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UClncR: Ultrafast and comprehensive long non-coding RNA detection from RNA-seq.
Zhifu Sun1, Asha Nair2, Xianfeng Chen2,3
1Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, MN, 55905, USA. sun.zhifu@mayo.edu.
Scientific Reports
|October 29, 2017
Summary
UClncR is a new pipeline for discovering and quantifying long non-coding RNAs (lncRNAs) from RNA-seq data. This ultrafast tool accurately identifies novel lncRNAs and aids in understanding their role in disease.
Area of Science:
- Genomics
- Bioinformatics
- Molecular Biology
Background:
- Long non-coding RNAs (lncRNAs) are key gene regulators with many yet to be discovered.
- Analyzing massive RNA-seq data for novel lncRNA identification and quantification presents significant challenges.
Purpose of the Study:
- To introduce UClncR, an Ultrafast and Comprehensive lncRNA detection pipeline.
- To address the challenges of discovering and quantifying lncRNAs from large-scale RNA-seq datasets.
Main Methods:
- UClncR processes RNA-seq alignment files for transcript assembly, lncRNA prediction, quantification, and annotation.
- The pipeline supports both stranded and un-stranded RNA-seq data, enabling accurate prediction and quantification of overlapping lncRNAs.
- UClncR is designed for parallel processing in cluster environments but can also run samples sequentially.
Main Results:
- UClncR processes typical RNA-seq samples in minutes and hundreds of samples in hours.
- Analysis of test datasets demonstrated UClncR's accuracy in predicting lncRNAs.
- The identified lncRNAs showed relevance to sample clinical phenotypes.
Conclusions:
- UClncR significantly facilitates novel lncRNA discovery for researchers.
- The pipeline provides accurate and efficient analysis of lncRNAs from RNA-seq data.
- UClncR is publicly available to support the research community.
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