Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Input control
Antigen
Input control

Cell type

Cell type Class
Pluripotent stem cell
Cell type
ES cells
NA
NA

Attributes by original data submitter

Sample

source_name
mouse ES cells E14Tg2a
strain
129/Ola, XY
genotype
CTCF-AID, Tir1
chip epitope
Input for CTCF ChIP-seq

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
For ChIP-seq cells were trypsinized and fixed in suspension; For Chromosome Conformation Capture cells were fixed in tissue culture plates and scrapped off; For RNA-seq cells werre washed once with PBS and lysed in Trizol in the tissue culture plate. ChIP libraries were prepared using standard Illumina protocols; RNA-seq libraries were assembled using the non-stranded kit E7530L from NEB; 5C (in-situ ligation) and Hi-C (dilution ligation) were assembled based on Illumina-compatible protocols. Detailed experimental procedures can be found in the supplementary information of Nora et al. 2017 Cell ChIP-seq, ChIP-exo, RNA-seq, Hi-C, 5C

Sequencing Platform

instrument_model
NextSeq 500

mm10

Number of total reads
23891341
Reads aligned (%)
97.9
Duplicates removed (%)
13.2
Number of peaks
405 (qval < 1E-05)

mm9

Number of total reads
23891341
Reads aligned (%)
97.7
Duplicates removed (%)
13.2
Number of peaks
355 (qval < 1E-05)

Base call quality data from DBCLS SRA