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Sample GSM8212669 Query DataSets for GSM8212669
Status Public on May 01, 2024
Title RNA-seq_KO1
Sample type SRA
 
Source name macrophage
Organism Mus musculus
Characteristics cell type: macrophage
genotype: G3bp1mac-/-
Growth protocol DMEM, 10% fetal bocine serum, 1×penicilin/streptomycin. Cells were cultured at 37℃ with 5% CO2.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using Trizol reagent
Total RNA was extracted followed by library preparation according to Illumina standard instruction (VAHTS Universal V6 RNA-seq Library Prep Kit for Illumina® ). Agilent 4200 bioanalyzer was employed to evaluate the concentration and size distribution of cDNA library before sequencing with an Illumina novaseq6000. The protocol of high-throughput sequencing was fully according to the manufacturer's instructions (Illumina).
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina NovaSeq 6000
 
Data processing The RNA is purified by phenol:chloroform extraction.
The raw reads were filtered by Seqtk before mapping to genome using Hisat2 (version:2.0.4). The fragments of genes were counted using stringtie(v1.3.3b) followed by TMM (trimmed mean of M values) normalization. Significant differential expressed genes (DEGs) were identified as those with a False Discovery Rate (FDR) value above the threshold (Q< 0.05)
Assembly: mm39
Supplementary files format and content: tab-delimited with raw counts and FPKM
 
Submission date Apr 16, 2024
Last update date May 01, 2024
Contact name Ye Zhou
E-mail(s) yzhou1989@126.com
Organization name Naval Medical University
Department National Key Laboratory of Immunity & Inflammation
Street address Xiangyin Road
City Shanghai
ZIP/Postal code 200433
Country China
 
Platform ID GPL24247
Series (1)
GSE264134 Stress granule assembly impairs macrophage efferocytosis [RNA-seq]
Relations
BioSample SAMN40985903
SRA SRX24276676

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

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