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Using Phylogenetic Analysis to Investigate Eukaryotic Gene Origin
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Constructing phylogenetic trees for microbiome data analysis: A mini-review.

Ruitao Liu1, Xi Qiao1, Yushu Shi2

  • 1Department of Population and Quantitative Health Sciences, School of Medicine, Case Western Reserve University, 10900 Euclid Avenue, Cleveland, 44106, OH, United States.

Computational and Structural Biotechnology Journal
|November 18, 2024
PubMed
Summary
This summary is machine-generated.

This review simplifies phylogenetic tree construction for microbiome data analysis. It guides researchers in using these essential tools for more accurate insights from 16S rRNA and whole-genome shotgun sequencing data.

Keywords:
16S sequencingAlignmentMicrobiomePhylogenetic treesShotgun sequencing

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Area of Science:

  • Microbiome Research
  • Bioinformatics
  • Computational Biology

Background:

  • Next-generation sequencing generates vast microbiome data, necessitating advanced analysis methods.
  • Phylogenetic information is crucial for accurate microbiome analysis, but constructing trees from metagenomic data is challenging.
  • Existing phylogenetic tree construction tools are often difficult for downstream researchers to use, and public datasets frequently lack these trees.

Purpose of the Study:

  • To provide a comprehensive review of phylogenetic tree construction techniques for microbiome data.
  • To outline the strengths and limitations of current methods for 16S rRNA and whole-genome shotgun sequencing.
  • To offer guidance for making these tools more accessible and applicable in quantitative microbiome analysis.

Main Methods:

  • Review of existing literature on phylogenetic tree construction methods for microbiome data.
  • Analysis of challenges in marker gene identification for metagenomic and whole-genome shotgun sequencing.
  • Assessment of the usability and accessibility of current bioinformatics tools for downstream researchers.

Main Results:

  • Established methods exist for 16S rRNA gene sequencing, but robust tools for metagenomic and whole-genome shotgun sequencing are scarce.
  • Downstream researchers often lack awareness or face difficulties using available phylogenetic tree construction tools.
  • Public microbiome datasets commonly provide only abundance and taxonomic data, omitting phylogenetic trees.

Conclusions:

  • There is a need for more accessible and user-friendly phylogenetic tree construction tools for diverse microbiome sequencing data.
  • Guidance and expert insights are required to bridge the gap between upstream bioinformatics and downstream data analysis.
  • Improved accessibility of phylogenetic trees will enhance the accuracy and depth of quantitative microbiome research.