Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Input control
Antigen
Input control

Cell type

Cell type Class
Kidney
Cell type
293
Primary Tissue
Kidney
Tissue Diagnosis
Normal

Attributes by original data submitter

Sample

source_name
HEK 293T cells
cell line
HEK 293T cells
chip antibody
none

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
The chromatin fraction was prepared according to the fanChIP method described in our previous report [Nucleic Acids Research 42:7 4241-4256 (2014)], and DNA/protein complexes were isolated by anti-HA antibody (3F10, Roche). The fanChIP libraries were constructed using a TruSeq ChIP Sample Prep Kit [iIllumina] following the manufacturer's instructions. The quality and quantity of these libraries were checked using Agilent TapeStation D1000 and KAPA Library Quantification Kits [KAPA BioSystems] / Real-time PCR Systems Step One Plus [Applied Biosystems]. The libraries were sequenced on the Illumina HiSeq 2500 System with 50-bp single-end reads according to the manufacturer's protocol at the core facility of Hiroshima University.

Sequencing Platform

instrument_model
Illumina HiSeq 2500

hg38

Number of total reads
34117116
Reads aligned (%)
85.1
Duplicates removed (%)
2.1
Number of peaks
749 (qval < 1E-05)

hg19

Number of total reads
34117116
Reads aligned (%)
84.5
Duplicates removed (%)
3.4
Number of peaks
854 (qval < 1E-05)

Base call quality data from DBCLS SRA