mouse-diet-two-factors-PTM-VIS.qmd

# Wrapup: Factorial design with two factors {-}

```{r, echo = FALSE}
source("R/knitr_setup.R")
```

# Background 

With the PXD059421 data deposited on ProteomeXchange researchers study the molecular effects of dietary DINCH exposure, on the proteome, phosphoproteome and acetylome profiles of visceral (VIS) and subcutaneous (SC) adipose tissue in a model of diet-induced obesity in male and female C57BL/6N mice. This study includes data on visceral and subcutaneous adipose tissue of female and male mice that were either fed a standard plant-based diet (chow), a standard high-fat diet (HFD) or two HFD diets including doses of DINCH (4,500 ppm and 15,000 ppm). Three female and three male mice were used for each diet [@AldehoffEtAl2025].

The data were downloaded from Pride and reprocessed using spectronaut. 
Here, we will focus on the proteomics data from the visceral tissue of mice subjected to the low and high DINCH diet. 

# Load packages

We load the `msqrob2` package, along with additional packages for
data manipulation and visualisation.

```{r load_libraries}
library("QFeatures")  
library("dplyr") 
library("tidyr")
library("ggplot2")
library("msqrob2")    
library("stringr")
library("ExploreModelMatrix")
library("MsCoreUtils") 
library("matrixStats")
library("patchwork")
library("kableExtra")
library("ComplexHeatmap")
library("purrr")
library("tibble")
library("scater")
```

# Data

## Precursor table

We load the output from Spectronaut parquet file. Can be file path to local file or url to file that lives on the web.

```{r import_data}
precursorFile = "data/mouseDiet-spectronaut.parquet"
precursorFilePTM = "data/mouseDiet-phospho-spectronaut.parquet"
```


We can import the report.parquet file using the `read_parquet` function from the `arrow` package. 

```{r}
precursors <- arrow::read_parquet(precursorFile) # function from the arrow package
precursorsPTM <- arrow::read_parquet(precursorFilePTM) # function from the arrow package
#precursors <- data.table::fread(precursorFile) # For older versions the results are stored as tsv files. 
```

Note, that by default the spectronaut output is stored as a tsv file. In that case a `.` occurs in the column variables instead of a "_" upon importing with fread. 

Each row in the precursor data table is in "long format" and contains information about one precursor in a specific run (the table below shows the first 6 rows). 
The columns contains various descriptors about the precursor, such as its sequence, its charge, run, etc. 


```{r, echo=FALSE}
knitr::kable(head(precursors))
```


(Note, that by default the spectronaut output is stored as a tsv file. In that case a `.` occurs in the column variables instead of a "_" upon importing with fread.) 



No precursor Id and norm factors are present in the file. 
We can make the former using the EG_ModifiedSequence and FG_Charge, and the latter using FG_MS2RawQuantity and FG_Quantity.

```{r}
precursors <- precursors |> 
  mutate(EG_PrecursorId = paste0(EG_ModifiedSequence, FG_Charge),
         EG_NormalizationFactor = FG_Quantity/FG_MS2RawQuantity #Normalisation.Factor
)
precursorsPTM <- precursorsPTM |> 
  mutate(EG_PrecursorId = paste0(EG_ModifiedSequence, FG_Charge),
         EG_NormalizationFactor = FG_Quantity/FG_MS2RawQuantity,
         EG_IsDecoy = FALSE#Normalisation.Factor
)
```

## Subset phospho

```{r}
precursorsPTM <- precursorsPTM |>
  filter(grepl(pattern = "Phospho", EG_ModifiedSequence))
```

## Subset for low and high diets

Subset the data from the male and female mice subjected to Low and High diets

```{r}
precursors <- precursors |> 
  filter(grepl("VIS", R_FileName) & 
           (grepl("low",R_FileName) | grepl("high",R_FileName))
  )
precursorsPTM <- precursorsPTM |> 
  filter(grepl("VIS", R_FileName) & 
           (grepl("low",R_FileName) | grepl("high",R_FileName))
  )
```


```{r}
precursors <- precursors |> 
  select(
         R_FileName, #Run,
         EG_PrecursorId,
         EG_ModifiedSequence, #Modified.Sequence, 
         PEP_StrippedSequence, #Stripped.Sequence, 
         FG_Charge, #PrecursoR_Charge, 
         PG_ProteinGroups, #Protein.Group, 
         PG_Genes, #Genes,
         FG_MS2RawQuantity, #PrecursoR_Quantity,
         FG_Quantity,
         EG_NormalizationFactor,
         EG_Qvalue, #Q.Value, 
         #No spectronaut counterpart #Lib.Q.Value,
         PG_Qvalue, # PG_Q.Value,
         #No spectronaut counterpart #Lib.PG_Q.Value
         PEP_IsProteotypic, #Proteotypic,
         EG_IsDecoy, #Decoy,
         EG_ApexRT,#RT
         EG_IsImputed)
precursorsPTM <- precursorsPTM |> 
  select(
         R_FileName, #Run,
         EG_PrecursorId,
         EG_ModifiedSequence, #Modified.Sequence, 
         PEP_StrippedSequence, #Stripped.Sequence, 
         FG_Charge, #PrecursoR_Charge, 
         PG_ProteinGroups, #Protein.Group, 
         PG_Genes, #Genes,
         FG_MS2RawQuantity, #PrecursoR_Quantity,
         FG_Quantity,
         EG_NormalizationFactor,
         EG_Qvalue, #Q.Value, 
         #No spectronaut counterpart #Lib.Q.Value,
         PG_Qvalue, # PG_Q.Value,
         #No spectronaut counterpart #Lib.PG_Q.Value
         PEP_IsProteotypic, #Proteotypic,
         EG_IsDecoy, #Decoy,
         #EG_ApexRT,#RT
         EG_IsImputed)
```

Quick check on distribution of precursors MS2 intensities.

```{r}
precursors |> 
  ggplot(aes(x = log2(FG_MS2RawQuantity))) +
  geom_density() +
  theme_minimal()
```

```{r}
precursorsPTM |> 
  ggplot(aes(x = log2(FG_MS2RawQuantity))) +
  geom_density() +
  theme_minimal()
```

Seems no imputation has been done. 

