Application of PepsNMR on the Human Serum dataset
2021-01-14
Package
PepsNMR 1.8.1
1 Introduction
This document provides a brief summary on how to use the PepsNMR package. In this package, pre-processing functions transform raw FID signals from 1H NMR spectroscopy into a set of interpretable spectra.
2 Installation
The PepsNMR package is available on Bioconductor and can be installed via BiocManager::install:
if (!requireNamespace("BiocManager", quietly = TRUE))
install.packages("BiocManager")
BiocManager::install("PepsNMR",
dependencies = c("Depends", "Imports", "Suggests"))Note tha installing the Suggests dependencies will install the PepsNMRData package to run the demo below.
The package needs to be loaded once installed to be used:
library(PepsNMR)The package development version is available on Github (Master branch): https://github.com/ManonMartin/PepsNMR, although it is highly recommended to rely on the Bioconductor release version of the package to avoid any package version mismatch.
3 Data importation
The first step is meant to access the raw data files. To import Free Induction Decays (FIDs) in Bruker format, use the ReadFids function. This function will return a list with the FID data matrix (saved in Fid_data) and metadata about these FIDs (saved in Fid_info).
fidList <- ReadFids(file.path(path,dataset_name))
Fid_data <- fidList[["Fid_data"]]
Fid_info <- fidList[["Fid_info"]]The possible directory structures are illustrated here:
Figure 1: Accepted directory structures for the raw Bruker files
And is to be linked with the possible options of the ReadFids function:
- If use of title file and presence of sub-directories: set the FID Title line,
subdirs = TRUE,dirs.names = FALSE - If use of title file and no sub-directories: set the FID Title line,
subdirs = FALSE,dirs.names = FALSE - If no use of title file and presence of sub-directories:
subdirs = TRUE,dirs.names = TRUE - If no use of title file and no sub-directories:
subdirs = FALSE,dirs.names = TRUE
4 Pre-processing steps
Here is the recommended pre-processing workflow on the FIDs and the spectra once the raw data have been loaded in R:
| Steps | Description |
|---|---|
| Group Delay Correction | Correct for the Bruker Group Delay. |
| Solvent Suppression | Remove the solvent signal from the FIDs. |
| Apodization | Increase the Signal-to-Noise ratio of the FIDs. |
| ZeroFilling | Improve the visual representation of the spectra. |
| Fourier Transform | Transform the FIDs into a spectrum and convert the frequency scale (Hz -> ppm). |
| Zero Order Phase Correction | Correct for the zero order phase dephasing. |
| Internal Referencing | Calibrate the spectra with an internal reference compound. Referencing with an internal (e.g. TMSP at 0 ppm) |
| Baseline Correction | Remove the spectral baseline. |
| Negative Values Zeroing | Set negatives values to 0. |
| Warping | Warp the spectra according to a reference spectrum. |
| Window Selection | Select the informative part of the spectrum. |
| Bucketing | Data reduction. |
| Region Removal | Set a desired spectral region to 0. |
| Zone Aggregation | Aggregate a spectral region into a single peak. |
| Normalization | Normalize the spectra. |
Information on each function is provided in R, (e.g. type ?ReadFids in the R console) and methodological details are found in Martin et al. (2018).
5 Available datasets
Human serum (HS) and urine (HU) datasets are available as raw data (FIDs in Bruker format) and as (partially) pre-processed signals/spectra in the ad hoc PepsNMRData package that is automatically installed with PepsNMR (through ).
Here are examples of available datasets:
library(PepsNMRData)
str(FidData_HU)
#> cplx [1:24, 1:29411] 0+0i 0+0i 0+0i ...
#> - attr(*, "dimnames")=List of 2
#> ..$ : chr [1:24] "S1-D0-E1" "S1-D0-E2" "S1-D1-E2" "S2-D0-E2" ...
