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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: NA
wikigenes
PDBj
CellType: STAP cells
ATCC
MeSH
RIKEN BRC
SRX472662
Low pH treated CD45 positive Cells ; ChIPSeq input
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
No description
Antigen
NA
Cell type
Cell type Class
Pluripotent stem cell
Cell type
STAP cells
NA
NA
Attributes by original data submitter
Sample
strain
C57BL/6 x 129/sv
dev_stage
Oct3/4 expressing cells
sample_type
ChIPSeq
label
STAP_input DNA
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
Sequencing Platform
instrument_model
Illumina HiSeq 1500
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
38924902
Reads aligned (%)
98.5
Duplicates removed (%)
11.8
Number of peaks
577 (qval < 1E-05)
mm9
Number of total reads
38924902
Reads aligned (%)
98.2
Duplicates removed (%)
11.8
Number of peaks
613 (qval < 1E-05)
Base call quality data from
DBCLS SRA