RMassBank is a two-part computational mass spectrometry workflow:
This vignette describes basic usage with the standard workflow. The package is flexible and allows for different advanced use cases. Examples of specialized applications of RMassBank are available at the RMassBank message board hosted by the Metabolomics-Forum: (http://www.metabolomics-forum.com/viewforum.php?f=29).
The library is available from Bioconductor ((http://www.bioconductor.org)). In addition to the library itself, it is recommended to install the OpenBabel chemical toolkit, available from (http://www.openbabel.org) for various platforms (or via Linux package distribution systems).
The library is loaded as follows
## Loading required package: Rcpp
The data used in the following example is available as a package RMassBankData, which must be installed separately and is loaded using
RMassBank handles high-resolution LC/MS spectra in mzML format in centroid1 The term “centroid” here refers to any kind of data which are not in profile mode, i.e. don’t have continuous m/z data. It does not refer to the (mathematical) centroid peak, i.e. the area-weighted mass peak. or in profile mode.
Data in the examples was acquired using an LTQ Orbitrap XL instrument in profile mode, and converted from profile-mode RAW into centroid-mode mzML using MSConvertGUI from ProteoWizard. The settings were as shown in the screenshot below (note the “Peak Picking” filter.)
Fig. 1: ProteoWiz settings for conversion to mzML
In the standard workflow, the file names are used to identify a
compound: file names must be in the format
where the xxx parts denote anything and the 1234 part denotes the compound ID in
the compound list (see below). Advanced and alternative uses can be implemented;
consult the implementation of
A compound list in CSV format is required to identify all compounds unambiguously.
The CSV file is required to have at least the following columns, which are used for
further processing and must be named correctly (but present in any order):
ID, Name, SMILES, RT, CAS. The columns
SMILES must be filled, the other columns
must be present in the file but do not need to be filled.
ID specifies an (arbitrary) numeric ID code which must be < 4 digits long;
a SMILES code with the chemical structure of the compound (and is used to extract the
molecular formula, for calculation of molecular masses, for database searching in CTS etc.)
Although the columns
Name, RT, CAS have to be present, the
information in the columns is only used if the cells are filled.
RT, if present, specifies the retention time (in minutes; \(\pm\) a window specified in the RMassBank options, see below)
where a LC/MS file is searched for the compound spectra.
are used as additional information while retrieving annotations from CTS. The
compound list doesn’t have to be ordered in any particular way. It can contain large numbers of compounds,
even compounds which will not be actively used by the script (Note: Unused compounds
don’t require a SMILES code, since they will not be accessed.)
An example list is provided with the RMassBankData package, and can be copied into a local folder, viewed and edited:
file.copy(system.file("list/NarcoticsDataset.csv", package="RMassBankData"), "./Compoundlist.csv")
##  TRUE
A number of different settings influence RMassBank. They are partly parameters for data processing and partly constants used for annotation.
A settings template file, to be edited by hand, can be generated using
mysettings.ini is the file that will be generated. This file
should then be edited. Important settings are:
deprofile: Whether to use a deprofiling algorithm to work with profile-mode data. Default is
NAfor use with centroid-mode data. Allowed settings for profile-mode data include
deprofile.fwhm(full-width half-maximum algorithm),
deprofile.spline(cubic spline algorithm),
deprofile.localmax(local maximum). See the respective help pages for detailed information.
rtMargin: The deviation allowed for retention times (in minutes) when extracting spectra from raw data files.
rtShift: The systematic retention time shift (in minutes) in the LC-MS data compared to the values in the compound list.
babeldir: The directory pointing to the OpenBabel binaries.
use_version: which MassBank data format to use. The default is the newer version 2; alternatively, the (deprecated) version 1 can be specified for MassBank servers running old versions of the server software.
use_rean_peaks: Whether or not peaks from reanalysis should be used (see below for details.)
add_annotation: Whether or not fragments should be annotated with the (tentative) molecular formula in MassBank records.
annotations: A list of annotation data used in the MassBank records.
compound_class: values for the corresponding MassBank fields
confidence_comment: A commentary field about “compound confidence” which is added like “COMMENT: CONFIDENCE standard compound” in the MassBank record.
internal_id_fieldname: The name for an internal ID field in the MassBank record where to store the compound ID (in the compound list). For
internal_id_fieldname= “MY_ID”, the ID will be stored like “COMMENT: MY_ID 1234”.
entry_prefix: The (2-letter) prefix for MassBank accession IDs.
lc_*: Annotations for the LC and MS information fields in the MassBank records.
ms_dataprocessing: Tags added to describe the data processing. In addition to the tags specified here, MS$DATA_PROCESSING: WHOLE RMassBank will be added (corresponding to a list(“WHOLE” = “RMassBank”) entry for this option.)
annotator: For advanced users: option to select your own custom annotator. Check ?annotator.default and the source code for details.