#> ..$ : chr [1:29411] "0" "5.1e-05" "0.000102" "0.000153" ...
str(FinalSpectra_HS)
#> cplx [1:32, 1:500] 0-371030i 0-362686i 0-216899i ...
#> - attr(*, "dimnames")=List of 2
#> ..$ : chr [1:32] "J1-D1-1D-T1" "J3-D2-1D-T8" "J3-D3-1D-T9" "J3-D4-1D-T14" ...
#> ..$ : chr [1:500] "9.98986984692192" "9.97027064485524" "9.95067144278856" "9.93107224072187" ...Information for each dataset is available, (e.g. enter ?FidData_HS in the R Console).
6 Demo on the HSerum dataset
6.1 Load the data
Raw Bruker FIDs can be loaded from where PepsNMRData has been intalled:
data_path <- system.file("extdata", package = "PepsNMRData")
dir(data_path)
#> [1] "Group_HS.csv" "HumanSerum"6.2 Read the FID data file
To import FIDs in Bruker format, the ReadFids function is used. This function will return a list with the FID data matrix (here saved as Fid_data) and information about these FIDs (here saved as Fid_info).
# ==== read the FIDs and their metadata =================
fidList <- ReadFids(file.path(data_path, "HumanSerum"))
Fid_data0 <- fidList[["Fid_data"]]
Fid_info <- fidList[["Fid_info"]]
kable(head(Fid_info))| TD | BYTORDA | DIGMOD | DECIM | DSPFVS | SW_h | SW | O1 | DTYPA | DT | |
|---|---|---|---|---|---|---|---|---|---|---|
| J1-D1-1D-T1 | 65536 | 1 | 1 | 16 | 12 | 10245.9 | 20.48638 | 2352.222 | 0 | 4.88e-05 |
| J3-D2-1D-T8 | 65536 | 1 | 1 | 16 | 12 | 10245.9 | 20.48638 | 2352.222 | 0 | 4.88e-05 |
| J3-D3-1D-T9 | 65536 | 1 | 1 | 16 | 12 | 10245.9 | 20.48638 | 2352.222 | 0 | 4.88e-05 |
| J3-D4-1D-T14 | 65536 | 1 | 1 | 16 | 12 | 10245.9 | 20.48638 | 2352.222 | 0 | 4.88e-05 |
| J4-D1-1D-T4 | 65536 | 1 | 1 | 16 | 12 | 10245.9 | 20.48638 | 2352.222 | 0 | 4.88e-05 |
| J4-D2-1D-T7 | 65536 | 1 | 1 | 16 | 12 | 10245.9 | 20.48638 | 2352.222 | 0 | 4.88e-05 |
Figure 2: Raw FID
6.3 Group Delay Correction
The Bruker’s digital filter originally produces a Group Delay that is removed during this step.
# ==== GroupDelayCorrection =================
Fid_data.GDC <- GroupDelayCorrection(Fid_data0, Fid_info)
Figure 3: Signal before and after the Group Delay removal
6.4 Solvent Suppression
Pre-acquisition techniques for solvent suppression can be unsufficient to remove the solvent signal from the FIDs. SolventSuppression estimates and removes this residual solvent signal based on a Whittaker smoother.
# ==== SolventSuppression =================
SS.res <- SolventSuppression(Fid_data.GDC, returnSolvent=TRUE)
Fid_data.SS <- SS.res[["Fid_data"]]
SolventRe <- SS.res[["SolventRe"]]
Figure 4: Signal before and after the Residual Solvent Removal
6.5 Apodization
The apodization step increases the spectral Signal-to-Noise ratio by multiplying the FIDs by an appropriate factor (by default a negative exponential).
# ==== Apodization =================
Fid_data.A <- Apodization(Fid_data.SS, Fid_info)
Figure 5: Signal before and after Apodization
6.6 Zero Filling
The zero filling adds 0 to the end of the FIDs to improve the visual representation of spectra.
