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Sample GSM5134368 Query DataSets for GSM5134368
Status Public on Jun 01, 2022
Title Control_Male_Rat18_AS
Sample type SRA
 
Source name placental tissue
Organism Rattus norvegicus
Characteristics strain:
tissue: placenta
dam: dam 18
Sex: male
treatment: vehicle control (corn oil)
treatment duration: gestation days 6-16
Treatment protocol Timed-pregnant Wistar rats were exposed to 480 mg TCE mg/kg/day, 200 mg/kg/day NAC or co-exposure with both chemicals via ingestion (treated mini vanilla wafer) on gestation days 6-16 (tissue collection day).
Extracted molecule total RNA
Extraction protocol RNA was extracted from placental tissue using the RNeasy Plus Mini Kit (Qiagen) following the manufacturer’s recommended protocol with a modification. A FastPrep-24 tissue lyser (MP Biomedicals; Solon, OH, USA) was utilized prior to the gDNA elimination step to achieve maximum quality tissue homogenization. DNA was extracted from placental using the NucleoSpin Tissue kit (Machery-Nagel; Düren, Germany) according to the manufacture’s recommended protocol. RNA and DNA concentrations were determined using a NanoDrop 2000 Spectrophotometer (Thermo Fisher Scientific; Waltham, MA, USA). Isolated nucleic acids were subsequently stored at -80°C until further processing.
RNA libraries were prepared for sequencing using standard Illumina protocols
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NovaSeq 6000
 
Data processing Reads were aligned to the rat genome using STAR, with the options "outFilterMultimapNmax 10" and "sjdbScore 2".
Aligned reads were assigned to Rnor_6.0 genes using featureCounts.
Genes with mean read counts-per-million less than six across all samples were filtered out and excluded from the analysis to reduce dispersion due to low expression levels.
Data were normalized using the median of ratios method .
RUV(Remove Unwanted Variation) normalization factors were generated for each sample using the RUVSeq package RUVr function
Differential gene expression testing was performed using the DESeq2 package (version 1.28.1) for R statistical computing. Negative binomial general linear modeling was used for differential gene expression testing.
Genome_build: rn6
 
Submission date Mar 04, 2021
Last update date Jun 01, 2022
Contact name Elana Elkin
Organization name University of Michigan
Department Department of Environmental Health Sciences
Lab Bakulski
Street address 1415 Washington Heights
City Ann Arbor
State/province MI
ZIP/Postal code 48109
Country USA
 
Platform ID GPL25947
Series (1)
GSE168232 Transcriptional responses to maternal trichloroethylene and/or N-acetyl cysteine exposure in Wistar rat placental tissue
Relations
BioSample SAMN18138826
SRA SRX10237675

Supplementary file Size Download File type/resource
GSM5134368_Sample_577-EE-3_counts.txt.gz 2.8 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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