| Literature DB >> 33396959 |
Athanasios Alexiou1,2, Dimitrios Zisis2, Ioannis Kavakiotis1, Marios Miliotis1,2, Antonis Koussounadis3, Dimitra Karagkouni1,2, Artemis G Hatzigeorgiou1,2,3.
Abstract
microRNAs (miRNAs) are small non-coding RNAs (~22 nts) that are considered central post-transcriptional regulators of gene expression and key components in many pathological conditions. Next-Generation Sequencing (NGS) technologies have led to inexpensive, massive data production, revolutionizing every research aspect in the fields of biology and medicine. Particularly, small RNA-Seq (sRNA-Seq) enables small non-coding RNA quantification on a high-throughput scale, providing a closer look into the expression profiles of these crucial regulators within the cell. Here, we present DIANA-microRNA-Analysis-Pipeline (DIANA-mAP), a fully automated computational pipeline that allows the user to perform miRNA NGS data analysis from raw sRNA-Seq libraries to quantification and Differential Expression Analysis in an easy, scalable, efficient, and intuitive way. Emphasis has been given to data pre-processing, an early, critical step in the analysis for the robustness of the final results and conclusions. Through modularity, parallelizability and customization, DIANA-mAP produces high quality expression results, reports and graphs for downstream data mining and statistical analysis. In an extended evaluation, the tool outperforms similar tools providing pre-processing without any adapter knowledge. Closing, DIANA-mAP is a freely available tool. It is available dockerized with no dependency installations or standalone, accompanied by an installation manual through Github.Entities:
Keywords: NGS; analysis; bioinformatics; expression; microRNA; pipeline; quantification; small RNA-Seq
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Year: 2020 PMID: 33396959 PMCID: PMC7823405 DOI: 10.3390/genes12010046
Source DB: PubMed Journal: Genes (Basel) ISSN: 2073-4425 Impact factor: 4.096