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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: DNase-Seq
wikigenes
PDBj
CellType: mESC derived mesodermal cells
ATCC
MeSH
RIKEN BRC
SRX2911517
GSM2665584: DHSseq WT FLK; Mus musculus; DNase-Hypersensitivity
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
DNase-seq
Antigen
DNase-Seq
Cell type
Cell type Class
Pluripotent stem cell
Cell type
mESC derived mesodermal cells
NA
NA
Attributes by original data submitter
Sample
source_name
Flk-1+ cells
cell type
ES cell derived Flk-1+ cells
genotype
WT
Sequenced DNA Library
library_strategy
DNase-Hypersensitivity
library_source
GENOMIC
library_selection
DNase
library_construction_protocol
RNA extraction using collumns; AmPure beads for the ChIP-Seq; Qiagen MinElute for the DHS-seq According to Illumina Sample 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
35969077
Reads aligned (%)
94.6
Duplicates removed (%)
8.1
Number of peaks
17892 (qval < 1E-05)
mm9
Number of total reads
35969077
Reads aligned (%)
94.5
Duplicates removed (%)
8.1
Number of peaks
17888 (qval < 1E-05)
Base call quality data from
DBCLS SRA