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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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Analyze
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: NGP
ATCC
MeSH
RIKEN BRC
Variation
TogoVar
SRX1690212
GSM2113528: NGP INPUT; Homo sapiens; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Neural
Cell type
NGP
NA
NA
Attributes by original data submitter
Sample
source_name
NGP_Neuroblastoma
cell line
NGP
cell type
neuroblastoma cell line
growth condition
10% FBS, DMEM
treated with
None
chip antibody
NA
chip antibody vendor
NA
input
NA
barcode
CGATGT
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Lysates were clarified from sonicated nuclei and histone-DNA complexes were isolated with antibody. Libraries were prepared using the Rubicon Thruplex FD library preparation kit (cat#: 400427) per manufacturers instructions.
Sequencing Platform
instrument_model
NextSeq 500
Where can I get the processing logs?
Read processing pipeline
log
hg38
Number of total reads
43373072
Reads aligned (%)
95.5
Duplicates removed (%)
7.1
Number of peaks
693 (qval < 1E-05)
hg19
Number of total reads
43373072
Reads aligned (%)
95.1
Duplicates removed (%)
7.9
Number of peaks
787 (qval < 1E-05)
Base call quality data from
DBCLS SRA