ChIP-seq for NF-YA and Pbx4 on whole zebrafish embryos at 3.5hpf
收藏官方服务：
资源简介：
ChIP-seq for NF-YA and Pbx4 on whole zebrafish embryos at 3.5hpf
应用场景：
创建时间：
2020-04-28
相关数据集
ZSCAN5B and its primate-specific paralogs bind RNA polymerase III genes and extra-TFIIIC (ETC) sites to modulate mitotic progression [Human cell line ChIP-Seq data set]. Homo sapiens
Particularly in the context of differentiation and development, the importance of three-dimensional chromatin architecture to gene regulatory mechanisms is becoming increasingly clear. The most ancien
NIAID Data Ecosystem80
NF-Y Binding Site Architecture Defines a C-Fos Targeted Promoter Class
ChIP-seq experiments detect the chromatin occupancy of known transcription factors in a genome-wide fashion. The comparisons of several species-specific ChIP-seq libraries done for different transcrip
NIAID Data Ecosystem30
TF ChIP-seq from whole organism (ENCSR197UZT)
ChIP-seq against CEH-16 in L3 larva worms. 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_f
NIAID Data Ecosystem10
ChIP-seq of AP4 binding in human colorectal cancer cells DLD-1.
In order to comprehensively identify genes directly regulated by AP4, a genome-wide chromatin-immunoprecipitation analysis (ChIP) followed by next generation sequencing (ChIP-seq) was performed after
NIAID Data Ecosystem30
HIF1A ChIP-seq from HCT116, RKO, A549, and H460 cells in normoxia and hypoxia
ChIP-seq analysis was used to identify HIF1A binding sites in normoxia and hypoxia in HCT116, RKO, A549, and H460 cells Two independent biological replicates each of HCT116, RKO, A549, and H460 cells
NIAID Data Ecosystem20
