2.1 General case

The very first step to use this package is to have a dataframe containing at least a taxid column containing NCBI format TaxIds. This dataframe can also contain other data that you might want to visualise.

## Le chargement a nécessité le package : LifemapR

##    taxid                  sci_name zoom       lat       lon
## 6   2836           Bacillariophyta   13 -8.303813 -11.45440
## 7   2849             Phaeodactylum   22 -8.350041 -11.49067
## 8   2850 Phaeodactylum tricornutum   24 -8.349969 -11.49059
## 9   2857                 Nitzschia   19 -8.342116 -11.49004
## 10  2864               Dinophyceae   12 -6.949512 -12.25927

You can then transform this dataframe into a format suitable for the visualisation functions of the package with the build_Lifemap function.

require("LifemapR")

LM <- build_Lifemap(data)

After that, you get a lifemap object that takes the form of a list containing the following informations :

• df : containing the augmented dataframe obtained after the first step.
• basemap : which basemap was used to fetch the data.

You can then visualise your data with lifemap() associated with one or more of the following functions :

• lm_markers(), to represent data as circles.
• lm_branches(), to represent the data’s subtree.
• lm_discret(), to represent discret data as piecharts.

Each one of these three function adds a layer to the visualisation. These layers are combined with the + symbol.

# Example with default representation

# one layer
lifemap(LM) + lm_markers()

# three different layers 
lifemap(LM) + lm_markers() + lm_branches()

These function also allow the user to represent data by modifying characteristics of representations as we’ll see later in the examples.

The output is a shiny interface where the user can move and zoom freely.

Please note that the following examples have been done in may 2023, if you try them you may not have the same values due to database update

2.2 Analyse of Kraken2 results

This dataset is the result of a classification by Kraken (Derrick E. Wood, J. Lu, 2019) on a metagenomic sample coming from a controlled set of 12 known bacterial species (V. Sevim, J. Lee, 2019).

First of all, we load the data and transform it into the LifemapR format.

data(kraken_res)

LM_kraken <- build_Lifemap(df = kraken_res, basemap = "ncbi")

Then we can began to visualize our data.

We can for example represent the number of read that was assigned to each TaxID by the color of the markers with the following command.

lifemap(LM_kraken) + 
  lm_markers(var_fillColor = "coverage_percent", fillColor = "PiYG")

visualisation of kraken data

With this representation, the markers are displayed if the if the associated node is close enough.

It is possible to change the way markers are displayed with the display argument.

# All the nodes that were requested by the user
lifemap(LM_kraken) + 
  lm_markers(var_fillColor = "coverage_percent", fillColor = "PiYG", display = "requested")

# Only the nodes that have no descendants
lifemap(LM_kraken) + 
  lm_markers(var_fillColor = "coverage_percent", fillColor = "PiYG", display = "leaves")

left : display = “requested”, right : display = “leaves”

Informations can also be displayed for the user with the popup or label arguments.

# When clicking on a node, display the desired information
lifemap(LM_kraken) + 
  lm_markers(var_fillColor = "coverage_percent", fillColor = "PiYG", popup = "name")

Usage of the popup argument

Finally, it is also possible to represent data with a subtree, either by the size of the branches or their color.

# Information on branche's color
lifemap(LM_kraken) + 
  lm_branches(var_color = "coverage_percent", color = "PiYG")

# Information on branche's size
lifemap(LM_kraken) + 
  lm_branches(size = "coverage_percent")

left : branche’s color, right : branche’s size

2.3 comparative genomic data on genome sizes and transposable elements

This dataset contains informations about the genome size and the Transposable Elements content for molluscs, insects and vertebrates.

First of all, we load the data and transform it into the LifemapR format.

data(gen_res)

LM_gen <- build_Lifemap(df = gen_res, basemap = "ncbi")

Then we can began to visualize our data.

Here we have two characteristics to visualise, we can do so with the following command.

However, unlike the precedent data set, we don’t have informations for all the nodes. Here we only have data for the leaves so it will be necessary to infere values to the nodes where the information is missing with the FUN argument.

# Visualisation of the Genome size on the fillColor and the TEcontent on the size of markers.
lifemap(LM_gen) + 
  lm_markers(var_fillColor = "Genome_size", fillColor = "PiYG", radius  = "TEcontent_bp", FUN = mean)

visualisation of genomics data

We can also represent markers and subtree at the same time

# Visualisation of the Genome size on the fillColor and the TEcontent on the size of markers.
lifemap(LM_gen) + 
  lm_branches()
  lm_markers(var_fillColor = "Genome_size", fillColor = "PiYG", radius  = "TEcontent_bp", FUN = mean) 

visualisation of genomics data with markers and subtree

2.4 dataset of eukaryotes from NCBI database

This dataset contains informations about around 1 000 eukaryotes randomly fetched from the NCBI database.

First of all, we load the data and transform it into the LifemapR format.

data(eukaryotes_1000)

LM_eukaryotes <- build_Lifemap(df = eukaryotes_1000, basemap = "ncbi")

Then we can began to visualize our data.

# Visualisation of eukaryotes data.
lifemap(LM_eukaryotes) + 
  lm_markers()

Basic visualisation

We can also choose to visualise only a part of our data. To do this, we can either sort our data in advance or use the data argument to do so.

# Visualisation of Plants.
lifemap(LM_eukaryotes) + 
  lm_markers(data = LM_eukaryotes$df[LM_eukaryotes$df$Group %in% "Plants",])

Visualisation of Plants

Finally we can visualise discret variables with the lm_piechats() function as following.

# Visualisation of the maximum assembly level.
lifemap(LM_eukaryotes) + 
  lm_piecharts(param = "Group")

Visualisation of the maximum assembly level