nf-core/circrna: a portable workflow for the quantification, miRNA target prediction and differential expression analysis of circular RNAs

被引:5
作者
Digby, Barry [1 ]
Finn, Stephen P. [2 ]
Broin, Pilib O. [1 ]
机构
[1] Natl Univ Ireland, Sch Math & Stat Sci, Galway, Ireland
[2] Trinity Translat Med Inst, Dept Histopathol & Morbid Anat, Dublin, Ireland
基金
爱尔兰科学基金会;
关键词
Circular RNA; ceRNA; Nextflow; nf-core; Portable analysis workflow; LANDSCAPE; MICRORNA; HISAT;
D O I
10.1186/s12859-022-05125-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Circular RNAs (circRNAs) are a class of covalenty closed non-coding RNAs that have garnered increased attention from the research community due to their stability, tissue-specific expression and role as transcriptional modulators via sequestration of miRNAs. Currently, multiple quantification tools capable of detecting circRNAs exist, yet none delineate circRNA-miRNA interactions, and only one employs differential expression analysis. Efforts have been made to bridge this gap by way of circRNA workflows, however these workflows are limited by both the types of analyses available and computational skills required to run them. Results: We present nf-core/circrna, a multi-functional, automated high-throughput pipeline implemented in nextflow that allows users to characterise the role of circRNAs in RNA Sequencing datasets via three analysis modules: (1) circRNA quantification, robust filtering and annotation (2) miRNA target prediction of the mature spliced sequence and (3) differential expression analysis. nf-core/circrna has been developed within the nf-core framework, ensuring robust portability across computing environments via containerisation, parallel deployment on cluster/cloud-based infrastructures, comprehensive documentation and maintenance support. Conclusion: nf-core/circrna reduces the barrier to entry for researchers by providing an easy-to-use, platform-independent and scalable workflow for circRNA analyses.
引用
收藏
页数:15
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