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Engineered yeast genomes accurately assembled from pure and mixed samples

Author

Listed:
  • Joseph H. Collins

    (Worcester Polytechnic Institute)

  • Kevin W. Keating

    (Worcester Polytechnic Institute)

  • Trent R. Jones

    (Worcester Polytechnic Institute)

  • Shravani Balaji

    (Worcester Polytechnic Institute)

  • Celeste B. Marsan

    (Worcester Polytechnic Institute)

  • Marina Çomo

    (Worcester Polytechnic Institute)

  • Zachary J. Newlon

    (Worcester Polytechnic Institute)

  • Tom Mitchell

    (Raytheon BBN Technologies)

  • Bryan Bartley

    (Raytheon BBN Technologies)

  • Aaron Adler

    (Raytheon BBN Technologies)

  • Nicholas Roehner

    (Raytheon BBN Technologies)

  • Eric M. Young

    (Worcester Polytechnic Institute)

Abstract

Yeast whole genome sequencing (WGS) lacks end-to-end workflows that identify genetic engineering. Here we present Prymetime, a tool that assembles yeast plasmids and chromosomes and annotates genetic engineering sequences. It is a hybrid workflow—it uses short and long reads as inputs to perform separate linear and circular assembly steps. This structure is necessary to accurately resolve genetic engineering sequences in plasmids and the genome. We show this by assembling diverse engineered yeasts, in some cases revealing unintended deletions and integrations. Furthermore, the resulting whole genomes are high quality, although the underlying assembly software does not consistently resolve highly repetitive genome features. Finally, we assemble plasmids and genome integrations from metagenomic sequencing, even with 1 engineered cell in 1000. This work is a blueprint for building WGS workflows and establishes WGS-based identification of yeast genetic engineering.

Suggested Citation

  • Joseph H. Collins & Kevin W. Keating & Trent R. Jones & Shravani Balaji & Celeste B. Marsan & Marina Çomo & Zachary J. Newlon & Tom Mitchell & Bryan Bartley & Aaron Adler & Nicholas Roehner & Eric M. , 2021. "Engineered yeast genomes accurately assembled from pure and mixed samples," Nature Communications, Nature, vol. 12(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-21656-9
    DOI: 10.1038/s41467-021-21656-9
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