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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)
Error connecting to IGV?
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: dpy-27
wikigenes
PDBj
CellType: L3
ATCC
MeSH
RIKEN BRC
SRX063960
GSM727909: DPY-27
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
TFs and others
Antigen
dpy-27
Cell type
Cell type Class
Larvae
Cell type
L3
NA
NA
Attributes by original data submitter
Sample
source_name
L3 embyros
strain
N2
developmental stage
L3
chip antibody
DPY-27
Sequenced DNA Library
library_name
GSM727909: DPY-27
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
Sequencing Platform
instrument_model
Illumina Genome Analyzer II
Where can I get the processing logs?
Read processing pipeline
log
ce11
Number of total reads
17659150
Reads aligned (%)
93.9
Duplicates removed (%)
49.5
Number of peaks
811 (qval < 1E-05)
ce10
Number of total reads
17659150
Reads aligned (%)
93.9
Duplicates removed (%)
49.5
Number of peaks
846 (qval < 1E-05)
Base call quality data from
DBCLS SRA