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Install and launch IGV before selecting data to visualize
For dm6
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For dm3
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
Error connecting to IGV?
Analyze
For dm6
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
For dm3
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
Download
For dm6
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For dm3
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: Dfd
wikigenes
PDBj
CellType: 0-8h embryos
ATCC
MeSH
RIKEN BRC
SRX026861
GSM594216: NW-GFP-Goat[Dfd] ChIPSeq 1 and 2
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
TFs and others
Antigen
Dfd
Cell type
Cell type Class
Embryo
Cell type
0-8h embryos
NA
NA
Attributes by original data submitter
Sample
source_name
E0-8h
developmental stage
E0-8h
antibody name
NW-GFP-Goat[Dfd]
antibody manufacturer
White Lab
catalog
Custom
Sequenced DNA Library
library_name
GSM594216: NW-GFP-Goat[Dfd]_ChIPSeq_1 and 2
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
Sequencing Platform
instrument_model
Illumina Genome Analyzer
Where can I get the processing logs?
Read processing pipeline
log
dm6
Number of total reads
43433932
Reads aligned (%)
94.8
Duplicates removed (%)
60.1
Number of peaks
3203 (qval < 1E-05)
dm3
Number of total reads
43433932
Reads aligned (%)
96.7
Duplicates removed (%)
52.7
Number of peaks
16390 (qval < 1E-05)
Base call quality data from
DBCLS SRA