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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: NA
wikigenes
PDBj
CellType: Unclassified
ATCC
MeSH
RIKEN BRC
SRX4546294
DNA-seq of drosophila
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
No description
Antigen
NA
Cell type
Cell type Class
Unclassified
Cell type
Unclassified
NA
NA
Attributes by original data submitter
Sample
isolate
NA
breed
NA
cultivar
NA
ecotype
NA
age
NA
dev_stage
NA
sex
NA
tissue
NA
biomaterial_provider
NA
Sequenced DNA Library
library_name
3_AGGCAGAA_L007_R1_001.fastq.gz
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
Sequencing Platform
instrument_model
Illumina HiSeq 4000
Where can I get the processing logs?
Read processing pipeline
log
dm6
Number of total reads
39511577
Reads aligned (%)
93.8
Duplicates removed (%)
29.3
Number of peaks
19563 (qval < 1E-05)
dm3
Number of total reads
39511577
Reads aligned (%)
94.0
Duplicates removed (%)
27.7
Number of peaks
19959 (qval < 1E-05)
Base call quality data from
DBCLS SRA