Mitoclone2: an R package for elucidating clonal structure in single-cell RNA-sequencing data using mitochondrial variants

Author:

Story Benjamin12ORCID,Velten Lars3,Mönke Gregor4,Annan Ahrmad5ORCID,Steinmetz Lars167ORCID

Affiliation:

1. Genome Biology Unit, European Molecular Biology Laboratory (EMBL) , Heidelberg, Germany

2. Department of Biosystems Science and Engineering , ETH Zurich, Basel,  Switzerland

3. Center for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology , Barcelona, Spain

4. Developmental Biology Unit, European Molecular Biology Laboratory (EMBL) , Heidelberg, Germany

5. Department of Computational Biology, University of Lausanne , Lausanne, Switzerland

6. Department of Genetics, Stanford University School of Medicine , Stanford, CA, USA

7. Stanford Genome Technology Center , Palo Alto, CA, USA

Abstract

Abstract Clonal cell population dynamics play a critical role in both disease and development. Due to high mitochondrial mutation rates under both healthy and diseased conditions, mitochondrial genomic variability is a particularly useful resource in facilitating the identification of clonal population structure. Here we present mitoClone2, an all-inclusive R package allowing for the identification of clonal populations through integration of mitochondrial heteroplasmic variants discovered from single-cell sequencing experiments. Our package streamlines the investigation of this phenomenon by providing: built-in compatibility with commonly used tools for the delineation of clonal structure, the ability to directly use multiplexed BAM files as input, annotations for both human and mouse mitochondrial genomes, and helper functions for calling, filtering, clustering, and visualizing variants.

Funder

Emerson Collective

Publisher

Oxford University Press (OUP)

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