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Sample GSM4637155 Query DataSets for GSM4637155
Status Public on Jul 10, 2020
Title Treated48_2
Sample type SRA
 
Source name Choroid Plexus Epithelia
Organism Homo sapiens
Characteristics cell type: Primary choroid plexus epithelial cells
treatment: B. burgdorferi infected - 48 hours
Treatment protocol Cell cultures were grown to approximately 80% confluency, washed, and medium replaced. B. burgdorferi was added to each flask at a 10:1 multiplicity of infection (10 bacteria: 1 cell) for 48 hours.
Growth protocol Primary human choroid plexus epithelial cells were obtained from ScienCell (Catalog #1310). Cells were maintained in tissue-treated T-75 flasks in epithelial cell medium (ScienCell, catalog #4101), supplemented with 2% FBS and EpiCGS (ScienCell, catalog #4125).
Extracted molecule total RNA
Extraction protocol Cell cultures were thoroughly washed, and RNA was harvested by phenol-chloroform extraction via Trizol. The Rneasy Mini kit from Qiagen (catalog #74106) was used for isolation following manufacterer's instructions.
RNA libraries were prepared using the NEBNext Ultra II RNA-seq library kit (catalog #7775S) for Illumina sequencing following manufacterer's instructions.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 4000
 
Data processing Raw data was provided in Fastq format
Reads were trimmed for adaptor and poor quality using Trimmomatic and quality assessed by FASTQC before and after trimming.
Reads were aligned to the human (hg19) assembly using Hisat2 version 2.1.0 and indexed by Samtools version 1.9
Differential gene expression was performed using DESeq2 version 1.24.0. Differential genes were considered statistically significant if FDR < 0.05.
Genome_build: hg19
Supplementary_files_format_and_content: Tab-delimited text files. A single file that includes counts, FDR values, fold change, and gene annotation for all samples. Individual files for each sample that contain counts and annotations.
 
Submission date Jun 25, 2020
Last update date Jul 11, 2020
Contact name Derick Thompson
E-mail(s) [email protected]
Organization name University of North Dakota
Department Biomedical Sciences
Street address 504 Hamline Street
City Grand Forks
State/province ND
ZIP/Postal code 58203
Country USA
 
Platform ID GPL20301
Series (1)
GSE153261 The Lyme disease bacterium, Borrelia burgdorferi, stimulates an inflammatory response in human choroid plexus epithelial cells
Relations
BioSample SAMN15369434
SRA SRX8617532

Supplementary file Size Download File type/resource
GSM4637155_Treated48_2_Count.txt.gz 2.5 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record
Raw data provided as supplementary file

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