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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: Unclassified
wikigenes
PDBj
CellType: Trophoblast stem cells
ATCC
MeSH
RIKEN BRC
SRX1817734
GSM2186407: K9m3 TS rep1; Mus musculus; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Unclassified
Antigen
Unclassified
Cell type
Cell type Class
Placenta
Cell type
Trophoblast stem cells
NA
NA
Attributes by original data submitter
Sample
source_name
trophoblast stem cell
strain
TS6.5, B5/EGFP, Tanaka et al. 1998
illumina platform
NextSeq500
read type
PE150
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
H3K9me3 native ChIP as described in Karimi et al. 2012 Truseq adapters, https://ethanomics.wordpress.com/chip-seq-library-construction-using-the-illumina-TruSeq-adapters
Sequencing Platform
instrument_model
NextSeq 500
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
21630803
Reads aligned (%)
70.4
Duplicates removed (%)
30.9
Number of peaks
107 (qval < 1E-05)
mm9
Number of total reads
21630803
Reads aligned (%)
70.2
Duplicates removed (%)
31.3
Number of peaks
91 (qval < 1E-05)
Base call quality data from
DBCLS SRA