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SRX523243: GSM1372154: in vivo rep2; Burkholderia glumae BGR1; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 21.6M spots, 4.4G bases, 2.6Gb downloads

Submitted by: Gene Expression Omnibus (GEO)
Study: RNAseq analyses of pathogenic Burkholderia glumae under in vitro and in vivo conditions
show Abstracthide Abstract
We analyzed B. glumae transcriptome from infected rice tissue using an RNAseq technique. To identify unique expression of B. glumae genes within rice tissues, we compared in vivo transcriptome data of B. glumae to in vitro data. To accomplish this, we analyzed differentially expressed genes (DEGs) and identified 2,906 transcripts that were significantly altered. Overall design: Three in vitro (culture) and three in vivo (in plant) RNAseqs in B. glumae
Sample: in vivo rep2
SAMN02731481 • SRS595404 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: The infected rice stem segments were centrifuged directly at 4°C and 2,000 × g for 5 min in 15-ml conical tubes to obtain bacteria pellets. Each pellet contained 2.5 × 108 to 3.3 × 108 CFU/ml, which was primarily composed of B. glumae BGR1 (data not shown). For later RNA extraction, the collected pellets were suspended in 2 ml of RNAprotectTM Bacteria Reagent (Qiagen, Valencia, CA). RNA libraries were prepared for sequencing using standard Illumina protocols
Experiment attributes:
GEO Accession: GSM1372154
Links:
External link:
Runs: 1 run, 21.6M spots, 4.4G bases, 2.6Gb
Run# of Spots# of BasesSizePublished
SRR125817621,625,2374.4G2.6Gb2014-08-21

ID:
723708

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