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SRX4408665: GSM3291872: MARV_WT_3hr_rep1; Rousettus aegyptiacus; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 30.7M spots, 8.2G bases, 3.4Gb downloads

Submitted by: NCBI (GEO)
Study: Infection of RoNi cells with Sendai Cantell virus, MARV371bat virus, and VP35 mutant MARV371bat-R301A virus at MOI of 1.0
show Abstracthide Abstract
Study was performed in order to determine the scope of antiviral response of Rousettus aegyptiacus-derived fibroblasts to Sendai and Marburg virus infection. This study aids in understanding the function of the expanded immune repertoire of Rosettus aegyptiacus. Overall design: 3 timepoints, three replicates. Mock, SeV, MARV, and MARV VP35mut infected samples. 36 total samples.
Sample: MARV_WT_3hr_rep1
SAMN09692177 • SRS3562310 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Harvested in 1x RNA Lysis/Binding Solution Concentrate (Thermo Fisher Scientific) at 3hr, 8hr and 24hr post-infection, followed by magnetic bead purification and TURBO DNase treatment using the MagMAX-96 Total RNA Isolation Kit (Ambion) according to manufacturer guidelines. RNA extractions were performed on a MagMAX Express 96 Magnetic Particle Processor (Applied Biosystems) Libraries were generated on the Sciclone G3 Liquid Handling Robot (PerkinElmer) using the TruSeq Stranded Total RNA Library Prep Kit (Illumina). Library quality was evaluated on the Agilent 2200 TapeStation 2200 and quantified by qPCR using the KAPA Complete (Universal) qPCR kit (Kapa Biosystems) for Illumina libraries. Libraries were diluted to 12 pM and cluster generation was performed on the Illumina cBot. Libraries were sequenced on the Illumina HiSeq 2500 using the paired end 2x125 bp, dual-index format.
Experiment attributes:
GEO Accession: GSM3291872
Links:
Runs: 1 run, 30.7M spots, 8.2G bases, 3.4Gb
Run# of Spots# of BasesSizePublished
SRR754803730,700,5098.2G3.4Gb2018-11-02

ID:
5990744

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