ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR253/006/ERR2537886/ERR2537886.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR253/000/ERR2537890/ERR2537890.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR253/008/ERR2537888/ERR2537888.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR253/004/ERR2537894/ERR2537894.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR253/002/ERR2537882/ERR2537882.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR253/003/ERR2537883/ERR2537883.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR253/005/ERR2537885/ERR2537885.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR253/000/ERR2537880/ERR2537880.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR253/007/ERR2537887/ERR2537887.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR253/001/ERR2537891/ERR2537891.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR253/003/ERR2537893/ERR2537893.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR253/005/ERR2537895/ERR2537895.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR253/001/ERR2537881/ERR2537881.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR253/009/ERR2537889/ERR2537889.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR253/002/ERR2537892/ERR2537892.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/ERR253/004/ERR2537884/ERR2537884.fastq.gzprimaryOK200GenomicsEUROPEAN MOLECUALR BIOLOGY LABORATORY, GENOME BIOLOGY UNITEMBLhttps://www.ebi.ac.uk/ena/browser/view/PRJEB26442MCF7 cells were crosslinked with 0.2 J/cm^2 UV254nm and extracted with XRNAX. XRNAX extracts were fragmented by ultrasonication and subjected to a CLIP-seq variation using a size-matched input control (SMI). Library preparation from purified RNA fragments occurred with the NextFlex Small RNA 3.0 kit (Bioo Scientific), which uses unique molecular identifiers (UMIs). For LMNB1 XRNAX-CLIP-seq was preformed on untreated MCF7 cells. For EXOSC2 XRNAX-CLIP-seq was preformed on untreated MCF7 cells and cells treated with sodium arsenite for 5 and 30 minutes.ENAfalse"XRNAX-CLIP-seq on MCF7 cells for LMNB1 and EXOSC2"2018-04-262018-12-06PRJEB26442