## Sample annotation table

The [sample annotation table](#sec-annotation_table)) is not available
and can be generated from the run labels, as the researchers included information on the design in the filenames.

```{r create_metadata}
annot <- precursors |> 
  dplyr::distinct(R_FileName) |> 
  separate(R_FileName, into = c('f1','tissue','f2','diet','rep'), sep = '_', remove=FALSE) |>
    mutate(runCol=R_FileName,
           sex = stringr::str_sub(diet,1,1),
           diet = stringr::str_sub(diet,2),
           rep = paste(diet, sex, rep, sep='_'),
           sampleGroup = paste(tissue,diet,sex,sep='_'),
           sampleId = paste(tissue,rep, sep="_")) |>
    dplyr::select(-c(R_FileName,f1,f2)) |> 
  relocate("runCol")
annot
```

```{r}
annotPTM <- precursorsPTM |> 
  dplyr::distinct(R_FileName) |> 
  separate(R_FileName, into = c('f1','tissue','f2','diet','rep'), sep = '_', remove=FALSE) |>
    mutate(runCol=R_FileName,
           sex = stringr::str_sub(diet,1,1),
           diet = stringr::str_sub(diet,2),
           rep = paste(diet, sex, rep, sep='_'),
           sampleGroup = paste(tissue,diet,sex,sep='_'),
           sampleId = paste(tissue,rep, sep="_")) |>
    dplyr::select(-c(R_FileName,f1,f2)) |> 
  relocate("runCol")
annotPTM
```

## Convert to QFeatures
First, recall that the precursor table is file in long format. 
Every quantitative column in the precursor table contains
information for multiple runs. Therefore, the function split the table
based on the run identifier, given by the `runCol` argument (for
Spectronaut, that identifier is contained in `run`). 
So, the
`QFeatures` object after import will contain as many sets as there are
runs. 
Next, the function links the annotation table with the PSM data.
To achieve this, the annotation table must contain a `runCol` column
that provides the run identifier in which each sample has been
acquired, and this information will be used to match the identifiers
in the `Run` column of the precursor table. 

Here, we will use the `FG_MS2Quantity` column as quantification input. 

We first combine the precursor and precursorPTM table in a list of QFeatures objects, which we subsequently reduce in one QFeatures object. 

```{r}
(qf <- list(
  readQFeatures(assayData = precursors,  
                              colData = annot,
                              quantCols = "FG_MS2RawQuantity",
                              runCol = "R_FileName",
                              fnames = "EG_PrecursorId"),
 readQFeatures(assayData = precursorsPTM,  
                              colData = annotPTM,
                              quantCols = "FG_MS2RawQuantity",
                              runCol = "R_FileName",
                              fnames = "EG_PrecursorId")
 ) |> reduce(c)
)
```


# Data preprocessing{#sec-basic_preprocess}

The data preprocessing workflow for DIA data is similar to the workflow for DDA-LFQ data, but there are suble differences as we start from precursor level data and have additional columns. 

## Encoding missing values

We first replace any zero in the quantitative data
with an `NA`. 

```{r}
qf <- zeroIsNA(qf, names(qf))
```

Note that `msqrob2` can handle missing data without having to rely on
hard-to-verify imputation assumptions, which is our general recommendation. However, `msqrob2` does not
prevent users from using imputation, which can be performed with
`impute()` from the `QFeatures` package. 

## Precursor Filtering 

Filtering removes low-quality and unreliable precursors that would otherwise introduce noise and artefacts in the data. 

### Remove questionable identifications


We apply standard filtering: 

1. q-value threshold of 0.01 for the identification of precursors (`EG_Qvalue`) and protein groups (`PG_Qvalue`). 

2. Remove precursors that could not be mapped, i.e. when `EG_PrecursorId` column is an empty string.  

3. Filter decoys, i.e. only keep precursors for which the `EG_IsDecoy` column equals 0. 

4. Keeping only proteotypic peptides, which map uniquely to a specific protein.

5. Only keep non-imputed intensities: `EG_IsImputed` equals 0.


```{r}
qf <-  qf |>
  filterFeatures(~ EG_Qvalue <= 0.01 & #1.
                     PG_Qvalue <= 0.01 &  #1.
#                     Lib.Q.Value <= 0.01 & #1.
#                     Lib.PG_Q.Value <= 0.01 & #1.
                     EG_PrecursorId != "" & #2.
                     EG_IsDecoy == 0 & #3.
                     PEP_IsProteotypic == 1 & #4
                     EG_IsImputed == 0) #5 
```


Note, that it is important that the filtering criteria are not distorting the distribution of the test statistics in the downstream analysis for features that are non-DA. 
It can be shown that filtering will not induce bias results when the filtering criterion is independent of test statistic. The criteria that we proposed above are all based on the results of the identification step, hence, they are independent of the downstream test statistics that will be used to prioritize DA proteins. 

### Assay joining

Up to now, the data from different runs were kept in separate assays. We can now join the normalised sets into an precursor set using joinAssays(). Sets are joined by stacking the columns (samples) in a matrix and rows (features) are matched according to a row identifier, here the `EG_PrecursorId`.
We will store the result in the assay with name: `precursor`.

```{r}
qf <- joinAssays(
  x = qf,
  i = grep("FP",names(qf), value = TRUE),
  fcol = "EG_PrecursorId",
  name = "precursors"
  )
(qf <- joinAssays(
  x = qf,
  i = grep("PP",names(qf), value = TRUE),
  fcol = "EG_PrecursorId",
  name = "precursorsPTM"
  )
)
```

### Filtering: Remove highly missing precursors

We keep peptides that were observed at last 6 times out of the $n
= 48$ samples, so that we can estimate the peptide characteristics. 

```{r}
nObs <- 6
n <- ncol(qf[["precursors"]])

(qf <- filterNA(qf, i = c("precursors", "precursorsPTM"), pNA = (n - nObs) / n))
```


### Filter one-hit wonders

Here, we remove proteins that can only be found by one peptide, as such proteins may not be trustworthy.

1. We first calculate how many distinct peptides map to each protein group (`PG_ProteinGroups`). We use the stripped precursor sequence, i.e. sequence of the base peptide for this purpose. 

2. We store this information in the row data of the precursors assay

3. We filter precursors of one-hit wonder proteins.  

We only do this for the proteins assay 

```{r}
# Filter for peptides per protein
pepsPerProtDf <- qf[["precursors"]] |> 
    rowData() |> 
    data.frame() |>
    dplyr::select("PEP_StrippedSequence", "PG_ProteinGroups") |>
    group_by(PG_ProteinGroups) |>
    mutate(pepsPerProt = PEP_StrippedSequence |>
               unique() |> length()
           ) #1.

rowData(qf[["precursors"]])$pepsPerProt <- pepsPerProtDf$pepsPerProt #2. 

qf <- filterFeatures(qf, 
                              ~ pepsPerProt > 1, 
                              keep = TRUE) #3.
```

## Log-transformation 


We perform log2-transformation with `logTransform()` from the
`QFeatures` package. We use `base = 2` and store the result in a new summarized experiment named `precursors_log`

```{r}
qf <- logTransform(qf, 
                            base = 2, 
                            i = "precursors", 
                            name = "precursors_log")
qf <- logTransform(qf, 
                            base = 2, 
                            i = "precursorsPTM", 
                            name = "precursorsPTM_log")
```

