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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)
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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)
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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: Input control
wikigenes
PDBj
CellType: Adult body
ATCC
MeSH
RIKEN BRC
SRX7217778
GSM4193041: HDA-1 input (L4440) rep1; Caenorhabditis elegans; ChIP-Seq
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Input control
Antigen
Input control
Cell type
Cell type Class
Adult
Cell type
Adult body
NA
NA
Attributes by original data submitter
Sample
source_name
the whole organism
strain
hda-1p::hda-1::gfp; glp-4(bn2)
developmental stage
Day1 of adulthood
chip antibody
none
knockdown
L4440 RNAi
Sequenced DNA Library
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Worms were cross-linked by formaldehyde and homogenized by a glass homogenizer.Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibody. Libraries were prepared by DNA Sample Kit (NEB, E7370).
Sequencing Platform
instrument_model
HiSeq X Ten
Where can I get the processing logs?
Read processing pipeline
log
ce11
Number of total reads
7928426
Reads aligned (%)
86.3
Duplicates removed (%)
14.2
Number of peaks
306 (qval < 1E-05)
ce10
Number of total reads
7928426
Reads aligned (%)
86.3
Duplicates removed (%)
14.2
Number of peaks
307 (qval < 1E-05)
Base call quality data from
DBCLS SRA