Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Unclassified
Antigen
Unclassified

Cell type

Cell type Class
Uterus
Cell type
HeLa
Primary Tissue
Cervix
Tissue Diagnosis
Adenocarcinoma

Attributes by original data submitter

Sample

source_name
Hela cell
cell line
Hela cell
genotype
siNC
chip antibody
BD, BD44, S2
library strategy
ChIP-seq

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Cells were first crosslinked by formaldehyde, then sonicated in SDS containing buffer to dissolve the chromatin. The clarified chromatin were immunoprecipitated with dyno beas conjucated with antibodies. For ORC1 ChIP, the chromatin were immunoprecipitated with streptavidin dyno beads( Invitrogent, M280). For native ChIP-seq, cells were collected and digested by MNase to get the mono-nucleosome. For BrdU-IP-seq, genomic DNA were extracted from cells and then sonicated to 200-500bp. The ChIP-seq antibodies are as following: Anti-H2A.Z, Abcam, ab4174; Anti-BrdU, BD, BD44; Anti-H4K20me1, Abcam, ab9051; Anti-H4K20me2, Abcam, ab9052; Anti-H4K20me3, Abcam, ab9053. H2A.Z, H4K20me, ORC1,BrdU Libraries(sample 1-22, 35-44, 49-52) were prepared according to NEBNext Ultra DNA Library Prep Kit for Illumina (E7370L) and were sequenced using HiSeq2000 or Nova seq.

Sequencing Platform

instrument_model
Illumina HiSeq 2000

hg38

Number of total reads
22504228
Reads aligned (%)
98.9
Duplicates removed (%)
0.8
Number of peaks
116 (qval < 1E-05)

hg19

Number of total reads
22504228
Reads aligned (%)
98.7
Duplicates removed (%)
1.0
Number of peaks
140 (qval < 1E-05)

Base call quality data from DBCLS SRA