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Install and launch IGV before selecting data to visualize
For mm10
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For mm9
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
Error connecting to IGV?
Analyze
For mm10
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
For mm9
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
Download
For mm10
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For mm9
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
Link Out
Sequence Read Archive
DBCLS SRA
NCBI SRA
ENA
Antigen: Cebpa
wikigenes
PDBj
CellType: B cells
ATCC
MeSH
RIKEN BRC
SRX377484
GSM1264230: Bcells 18hEstradiol ChIPseq Cebpa; Mus musculus; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
TFs and others
Antigen
Cebpa
Cell type
Cell type Class
Blood
Cell type
B cells
NA
NA
Attributes by original data submitter
Sample
source_name
primary Bcell after 18h treatment of estradiol
cell type
primary B cells
treatment
Estradiol for 18h
chip antibody
anti-Cebpa (Santa Cruz, catalog: sc-61, lot: k1009)
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
ChIP experiments were performed as described previously (van Oevelen et al, 2008, PMID:20956564). DNA libraries of C/EBPa enriched chromatin fragments were prepared using Illumina's reagents and instructions.
Sequencing Platform
instrument_model
Illumina HiSeq 2000
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
29435701
Reads aligned (%)
93.6
Duplicates removed (%)
27.6
Number of peaks
565 (qval < 1E-05)
mm9
Number of total reads
29435701
Reads aligned (%)
93.2
Duplicates removed (%)
27.5
Number of peaks
606 (qval < 1E-05)
Base call quality data from
DBCLS SRA