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Install and launch IGV before selecting data to visualize
For dm3
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For dm6
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
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For dm3
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
For dm6
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
Download
For dm3
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For dm6
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: ph-d
wikigenes
PDBj
CellType: 16-18h embryos
ATCC
MeSH
RIKEN BRC
SRX1872292
GSM2211687: PH WT rep2 ChIPSeq; Drosophila melanogaster; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
TFs and others
Antigen
ph-d
Cell type
Cell type Class
Embryo
Cell type
16-18h embryos
NA
NA
Attributes by original data submitter
Sample
source_name
Embryo 16h-18h
genotype
WT
tissue
Embryo
age
16-18
antibody
PH
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Chromatin prepared from Drosophila embryos was immunoprecipitated with specific antibodies and precipitated DNA was isolated (see mat and methods for details) Libraries were prepared according to Illumina's instructions
Sequencing Platform
instrument_model
Illumina HiSeq 2000
Where can I get the processing logs?
Read processing pipeline
log
dm3
Number of total reads
52116026
Reads aligned (%)
64.5
Duplicates removed (%)
80.5
Number of peaks
3799 (qval < 1E-05)
dm6
Number of total reads
52116026
Reads aligned (%)
63.5
Duplicates removed (%)
82.2
Number of peaks
3485 (qval < 1E-05)
Base call quality data from
DBCLS SRA