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Sample GSM3687989 Query DataSets for GSM3687989
Status Public on Jul 09, 2019
Title LPS+DEF rep3
Sample type SRA
 
Source name Macrophage
Organism Homo sapiens
Characteristics cell type: Macrophage
treatment: LPS+DEF
treatment time: 16h (DEF); 3h (LPS)
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using Trizol and Rneasy mini kit with an additional purification step by on-column DNAse treatment using Rnase-free Dnase Kit (Qiagen)
RNA libraries were prepared for sequencing using NEBNext Ultra II Directional RNA Library Prep kit for Illumina
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Description TDC_16
Data processing Illumina CASAVA-1.8.4 software used for basecalling.
Sequencing adapters were removed using Trimmomatic (v.0.36) and the reads quality was checked using FastQC (v.0.11.2) before and after trimming. Reads were aligned to the human genome (GRCh38.primary_assembly.genome.fa; annotation: gencode.v25.annotation.gtf) using tophat2 package (v.2.1.0: -b2-sensitive,--library-type fr-firststrand). Mapping quality, read distribution, gene body coverage, GC content and rRNA contamination, were checked using picard (v.2.6.0) software.
Gene level read counts were computed using HT-Seq-count (v.0.6.1, annotation: gencode.v25.annotation.gtf)1 with strict "-m intersection-strict” mode. Genes with less than 10 aligned reads across all samples were filtered out as lowly expressed genes.
Differential gene expression analysis between groups was performed using DESeq2 (v.1.14.1)4 and significantly differentially expressed genes were reported using fold-change at 1.5 times and below 1 % Benjamini-Hochberg (BH) adjusted p-value.
In order to visualize the similarities between samples, unsupervised hierarchical clustering and principal component analysis (PCA) were performed using pcaExplorer (v.2.6.0, https://github.com/federicomarini/pcaExplorer) and pheatmap (v 1.0.10, https://CRAN.R-project.org/package=pheatmap) packages respectively. Volcano plots of differentially expressed genes were generated using ggplot2 (v.3.0.0, https://cran.r-project.org/web/packages/ggplot2/index.html) package.
Genome_build: GRCh38.primary_assembly.genome.fa; annotation: gencode.v25.annotation.gtf)
 
Submission date Mar 26, 2019
Last update date Sep 13, 2023
Contact name Norzawani Binti Buang
E-mail(s) n.buang13@imperial.ac.uk
Phone 07716497826
Organization name Imperial College London
Street address 9N15 Commonwealth Buidling, Ducane Road
City London, United Kingdom
State/province London
ZIP/Postal code W12 0NN
Country United Kingdom
 
Platform ID GPL16791
Series (1)
GSE128885 RNA sequencing of human macrophages treated with iron chelator deferiprone (DEF), with and without lipopolysaccharide (LPS)
Relations
BioSample SAMN11258674
SRA SRX5577120

Supplementary file Size Download File type/resource
GSM3687989_TDC_16_total.count.txt.gz 230.1 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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