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Sample GSM8279169 Query DataSets for GSM8279169
Status Public on May 23, 2024
Title Saos2, 40 nM Roc, biol replicate 1
Sample type SRA
 
Source name Saos2
Organism Homo sapiens
Characteristics cell line: Saos2
cell type: osteosarcoma
genotype: WT
treatment: 40 nM Roc
treatment: 24 hours
Treatment protocol Cells were treated with 0.04% DMSO as a vehicle control or 1x growth-inhibitory IC50 concentration of Roc or DDR for 24 hours. Cells were harvested by scraping down on ice, cell pellets rinsed with cold PBS, and snap-frozen on dry ice
Growth protocol Human osteosarcoma cell lines MG-63 and Saos2 were grown in standard 10-centimeter dishes in high-glucose DMEM with glutamine and 10% heat-inactivated FBS at 37° C in a 5% CO2 humifiied incubator.
Extracted molecule total RNA
Extraction protocol Maxwell RSC simplyRNA Cells kit (Cat. #AS1390; Promega).
Illumina TruSeq stranded mRNA kit
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NovaSeq 6000
 
Data processing Non-polyA-tailed RNA species, including mitochondrial transcripts, rRNAs, and tRNAs, were filtered out using Bowtie 2 (v.2.5.1).
STAR v2.7.3a was used to align reads to the GRCh37/hg19 reference human genome (released February 2009). Raw read counts were estimated via HTSeq v0.11.225 and normalized with the DESeq2 package26. Cufflinks v2.2.1 was used to estimate the gene expression levels27, and the values were reported as FPKM (fragments per kilobase per million) units per gene. DESeq2 was employed to estimate the differential expression of gene counts relative to the DMSO-treated controls.
Raw read counts were estimated via HTSeq v0.11.2 and normalized with the DESeq2 package. Cufflinks v2.2.1 was used to estimate the gene expression levels27, and the values were reported as FPKM (fragments per kilobase per million) units per gene. DESeq2 was employed to estimate the differential expression of gene counts relative to the DMSO-treated controls.
Cufflinks v2.2.1 was used to estimate the gene expression levels, and the values were reported as FPKM (fragments per kilobase per million) units per gene. DESeq2 was employed to estimate the differential expression of gene counts relative to the DMSO-treated controls.
DESeq2 was used to estimate the differential expression of gene counts relative to the DMSO-treated controls.
Assembly: GRCh37/hg19 reference human genome (released February 2009)
Supplementary files format and content: Excel (xlsx) file containing the raw and normalized counts (in FPKM) for all replicates
Supplementary files format and content: Excel (xlsx) file containing the log2-fold change (log2FC) of DDR- and Roc-treated cells compared to DMSO-treated control cells, statstics including P-values and adjusted P-values, and raw and normalized FPKM counts for replicates
 
Submission date May 18, 2024
Last update date May 23, 2024
Contact name Long-Sheng Chang
E-mail(s) Long-Sheng.Chang@nationwidechildrens.org
Phone 6143552658
Organization name Research Institute at Nationwide Children's Hospital
Department Center for Childhood Cancer
Lab Chang Lab
Street address 575 Children's Crossroad, WC-5574, Ctr for Childhood Cancer & Dept of Pediatrics, Nationwide Children's Hosp & The Ohio State U
City Columbus
State/province Ohio
ZIP/Postal code 43215
Country USA
 
Platform ID GPL24676
Series (1)
GSE267810 Anti-tumor effects of the eIF4A Inhibitor didesmethylrocaglamide and its derivatives in human and canine osteosarcomas
Relations
BioSample SAMN41447735
SRA SRX24600914

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA

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