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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: Intestinal crypt
ATCC
MeSH
RIKEN BRC
SRX1771658
GSM2157530: Input#1+2+3 Sample#1; Mus musculus; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Digestive tract
Cell type
Intestinal crypt
NA
NA
Attributes by original data submitter
Sample
source_name
Input#1+2+3
genotype
wild type
age
6 weeks
treated with
beta-naphthoflavone for 6 weeks
cell type
small intestinal crypts
chip antibody
none (input)
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Protein A-G magnetic beads (Dynabeads, Thermo Fisher Scientific) were used to pull down immunocomplexes. Illumina compatible libraries were prepared using Diagenode's MicroPlex v2 Library Preparation™ kit.
Sequencing Platform
instrument_model
Illumina HiSeq 2500
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
2771916
Reads aligned (%)
96.9
Duplicates removed (%)
9.6
Number of peaks
62 (qval < 1E-05)
mm9
Number of total reads
2771916
Reads aligned (%)
96.7
Duplicates removed (%)
10.1
Number of peaks
54 (qval < 1E-05)
Base call quality data from
DBCLS SRA