|
Status |
Public on Dec 31, 2016 |
Title |
Input_NUP98 |
Sample type |
SRA |
|
|
Source name |
HEK293FT cell line
|
Organism |
Homo sapiens |
Characteristics |
cell line: HEK293FT tag: none cell type: embryonal kidney chip antibody: none
|
Growth protocol |
HEK293FT cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM), supplemented with 10% fetal bovine serum (FBS) and 1% penicillin-streptomycin (Invitrogen)
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with the antibody. Libraries were constructed using the ChIP-seq sample preparation kit (Illumina, San Diego, California, USA)
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina Genome Analyzer II |
|
|
Data processing |
Samples were sequenced in a Genome Analyzer IIx (GA2, Illumina) single 40-base read run. Alignment to the human sequence assembly (GRCh37/hg19, Feb 2009) was performed using BWA with default settings, permitting alignments with 1 mismatch in 40 base reads. Peak detection was performed using MACS 2.020 following the developer’s technical recommendations (p-value cutoff for peak detection = 10-5). Significant ChIP-seq peaks were established at FDR ≤ 5%. Genome_build: GRCh37/hg19 Supplementary_files_format_and_content: wig files with alignments, bed files with peaks provided by MACS
|
|
|
Submission date |
Oct 22, 2014 |
Last update date |
May 15, 2019 |
Contact name |
Ana Del Rio |
E-mail(s) |
[email protected]
|
Organization name |
CNIO
|
Street address |
Calle Melchor Fernandez Almagro 3
|
City |
Madrid |
State/province |
Madrid |
ZIP/Postal code |
28029 |
Country |
Spain |
|
|
Platform ID |
GPL9115 |
Series (2) |
GSE62586 |
Evaluation of the NUP98-HOXA9 role as oncogenic transcription factor |
GSE62587 |
NUP98-HOXA9 role as oncogenic transcription factor |
|
Relations |
BioSample |
SAMN03135230 |
SRA |
SRX738221 |