## Normalisation {#sec-norm}


```{r}
qf[, , "precursors_log"] |> #1.
  longForm(colvars = colnames(colData(qf))) |>  #2. 
  data.frame() |> 
  filter(!is.na(value)) |>
  ggplot() + #3.
  aes(x = value,
      colour = sampleGroup,
      group = colname) +
  geom_density() +
  labs(subtitle = "precursors") +
  theme_minimal()
  
qf[, , "precursorsPTM_log"] |> #1.
  longForm(colvars = colnames(colData(qf))) |>  #2. 
  data.frame() |> 
  filter(!is.na(value)) |>
  ggplot() + #3.
  aes(x = value,
      colour = sampleGroup,
      group = colname) +
  geom_density() +
  labs(subtitle = "PTM - precursors") +
  theme_minimal()
```
Normalisation is required. For this dataset we use median of ratio normalisation because we noticed severe differences in compositionality see [Wrap-up normalisation](02-normalisation-wrapup.html). 

```{r}
qf <- sweep( #4. Subtract log2 norm factor column-by-column (MARGIN = 2)
  qf,
  MARGIN = 2,
  STATS = nf_log_medrat(qf,"precursors_log"),
  i = "precursors_log",
  name = "precursors_norm"
)
qf <- sweep( #4. Subtract log2 norm factor column-by-column (MARGIN = 2)
  qf,
  MARGIN = 2,
  STATS = nf_log_medrat(qf,"precursorsPTM_log"),
  i = "precursorsPTM_log",
  name = "precursorsPTM_norm"
)
```


We explore the effect of the global normalisation in the subsequent plot. 

Formally, the function applies the following operation on each sample
$i$ across all precursors $p$:

$$
y_{ip}^{\text{norm}} = y_{ip} - \log_2(nf_i)
$$

with $y_ip$ the log2-transformed intensities and $nf_i$ the log2-transformed norm factor. Upon normalisation, we can see
that the distribution of the $y_{ip}^{\text{norm}}$ nicely overlap (using the same code as above)

```{r}
qf[, , "precursors_norm"] |>
  longForm(colvars = colnames(colData(qf))) |> 
  data.frame() |> 
  filter(!is.na(value)) |>
  ggplot() + 
  aes(x = value,
      colour = sampleGroup,
      group = colname) +
  geom_density() +
  labs(subtitle = "Median normalisation precursors") +
  theme_minimal()
qf[, , "precursorsPTM_norm"] |>
  longForm(colvars = colnames(colData(qf))) |> 
  data.frame() |> 
  filter(!is.na(value)) |>
  ggplot() + 
  aes(x = value,
      colour = sampleGroup,
      group = colname) +
  geom_density() +
  labs(subtitle = "Median normalisation PTM precursors") +
  theme_minimal()
```

We also explore the normalisation for the common precursors. 


```{r}
precursorsCommon <- assay(qf[, , "precursors_log"]) |> na.exclude() |> rownames()
precursorCommonDens <- qf[precursorsCommon, , "precursors_norm"] |>
  longForm(colvars = colnames(colData(qf))) |> 
  data.frame() |> 
  filter(!is.na(value)) |>
  ggplot() + 
  aes(x = value,
      colour = sampleGroup,
      group = colname) +
  geom_density() +
  theme_minimal() +
   labs(subtitle = "Median normalised log2 precursor intensities (common)")
precursorCommonDens
precursorsCommonPTM <- assay(qf[, , "precursorsPTM_log"]) |> na.exclude() |> rownames()
precursorCommonDensPTM <- qf[precursorsCommonPTM, , "precursorsPTM_norm"] |>
  longForm(colvars = colnames(colData(qf))) |> 
  data.frame() |> 
  filter(!is.na(value)) |>
  ggplot() + 
  aes(x = value,
      colour = sampleGroup,
      group = colname) +
  geom_density() +
  theme_minimal() +
   labs(subtitle = "Median normalised log2 precursor intensities (common)")
precursorCommonDensPTM
```

## Summarisation

Here, we summarise the precursor-level data into protein intensities using maxLFQ. 
maxLFQ first calculates all pairwise log ratio's between samples only using their shared precursors.
Particularly, it uses the median of the log ratio's between the shared precursors s, i.e. 
$$r_{ij} = median(y_{sj}-y_{si})$$.  
Hence, it first eliminates peptide effects. 
It then estimates the summaries by solving 

$$
\sum_i\sum_j(y^{prot}_j - y^{prot}_i - r_ij)^2
$$
It is implemented in the `maxLFQ` function of the `iq` package. 

`aggregateFeatures()` streamlines summarisation. It requires the name
of a `rowData` column to group the precursors into proteins (or
protein groups), here `PG_ProteinGroups`. We provide the summarisation
approach through the `fun` argument. Other summarisation methods
are available from the `MsCoreUtils` package, see `?aggregateFeatures`
for a comprehensive list. The function will return a `QFeatures`
object with a new set that we called `proteins`.

```{r, warning=FALSE}
(qf <- aggregateFeatures(
  qf, i = "precursors_norm", 
  name = "proteins",
  fcol = "PG_ProteinGroups", 
  fun = function(X) iq::maxLFQ(X)$estimate
))
```


# Data exploration and QC regular assay

Data exploration aims to highlight the main sources of variation in
the data prior to data modelling and can pinpoint to outlying or
off-behaving samples. 

## Marginal distribution at precursor and protein level 


```{r}
precursorDens <- qf[, , "precursors_norm"] |>
  longForm(colvars = colnames(colData(qf))) |> 
  data.frame() |> 
  filter(!is.na(value)) |>
  ggplot() + 
  aes(x = value,
      colour = sampleGroup,
      group = colname) +
  geom_density() +
  theme_minimal() +
   labs(subtitle = "Median normalised log2 precursor intensities")
precursorDens
```

```{r}
qf[, , "precursors_norm"] |>
  longForm(colvars = colnames(colData(qf))) |> 
  data.frame() |> 
  filter(!is.na(value)) |>
  ggplot() + 
  aes(x = sampleId,
      y = value,
      colour = sampleGroup,
      group = colname) +
  xlab("sample") +
  geom_boxplot() +
  theme_minimal() +
   labs(subtitle = "Median normalised log2 precursor intensities")
```


```{r}
qf[, , "proteins"] |>
  longForm(colvars = colnames(colData(qf))) |> 
  data.frame() |> 
  filter(!is.na(value)) |>
  ggplot() + 
  aes(x = sampleId,
      y = value,
      colour = sampleGroup,
      group = colname) +
  xlab("sample") +
  geom_boxplot() +
  theme_minimal() +
   labs(subtitle = "log2 protein intensities (median normalised precursors)")
```

```{r}
protDens <- qf[, , "proteins"] |>
  longForm(colvars = colnames(colData(qf))) |> 
  data.frame() |> 
  filter(!is.na(value)) |>
  ggplot() + 
  aes(x = value,
      colour = sampleGroup,
      group = colname) +
  geom_density() +
  theme_minimal() +
   labs(subtitle = "log2 protein intensities (median normalised precursors)")
protDens
```

## Charge state 

```{r}
qf[, , "precursors_norm"] |>
  longForm(colvars = colnames(colData(qf)), rowvars = "FG_Charge") |>
  as.data.frame() |>
  filter(!is.na(value)) |>
  filter(FG_Charge<=4) |> 
ggplot(aes(x = sampleId)) +
  geom_bar(aes(fill = factor(FG_Charge, levels = 4:1)),
           colour = "black") +
  labs(title = "Peptide types per sample",
       x = "Sample",
       fill = "Charge state") +
  theme_bw()
```

