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Sample GSM8335828 Query DataSets for GSM8335828
Status Public on Jun 18, 2024
Title H2023 Replicate 2
Sample type SRA
 
Source name NCI-H2023
Organism Homo sapiens
Characteristics cell line: NCI-H2023
cell type: Non-small cell lung cancer
genotype: PTPRH Endogenous
treatment: FBS stimulation
Treatment protocol Cells were serum starved for 24 hours, followed by FBS stimulation (5% or 10% in complete media for NCI-H2023 and NCI-H23 derived cells, respectively) for 16 hours prior to collection of total RNA.
Growth protocol Each cell line was seeded in 6-wells plates (n=3/group) and the total RNA was extracted when cells reached ~80% confluency.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using the RNeasy Mini Kit (Qiagen #74104) according to the manufacturer's instructions.
Messenger RNA was purified from total RNA using poly-T oligo-attached magnetic beads. After fragmentation, the first strand cDNA was synthesized using random hexamer primers, followed by the second strand cDNA synthesis using either dUTP for directional library. For the directional library, it was ready after end repair, A-tailing, adapter ligation, size selection, USER enzyme digestion, amplification, and purification. Paired-end RNA sequencing (Illumina PE150) were conducted using NovaSeq X Plus Series (Illumina) with a minimum coverage of 30M reads per sample
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NovaSeq X Plus
 
Description MC2
Data processing The quality of the raw reads was assessed through FastQC 0.11.7 and trimmed using Trimmomatic 0.39. Trimmed reads were aligned against the human genome (grch38) using Hisat2 2.1.0 and a count matrix of raw reads to be used as input for DESeq2 was generated by StringTie 2.1.3 as described in the StringTie documentation.
Assembly: Trimmed reads were aligned against the human genome (grch38) using Hisat2 2.1.0
Supplementary files format and content: gene_count_matrix.csv includes matrix of raw counts for each sample.
Supplementary files format and content: phenodata.csv included phenodata information for each sample.
 
Submission date Jun 18, 2024
Last update date Jun 21, 2024
Contact name Mylena M.O. Ortiz
E-mail(s) [email protected]
Organization name Michigan State University
Department Genetics and Genomics Sciences
Lab Eran Andrechek
Street address 567 Wilson Road
City East Lansing
State/province Michigan
ZIP/Postal code 48824
Country USA
 
Platform ID GPL34284
Series (1)
GSE270167 Effects of the receptor-like protein tyrosine phosphatase PTPRH overexpression on gene expression in non-small cell lung cancer cell lines
Relations
SRA SRX24967207
BioSample SAMN41896188

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

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