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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: BEko
ATCC
MeSH
RIKEN BRC
SRX4670703
GSM3383947: Beko Input GSI; Mus musculus; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Blood
Cell type
BEko
NA
NA
Attributes by original data submitter
Sample
source_name
Beko pre-T cell line
cell line
Beko pre-T
chip antibody
none
treatment
24 hours with 10 mg/ml DAPT (GSI).
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
ChIP was done essentially as previously described (Giaimo et al. Jove 2017, doi: 10.3791/55907) Lybrary-prep kit: Diagenode MicropPlex Library Preparation kit v2 (C05010012)
Sequencing Platform
instrument_model
Illumina HiSeq 2500
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
32898789
Reads aligned (%)
97.5
Duplicates removed (%)
17.8
Number of peaks
876 (qval < 1E-05)
mm9
Number of total reads
32898789
Reads aligned (%)
97.4
Duplicates removed (%)
18.1
Number of peaks
864 (qval < 1E-05)
Base call quality data from
DBCLS SRA