Assisted Selection of Biomarkers by Linear Discriminant Analysis Effect Size (LEfSe) in Microbiome Data

Summary

LEfSe (LDA Effect Size) is a tool for high-dimensional biomarker mining to identify genomic features (such as genes, pathways, and taxonomies) that significantly characterize two or more groups in microbiome data.

Abstract

There is growing attention toward closed biological genomes in the environment and in health. To explore and reveal the intergroup differences among different samples or environments, it is crucial to discover biomarkers with statistical differences among groups. The application of Linear discriminant analysis Effect Size (LEfSe) can help find good biomarkers. Based on the original genome data, quality control, and quantification of different sequences based on taxa or genes are carried out. First, the Kruskal-Wallis rank test was used to distinguish between specific differences among statistical and biological groups. Then, the Wilcoxon rank test was performed between the two groups obtained in the previous step to assess whether the differences were consistent. Finally, a linear discriminant analysis (LDA) was conducted to evaluate the influence of biomarkers on significantly different groups based on LDA scores. To sum up, LEfSe provided the convenience for identifying genomic biomarkers that characterize statistical differences among biological groups.

Introduction

Biomarkers are biological characteristics that can be measured and can indicate some phenomena such as infection, disease, or environment. Among them, functional biomarkers may be specific biological functions of single species or common to some species, such as gene, protein, metabolite and pathways. Besides, taxonomic biomarkers indicate an unusual species, a group of organisms (kingdom, phylum, class, order, family, genus, species), the Amplicon Sequence Varient (ASV)¹, or the Operational Taxonomic Unit (OTU)². In order to find biomarkers more quickly and accurately, a tool for analyzing the biological data is necessary. The differences between classes can be explained by LEfSe coupled with standard tests for statistical significance and additional tests encoding biological consistency and effect relevance³. LEfSe is available as a galaxy module, a conda formula, a docker image, and included in bioBakery (VM and cloud)⁴. Generally, the analysis of microbial diversity often uses a non-parametric test for the uncertain distribution of a sample community. The rank sum test is a non-parametric test method, which uses the rank of samples to replace the value of samples. According to the difference of sample groups, it can be divided into two samples with the Wilcoxon rank sum test and into multiple samples with the Kruskal-Wallis test^5,6. Notably, when there are significant differences among multiple groups of samples, a rank-sum test of pairwise comparison of multiple samples should be performed. LDA (which stands for Linear Discriminant Analysis) invented by Ronald Fisher in 1936, is a type of supervised learning, also known as Fisher’s Linear Discriminant⁷. It is a classic and popular algorithm in the current field of machine learning data mining.

Here, the LEfSe assay has been optimized by Conda and Galaxy servers. Three groups of 16S rRNA gene sequences are analyzed to demonstrate the significant differences between different groups with LDA scores of microbial communities and visualization results.

Protocol

NOTE: The protocol was sourced and modified from the research of Segata et al.³. The method is provided at https://bitbucket.org/biobakery/biobakery/wiki/lefse.

1. Preparation of input file for analysis

1. Prepare the input file (Table 1) of LEfSe, which could be easily generated by many workflows⁸ or previous protocols⁹ with the original files (sample file and corresponding species annotation file).

