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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)
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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: GFP
wikigenes
PDBj
CellType: 7h embryos
ATCC
MeSH
RIKEN BRC
SRX4047186
GSM3132650: Pnt-GFP ChIP yanmutant; Drosophila melanogaster; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
TFs and others
Antigen
GFP
Cell type
Cell type Class
Embryo
Cell type
7h embryos
NA
NA
Attributes by original data submitter
Sample
source_name
Stage 11 embryos
chip antibody
rabbit anti-GFP antibody (1:100), Invitrogen A6455, Lot# 1603336
genotype
yan-/-(yanE833), Pbac{pnt-GFP.FPTB}VK00037
Stage
stage 11 embryo
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Hand-selected embryos were fixed with 1.8% formaldehyde. Lysates were clarified from sonicated nuclei andTF-DNA complexes isolated with an antibody. Libraries were prepared for sequencing using standard Illumina protocols.
Sequencing Platform
instrument_model
Illumina HiSeq 2000
Where can I get the processing logs?
Read processing pipeline
log
dm6
Number of total reads
57197110
Reads aligned (%)
39.1
Duplicates removed (%)
27.9
Number of peaks
8242 (qval < 1E-05)
dm3
Number of total reads
57197110
Reads aligned (%)
39.3
Duplicates removed (%)
26.4
Number of peaks
7666 (qval < 1E-05)
Base call quality data from
DBCLS SRA