spectraList: The list of data-dependent scans triggered by a MS1 scan in their order; used for annotation of MassBank records. See the template file for description.
accessionBuilderType: A string (either “standard”, “simple” or “selfDefined”) to determine how to generate MassBank record accession numbers (optional, default: “standard”). RMassBank generates an accession number for each record. The structure and generation of this number varies based on
annotations$entry_prefix, the first four digits are given by the compound ID. The last two digits are generated from the position of the spectrum in
spectraListand the shift defined in
accessionNumberShiftsfor the selected ion type (Example: the compound with ID 2112, processed in “pNa” mode ([M+Na]+), will have accession numbers XX211233, XX211234 … etc in for the first, second… spectrum in the data-dependent scan, if the “pNa” shift is set to 32.)
annotations$entry_prefix, the 6 digit code is generated from the position of the spectrum in
spectraListand the shift given in
accessionNumberStart. Leading zeros are added if necessary. (Example: accession numbers XX000043, XX000045 … will be generated for the first, second … spectrum in the data-dependent scan if
accessionNumberStartis set to 32.)
accessionBuilderFile. In particular, there is no constraint on the prefix and
annotations$entry_prefixwill be ignored, if this option is chosen. The function definition must be in the form
accessionBuilder <- function(cpd, spectrm, subscan). Note: This functionality is quite advanced. If you really want to specify your own
accessionBuilderinstead of using the “simple” or “standard” option, we highly encourage you to familiarize yourself with the source code of the function
accessionNumberShifts: A list defining the starting points for generating MassBank record accession numbers. This will be used if
accessionBuilderTypeis unspecified or “standard” (see
accessionBuilderFile: A file with a user-defined function to generate MassBank record accession numbers. This will be used if
accessionBuilderTypeis “selfDefined” (see
accessionNumberStart: An integer < 1000000 defining the starting point of MassBank record accession numbers. This will be used if
accessionBuilderTypeis “simple”. (see
recalibrateBy: Which parameter to use for recalibration:
dppm(recalibrate the deviation in ppm) or
dmz(recalibrate the m/z deviation).
recalibrateMS1: Whether to recalibrate MS1 data points separately from MS2 data points (
"separate"), with the same recalibration curve as the MS2 data points (
"common") or not at all (
"none"). Note that the MS1 datapoints points will be used to generate the MS2 recalibration curve in all cases (since this makes the recalibration curve in high-m/z regions better-defined) but may be recalibrated independently themselves, if desired.
recalibrator: Sets the functions to use for recalibration. Defaults to
list(MS1="recalibrate.loess", MS2="recalibrate.loess")which uses a Loess non-parametric fit to generate a recalibration curve. Any custom function may be specified. The function is expected to accept a dataset with variables
mzFoundand to return an object which can be used with
predict(). The input
recalfieldis the value to be estimated by recalibration - it will either contain delta ppm values or absolute mass deviations, depending on the setting for
recalibrateBy. In addition to
recalibrate.MS1is predefined, which uses a GAM model for recalibration and appears to work well for pure MS1 datapoints. However, common recalibration for MS1 and MS2 appears to be the best option in general.
multiplicityFilter: Define the multiplicity filtering level. Default is 2, a value of 1 is off (no filtering) and >2 is harsher filtering.
titleFormat: The title of MassBank records is a mini-summary of the record, for example “Dinotefuran; LC-ESI-QFT; MS2; CE: 35%; R=35000; [M+H]+”. By default, the first compound name
CH$NAME, instrument type
AC$INSTRUMENT_TYPE, MS/MS type
AC$MASS_SPECTROMETRY: MS_TYPE, collision energy
AC$MASS_SPECTROMETRY: RESOLUTIONand precursor
MS$FOCUSED_ION: PRECURSOR_TYPEare used. If alternative information is relevant to differentiate acquired spectra, the title should be adjusted. For example, many TOFs do not have a resolution setting. See MassBank documentation for more.
filterSettings: A list of settings that affect the MS/MS processing.
ppmLowMass: values for pre-processing, prior to recalibration. The default settings (for e.g. Orbitrap) is 10 ppm for high mass range, 15 ppm for low mass range (defined by
massRangeDivision: The m/z value defining the split between
ppmLowMassabove. The default m/z 120 is recommended for Orbitraps.
ppmFine: This defines the ppm cut-off post recalibration. The default value of 5 ppm is recommended for Orbitraps.
prelimCutRatio: Intensity cut-off and cut-off ratio (in % of the most intense peak) for pre-processing. Affects peak selection for the recalibration only. Careful: the default 1e4 for Orbitrap LTQ positive could remove all peaks for TOF data and will remove too many peaks for Orbitrap LTQ negative mode spectra!
specOKLimit: MS/MS must have at least one peak above this limit present to be processed.
dbeMinLimit: The minimum allowable ring and double bond equivalent (DBE) allowed for assigned formulas. Assumes maximum valences for elements with multiple possible valences. Default is -0.5 (accounting for fragment peaks being ions).
