|
Status |
Public on Sep 04, 2020 |
Title |
PeTa_100nM_GSK_d6_R2 [ATACseq] |
Sample type |
SRA |
|
|
Source name |
PeTa_100nM_GSK_d6
|
Organism |
Homo sapiens |
Characteristics |
cell line: PeTa cell type: Merkel cell carcinoma cell line treatment: GSK-LSD1 drug concentration: 100nM
|
Treatment protocol |
Cells were treated for 6 days with either 100nM GSK-LSD1 or DMSO.
|
Growth protocol |
Cells were cultured as suspension cells in RPMI-1640 supplemented with 10% FBS, 2 mM L-glutamine, 50 U/mL penicillin and 50 mg/mL streptomycin.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
100,000 viable cells were harvested and nuclei isolated for transposition reaction according to the Omni-ATACseq protocol. Sequencing libraries were barcoded using Illumina Nextera Indexing
|
|
|
Library strategy |
ATAC-seq |
Library source |
genomic |
Library selection |
other |
Instrument model |
NextSeq 550 |
|
|
Data processing |
ATACseq data was analyzed using the nf-core/ATACseq pipeline (Patel et al, 2019) aligning against the human genome hg38 and calling peaks with MACS2 in narrow- and broad-peak mode. Aligned reads of the individual replicates were merged using samtools v1.9 (Li et al, 2009) and RPGC-normalized tracks were calculated and plotted as composite density plots using deeptools v3.1.2 (Ramírez et al, 2016).
Genome_build: hg38
Supplementary_files_format_and_content: BigWig file format with genome-wide ATACseq profiles.
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|
|
Submission date |
Mar 31, 2020 |
Last update date |
Sep 05, 2020 |
Contact name |
Anna Obenauf |
Organization name |
IMP - Research Institute of Molecular Pathology
|
Lab |
Anna Obenauf
|
Street address |
Campus-Vienna-Biocenter 1
|
City |
Vienna |
State/province |
Vienna |
ZIP/Postal code |
1030 |
Country |
Austria |
|
|
Platform ID |
GPL21697 |
Series (2) |
GSE147814 |
Genome-wide chromatin accessibility mapping upon pharmacological LSD1 inhibition in MCC [ATACseq] |
GSE147817 |
Pharmacological LSD1 inhibition in MCC |
|
Relations |
BioSample |
SAMN14501397 |
SRA |
SRX8036449 |