## Identifications per sample 

```{r}
qf[,,"precursors_norm"] |> 
  longForm(colvars = colnames(colData(qf)), 
           rowvars= c("EG_PrecursorId", 
                      "PG_ProteinGroups")) |>
  data.frame() |>
  filter(!is.na(value)) |>
  group_by(sampleGroup, sampleId) |>
  summarise(Precursors = length(unique(EG_PrecursorId)),
            `Protein Groups` = length(unique(PG_ProteinGroups))) |> 
  pivot_longer(-(1:2),
               names_to = "Feature",
               values_to = "IDs") |> 
  ggplot(aes(x = sampleId, y = IDs, fill = sampleGroup)) +
  geom_col() +
  #scale_fill_observable() +
  facet_wrap(~Feature,
             scales = "free_y") +
  labs(title = "Precursor and protein group identificiations per sample",
       x = "Sample",
       y = "Identifications") +
  theme_bw() + 
  theme(axis.text.x = element_text(angle = 90))
# Data Modeling (Robust Regression){#sec-modelling}
```

## Dimensionality reduction plot 

A common approach for data exploration is to
perform dimension reduction, such as Multi Dimensional Scaling (MDS).
We will first extract the set to explore along the sample annotations
(used for plot colouring).

```{r}
protMDS <- getWithColData(qf, "proteins") |> 
  as("SingleCellExperiment") |> 
  runMDS(exprs_values = 1) |> 
  plotMDS(colour_by = "sampleGroup") + 
  labs(title = "Median normalisation")
protMDS
```




# Data exploration and QC PTM assay

Data exploration aims to highlight the main sources of variation in
the data prior to data modelling and can pinpoint to outlying or
off-behaving samples. 

## Marginal distribution at precursor and protein level 


```{r}
precursorDensPTM <- qf[, , "precursorsPTM_norm"] |>
  longForm(colvars = colnames(colData(qf))) |> 
  data.frame() |> 
  filter(!is.na(value)) |>
  ggplot() + 
  aes(x = value,
      colour = sampleGroup,
      group = colname) +
  geom_density() +
  theme_minimal() +
   labs(subtitle = "Median normalised log2 PTM precursor intensities")
precursorDensPTM
```

```{r}
qf[, , "precursorsPTM_norm"] |>
  longForm(colvars = colnames(colData(qf))) |> 
  data.frame() |> 
  filter(!is.na(value)) |>
  ggplot() + 
  aes(x = sampleId,
      y = value,
      colour = sampleGroup,
      group = colname) +
  xlab("sample") +
  geom_boxplot() +
  theme_minimal() +
   labs(subtitle = "Median normalised log2 PTM precursor intensities")
```


## Charge state 

```{r}
qf[, , "precursorsPTM_norm"] |>
  longForm(colvars = colnames(colData(qf)), rowvars = "FG_Charge") |>
  as.data.frame() |>
  filter(!is.na(value)) |>
  filter(FG_Charge<=4) |> 
ggplot(aes(x = sampleId)) +
  geom_bar(aes(fill = factor(FG_Charge, levels = 4:1)),
           colour = "black") +
  labs(title = "Peptide types per sample",
       x = "Sample",
       fill = "Charge state") +
  theme_bw()
```

## Identifications per sample 

```{r}
qf[,,"precursorsPTM_norm"] |> 
  longForm(colvars = colnames(colData(qf)), 
           rowvars= c("EG_PrecursorId", 
                      "PG_ProteinGroups")) |>
  data.frame() |>
  filter(!is.na(value)) |>
  group_by(sampleGroup, sampleId) |>
  summarise(Precursors = length(unique(EG_PrecursorId)),
            `Protein Groups` = length(unique(PG_ProteinGroups))) |> 
  pivot_longer(-(1:2),
               names_to = "Feature",
               values_to = "IDs") |> 
  ggplot(aes(x = sampleId, y = IDs, fill = sampleGroup)) +
  geom_col() +
  #scale_fill_observable() +
  facet_wrap(~Feature,
             scales = "free_y") +
  labs(title = "Precursor and protein group identificiations per PTM sample",
       x = "Sample",
       y = "Identifications") +
  theme_bw() + 
  theme(axis.text.x = element_text(angle = 90))
# Data Modeling (Robust Regression){#sec-modelling}
```

## Dimensionality reduction plot 

A common approach for data exploration is to
perform dimension reduction, such as Multi Dimensional Scaling (MDS).
We will first extract the set to explore along the sample annotations
(used for plot colouring).

```{r}
precursorPTMMDS <- getWithColData(qf, "precursorsPTM_norm") |> 
  as("SingleCellExperiment") |> 
  runMDS(exprs_values = 1) |> 
  plotMDS(colour_by = "sampleGroup") + 
  labs(title = "Median normalisation")
precursorPTMMDS
```

# Data Modeling at protein-level (Robust Regression){#sec-modelling}

## Model estimation

1. We first define the model. We only have one sources of variability in the experiment that we can model, i.e. the effect of the spike-in condition. 

2. We fit the model to each protein in the `proteins` summarised experiment of the QFeatures object `qf` using the msqrob function. 

```{r warning=FALSE}
model <- ~ diet * sex 
qf <- msqrob(
  qf,
  i = "proteins",
  formula = model,
  robust = TRUE)
```

We enabled M-estimation (`robust = TRUE`) for improved robustness
against outliers. 

## Inference

We can now convert the research question "do the spike-in
conditions affect the protein intensities?" into a statistical
hypothesis. 

In other words, we need to translate this question in a null and alternative hypothesis on a single model parameter or a linear combination of model parameters, which is also referred to with a [contrast](#sec-inference).

To aid defining contrasts, we will visualise the experimental design using the `ExploreModelMatrix` package.

```{r}

vd <- ExploreModelMatrix::VisualizeDesign(
    sampleData =  colData(qf),
    designFormula = model,
    textSizeFitted = 4
)
vd$plotlist
```
We have 4 interesting research questions related to the diet. 

1. Is there an effect of diet on in female mice / prioritise proteins that are differentially abundant (DA) between low and high diet for female mice.
2. Is there an effect of diet in male mice / prioritise proteins that are DA between low and high diet for male mice
3. Is the effect of diet different in male and female mice / prioritise proteins for which the log2 FC between low and high diet differs between male and female mice (interaction)
4. Prioritise proteins that are differentially abundant (DA) between low and high diet in mice. Here we will average the log2 FC over male and female mice. This would prioritise proteins that would be picked up according to diet if we were to remove the interaction term from the model. 

Each of these contrasts can be translated in a log2 FC or a difference in log2 FC and can be estimated with one or a linear combination of the model parameters. 

