ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR654/005/ERR6548335/ERR6548335.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR654/004/ERR6548334/ERR6548334.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR654/003/ERR6548333/ERR6548333.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR654/001/ERR6548331/ERR6548331.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR654/006/ERR6548336/ERR6548336.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR654/002/ERR6548332/ERR6548332.fastq.gzprimaryOK200GenomicsPh.D. Postdoctoral ResearcherEuropean Bioinformatics Institutehttps://www.ebi.ac.uk/ena/browser/view/PRJEB47141ArrayExpressIn this experiment, we carried out a global analysis of specific RNAs that are bound to the RelA protein. CLIP-Seq experiment was carried out with E. coli RelA wild type and RelA::C289Y mutant strains. Libraries were prepared and high throughput sequencing was done.ENAfalseCLIP-Seq experiment of Escherichia coli RelA wild type and RelA::C289Y mutant strains to identify specific RNAs that bind RelACLIP-Seq experiment of Escherichia coli RelA wild type and RelA::C289Y mutant strains to identify specific RNAs that bind RelA2021-09-162021-09-16PRJEB47141