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Install and launch IGV before selecting data to visualize
For ce11
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For ce10
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
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Analyze
For ce11
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
For ce10
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
Download
For ce11
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For ce10
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: GFP
wikigenes
PDBj
CellType: Whole worm
ATCC
MeSH
RIKEN BRC
SRX7627595
GSM4283792: GFP2 ChIPSeq; Caenorhabditis elegans; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
TFs and others
Antigen
GFP
Cell type
Cell type Class
Adult
Cell type
Whole worm
NA
NA
Attributes by original data submitter
Sample
source_name
whole animal
cell type
whole animal
passages
ND
strain
Bristol
chip antibody
GFP
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Animal lysates were prepared following the protocol of Berkseth et al., 2013. Libraries were prepared with the kapa hyper prep kit.
Sequencing Platform
instrument_model
Illumina HiSeq 3000
Where can I get the processing logs?
Read processing pipeline
log
ce11
Number of total reads
13642872
Reads aligned (%)
60.3
Duplicates removed (%)
16.9
Number of peaks
704 (qval < 1E-05)
ce10
Number of total reads
13642872
Reads aligned (%)
60.3
Duplicates removed (%)
16.9
Number of peaks
703 (qval < 1E-05)
Base call quality data from
DBCLS SRA