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Published on: May 19, 2019
FEELnc: a tool for long non-coding RNA annotation and its application to the dog transcriptome
Valentin Wucher1, Fabrice Legeai2,3, Benoît Hédan1
1Institut Génétique et Développement de Rennes, CNRS, UMR6290, University Rennes1, Rennes, Cedex 35043, France.
FEELnc accurately identifies long non-coding RNAs (lncRNAs) using an alignment-free method. This tool enhances RNA sequencing analysis by distinguishing lncRNAs from messenger RNAs (mRNAs), expanding genome annotation.
Area of Science:
- Genomics
- Bioinformatics
- Molecular Biology
Background:
- Whole transcriptome sequencing (RNA-seq) is crucial for RNA analysis.
- Distinguishing long non-coding RNAs (lncRNAs) from messenger RNAs (mRNAs) remains a challenge.
- Accurate annotation of RNA classes is essential for understanding gene regulation.
Purpose of the Study:
- To introduce FEELnc, a novel alignment-free program for accurate lncRNA annotation.
- To provide a flexible and standardized solution for classifying RNA types.
- To expand genome annotation using RNA-seq data.
Main Methods:
- Developed FEELnc, an alignment-free program utilizing a Random Forest model.
- Incorporated features like k-mer frequencies and relaxed open reading frames for classification.
- Benchmarked FEELnc against five state-of-the-art tools using GENCODE and NONCODE datasets.
- Included modules for fine-tuning accuracy and annotating lncRNA classes without a training set.
Main Results:
- FEELnc demonstrated comparable or superior performance to existing tools.
- Applied FEELnc to canine RNA-seq data, identifying 10,374 novel lncRNAs.
- Discovered 58,640 novel mRNA transcripts in the canine genome.
- Successfully expanded canine genome annotation significantly.
Conclusions:
- FEELnc offers a standardized and comprehensive approach to lncRNA annotation.
- The tool effectively distinguishes lncRNAs from mRNAs, improving RNA-seq data interpretation.
- FEELnc facilitates substantial expansion of genome annotations, particularly for non-model organisms.
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