We reported the application of NGS technology for high-throughput transcription profiling of S. aureus in the presence of V12CBD, the binding domain from bacteriophage lysin PlyV12. In summary, a tota
RNA-Seq reads of DrosDel deficiency (Df/+) and parental strain diploid flies along with spike-in controls was performed on the SOLiD platform. Samples are named in this dataset according to the follow
RNAseq to evaluate the effect of the deletion of a transcription factor encoded in the suf operon (ZMO0422) in Z. mobilis. Grown in minimal medium under anaerobic conditions
