ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR765/000/SRR7657990/SRR7657990_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR765/001/SRR7657991/SRR7657991_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR765/009/SRR7657989/SRR7657989_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR765/000/SRR7657990/SRR7657990_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR765/001/SRR7657991/SRR7657991_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR765/008/SRR7657988/SRR7657988_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR765/008/SRR7657988/SRR7657988_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR765/009/SRR7657989/SRR7657989_2.fastq.gzprimary200OKGenomics2nd Faculty of Medicine, Charles University and Motol University Hospitalhttps://www.ebi.ac.uk/ena/browser/view/PRJNA484696Burkholderia cenocepaciaRNA was isolated from log-phase planctonic cultures of B. cenocepacia J2315 20 mins post exposure to sub- and suprainhibitory concentrations of 11026103 and subjected to RNA-Seq analysis in order to characterize the effect of the compound on bacterial transcription.pathogen:prioritypathogen:bacteriumxref:EuropePMC:PMC6963507pathogenENAbacteriafalseBurkholderia cenocepaciaEffect of 11026103 on Burkholderia cenocepacia transcriptome2025-09-222018-08-08PRJNA48469695486