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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)
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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: H3K27ac
wikigenes
PDBj
CellType: Lung cancer
ATCC
MeSH
RIKEN BRC
SRX5083727
GSM3497805: mNSCLC-H3K27ac 4; Mus musculus; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Histone
Antigen
H3K27ac
Cell type
Cell type Class
Lung
Cell type
Lung cancer
NA
NA
Attributes by original data submitter
Sample
source_name
in vivo
disease state
NSCLC
cell type
lung tumor
genotype
KrasG12D/+;Trp53-/-;GFPi-GFP-2A-rTA;Luc
chip antibody
anti-H3K27ac ab4729 Abcam
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Trypsin/Collegenase/Hyarulonydase/DNaseI digestion followed by SDS buffer lysis. ChIP-seq was performed as previously described (Serresi et al., 2016). Libraries were prepared according to Illumina's instructions.
Sequencing Platform
instrument_model
NextSeq 500
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
22692515
Reads aligned (%)
89.6
Duplicates removed (%)
66.1
Number of peaks
22033 (qval < 1E-05)
mm9
Number of total reads
22692515
Reads aligned (%)
89.5
Duplicates removed (%)
66.2
Number of peaks
21974 (qval < 1E-05)
Base call quality data from
DBCLS SRA