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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: Input control
wikigenes
PDBj
CellType: AML12
ATCC
MeSH
RIKEN BRC
SRX6481997
GSM3959433: PML ChIP-seq Input-1; Mus musculus; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Liver
Cell type
AML12
Tissue
Liver
Cell Type
Hepatocyte
Disease
Normal
Attributes by original data submitter
Sample
source_name
shCtrl
cell line
AML12 cells
genotype/variation
shCtrl
chip antibody
none (input)
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
PML ChIP was done as previously described (Lund et al., 2014) from 5×10^6 cells. Illumina sequencing library were prepared according to the standard Illumina protocol.
Sequencing Platform
instrument_model
Illumina HiSeq X Ten
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
35037092
Reads aligned (%)
96.2
Duplicates removed (%)
31.5
Number of peaks
652 (qval < 1E-05)
mm9
Number of total reads
35037092
Reads aligned (%)
96.0
Duplicates removed (%)
31.6
Number of peaks
637 (qval < 1E-05)
Base call quality data from
DBCLS SRA