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Sample GSM3532971 Query DataSets for GSM3532971
Status Public on Nov 26, 2019
Title 3_ATRA+GSK-LSD1
Sample type SRA
 
Source name acute myeloid leukemia
Organism Homo sapiens
Characteristics cell type: HL-60
perturbation: ATRA (100 nM)
Treatment protocol 1.5 x 10^6 cells were treated with respective compounds for 3 hours.
Growth protocol Cells were cultured in humidified incubator at 37°C and 5% CO2 in RPMI 1640 (supplemented: 1 mM sodium pyruvate, 10% FCS).
Extracted molecule total RNA
Extraction protocol Total RNA was isolated and purified using Direct-zol™ RNA Kit (Zymo Research)
Library preparation was done using Illumina's TruSeq Stranded mRNA Library Preparation Kit following the manufacturer's instruction.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Data processing Basecalls performed using bcl2FastQ v1.8.4.
Reads were aligned to the hg19 genome assembly using HISAT2.
Gene counts were quantified using htseq-count.
Genome_build: GRCh37/hg19 and respective gene annotation.
Supplementary_files_format_and_content: The Excel file includes raw counts of all genes for each sample.
 
Submission date Dec 27, 2018
Last update date Nov 26, 2019
Contact name Marco Groth
E-mail(s) dnaseq@leibniz-fli.de
Organization name Leibniz Institute on Aging - FLI
Department Core Facility - Next Generation Sequencing
Street address Beutenbergstraße 11
City Jena
ZIP/Postal code 07747
Country Germany
 
Platform ID GPL16791
Series (2)
GSE124422 RNA-seq of HL-60 cells following treatment with different compounds
GSE124423 HL-60 cells following treatment with different compounds
Relations
BioSample SAMN10655790
SRA SRX5184923

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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