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dc.contributor.authorMcBee, Megan E.
dc.contributor.authorSu, Dan
dc.contributor.authorPang, Yan Ling Joy
dc.contributor.authorGu, Chen
dc.contributor.authorPrestwich, Erin
dc.contributor.authorDedon, Peter C.
dc.contributor.authorChionh, Yok Hian
dc.contributor.authorHo, Chia-Hua
dc.contributor.authorPruksakorn, Dumnoensun
dc.contributor.authorIndrakanti, Ramesh Babu
dc.contributor.authorNg, Chee Sheng
dc.contributor.authorHia, Fabian
dc.contributor.authorDong, Hongping
dc.contributor.authorShi, Pei-Yong
dc.contributor.authorPreiser, Peter Rainer
dc.contributor.authorAlonso, Sylvie
dc.date.accessioned2013-10-07T14:22:04Z
dc.date.available2013-10-07T14:22:04Z
dc.date.issued2013-08
dc.date.submitted2013-07
dc.identifier.issn0305-1048
dc.identifier.issn1362-4962
dc.identifier.urihttp://hdl.handle.net/1721.1/81340
dc.description.abstractA renewed interest in non-coding RNA (ncRNA) has led to the discovery of novel RNA species and post-transcriptional ribonucleoside modifications, and an emerging appreciation for the role of ncRNA in RNA epigenetics. Although much can be learned by amplification-based analysis of ncRNA sequence and quantity, there is a significant need for direct analysis of RNA, which has led to numerous methods for purification of specific ncRNA molecules. However, no single method allows purification of the full range of cellular ncRNA species. To this end, we developed a multidimensional chromatographic platform to resolve, isolate and quantify all canonical ncRNAs in a single sample of cells or tissue, as well as novel ncRNA species. The applicability of the platform is demonstrated in analyses of ncRNA from bacteria, human cells and plasmodium-infected reticulocytes, as well as a viral RNA genome. Among the many potential applications of this platform are a system-level analysis of the dozens of modified ribonucleosides in ncRNA, characterization of novel long ncRNA species, enhanced detection of rare transcript variants and analysis of viral genomes.en_US
dc.description.sponsorshipSingapore-MIT Alliance for Research and Technologyen_US
dc.description.sponsorshipNational Institute of Environmental Health Sciences (ES017010)en_US
dc.description.sponsorshipNational Institute of Environmental Health Sciences (ES002109)en_US
dc.language.isoen_US
dc.publisherOxford University Pressen_US
dc.relation.isversionofhttp://dx.doi.org/10.1093/nar/gkt668en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/en_US
dc.sourceOxford University Pressen_US
dc.titleA multidimensional platform for the purification of non-coding RNA speciesen_US
dc.typeArticleen_US
dc.identifier.citationChionh, Y. H., C.-H. Ho, D. Pruksakorn, I. Ramesh Babu, C. S. Ng, F. Hia, M. E. McBee, et al. “A multidimensional platform for the purification of non-coding RNA species.” Nucleic Acids Research 41, no. 17 (September 25, 2013): e168-e168.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Center for Environmental Health Sciencesen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.mitauthorMcBee, Megan E.en_US
dc.contributor.mitauthorSu, Danen_US
dc.contributor.mitauthorPang, Yan Ling Joyen_US
dc.contributor.mitauthorGu, Chenen_US
dc.contributor.mitauthorPrestwich, Erinen_US
dc.contributor.mitauthorDedon, Peter C.en_US
dc.contributor.mitauthorIndrakanti, Ramesh Babuen_US
dc.relation.journalNucleic Acids Researchen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsChionh, Y. H.; Ho, C.-H.; Pruksakorn, D.; Ramesh Babu, I.; Ng, C. S.; Hia, F.; McBee, M. E.; Su, D.; Pang, Y. L. J.; Gu, C.; Dong, H.; Prestwich, E. G.; Shi, P.-Y.; Preiser, P. R.; Alonso, S.; Dedon, P. C.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-2673-5606
dc.identifier.orcidhttps://orcid.org/0000-0003-0011-3067
dc.identifier.orcidhttps://orcid.org/0000-0001-8533-2706
dc.identifier.orcidhttps://orcid.org/0000-0001-9920-2080
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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