The targets of small regulatory RNAs can be mapped using High‐throughput Global sRNA target Identifi cation by Ligation and Sequencing (Hi‐GRIL‐seq). The position on the x and y axes identifies the genome coordinates of the interacting RNAs. Highlighted chimeras include those containing either the prrF1/2 sRNAs (blue) or the oprD (red) or pagL (green) mRNAs. For details, see the article

Abstract

Molecular MicrobiologyVolume 106, Issue 6 p. i-i Front CoverFree Access The targets of small regulatory RNAs can be mapped using High-throughput Global sRNA target Identifi cation by Ligation and Sequencing (Hi-GRIL-seq). The position on the x and y axes identifies the genome coordinates of the interacting RNAs. Highlighted chimeras include those containing either the prrF1/2 sRNAs (blue) or the oprD (red) or pagL (green) mRNAs. For details, see the article by Zhang et al. on pp. 919–937 of this issue. First published: 07 December 2017 https://doi.org/10.1111/mmi.13523AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article. Volume106, Issue6December 2017Pages i-i RelatedInformation