1. $\log_2 FC_\text{low - high}^\text{f} = (Intercept) + dietlow- (Intercept) = dietlow$
2. $\log_2 FC_\text{low - high}^\text{m} = (Intercept) + dietlow + sexm + dietlow:sexm - ((Intercept) + sexm) = dietlow + dietlow:sexm$
3. $\log_2 FC_\text{low - high}^\text{m} - \log_2 FC_\text{low - high}^\text{f} = dietlow:sexm$
4. $0.5 \times \log_2 FC_\text{low - high}^\text{m} + 0.5 \times \log_2 FC_\text{low - high}^\text{f} = dietlow + 0.5 \times dietlow:sexm $

Below we define the contrast and construct the corresponding contrast matrix. 

```{r}
contrast <- c("dietlow = 0", "dietlow + dietlow:sexm = 0", "dietlow:sexm = 0", "dietlow + 0.5* dietlow:sexm = 0")
(L <- makeContrast(
  contrast,
   parameterNames = colnames(vd$designmatrix)
))
```


We assess the contrast for each protein. 

```{r warning=FALSE}
qf <- hypothesisTest(qf, i = "proteins", contrast = L, overwrite = TRUE)
```

We extract the results table from the `proteins` summarised experiment in the `qf` object. 

```{r}
inferences <- 
  msqrobCollect(qf[["proteins"]], L)
```

## Report results

We report the results using a results table, volcano plots and heatmaps. 

### Results table

We use the 5% nominal FDR level to report results 
```{r}
alpha <- 0.05
```

```{r}
#| results: asis
for (j in colnames(L)) {

  inference <- inferences |> 
    dplyr::filter(adjPval < alpha & contrast == j)

  cat("**Median - Contrast:**", j, "= 0 (", nrow(inference),
      "significant proteins)\n\n")

  cat('<div style="max-height:300px; overflow-y:auto;">')

  print(
    kable(
      inference |>
        dplyr::arrange(pval) |>
        dplyr::relocate(feature),
      row.names = FALSE
    )
  )

  cat('</div>')

  cat("\n\n\n---\n\n")
}
```

### Volcanoplots 

```{r}
volcanoplot <- plot_volcano(inferences) + 
  facet_wrap(~contrast) + 
  labs(title = "Protein-level")
volcanoplot
```

Note that the volcanoplots are still slightly asymmetric, which can probe issues w.r.t. normalisation. 


```{r}
inferences |> 
  filter(adjPval < alpha) |> 
  mutate(DA = sign(logFC) |> as.factor() |> recode("-1"= "down","1" = "up")) |>
  group_by(contrast, DA) |> 
  ggplot(aes(x = contrast)) +
  geom_bar(aes(fill = factor(DA)),
           colour = "black") +
  theme_minimal()
```

### Heatmaps

```{r}
heatmaps <- lapply(colnames(L),
                   function(contrast, se, alpha)
                   {
                     sig <- rowData(se)[[contrast]] |> 
                       filter(adjPval < alpha) |> 
                       rownames()
                     quants <- t(scale(t(assay(se[sig,]))))
                     colnames(quants) <- se$sampleId #specific to this dataset to get short colnames
                     annotations <- columnAnnotation(
                       group = se$sampleGroup
                       ) #3.
                     set.seed(1234) ## annotation colours are randomly generated by default
                     return(
                       Heatmap(
                       quants, 
                       name = "log2 intensity",
                       top_annotation = annotations, 
                       column_title = paste0(contrast, " = 0")
                       )
                     )
                   },
                   se = getWithColData(qf, "proteins"),
                   alpha = alpha)
heatmaps
```


### Detail plots

We can explore the data for a protein to validate the statistical inference results. For example, let’s explore the normalised precursor and the summarised protein intensities for the protein with the most significant log2 fold change.

```{r}
(target_feature <- inferences |> 
   dplyr::slice(which.min(pval)) |> 
   pull(feature)
)
inferences |> 
  filter(feature == target_feature)
```

To obtain the required data, we perform a little data manipulation pipeline:

We use the QFeatures subsetting functionality to retrieve all data related to and focusing on the peptides_log and proteins sets that contains the peptide ion data used for model fitting. We then convert the data with longForm() for plotting. Finally, we plot the log2 normalised intensities for each sample at the protein and at the peptide level. Since multiple peptides are recorded for the protein, we link peptides across samples using a grey line. Samples are colored according to E. coli spike-in condition.

```{r}
qf[target_feature, , c("precursors_log","precursors_norm", "proteins")] |> #1
  longForm(colvars = colnames(colData(qf))) |> #2
  data.frame() |> 
  ggplot() +
  aes(x = colname,
      y = value) +
  geom_line(aes(group = rowname), linewidth = 0.1) +
  geom_point(aes(colour = sampleGroup)) +
  facet_wrap(~ assay, scales = "free") +
  ggtitle(target_feature) +
  theme_minimal() +
  theme(axis.text.x = element_blank())
```

```{r}
qf[target_feature, , c("precursors_log","precursors_norm", "proteins")] |> #1
  longForm(colvars = colnames(colData(qf))) |> #2
  data.frame() |>
  filter(!is.na(value)) %>% 
  {
  ggplot(.) +
  aes(x = sampleGroup,
      y = value) +
  geom_boxplot(aes(colour = sampleGroup)) +
  facet_wrap(~ assay, scales = "free") +
  geom_jitter(aes(shape = rowname)) +
  scale_shape_manual(values = seq_len(dplyr::n_distinct(.$rowname))) +
  ggtitle(target_feature) +
  theme_minimal() +
  theme(axis.text.x = element_blank()) +
  guides(shape = "none")
  }
```

# Data Modeling at phospho-peptidoform-level (Robust Regression){#sec-modelling}

## Model estimation

1. We first define the model. We only have one sources of variability in the experiment that we can model, i.e. the effect of the spike-in condition. 

2. We fit the model to each protein in the `proteins` summarised experiment of the QFeatures object `qf` using the msqrob function. 

```{r warning=FALSE}
model <- ~ diet * sex 
qf <- msqrob(
  qf,
  i = "precursorsPTM_norm",
  formula = model,
  robust = TRUE)
```

We enabled M-estimation (`robust = TRUE`) for improved robustness
against outliers. 

## Inference

We can now convert the research question "do the spike-in
conditions affect the protein intensities?" into a statistical
hypothesis. 

In other words, we need to translate this question in a null and alternative hypothesis on a single model parameter or a linear combination of model parameters, which is also referred to with a [contrast](#sec-inference).

To aid defining contrasts, we will visualise the experimental design using the `ExploreModelMatrix` package.

```{r}

vd <- ExploreModelMatrix::VisualizeDesign(
    sampleData =  colData(qf),
    designFormula = model,
    textSizeFitted = 4
)
vd$plotlist
```
We have 4 interesting research questions related to the diet. 

