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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)
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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: RNA polymerase II
wikigenes
PDBj
CellType: ES cells
ATCC
MeSH
RIKEN BRC
SRX7786269
GSM4333025: WT Pol2 ChIP B1T2; Mus musculus; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
RNA polymerase
Antigen
RNA polymerase II
Cell type
Cell type Class
Pluripotent stem cell
Cell type
ES cells
NA
NA
Attributes by original data submitter
Sample
source_name
mouse embryonic stem cells
cell line
V6.5
cell line
mouse embryonic stem cells
treatment
WT untreated mES
chip antibody
Pol2
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Lysates were clarified from MNase digested and sonicated nuclei and protein-DNA complexes were isolated with specific antibody. ChIP DNA were used to construct Illumina sequencing libraries using TELP method from (Peng et al., 2015).
Sequencing Platform
instrument_model
HiSeq X Ten
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
43241389
Reads aligned (%)
63.4
Duplicates removed (%)
10.8
Number of peaks
14232 (qval < 1E-05)
mm9
Number of total reads
43241389
Reads aligned (%)
63.3
Duplicates removed (%)
10.8
Number of peaks
14172 (qval < 1E-05)
Base call quality data from
DBCLS SRA