Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Input control
Antigen
Input control

Cell type

Cell type Class
Blood
Cell type
Bone marrow nuclear cells
NA
NA

Attributes by original data submitter

Sample

source_name
AML patient 1 bone marrow nuclear cells
tissue
Bone marrow
chip antibody
None

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Lysates were clarified from sonicated nuclei and protein-DNA complexes were precipitated with antibody. ChIP-seq library preparation was performed using TruSeqChIP Sample Prep Kit (Illumina) according to the manufacturer's instructions.10ng of input ChIP-enriched DNA was used for ChIP-seq library preparation. Final libraries were checked using High Sensitivity chips in 2100 Bioanalyzer (Agilent). Average fragment size of final libraries was found to be 280 ± 8bp. Paired-end sequencing (2 x 100 bp) of these libraries were performed in HiSeq-2500 (Illumina) according to the manufacturer's protocols.

Sequencing Platform

instrument_model
Illumina HiSeq 2500

hg38

Number of total reads
33887273
Reads aligned (%)
98.3
Duplicates removed (%)
64.5
Number of peaks
905 (qval < 1E-05)

hg19

Number of total reads
33887273
Reads aligned (%)
97.1
Duplicates removed (%)
65.3
Number of peaks
438 (qval < 1E-05)

Base call quality data from DBCLS SRA