1. Is there an effect of diet on in female mice / prioritise proteins that are differentially abundant (DA) between low and high diet for female mice.
2. Is there an effect of diet in male mice / prioritise proteins that are DA between low and high diet for male mice
3. Is the effect of diet different in male and female mice / prioritise proteins for which the log2 FC between low and high diet differs between male and female mice (interaction)
4. Prioritise proteins that are differentially abundant (DA) between low and high diet in mice. Here we will average the log2 FC over male and female mice. This would prioritise proteins that would be picked up according to diet if we were to remove the interaction term from the model. 

Each of these contrasts can be translated in a log2 FC or a difference in log2 FC and can be estimated with one or a linear combination of the model parameters. 

1. $\log_2 FC_\text{low - high}^\text{f} = (Intercept) + dietlow- (Intercept) = dietlow$
2. $\log_2 FC_\text{low - high}^\text{m} = (Intercept) + dietlow + sexm + dietlow:sexm - ((Intercept) + sexm) = dietlow + dietlow:sexm$
3. $\log_2 FC_\text{low - high}^\text{m} - \log_2 FC_\text{low - high}^\text{f} = dietlow:sexm$
4. $0.5 \times \log_2 FC_\text{low - high}^\text{m} + 0.5 \times \log_2 FC_\text{low - high}^\text{f} = dietlow + 0.5 \times dietlow:sexm $

Below we define the contrast and construct the corresponding contrast matrix. 

```{r}
contrast <- c("dietlow = 0", "dietlow + dietlow:sexm = 0", "dietlow:sexm = 0", "dietlow + 0.5* dietlow:sexm = 0")
(L <- makeContrast(
  contrast,
   parameterNames = colnames(vd$designmatrix)
))
```


We assess the contrast for each protein. 

```{r warning=FALSE}
qf <- hypothesisTest(qf, i = "precursorsPTM_norm", contrast = L, overwrite = TRUE)
```

We extract the results table from the `proteins` summarised experiment in the `qf` object. 

```{r}
inferencesPTM <- 
  msqrobCollect(qf[["precursorsPTM_norm"]], L)
```

## Report results

We report the results using a results table, volcano plots and heatmaps. 

### Results table

We use the 5% nominal FDR level to report results 
```{r}
alpha <- 0.05
```

#### median 

```{r}
#| results: asis
for (j in colnames(L)) {

  inference <- inferencesPTM |> 
    dplyr::filter(adjPval < alpha & contrast == j)

  cat("**Median - Contrast:**", j, "= 0 (", nrow(inference),
      "significant proteins)\n\n")

  cat('<div style="max-height:300px; overflow-y:auto;">')

  print(
    kable(
      inference |>
        dplyr::arrange(pval) |>
        dplyr::relocate(feature),
      row.names = FALSE
    )
  )

  cat('</div>')

  cat("\n\n\n---\n\n")
}
```

### Volcanoplots 

```{r}
volcanoplotPTM <- plot_volcano(inferencesPTM) + 
  facet_wrap(~contrast) + 
  labs(title = "Median normalisation")
volcanoplotPTM
```

Note that the volcanoplots are still slightly asymmetric, which can probe issues w.r.t. normalisation. 


```{r}
inferencesPTM |> 
  filter(adjPval < alpha) |> 
  mutate(DA = sign(logFC) |> as.factor() |> recode("-1"= "down","1" = "up")) |>
  group_by(contrast, DA) |> 
  ggplot(aes(x = contrast)) +
  geom_bar(aes(fill = factor(DA)),
           colour = "black") +
  theme_minimal()
```

### Heatmaps

```{r}
heatmaps <- lapply(colnames(L),
                   function(contrast, se, alpha)
                   {
                     sig <- rowData(se)[[contrast]] |> 
                       filter(adjPval < alpha) |> 
                       rownames()
                     quants <- t(scale(t(assay(se[sig,]))))
                     colnames(quants) <- se$sampleId #specific to this dataset to get short colnames
                     annotations <- columnAnnotation(
                       group = se$sampleGroup
                       ) #3.
                     set.seed(1234) ## annotation colours are randomly generated by default
                     return(
                       Heatmap(
                       quants, 
                       name = "log2 intensity",
                       top_annotation = annotations, 
                       column_title = paste0(contrast, " = 0")
                       )
                     )
                   },
                   se = getWithColData(qf, "precursorsPTM_norm"),
                   alpha = alpha)
heatmaps
```


### Detail plots

We can explore the data for a protein to validate the statistical inference results. For example, let’s explore the normalised precursor and the summarised protein intensities for the protein with the most significant log2 fold change.

```{r}
(target_feature <- inferencesPTM |> 
   dplyr::slice(which.min(pval)) |> 
   pull(feature)
)
inferencesPTM |> 
  filter(feature == target_feature)
```

To obtain the required data, we perform a little data manipulation pipeline:

We use the QFeatures subsetting functionality to retrieve all data related to and focusing on the peptides_log and proteins sets that contains the peptide ion data used for model fitting. We then convert the data with longForm() for plotting. Finally, we plot the log2 normalised intensities for each sample at the protein and at the peptide level. Since multiple peptides are recorded for the protein, we link peptides across samples using a grey line. Samples are colored according to E. coli spike-in condition.

```{r}
qf[target_feature, , c("precursorsPTM_log","precursorsPTM_norm")] |> #1
  longForm(colvars = colnames(colData(qf))) |> #2
  data.frame() |> 
  ggplot() +
  aes(x = colname,
      y = value) +
  geom_line(aes(group = rowname), linewidth = 0.1) +
  geom_point(aes(colour = sampleGroup)) +
  facet_wrap(~ assay, scales = "free") +
  ggtitle(target_feature) +
  theme_minimal() +
  theme(axis.text.x = element_blank())
```

```{r}
qf[target_feature, , c("precursorsPTM_log","precursorsPTM_norm")] |> #1
  longForm(colvars = colnames(colData(qf))) |> #2
  data.frame() |>
  filter(!is.na(value)) %>% 
  {
  ggplot(.) +
  aes(x = sampleGroup,
      y = value) +
  geom_boxplot(aes(colour = sampleGroup)) +
  facet_wrap(~ assay, scales = "free") +
  geom_jitter(aes(shape = rowname)) +
  scale_shape_manual(values = seq_len(dplyr::n_distinct(.$rowname))) +
  ggtitle(target_feature) +
  theme_minimal() +
  theme(axis.text.x = element_blank()) +
  guides(shape = "none")
  }
```


