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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: ATAC-Seq
wikigenes
PDBj
CellType: E10.5 embryos
ATCC
MeSH
RIKEN BRC
DRX131671
Illumina HiSeq 1500 paired end sequencing of SAMD00127798
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
ATAC-Seq
Antigen
ATAC-Seq
Cell type
Cell type Class
Embryo
Cell type
E10.5 embryos
NA
NA
Attributes by original data submitter
Sample
sample_name
Mm_E10_rep2
dev_stage
E10.5
replicate
biological replicate 2
tissue_type
embryo
Sequenced DNA Library
library_strategy
ATAC-seq
library_source
GENOMIC
library_selection
other
Sequencing Platform
instrument_model
Illumina HiSeq 1500
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
75427040
Reads aligned (%)
97.3
Duplicates removed (%)
57.8
Number of peaks
30142 (qval < 1E-05)
mm9
Number of total reads
75427040
Reads aligned (%)
97.2
Duplicates removed (%)
57.9
Number of peaks
30100 (qval < 1E-05)
Base call quality data from
DBCLS SRA