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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: Epitope tags
wikigenes
PDBj
CellType: S2
ATCC
MeSH
RIKEN BRC
SRX099637
GSM807218: no protein/D.mel PB-seq mock seqB; Drosophila melanogaster; other
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
TFs and others
Antigen
Epitope tags
Cell type
Cell type Class
Cell line
Cell type
S2
Source
Oregon R
Developmental Stage
late embryonic stage
Attributes by original data submitter
Sample
source_name
mock IP (no HSF)
library strategy
PB-Seq
library selection
immunoprecipitation
library source
naked, sheared genomic Drosophila S2 DNA
antibody
Anti-FLAG M2
Sequenced DNA Library
library_name
GSM807218: no_protein/D.mel_PB-seq_mock_seqB
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
Sequencing Platform
instrument_model
Illumina HiSeq 2000
Where can I get the processing logs?
Read processing pipeline
log
dm6
Number of total reads
11889914
Reads aligned (%)
43.3
Duplicates removed (%)
49.7
Number of peaks
2895 (qval < 1E-05)
dm3
Number of total reads
11889914
Reads aligned (%)
44.1
Duplicates removed (%)
45.4
Number of peaks
3714 (qval < 1E-05)
Base call quality data from
DBCLS SRA