| Literature DB >> 28053114 |
Valentin Wucher1, Fabrice Legeai2,3, Benoît Hédan1, Guillaume Rizk3, Lætitia Lagoutte1, Tosso Leeb4, Vidhya Jagannathan4, Edouard Cadieu1, Audrey David2, Hannes Lohi5,6, Susanna Cirera7, Merete Fredholm7, Nadine Botherel1, Peter A J Leegwater8, Céline Le Béguec1, Hille Fieten8, Jeremy Johnson9, Jessica Alföldi9, Catherine André1, Kerstin Lindblad-Toh9,10, Christophe Hitte1, Thomas Derrien1.
Abstract
Whole transcriptome sequencing (RNA-seq) has become a standard for cataloguing and monitoring RNA populations. One of the main bottlenecks, however, is to correctly identify the different classes of RNAs among the plethora of reconstructed transcripts, particularly those that will be translated (mRNAs) from the class of long non-coding RNAs (lncRNAs). Here, we present FEELnc (FlExible Extraction of LncRNAs), an alignment-free program that accurately annotates lncRNAs based on a Random Forest model trained with general features such as multi k-mer frequencies and relaxed open reading frames. Benchmarking versus five state-of-the-art tools shows that FEELnc achieves similar or better classification performance on GENCODE and NONCODE data sets. The program also provides specific modules that enable the user to fine-tune classification accuracy, to formalize the annotation of lncRNA classes and to identify lncRNAs even in the absence of a training set of non-coding RNAs. We used FEELnc on a real data set comprising 20 canine RNA-seq samples produced by the European LUPA consortium to substantially expand the canine genome annotation to include 10 374 novel lncRNAs and 58 640 mRNA transcripts. FEELnc moves beyond conventional coding potential classifiers by providing a standardized and complete solution for annotating lncRNAs and is freely available at https://github.com/tderrien/FEELnc.Entities:
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Year: 2017 PMID: 28053114 PMCID: PMC5416892 DOI: 10.1093/nar/gkw1306
Source DB: PubMed Journal: Nucleic Acids Res ISSN: 0305-1048 Impact factor: 16.971