# Usage (Robust Regression){#sec-modelling}

```{r}
calculate_usage_paired <- function(qf, i_precursor, i_protein = "proteins", fcol_precursor = "Protein.Group", fcol_protein = "Protein.Group", name = "precursors_usage", match_cols_precursor_to_protein = colnames(qf[[i_precursor]]))
{
    nf <- assay(qf[[i_precursor]])
    nf[,] <- NA
    match_precursor_to_protein_FC <- match(
      rowData(qf[[i_precursor]])[[fcol_precursor]], 
      rowData(qf[[i_protein]])[[fcol_protein]])
    idsMatch <- which(!is.na(match_precursor_to_protein_FC))
    nf[idsMatch, ] <- assay(qf[[i_protein]])[match_precursor_to_protein_FC[idsMatch], match_cols_precursor_to_protein]
    
    qf <- sweep( #4. Subtract log2 norm factor elementwise (MARGIN = 1:2)
      qf,
      MARGIN = 1:2,
      STATS = nf,
      i = i_precursor,
      name = name
      )
    match_name <- paste0("match_",i_precursor,"_to_",i_protein)
    rowData(qf[[name]])[[match_name]] <- match_precursor_to_protein_FC 
    qf <- filterFeatures(qf, i = name, filter = formula(paste0("~ !is.na(",match_name,")")))
}
```

```{r}
qf <- calculate_usage_paired(qf, i_precursor = "precursorsPTM_norm", i_protein = "proteins", fcol_precursor = "PG_ProteinGroups", fcol_protein = "PG_ProteinGroups", name = "usage", match_cols_precursor_to_protein = 1:ncol(qf[["precursorsPTM_norm"]]))
```

```{r}
qf[, , "usage"] |> #1.
  longForm(colvars = colnames(colData(qf))) |>  #2. 
  data.frame() |> 
  filter(!is.na(value)) |>
  ggplot() + #3.
  aes(x = value,
      colour = sampleGroup,
      group = colname) +
  geom_density() +
  labs(subtitle = "usage") +
  theme_minimal()
```
## Model estimation

1. We first define the model. We only have one sources of variability in the experiment that we can model, i.e. the effect of the spike-in condition. 

2. We fit the model to each protein in the `proteins` summarised experiment of the QFeatures object `qf` using the msqrob function. 

```{r warning=FALSE}
model <- ~ diet * sex 
qf <- msqrob(
  qf,
  i = "usage",
  formula = model,
  robust = TRUE,
  overwrite = TRUE)
```

We enabled M-estimation (`robust = TRUE`) for improved robustness
against outliers. 

## Inference

We can now convert the research question "do the spike-in
conditions affect the protein intensities?" into a statistical
hypothesis. 

In other words, we need to translate this question in a null and alternative hypothesis on a single model parameter or a linear combination of model parameters, which is also referred to with a [contrast](#sec-inference).

To aid defining contrasts, we will visualise the experimental design using the `ExploreModelMatrix` package.

```{r}

vd <- ExploreModelMatrix::VisualizeDesign(
    sampleData =  colData(qf),
    designFormula = model,
    textSizeFitted = 4
)
vd$plotlist
```
We have 4 interesting research questions related to the diet. 

1. Is there an effect of diet on in female mice / prioritise proteins that are differentially abundant (DA) between low and high diet for female mice.
2. Is there an effect of diet in male mice / prioritise proteins that are DA between low and high diet for male mice
3. Is the effect of diet different in male and female mice / prioritise proteins for which the log2 FC between low and high diet differs between male and female mice (interaction)
4. Prioritise proteins that are differentially abundant (DA) between low and high diet in mice. Here we will average the log2 FC over male and female mice. This would prioritise proteins that would be picked up according to diet if we were to remove the interaction term from the model. 

Each of these contrasts can be translated in a log2 FC or a difference in log2 FC and can be estimated with one or a linear combination of the model parameters. 

1. $\log_2 FC_\text{low - high}^\text{f} = (Intercept) + dietlow- (Intercept) = dietlow$
2. $\log_2 FC_\text{low - high}^\text{m} = (Intercept) + dietlow + sexm + dietlow:sexm - ((Intercept) + sexm) = dietlow + dietlow:sexm$
3. $\log_2 FC_\text{low - high}^\text{m} - \log_2 FC_\text{low - high}^\text{f} = dietlow:sexm$
4. $0.5 \times \log_2 FC_\text{low - high}^\text{m} + 0.5 \times \log_2 FC_\text{low - high}^\text{f} = dietlow + 0.5 \times dietlow:sexm $

Below we define the contrast and construct the corresponding contrast matrix. 

```{r}
contrast <- c("dietlow = 0", "dietlow + dietlow:sexm = 0", "dietlow:sexm = 0", "dietlow + 0.5* dietlow:sexm = 0")
(L <- makeContrast(
  contrast,
   parameterNames = colnames(vd$designmatrix)
))
```


We assess the contrast for each protein. 

```{r warning=FALSE}
qf <- hypothesisTest(qf, i = "usage", contrast = L, overwrite = TRUE)
```

We extract the results table from the `proteins` summarised experiment in the `qf` object. 

```{r}
inferencesUsage <- 
  msqrobCollect(qf[["usage"]], L)
```

## Report results

We report the results using a results table, volcano plots and heatmaps. 

### Results table

We use the 5% nominal FDR level to report results 
```{r}
alpha <- 0.05
```

```{r}
#| results: asis
for (j in colnames(L)) {

  inference <- inferencesUsage |> 
    dplyr::filter(adjPval < alpha & contrast == j)

  cat("**Median - Contrast:**", j, "= 0 (", nrow(inference),
      "significant proteins)\n\n")

  cat('<div style="max-height:300px; overflow-y:auto;">')

  print(
    kable(
      inference |>
        dplyr::arrange(pval) |>
        dplyr::relocate(feature),
      row.names = FALSE
    )
  )

  cat('</div>')

  cat("\n\n\n---\n\n")
}
```

### Volcanoplots 

```{r}
volcanoplot <- plot_volcano(inferencesUsage) + 
  facet_wrap(~contrast) + 
  labs(title = "Usage")
volcanoplot
```


```{r}
inferencesUsage |> 
  filter(adjPval < alpha) |> 
  mutate(DA = sign(logFC) |> as.factor() |> recode("-1"= "down","1" = "up")) |>
  group_by(contrast, DA) |> 
  ggplot(aes(x = contrast)) +
  geom_bar(aes(fill = factor(DA)),
           colour = "black") +
  theme_minimal()
```

### Heatmaps

```{r}
heatmaps <- lapply(colnames(L),
                   function(contrast, se, alpha)
                   {
                     sig <- rowData(se)[[contrast]] |> 
                       filter(adjPval < alpha) |> 
                       rownames()
                     quants <- t(scale(t(assay(se[sig,]))))
                     colnames(quants) <- se$sampleId #specific to this dataset to get short colnames
                     annotations <- columnAnnotation(
                       group = se$sampleGroup
                       ) #3.
                     set.seed(1234) ## annotation colours are randomly generated by default
                     return(
                       Heatmap(
                       quants, 
                       name = "log2 intensity",
                       top_annotation = annotations, 
                       column_title = paste0(contrast, " = 0")
                       )
                     )
                   },
                   se = getWithColData(qf, "usage"),
                   alpha = alpha)
heatmaps
```

### Detail plots

We can explore the data for a protein to validate the statistical inference results. For example, let’s explore the normalised precursor and the summarised protein intensities for the protein with the most significant log2 fold change.

```{r}
(target_feature <- inferencesUsage |> 
   dplyr::slice(which.min(pval)) |> 
   pull(feature)
)
inferencesUsage |> 
  filter(feature == target_feature)
```

