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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: iPSC intermediates
ATCC
MeSH
RIKEN BRC
SRX1178449
GSM1866648: ChIP seq ChaF1a 2122 day3 H3K9me3 input; Mus musculus; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Pluripotent stem cell
Cell type
iPSC intermediates
NA
NA
Attributes by original data submitter
Sample
source_name
OKSM reprogramming intermediates from Mouse Embryonic Fibroblasts
strain
Black6-129X1/SvJ
tissue
Mouse Embryonic Fibroblasts
age
E13.5 embryos
antibody
none
genotype
Col1a1::tetOP-OKSM ; R26-M2rtTA
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
see methods section in main text Libraries for sequencing were prepared using standard Illumina protocols.
Sequencing Platform
instrument_model
Illumina HiSeq 2500
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
21981699
Reads aligned (%)
98.5
Duplicates removed (%)
12.1
Number of peaks
365 (qval < 1E-05)
mm9
Number of total reads
21981699
Reads aligned (%)
98.3
Duplicates removed (%)
12.1
Number of peaks
393 (qval < 1E-05)
Base call quality data from
DBCLS SRA