodels the specificity landscape of transcription factors [84702_PhotoProduct_Antibody]
Somatic mutations are highly enriched at transcription factor (TF) binding sites, with the strongest trend being observed for ultraviolet light (UV)-induced mutations in melanomas. One of the main mec
NIAID Data Ecosystem40
Cut&Run analysis for transcription factors in MOLT-4 cells.
Cut&Run analysis was performed in MOLT-4 cells to analyze the basal level of H3K4me3 and DNA binding of RUNX1 and SMARCA4. Overall design: MOLT-4 cells were incubated with CUTANA pA/G-Mnase. Chromtin
NIAID Data Ecosystem20
Genome-wide mapping of SET-Nup214, mutant NPM1 (NPM1c), and CRM1-binding sites in human leukemia or mouse ES cell lines
We used ChIP-seq to examine the genome-wide binding of CRM1, SET-Nup214, and NPM1c in leukemia cell lines. Our analysis revealed that CRM1, SET-Nup214, and NPM1c are preferentially targeted to HOX clu
NIAID Data Ecosystem50
Two Residues in the Basic Region of the Yeast Transcription Factor Yap8 Are Crucial for Its DNA-Binding Specificity
In Saccharomyces cerevisiae, the transcription factor Yap8 is a key determinant in arsenic stress response. Contrary to Yap1, another basic region-leucine zipper (bZIP) yeast regulator, Yap8 has a ver
Figshare2016-01-18 更新20



