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BBmix: a Bayesian Beta-Binomial mixture model for accurate genotyping from RNA-sequencing

View ORCID ProfileElena Vigorito, View ORCID ProfileAnne Barton, Costantino Pitzalis, View ORCID ProfileMyles J. Lewis, View ORCID ProfileChris Wallace
doi: https://doi.org/10.1101/2022.12.02.518817
Elena Vigorito
1MRC Biostatistics Unit, University of Cambridge, Cambridge, UK
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  • ORCID record for Elena Vigorito
  • For correspondence: elena.vigorito@mrc-bsu.cam.ac.uk cew54@cam.ac.uk
Anne Barton
2Division of Musculoskeletal & Dermatological Sciences, University of Manchester, UK
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Costantino Pitzalis
3Centre for Experimental Medicine and Rheumatology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK
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Myles J. Lewis
4Centre for Experimental Medicine and Rheumatology, William Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK
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Chris Wallace
1MRC Biostatistics Unit, University of Cambridge, Cambridge, UK
5Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), Jeffrey Cheah Biomedical Centre, Cambridge Biomedical Campus, University of Cambridge, Cambridge
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  • For correspondence: elena.vigorito@mrc-bsu.cam.ac.uk cew54@cam.ac.uk
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Abstract

Motivation While many pipelines have been developed for calling genotypes using RNA-sequencing data, they all have adapted DNA genotype callers that do not model biases specific to RNA-sequencing such as reference panel bias or allele specific expression.

Results Here, we present BBmix, a Bayesian Beta-Binomial mixture model that first learns the expected distribution of read counts for each genotype, and then deploys those learned parameters to call genotypes probabilistically. We benchmarked our model on a wide variety of datasets and showed that our method generally performed better than competitors, mainly due to an increase of up to 1.4% in the accuracy of heterozygous calls. Moreover, BBmix can be easily incorporated into standard pipelines for calling genotypes. We further show that parameters are generally transferable within datasets, such that a single learning run of less than one hour is sufficient to call genotypes in a large number of samples.

Availability We implemented BBmix as an R package that is available for free under a GPL-2 licence at https://gitlab.com/evigorito/bbmix and accompanying pipeline at https://gitlab.com/evigorito/bbmix_pipeline.

Competing Interest Statement

CW holds research funding from GSK and MSD for an unrelated project and is a part-time employee of GSK. These companies had no involvement in or influence on this manuscript.

Footnotes

  • https://gitlab.com/evigorito/bbmix

  • https://gitlab.com/evigorito/bbmix_pipeline

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted December 03, 2022.
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BBmix: a Bayesian Beta-Binomial mixture model for accurate genotyping from RNA-sequencing
Elena Vigorito, Anne Barton, Costantino Pitzalis, Myles J. Lewis, Chris Wallace
bioRxiv 2022.12.02.518817; doi: https://doi.org/10.1101/2022.12.02.518817
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BBmix: a Bayesian Beta-Binomial mixture model for accurate genotyping from RNA-sequencing
Elena Vigorito, Anne Barton, Costantino Pitzalis, Myles J. Lewis, Chris Wallace
bioRxiv 2022.12.02.518817; doi: https://doi.org/10.1101/2022.12.02.518817

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