# ==== Zero Filling =================
Fid_data.ZF <- ZeroFilling(Fid_data.A, fn = ncol(Fid_data.A))
Figure 6: Signal before and after Apodization
6.7 FourierTransform
The Fourier Transform is applied to the FIDs to obtain spectra expressed in the frequency domain. The FourierTransform function further converts this frequency scale originally in hertz into parts per million (ppm).
# ==== FourierTransform =================
RawSpect_data.FT <- FourierTransform(Fid_data.ZF, Fid_info)
Figure 7: Spectrum after FT
6.8 Zero Order Phase Correction
After Fourier Transform, the spectra need to be phased for the real part to be in pure absoptive mode (i.e. with positive intensities).
# ==== ZeroOrderPhaseCorrection =================
Spectrum_data.ZOPC <- ZeroOrderPhaseCorrection(RawSpect_data.FT)
# with a graph of the criterion to maximize over 2pi
Spectrum_data.ZOPC <- ZeroOrderPhaseCorrection(RawSpect_data.FT,
plot_rms = "J1-D1-1D-T1")
Figure 8: Spectrum after Zero Order Phase Correction
6.9 Internal Referencing
During this step, the spectra are aligned with an internal reference compound (e.g. with the TMSP). The user determines the ppm value of the reference compound which is by default 0.
# ==== InternalReferencing =================
target.value <- 0
IR.res <- InternalReferencing(Spectrum_data.ZOPC, Fid_info,
ppm.value = target.value,
rowindex_graph = c(1,2))
# draws Peak search zone and location of the 2 first spectra
IR.res$plots
#> [[1]]
Spectrum_data.IR <- IR.res$Spectrum_data
Figure 9: Spectrum after Internal Referencing
6.10 Baseline Correction
The spectral baseline is estimated and removed from the spectral profiles with the Asymetric Least Squares smoothing algorithm.
# ==== BaselineCorrection =================
BC.res <- BaselineCorrection(Spectrum_data.IR, returnBaseline = TRUE,
lambda.bc = 1e8, p.bc = 0.01)
Figure 10: Spectrum before and after the Baseline Correction
6.11 Negative Values Zeroing
The remaining negative values are set to 0 since they cannot be interpreted.
# ==== NegativeValuesZeroing =================
Spectrum_data.NVZ <- NegativeValuesZeroing(Spectrum_data.BC)
Figure 11: Spectrum after Negative Values Zeroing
6.12 Warping
The spectra are realigned based on a reference spectrum with a Semi-Parametric Time Warping technique.
# ==== Warping =================
W.res <- Warping(Spectrum_data.NVZ, returnWarpFunc = TRUE,
reference.choice = "fixed")
Spectrum_data.W <- W.res[["Spectrum_data"]]
warp_func <- W.res[["Warp.func"]]
Figure 12: Spectrum before and after the Baseline Correction
6.13 Window Selection
During this step the user selects the part of the spectrum that is of interest and the other parts are removed from the spectral matrix.
# ==== WindowSelection =================
Spectrum_data.WS <- WindowSelection(Spectrum_data.W, from.ws = 10,
to.ws = 0.2)
Figure 13: Spectrum after Window Selection
6.14 Bucketing
The Bucketing function reduces the number of spectral descriptors by aggregating intensities into a series of buckets.
# ==== Bucketing =================
Spectrum_data.B <- Bucketing(Spectrum_data.WS, intmeth = "t")
Figure 14: Spectrum before and after Bucketing
6.15 Region Removal
By default, this step sets to zero spectral areas that are of no interest or have a sigificant and unwanted amount of variation (e.g. the water area).
# ==== RegionRemoval =================
Spectrum_data.RR <- RegionRemoval(Spectrum_data.B,
typeofspectra = "serum")
Figure 15: Spectrum after Region Removal
6.16 Normalization
The normalization copes with the dilution factor and other issues that render the spectral profiles non-comparable to each other.
