Data importation in PLNmodels

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Preliminaries

This vignette documents the data format used in PLNmodel by PLN and its variants. It also shows how to create an object in the proper format for further analyses from (i) tabular data, (ii) biom-class objects and (iii) phyloseq-class objects.

Format description

We illustrate the format using trichoptera data set, a full description of which can be found in the corresponding vignette.

library(PLNmodels)
data(trichoptera)

The trichoptera data set is a list made of two data frames: Abundance (hereafter referred to as the counts) and Covariate (hereafter the covariates).

str(trichoptera, max.level = 1)

The covariates include, among others, the wind, pressure and humidity.

names(trichoptera$Covariate)

In the PLN framework, we model the counts from the covariates, let's say wind and pressure, using a Poisson Log-Normal model. Most models in R use the so-called formula interface and it would thus be naturel to write something like

PLN(Abundance ~ Wind + Pressure, data = trichoptera)

Unfortunately and unlike many generalized linear models, the response in PLN is intrinsically multivariate: it has 17 dimensions in our example. The left hand side (LHS) must encode a multivariate response across multiple samples, using a 2D-array (e.g. a matrix or a data frame).

We must therefore prepare a data structure where Abundance refers to a count matrix whereas Wind and Pressure refer to vectors before feeding it to PLN. That's the purpose of prepare_data.

trichoptera2 <- prepare_data(counts     = trichoptera$Abundance, 
                             covariates = trichoptera$Covariate)
str(trichoptera2)

If you look carefully, you can notice a few difference between trichoptera and trichoptera2:

Computing offsets

It is common practice when modeling count data to introduce an offset term to control for different sampling efforts, exposures, baselines, etc. The proper way to compute sample-specific offsets in still debated and may vary depending on the field. There are nevertheless a few popular methods:

Each of these offset be computed from a counts matrix using the compute_offset function and changing its offset argument:

## same as compute_offset(trichoptera$Abundance, offset = "TSS")
compute_offset(trichoptera$Abundance) 

In this particular example, the counts are too sparse and sophisticated offset methods all fail (numeric output hidden)

compute_offset(trichoptera$Abundance, "CSS")
compute_offset(trichoptera$Abundance, "RLE")
compute_offset(trichoptera$Abundance, "GMPR")

We can mitigate this problem for the RLE offset by adding pseudocounts to the counts although doing so has its own drawbacks.

compute_offset(trichoptera$Abundance, "RLE", pseudocounts = 1)

Building data frame using prepare_data

We'll already learned that prepare_data can join counts and covariates into a single data.frame. It can also compute offset through compute_offset and does so by default with offset = "TSS", hence the Offset column in trichoptera2. You can change the offset method and provide additional arguments that will passed on to compute_offset.

str(prepare_data(trichoptera$Abundance, 
             trichoptera$Covariate, 
             offset = "RLE", pseudocounts = 1))

Different communities use different standard for the count data where samples are either or columns of the counts matrix. prepare_data uses heuristics to guess the direction of the counts matrix (or fail informatively doing so) and automatically transpose it if needed.

Finally, prepare_data enforces sample-consistency between the counts and the covariates and automatically trims away: - samples for which only covariates or only counts are available; - samples with no positive counts

For example, if we remove the first sample from the counts and the last one from the covariates, we end up with 49 - 2 = 47 samples left, as expected.

nrow(prepare_data(trichoptera$Abundance[-1, ], ## remove first sample
                  trichoptera$Covariate[-49,]  ## remove last sample
                  ))

Importing data from biom and phyloseq objects using prepare_data_from_[phyloseq|biom]

Community composition data are quite popular in microbial ecology and usually stored in flat files using the biom format and/or imported in R as phyloseq-class objects [@phyloseq] using the Bioconductor phyloseq package.

We show here how to import data from a biom file (or biom-class object) and form a phyloseq-class object.

Reading from a biom file

Reading from a biom file requires the bioconductor package biomformat. This package is not a standard dependency of PLNmodels and needs to be installed separately.

