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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: Unclassified
ATCC
MeSH
RIKEN BRC
SRX3343302
GSM2836180: Stage1 Rep1 [ATAC-Seq]; Mus musculus; ATAC-seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
ATAC-Seq
Antigen
ATAC-Seq
Cell type
Cell type Class
Unclassified
Cell type
Unclassified
NA
NA
Attributes by original data submitter
Sample
source_name
cells
strain
Mixed (C57BL/6 x 129)
marker
Oct4-GFP+
Stage
Stage 1 (day 6)
Sequenced DNA Library
library_strategy
ATAC-seq
library_source
GENOMIC
library_selection
other
library_construction_protocol
Cells were harvested and lysed at various stages of 3c enhanced reprogramming as previously described by Buenrostro et al., 2013. ATAC-Seq libraries were prepared as previously described by Buenrostro et al., 2013.
Sequencing Platform
instrument_model
Illumina HiSeq 2500
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
40715234
Reads aligned (%)
93.9
Duplicates removed (%)
40.0
Number of peaks
10913 (qval < 1E-05)
mm9
Number of total reads
40715234
Reads aligned (%)
93.9
Duplicates removed (%)
40.1
Number of peaks
10886 (qval < 1E-05)
Base call quality data from
DBCLS SRA