# ==== Normalization =================
Spectrum_data.N <- Normalization(Spectrum_data.RR, type.norm = "mean")
Figure 16: Spectrum before and after Normalization
Note: the function ZoneAggregation is not used here, but is can be applied e.g. to urine spectra to aggregate the citrate peak.
7 Final spectra visualisation
The Draw function enables to produce line plots with type.draw = "signal" or PCA results with type.draw = "pca" of FIDs or spectra. These plots can be saved as pdf files with the option output = "pdf", see ?Draw, ?DrawSignal and ?DrawPCA for more details on the other available options.
Draw(Spectrum_data.N[1:4,], type.draw = c("signal"),
subtype= "stacked", output = c("default"))
Figure 17: 4 first pre-processed spectra
Draw(Spectrum_data.N, type.draw = c("pca"),
output = c("default"), Class = Group_HS,
type.pca = "scores")
Figure 18: PCA scores of the pre-processed spectra
Draw(Spectrum_data.N, type.draw = c("pca"),
output = c("default"),
Class = Group_HS, type.pca = "loadings")
Figure 19: PCA loadings of the pre-processed spectra
8 Session info
sessionInfo()
#> R version 4.0.3 (2020-10-10)
#> Platform: x86_64-pc-linux-gnu (64-bit)
#> Running under: Ubuntu 18.04.5 LTS
#>
#> Matrix products: default
#> BLAS: /home/biocbuild/bbs-3.12-bioc/R/lib/libRblas.so
#> LAPACK: /home/biocbuild/bbs-3.12-bioc/R/lib/libRlapack.so
#>
#> locale:
#> [1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
#> [3] LC_TIME=en_US.UTF-8 LC_COLLATE=C
#> [5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
#> [7] LC_PAPER=en_US.UTF-8 LC_NAME=C
#> [9] LC_ADDRESS=C LC_TELEPHONE=C
#> [11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
#>
#> attached base packages:
#> [1] stats graphics grDevices utils datasets methods base
#>
#> other attached packages:
#> [1] PepsNMRData_1.8.0 PepsNMR_1.8.1 knitr_1.30 BiocStyle_2.18.1
#>
#> loaded via a namespace (and not attached):
#> [1] Rcpp_1.0.5 highr_0.8 plyr_1.8.6
#> [4] nloptr_1.2.2.2 compiler_4.0.3 pillar_1.4.7
#> [7] BiocManager_1.30.10 tools_4.0.3 digest_0.6.27
#> [10] evaluate_0.14 lifecycle_0.2.0 tibble_3.0.4
#> [13] gtable_0.3.0 lattice_0.20-41 pkgconfig_2.0.3
#> [16] rlang_0.4.10 Matrix_1.3-2 magick_2.6.0
#> [19] yaml_2.2.1 xfun_0.20 gridExtra_2.3
#> [22] stringr_1.4.0 dplyr_1.0.2 generics_0.1.0
#> [25] vctrs_0.3.6 grid_4.0.3 tidyselect_1.1.0
#> [28] glue_1.4.2 R6_2.5.0 ptw_1.9-15
#> [31] rmarkdown_2.6 bookdown_0.21 farver_2.0.3
#> [34] reshape2_1.4.4 ggplot2_3.3.3 purrr_0.3.4
#> [37] magrittr_2.0.1 matrixStats_0.57.0 scales_1.1.1
#> [40] htmltools_0.5.1 ellipsis_0.3.1 colorspace_2.0-0
#> [43] labeling_0.4.2 stringi_1.5.3 munsell_0.5.0
#> [46] crayon_1.3.4References
Martin, Manon, Benoît Legat, Justine Leenders, Julien Vanwinsberghe, Réjane Rousseau, Bruno Boulanger, Paul H. C. Eilers, Pascal De Tullio, and Bernadette Govaerts. 2018. “PepsNMR for 1H NMR Metabolomic Data Pre-Processing.” Analytica Chimica Acta 1019: 1–13. https://doi.org/10.1016/j.aca.2018.02.067.