You can easily prepare your data from a biom file using the following steps:

as illustrated below:

## If biomformat is not installed, uncomment the following lines
# if (!requireNamespace("BiocManager", quietly = TRUE)) {
#   install.packages("BiocManager")
# }
# BiocManager::install("biomformat")
library(biomformat)
biomfile <- system.file("extdata", "rich_dense_otu_table.biom", package = "biomformat")
biom <- biomformat::read_biom(biomfile)
## extract counts
counts <- as(biomformat::biom_data(biom), "matrix")
## extract covariates (or prepare your own)
covariates <- biomformat::sample_metadata(biom)
## prepare data
my_data <- prepare_data(counts = counts, covariates = covariates)
str(my_data)

Reading from a phyloseq-class object

Likewise, preparing data from a phyloseq-class object requires the bioconductor package phyloseq. This package is not a standard dependency of PLNmodels and needs to be installed separately.

You can easily prepare your data from a phyloseq object using the following steps:

as illustrated below:

## If biomformat is not installed, uncomment the following lines
# if (!requireNamespace("BiocManager", quietly = TRUE)) {
#   install.packages("BiocManager")
# }
# BiocManager::install("phyloseq")
library(phyloseq)
data("enterotype")
## extract counts
counts <- as(phyloseq::otu_table(enterotype), "matrix")
## extract covariates (or prepare your own)
covariates <- phyloseq::sample_data(enterotype)
## prepare data
my_data <- prepare_data(counts = counts, covariates = covariates)
str(my_data)

Mathematical details about the offsets

We detail here the mathematical background behind the various offsets and the way they are computed. Note $\mathbf{C} = (c_{ij})$ the counts matrix where $c_{ij}$ is the count of species $j$ in sample $i$. Assume that there are $J$ species in total. The offset of sample $i$ is noted $O_i$ and computed in the following way.

Total Sum Scaling

Offsets are simply the total counts of a sample: $$ O_i = \sum_{j=1}^J c_{ij} $$

Cumulative Sum Scaling

Positive counts are used to compute sample-specific quantiles $q_i^l$ and cumulative sums $s_i^l$ defined as $$ q_i^l = \min {q \text{ such that } \sum_j 1_{c_{ij} \leq q} \geq l \sum_j 1_{c_{ij} > 0} } \qquad s_i^l = \sum_{j: c_{ij} \leq q_i^l} c_{ij} $$ The sample-specific quantiles are then used to compute reference quantiles defined as $q^l = \text{median} {q^i_l}$ and median average deviation around the quantile $q^l$ as $d^l = \text{median} |q_i^l - q^l|$. The method then searches for the smallest quantile $l$ for which it detects instability, defined as large relative increase in the $d^l$. Formally, $\hat{l}$ is the smallest $l$ satisfying $\frac{d^{l+1} - d^l}{d^l} \geq 0.1$. The scaling sample-specific offset are then chosen as: $$ O_i = s_i^{\hat{l}} / \text{median}_i { s_i^{\hat{l}} } $$ Dividing by the median of the $s_i^{\hat{l}}$ ensures that offsets are centered around $1$ and compare sizes differences with respect to the reference sample. Note also that the reference quantiles $q^l$ can be computed using either the median (default, as in the original @CSS paper) or the mean, by specifying reference = mean, as implemented in metagenomeseq.

Relative Log Expression

A reference sample $(q_j)j$ is first built by computing the geometric means of each species count: $$ q_j = \exp \left( \frac{1}{n} \sum{i} \log(c_{ij})\right) $$ Each sample is then compared to the reference sample to compute one ratio per species and the final offset $O_i$ is the median of those ratios: $$ O_i = \text{median}j \frac{c{ij}}{q_j} $$ The method fails when no species is shared across all sample (as all $q_j$ are then $0$) or when a sample shares less than 50% of species with the reference (in which case the median of the ratios may be null or infinite). The problem can be alleviated by adding pseudocounts to the $c_{ij}$ with pseudocounts = 1.

Geometric Mean of Pairwise Ratio

This method is similar to RLE but does create a reference sample. Instead, each sample is compared to each other to compute a median ratio (similar to RLE) $$ r_{ii'} = {\text{median}}{j: c{ij}.c_{i'j} > 0} \frac{c_{ij}}{c_{i'j}} $$ The offset is then taken as the median of all the $r_{ii'}$: $$ O_i = \text{median}{i' != i} r{ii'} $$ The method fails when there is only one sample in the data set or when a sample shares no species with any other.

[^1]: although a data.frame is technically a list

References



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PLNmodels documentation built on Jan. 28, 2020, 1:07 a.m.