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Install and launch IGV before selecting data to visualize
For hg38
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For hg19
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
Error connecting to IGV?
Analyze
For hg38
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
For hg19
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
Download
For hg38
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For hg19
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: OCI-LY1
ATCC
MeSH
RIKEN BRC
Variation
TogoVar
SRX130605
GSM898057: OCI-LY1 NCOR-p300 INPUT
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Blood
Cell type
OCI-LY1
NA
NA
Attributes by original data submitter
Sample
source_name
Human DLBCL cel line
cell line
OCI-LY1
chip antibody
none (INPUT)
Sequenced DNA Library
library_name
GSM898057: OCI-LY1_NCOR-p300_INPUT
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
Sequencing Platform
instrument_model
Illumina Genome Analyzer IIx
Where can I get the processing logs?
Read processing pipeline
log
hg38
Number of total reads
51930521
Reads aligned (%)
87.3
Duplicates removed (%)
4.6
Number of peaks
1214 (qval < 1E-05)
hg19
Number of total reads
51930521
Reads aligned (%)
86.5
Duplicates removed (%)
6.3
Number of peaks
1355 (qval < 1E-05)
Base call quality data from
DBCLS SRA