To obtain the required data, we perform a little data manipulation pipeline:

We use the QFeatures subsetting functionality to retrieve all data related to and focusing on the peptides_log and proteins sets that contains the peptide ion data used for model fitting. We then convert the data with longForm() for plotting. Finally, we plot the log2 normalised intensities for each sample at the protein and at the peptide level. Since multiple peptides are recorded for the protein, we link peptides across samples using a grey line. Samples are colored according to E. coli spike-in condition.

```{r}
ptm <-  qf[target_feature, , c("precursorsPTM_norm", "usage")] |> #1
  longForm(colvars = colnames(colData(qf)), rowvars = "PG_ProteinGroups") |> #2
  data.frame()
protein <- qf[unique(ptm$PG_ProteinGroups), , c("proteins")] |> #1
  longForm(colvars = colnames(colData(qf)), rowvars = "PG_ProteinGroups") |> #2
  data.frame()

rbind(ptm, protein) |>
  ggplot() +
  aes(x = colname,
      y = value) +
  geom_line(aes(group = rowname), linewidth = 0.1) +
  geom_point(aes(colour = sampleGroup)) +
  facet_wrap(~ assay, scales = "free") +
  ggtitle(target_feature) +
  theme_minimal() +
  theme(axis.text.x = element_blank())
```

```{r}
rbind(ptm, protein) %>%
  {
  ggplot(.) +
  aes(x = sampleGroup,
      y = value) +
  geom_boxplot(aes(colour = sampleGroup)) +
  facet_wrap(~ assay, scales = "free") +
  geom_jitter(aes(shape = rowname)) +
  scale_shape_manual(values = seq_len(dplyr::n_distinct(.$rowname))) +
  ggtitle(target_feature) +
  theme_minimal() +
  theme(axis.text.x = element_blank()) +
  guides(shape = "none")
  }
```


```{r}
for (i in 1:10){
target_feature <- inferencesPTM |> 
  filter(feature %in% inferencesUsage$feature) |>
  filter(contrast == colnames(L)[1]) |>
  arrange(pval) |> 
  pull(feature)
target_feature <- target_feature[i]

ptm <-  qf[target_feature, , c("precursorsPTM_norm", "usage")] |> #1
  longForm(colvars = colnames(colData(qf)), rowvars = "PG_ProteinGroups") |> #2
  data.frame()
protein <- qf[unique(ptm$PG_ProteinGroups), , c("proteins")] |> #1
  longForm(colvars = colnames(colData(qf)), rowvars = "PG_ProteinGroups") |> #2
  data.frame()


ptm_protein <- rbind(ptm, protein)
ylims <- ptm_protein |> 
  group_by(assay) |> 
  summarise(cent = mean(range(value,na.rm=TRUE)), ampl = diff(range(value,na.rm=TRUE))) |> 
  mutate(lower = cent - max(ampl)/2, 
         upper = cent + max(ampl)/2) |> 
  select(-c(cent, ampl))

outplot <- ptm_protein |>
  ggplot() +
  aes(x = colname,
      y = value) +
  geom_line(aes(group = rowname), linewidth = 0.1) +
  geom_point(aes(colour = sampleGroup)) +
  facet_wrap(~ assay, scales = "free") +
  ggh4x::facetted_pos_scales(
    y = list(
      assay == ylims$assay[1] ~ scale_y_continuous(limits = unlist(ylims[1,c("lower","upper")])),
      assay == ylims$assay[2] ~ scale_y_continuous(limits = unlist(ylims[2,c("lower","upper")])),
      assay == ylims$assay[3] ~ scale_y_continuous(limits = unlist(ylims[3,c("lower","upper")]))
    )
    ) +
  ggtitle(target_feature) +
  theme_minimal() +
  theme(axis.text.x = element_blank())
print(outplot)
}
```

```{r}
for (i in 1:10){
target_feature <- inferencesPTM |> 
  filter(feature %in% inferencesUsage$feature) |>
  filter(contrast == colnames(L)[2]) |>
  arrange(pval) |> 
  pull(feature)
target_feature <- target_feature[i]

ptm <-  qf[target_feature, , c("precursorsPTM_norm", "usage")] |> #1
  longForm(colvars = colnames(colData(qf)), rowvars = "PG_ProteinGroups") |> #2
  data.frame()
protein <- qf[unique(ptm$PG_ProteinGroups), , c("proteins")] |> #1
  longForm(colvars = colnames(colData(qf)), rowvars = "PG_ProteinGroups") |> #2
  data.frame()

ptm_protein <- rbind(ptm, protein)
ylims <- ptm_protein |> 
  group_by(assay) |> 
  summarise(cent = mean(range(value,na.rm=TRUE)), ampl = diff(range(value,na.rm=TRUE))) |> 
  mutate(lower = cent - max(ampl)/2, 
         upper = cent + max(ampl)/2) |> 
  select(-c(cent, ampl))

outplot <- ptm_protein |>
  ggplot() +
  aes(x = colname,
      y = value) +
  geom_line(aes(group = rowname), linewidth = 0.1) +
  geom_point(aes(colour = sampleGroup)) +
  facet_wrap(~ assay, scales = "free") +
  ggh4x::facetted_pos_scales(
    y = list(
      assay == ylims$assay[1] ~ scale_y_continuous(limits = unlist(ylims[1,c("lower","upper")])),
      assay == ylims$assay[2] ~ scale_y_continuous(limits = unlist(ylims[2,c("lower","upper")])),
      assay == ylims$assay[3] ~ scale_y_continuous(limits = unlist(ylims[3,c("lower","upper")]))
    )
    ) +
  ggtitle(target_feature) +
  theme_minimal() +
  theme(axis.text.x = element_blank())
print(outplot)
}
```

```{r}
library(omicsGMF)
seP <- getWithColData(qf, "precursorsPTM_norm") |> 
  as("SingleCellExperiment")
X <- model.matrix(~diet*sex,colData(se))
seP <- runGMF(
    seP, 
    X = X,
    family = gaussian(), 
    ncomponents = 3, 
    name = "GMF")
# se <- runCVGMF(
#     se, 
#     X = X,                          # Covariate matrix
#     family = gaussian(),            # Gaussian model for proteomics data
#     ncomponents = c(1:5))  
```

```{r}
plotReducedDim(seP, dimred = "GMF", colour_by = "sampleGroup")
```


```{r}
library(omicsGMF)
se <- getWithColData(qf, "proteins") |> 
  as("SingleCellExperiment")
seN <- runGMF(
    se, 
    family = gaussian(), 
    ncomponents = 3, 
    name = "GMF")
# se <- runCVGMF(
#     se, 
#     X = X,                          # Covariate matrix
#     family = gaussian(),            # Gaussian model for proteomics data
#     ncomponents = c(1:5))  
```

```{r}
plotReducedDim(seN, dimred = "GMF", colour_by = "sampleGroup")
```