miRViz: a novel webserver application to visualize and interpret microRNA datasets

Author:

Giroux Pierre1,Bhajun Ricky2,Segard Stéphane2,Picquenot Claire2,Charavay Céline2,Desquilles Lise1,Pinna Guillaume3ORCID,Ginestier Christophe4ORCID,Denis Josiane1,Cherradi Nadia1ORCID,Guyon Laurent12ORCID

Affiliation:

1. Univ. Grenoble Alpes, CEA, IRIG, Inserm, BCI, 38000 Grenoble, France

2. Univ. Grenoble Alpes, CEA, IRIG, Inserm, BGE, 38000 Grenoble, France

3. Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS, University Paris-Sud, University Paris-Saclay, F-91191 Gif-sur-Yvette, France

4. Aix-Marseille Université, CNRS, INSERM, Institut Paoli-Calmettes, CRCM, Epithelial Stem Cells and Cancer lab, F-13273 Marseille, France

Abstract

Abstract MicroRNAs (miRNAs) are small non-coding RNAs that are involved in the regulation of major pathways in eukaryotic cells through their binding to and repression of multiple mRNAs. With high-throughput methodologies, various outcomes can be measured that produce long lists of miRNAs that are often difficult to interpret. A common question is: after differential expression or phenotypic screening of miRNA mimics, which miRNA should be chosen for further investigation? Here, we present miRViz (http://mirviz.prabi.fr/), a webserver application designed to visualize and interpret large miRNA datasets, with no need for programming skills. MiRViz has two main goals: (i) to help biologists to raise data-driven hypotheses and (ii) to share miRNA datasets in a straightforward way through publishable quality data representation, with emphasis on relevant groups of miRNAs. MiRViz can currently handle datasets from 11 eukaryotic species. We present real-case applications of miRViz, and provide both datasets and procedures to reproduce the corresponding figures. MiRViz offers rapid identification of miRNA families, as demonstrated here for the miRNA-320 family, which is significantly exported in exosomes of colon cancer cells. We also visually highlight a group of miRNAs associated with pluripotency that is particularly active in control of a breast cancer stem-cell population in culture.

Funder

Inserm

Publisher

Oxford University Press (OUP)

Subject

Genetics

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