Methplotlib: analysis of modified nucleotides from nanopore sequencing

Author:

De Coster Wouter1ORCID,Stovner Endre Bakken23,Strazisar Mojca1

Affiliation:

1. VIB, Center for Molecular Neurology, Antwerp 2610, Belgium

2. Department of Computer Science, Norwegian University of Science and Technology, Trondheim 7013, Norway

3. Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim 7013, Norway

Abstract

Abstract Summary Modified nucleotides play a crucial role in gene expression regulation. Here, we describe methplotlib, a tool developed for the visualization of modified nucleotides detected from Oxford Nanopore Technologies sequencing platforms, together with additional scripts for statistical analysis of allele-specific modification within-subjects and differential modification frequency across subjects. Availability and implementation The methplotlib command-line tool is written in Python3, is compatible with Linux, Mac OS and the MS Windows 10 Subsystem for Linux and released under the MIT license. The source code can be found at https://github.com/wdecoster/methplotlib and can be installed from PyPI and bioconda. Our repository includes test data, and the tool is continuously tested at travis-ci.com. Supplementary information Supplementary data are available at Bioinformatics online.

Funder

VIB Tech Watch Fund

Publisher

Oxford University Press (OUP)

Subject

Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability

Reference30 articles.

1. Diverse and dynamic DNA modifications in brain and diseases;Armstrong;Hum. Mol. Genet.,2019

2. Epigenetic control of alternative mRNA processing at the imprinted Herc3/Nap1l5 locus;Cowley;Nucleic Acids Res,2012

3. Structural variants identified by Oxford Nanopore PromethION sequencing of the human genome;De Coster;Genome Res,2019

4. An integrated encyclopedia of DNA elements in the human genome;Nature,2012

5. GENCODE reference annotation for the human and mouse genomes;Frankish;Nucleic Acids Res,2019

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