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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: NA
wikigenes
PDBj
CellType: Unclassified
ATCC
MeSH
RIKEN BRC
SRX278068
Illumina chromatin immunoprecipitates sequencing of genomic DNA library 'Solexa-8939' containing sample Control Input
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
Sample name
Control Input
geographic location (country and/or sea,region)
missing
isolation source
missing
strain
missing
BioSampleModel
Generic
Sequenced DNA Library
library_name
Solexa-8939
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
Sequencing Platform
instrument_model
Illumina Genome Analyzer II
Where can I get the processing logs?
Read processing pipeline
log
ce11
Number of total reads
16712402
Reads aligned (%)
26.0
Duplicates removed (%)
10.3
Number of peaks
449 (qval < 1E-05)
ce10
Number of total reads
16712402
Reads aligned (%)
26.0
Duplicates removed (%)
10.3
Number of peaks
442 (qval < 1E-05)
Base call quality data from
DBCLS SRA