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Article: UClncR: Ultrafast and comprehensive long non-coding RNA detection from RNA-seq

TitleUClncR: Ultrafast and comprehensive long non-coding RNA detection from RNA-seq
Authors
Issue Date2017
Citation
Scientific Reports, 2017, v. 7, n. 1, article no. 14196 How to Cite?
AbstractLong non-coding RNA (lncRNA) is a large class of gene transcripts with regulatory functions discovered in recent years. Many more are expected to be revealed with accumulation of RNA-seq data from diverse types of normal and diseased tissues. However, discovering novel lncRNAs and accurately quantifying known lncRNAs is not trivial from massive RNA-seq data. Herein we describe UClncR, an Ultrafast and Comprehensive lncRNA detection pipeline to tackle the challenge. UClncR takes standard RNA-seq alignment file, performs transcript assembly, predicts lncRNA candidates, quantifies and annotates both known and novel lncRNA candidates, and generates a convenient report for downstream analysis. The pipeline accommodates both un-stranded and stranded RNA-seq so that lncRNAs overlapping with other genes can be predicted and quantified. UClncR is fully parallelized in a cluster environment yet allows users to run samples sequentially without a cluster. The pipeline can process a typical RNA-seq sample in a matter of minutes and complete hundreds of samples in a matter of hours. Analysis of predicted lncRNAs from two test datasets demonstrated UClncR's accuracy and their relevance to sample clinical phenotypes. UClncR would facilitate researchers' novel lncRNA discovery significantly and is publically available at http://bioinformaticstools.mayo.edu/research/UClncR.
Persistent Identifierhttp://hdl.handle.net/10722/324496
PubMed Central ID
ISI Accession Number ID
Errata

 

DC FieldValueLanguage
dc.contributor.authorSun, Zhifu-
dc.contributor.authorNair, Asha-
dc.contributor.authorChen, Xianfeng-
dc.contributor.authorProdduturi, Naresh-
dc.contributor.authorWang, Junwen-
dc.contributor.authorKocher, Jean Pierre-
dc.date.accessioned2023-02-03T07:03:28Z-
dc.date.available2023-02-03T07:03:28Z-
dc.date.issued2017-
dc.identifier.citationScientific Reports, 2017, v. 7, n. 1, article no. 14196-
dc.identifier.urihttp://hdl.handle.net/10722/324496-
dc.description.abstractLong non-coding RNA (lncRNA) is a large class of gene transcripts with regulatory functions discovered in recent years. Many more are expected to be revealed with accumulation of RNA-seq data from diverse types of normal and diseased tissues. However, discovering novel lncRNAs and accurately quantifying known lncRNAs is not trivial from massive RNA-seq data. Herein we describe UClncR, an Ultrafast and Comprehensive lncRNA detection pipeline to tackle the challenge. UClncR takes standard RNA-seq alignment file, performs transcript assembly, predicts lncRNA candidates, quantifies and annotates both known and novel lncRNA candidates, and generates a convenient report for downstream analysis. The pipeline accommodates both un-stranded and stranded RNA-seq so that lncRNAs overlapping with other genes can be predicted and quantified. UClncR is fully parallelized in a cluster environment yet allows users to run samples sequentially without a cluster. The pipeline can process a typical RNA-seq sample in a matter of minutes and complete hundreds of samples in a matter of hours. Analysis of predicted lncRNAs from two test datasets demonstrated UClncR's accuracy and their relevance to sample clinical phenotypes. UClncR would facilitate researchers' novel lncRNA discovery significantly and is publically available at http://bioinformaticstools.mayo.edu/research/UClncR.-
dc.languageeng-
dc.relation.ispartofScientific Reports-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleUClncR: Ultrafast and comprehensive long non-coding RNA detection from RNA-seq-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1038/s41598-017-14595-3-
dc.identifier.pmid29079769-
dc.identifier.pmcidPMC5660178-
dc.identifier.scopuseid_2-s2.0-85032497731-
dc.identifier.volume7-
dc.identifier.issue1-
dc.identifier.spagearticle no. 14196-
dc.identifier.epagearticle no. 14196-
dc.identifier.eissn2045-2322-
dc.identifier.isiWOS:000413907000019-
dc.relation.erratumdoi:10.1038/s41598-018-23183-y-
dc.relation.erratumeid:eid_2-s2.0-85062541080-

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