ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR243/099/SRR24332099/SRR24332099.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR243/001/SRR24332101/SRR24332101.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR243/000/SRR24332100/SRR24332100.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR243/002/SRR24332102/SRR24332102.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR243/098/SRR24332098/SRR24332098.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR243/097/SRR24332097/SRR24332097.fastq.gzprimary200OKGenomicsUniversity of Würzburghttps://www.ebi.ac.uk/ena/browser/view/PRJNA962809Campylobacter jejuniRNA-seq was used to study gene expression profiles and potential processing sites in Campylobacter jejuni NCTC11168 wildtype and RNase Y (rny, Cj1209) deletion. Overall design: Total RNA was extracted from C. jejuni NCTC11168 WT and RNase Y deletion strains grown to exponential phase, genomic DNA was removed with DNase I and rRNA depleted, cDNA libraries were prepared at Vertis Biotechnologie AG, Freising, Germany, deep-sequencing was performed on an Illumina NextSeq 500 instrumentpathogen:prioritypathogen:bacteriumpathogenxref:PubMed:38897989bacteriaENAfalseInvestigation of the regulon and RNA targets of RNase Y in Campylobacter jejuniInvestigation of the regulon and RNA targets of RNase Y in Campylobacter jejuni2025-09-242024-06-23PRJNA962809GSE23083519738897989