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Install and launch IGV before selecting data to visualize
For ce11
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For ce10
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
Error connecting to IGV?
Analyze
For ce11
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
For ce10
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
Download
For ce11
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For ce10
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: L1
ATCC
MeSH
RIKEN BRC
SRX080090
GSM749401: pGES-1 EFL-1 YL418 5-31-10 L1 rep2 GFP CATT
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
TFs and others
Antigen
GFP
Cell type
Cell type Class
Larvae
Cell type
L1
NA
NA
Attributes by original data submitter
Sample
source_name
pGES-1 EFL-1:GFP:FLAG whole animal
strain
YL418
Stage
L1
chip antibody
GFP
Sequenced DNA Library
library_name
GSM749401: pGES-1_EFL-1_YL418_5-31-10_L1_rep2_GFP_CATT
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
Sequencing Platform
instrument_model
Illumina Genome Analyzer IIx
Where can I get the processing logs?
Read processing pipeline
log
ce11
Number of total reads
5139276
Reads aligned (%)
35.6
Duplicates removed (%)
16.5
Number of peaks
2108 (qval < 1E-05)
ce10
Number of total reads
5139276
Reads aligned (%)
35.6
Duplicates removed (%)
16.5
Number of peaks
2103 (qval < 1E-05)
Base call quality data from
DBCLS SRA