Abstract

BackgroundWith the development of DNA sequencing technology, static omics profiling in microbial communities, such as taxonomic and functional gene composition determination, has become possible. Additionally, the recently proposed in situ growth rate estimation method allows the applicable range of current comparative metagenomics to be extended to dynamic profiling. However, with this method, the applicable target range is presently limited. Furthermore, the characteristics of coverage depth during replication have not been sufficiently investigated.ResultsWe developed a probabilistic model that mimics coverage depth dynamics. This statistical model explains the bias that occurs in the coverage depth due to DNA replication and errors that arise from coverage depth observation. Although our method requires a complete genome sequence, it involves a stable to low coverage depth (>0.01×). We also evaluated the estimation using real whole-genome sequence datasets and reproduced the growth dynamics observed in previous studies. By utilizing a circular distribution in the model, our method facilitates the quantification of unmeasured coverage depth features, including peakedness, skewness, and degree of density, around the replication origin. When we applied the model to time-series culture samples, the skewness parameter, which indicates the asymmetry, was stable over time; however, the peakedness and degree of density parameters, which indicate the concentration level at the replication origin, changed dynamically. Furthermore, we demonstrated the activity measurement of multiple replication origins in a single chromosome.ConclusionsWe devised a novel framework for quantifying coverage depth dynamics. Our study is expected to serve as a basis for replication activity estimation from a broader perspective using the statistical model.

Highlights

  • The development of high-throughput DNA sequencers has enabled massive and exhaustive microbiome analyses

  • We constructed a statistical model for coverage depth dynamics based on circular distributions

  • A similar distorted structure was reproduced on a partial genome sequence that did not contain suspicious regions (Fig. 1B)

Read more

Summary

Introduction

The development of high-throughput DNA sequencers has enabled massive and exhaustive microbiome analyses. Probabilistic model based on circular statistics for quantifying coverage depth dynamics originating from DNA replication. DEMIC performed accurate estimation by using the coverage depths of multiple samples and estimating the appropriate position via principal component analysis (Gao & Li, 2018) Some studies using such pipelines have revealed associations between growth estimates and factors such as disease, 24-hour oscillations, and diet (Olm et al, 2017; Forsyth et al, 2018). Such an approach quantifying the growth of bacteria from coverage depth is expected to facilitate the investigation of new fields of microbial research. Our study is expected to serve as a basis for replication activity estimation from a broader perspective using the statistical model

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call