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For hg38
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For hg19
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
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For hg38
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
For hg19
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
Download
For hg38
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For hg19
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: KGN
ATCC
MeSH
RIKEN BRC
Variation
TogoVar
SRX8201618
GSM4504721: CON input; Homo sapiens; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Gonad
Cell type
KGN
Primary Tissue
Ovary
Tissue Diagnosis
Tumor Granulosa Cell
Attributes by original data submitter
Sample
source_name
human ovarian granulosa KGN cells
cell line
KGN
cell type
Ovarian granulosa cells
passages
5-8
treatment
Control
chip antibody
None
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
We used ChIP-seq kit (CST, Cat# 9003) to extract chromatins following the manufacturer instructions. Libraries were prepared according to Illumina's protocols. Libraries were sequenced on the Genome Analyzer following the manufacturer's protocols.
Sequencing Platform
instrument_model
Illumina Genome Analyzer
Where can I get the processing logs?
Read processing pipeline
log
hg38
Number of total reads
86830964
Reads aligned (%)
96.8
Duplicates removed (%)
18.3
Number of peaks
1764 (qval < 1E-05)
hg19
Number of total reads
86830964
Reads aligned (%)
96.0
Duplicates removed (%)
19.4
Number of peaks
622 (qval < 1E-05)
Base call quality data from
DBCLS SRA