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Install and launch IGV before selecting data to visualize
For mm10
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For mm9
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
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Analyze
For mm10
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
For mm9
Colocalization
Target Genes (TSS ± 1kb)
Target Genes (TSS ± 5kb)
Target Genes (TSS ± 10kb)
Download
For mm10
BigWig
Peak-call (q < 1E-05)
Peak-call (q < 1E-10)
Peak-call (q < 1E-20)
For mm9
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: Rorc
wikigenes
PDBj
CellType: Lymphoid organ
ATCC
MeSH
RIKEN BRC
SRX9690648
GSM4977289: WTIP; Mus musculus; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
TFs and others
Antigen
Rorc
Cell type
Cell type Class
Blood
Cell type
Lymphoid organ
NA
NA
Attributes by original data submitter
Sample
source_name
lymphoid organ
tissue
lymphoid organ
isolate
C57BL/6J
disease
NA
disease stage
NA
genotype
NA
chip antibody
polyclonal rabbit anti-RORgt antibodies (homemade)
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Lysates were clarified from sonicated PFA-fixed nuclei, and Twin-strep-tagged RORa-DNA complexes were isolated with Strep-Tactin. ChIP-Seq libraries were prepared with the KAPA HyperPlus Kit (Roche) following the manufacturer's protocols.
Sequencing Platform
instrument_model
Illumina HiSeq 4000
Where can I get the processing logs?
Read processing pipeline
log
mm10
Number of total reads
31877124
Reads aligned (%)
95.6
Duplicates removed (%)
10.1
Number of peaks
2970 (qval < 1E-05)
mm9
Number of total reads
31877124
Reads aligned (%)
95.4
Duplicates removed (%)
10.2
Number of peaks
3011 (qval < 1E-05)
Base call quality data from
DBCLS SRA