2. LEfSe native analysis (limited to the Linux server)

1. LEfSe Installation
   NOTE: The LEfSe pipeline is recommended to be installed with Conda¹⁰.
   1. Run the following commands to exclude the possibility of dependencies conflict. Create a conda environment for LEfSe (This step is recommended but not required.). -n stands for the environment name.
      $ conda create -n LEfSe-env
   2. To activate the LEfSe environment that was created, run:
      $ source activate LEfSe-env
   3. To install LEfSe with channel bioBakery where -c stands for channel name, run:
      $ conda install -c biobakery lefse
2. Format data for LEfSe
   1. Run the following command to format the original file to the internal format for LEfSe. Table.txt is the input file and Table-reformat.in is the output file. -c is used to set the feature, which is used as class (default 1) and -o is used to set the normalization value (default -1.0 meaning no normalization).
      $ format_input.py Table.txt Table-reformat.in -c 1 -o 1000000
3. Calculation of linear discriminant analysis (LDA) effect size
   1. Run the following command. The purpose of this step is to perform LDA of the previous result and generate the result file for the visualization. Table-reformat.in is generated using the previous step and is used as the input file in this step. Table-reformat.res is the result file.
      $ run_lefse.py Table-reformat.in Table-reformat.res
4. Visualization by plots
   1. Plot the LEfSe results. To plot the effect size of the biomarkers in a pdf file,.Table-reformat.res is generated using the previous step and the LDA.pdf is the plot file. –format is used to set the output file format.
      $ plot_res.py Table-reformat.res LDA.pdf --format pdf
   2. Plot the cladogram. To draw the species tree and display the biomarkers in a cladogram. cladogram.pdf is the output file.
      $ plot_cladogram.py Table-reformat.res cladogram.pdf --format pdf
   3. Plot one feature (optional) To plot the differences of a single biomarker among different groups. -f is used to set the features of plot. If one was set, the –feature_name must be given.
      $ plot_features.py -f one --feature_name "k__Bacteria.p__Firmicutes.c__Bacilli.o__Bacillales" --format pdf Table-reformat.in Table-reformat.res Bacillales.pdf
   4. Plot the differential features (optional) to draw all the features, but there is too much to be done with caution. --archive is used to choose whether to compress the results. ./ means the path of the results.
      $ plot_features.py -f diff --archive none --format pdf Table-reformat.in Table-reformat.res ./

3. LEfSe online analysis (galaxy)

1. Go to the huttenhower galaxy server¹¹: http://huttenhower.sph.harvard.edu/galaxy.
2. Upload the files. Press the Up arrow button on the left pane and upload the file. Click on Choose local file to select the input file and select the format tabular, and then click on the Start button.
   NOTE: Referred to the webpage (https://bitbucket.org/biobakery/biobakery/wiki/lefse), use the script (taxonomy_summary.R) to generate the input file of LEfSe, and the format (each column with a group name, each line with a different level of annotation separated by “|”) is required as shown in Table 1. A schematic overview of the uploading process is shown in Figure 1.
3. Format the data for LEfSe. Click on the LEfSe | Format Data for LEfSe link on the left pane, and select the specific rows for class in the file, and click on the Execute button. A schematic overview of the operational process and the parameters used are shown in Figure 2.
4. Calculate the LDA effect size. Click on the LEfSe | LDA Effect Size (LEfSe) link on the left pane, and select parameter values according to the analysis requirements. Click on Execute. A schematic overview of the operational process and the parameters used are shown in Figure 3.
5. Plot the LEfSe results. Click on the LEfSe | Plot LEfSe Results link on the left pane, and click on the Execute button. A schematic overview of the operational process and the parameters used are shown in Figure 4.
6. Plot the cladogram. Click on Plot Cladogram on the left pane, and click on the Execute button after selecting the parameter values. A schematic overview of the operational process and the parameters used are shown in Figure 5.
7. Plot one feature by clicking on Plot One Feature on the left pane, and clicking on the Execute button after selecting parameter values. A schematic overview of the operational process and the parameters used are shown in Figure 6.
8. Plot differential features by clicking on Plot Differential Features on the left pane, and clcking on the Execute button after selecting parameter values. A schematic overview of the operational process and the parameters used are shown in Figure 7.
   NOTE: These generated figures can be visualized and downloaded against the resulting output in the right pane.

Results

The LDA scores of microbial communities with significant differences in each group by analyzing the 16S rRNA gene sequences of three samples is shown in Figure 8. The color of the histogram represents different groups, while the length represents the LDA score, which is the influence of the species with significant differences between different groups. The histogram shows the species with significant differences whose LDA score is greater than the preset value. The default preset value is 2....

Discussion

Here, the protocol for the identification and characterization of biomarkers within different groups is described. This protocol can easily be adapted for other sample types, such as OTUs of microorganisms. The statistical method by LEfSe can find the characteristic microorganisms in each group (default is LDA >2), that is, the microorganisms that are more abundant in this group relative to the others¹². LEfSe is available in both native and web Linux versions where users can also perform LEfS...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
No materials used