Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Input control
Antigen
Input control

Cell type

Cell type Class
Blood
Cell type
MLL-AF9 leukemic cell
NA
NA

Attributes by original data submitter

Sample

source_name
MLL-AF9/NrasG12D murine cell line
cell line
MLL-AF9/NrasG12D AML cell line
treatment
DMSO
chip antibody
none

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Whole cell extracts were sonicated to solubilize the chromatin. 1x10^8 cells were sonicated at 21 watts in 20 second pulses for 3 min of sonication time. The chromatin extracts containing DNA fragments with an average size of 500 bp were prepared for sequencing according to a modified version of the Solexa Genomic DNA protocol. Fragmented DNA was end repaired and subjected to 18 cycles of LM-PCR using oligos provided by Illumina. Amplified fragments between 150 and 300bp (representing shear fragments between 50 and 200nt in length and ~100bp of primer sequence) were isolated by agarose gel electrophoresis and purified. All protocols for Illumina/Solexa sequence preparation, sequencing and quality control are provided by Illumina (http://www.illumina.com/pages.ilmn?ID=203).

Sequencing Platform

instrument_model
Illumina HiSeq 2000

mm10

Number of total reads
69632422
Reads aligned (%)
93.2
Duplicates removed (%)
36.4
Number of peaks
750 (qval < 1E-05)

mm9

Number of total reads
69632422
Reads aligned (%)
93.0
Duplicates removed (%)
36.4
Number of peaks
839 (qval < 1E-05)

Base call quality data from DBCLS SRA