satelliteIntLimit: Cut-off m/z and intensity values for satellite peak removal. All peaks within the m/z (default 0.5) and intensity ratio (default 0.05 or 5 %) of the respective peak will be removed. Applicable to Fourier Transform instruments (e.g. Orbitrap).
findMsMsRawSettings: Parameters for adjusting the raw data retrieval.
ppmFine: The ppm error to look for the precursor in the MS1 (parent) spectrum. Default is 10 ppm for Orbitrap.
mzCoarse: The error to search for the precursor specification in the MS2 spectrum. This is often only saved to 2 decimal places and thus inaccurate and may also depend on the isolation window. The default settings (for e.g. Orbitrap) is m/z=0.5 for
fillPrecursorScan: The default value (FALSE) assumes all necessary precursor information was available in the mzML file. A setting of TRUE tries to fill in the precursor data scan number if it is missing.
See also the manpage
?RmbSettings for a description of all RMassBank
In the first part of the workflow, spectra are extracted from the files and processed. In the following example, we will process the narcotics spectra from the RMassBankData package.
For the workflow to work correctly, a settings file (generated as above and edited accordingly) before must be loaded first.
## Warning in readLines(con): incomplete final line found on 'mysettings.ini'
(Note: the template file generated by
RmbSettingsTemplate() has no OpenBabel
Correspondingly, RMassBank will use the CACTUS service instead to generate MOL
files. For your actual use, it is strongly recommended to install OpenBabel and
specify its install directory in the settings! The CACTUS structures are
visually less appealing since they have all hydrogen atoms explicit, and CACTUS
is only a backup solution.)
First, create a workspace for the
w <- newMsmsWorkspace()
The full paths of the files must be loaded into the container in the array
files <- list.files(system.file("spectra", package="RMassBankData"), ".mzML", full.names = TRUE) basename(files)
##  "1_3_Chlorophenyl_piperazin_2818_pos.mzML" ##  "1_3_Trifluoromethylphenyl_piperazin_2819_pos.mzML" ##  "1_Benzylpiperazin_2820_pos.mzML" ##  "Amitriptylin_2821_pos.mzML" ##  "Amphetamin_2822_pos.mzML" ##  "Benzoylecgonin_2823_pos.mzML" ##  "Cocain_2817_pos.mzML" ##  "Dextromethorphan_2824_pos.mzML" ##  "EDDP_2_Ethyl_1_5_dimethyl_3_3_diphenylpyrrolinium_2825_pos.mzML" ##  "Ephedrin_2758_pos.mzML" ##  "Ketamin_2826_pos.mzML" ##  "Mephedron_4_Methylmethcathinon_2827_pos.mzML" ##  "Methadon_2828_pos.mzML" ##  "Methamphetamin_2829_pos.mzML" ##  "Naltrexon_2830_pos.mzML"
# To make the workflow faster here, we use only 2 compounds: w@files <- files[1:2]
Note the position of the compound IDs in the filenames. Historically, the “
pos” at the end was used to denote the polarity; it is obsolete now, but the ID must be terminated with an underscore.
Additionally, the compound list must be loaded using
using the formerly copied list from RMassBankData):
## Loaded compoundlist successfully
This creates a variable
compoundList in the global environment, which stores the compound data.
Now, we can start the complete workflow to extract [M+H]+ spectral data. The
workflow standard workflow consists of 8 steps.
archivename specifies the prefix under which to store the analyzed result
files. The argument
mode specifies the processing mode:
pH (positive H)
pNa specifies [M+Na]+,
pM specifies [M]+,
mFA specify [M-H]- and [M+FA]-, respectively. (I apologize for the naming of
which has absolutely nothing to do with chemical pH values.)
Basically, this runs through the entire workflow, which is explained in more detail below:
* Step 1: using the function
findMsMsHR, all the files in
files are searched for MS2 spectra of their respective compound. The found spectra are stored in the array
* Step 2: A molecular formula fit is attempted for every peak, using the molecular formula of the parent compound as limiting formula, using the function
analyzeMsMs. The results are stored in the array
* Step 3: The analyzed spectra from the array
analyzedSpecs are aggregated into the list
aggregatedSpecs. This uses the function
* Step 4: Using the function
recalibrateSpectra, a recalibration curve is calculated from the peaks in
aggregatedSpecs, and all spectra from
specs are recalibrated using this curve. The result is stored in
recalibratedSpecs. The recalibration curve is stored in
* Step 5: The recalibrated spectra (
recalibratedSpecs) are re-analyzed with
analyzeMsMs and the results stored in
* Step 6: The reanalyzed recalibrated spectra are aggregated with
aggregatedRcSpecs. Unmatched peaks in
aggregatedRcSpecs are cleaned from known electronic noise using
cleanElnoise. A backup copy of all present results is saved as
* Step 7: Using
reanalyzeFailpeaks, all unmatched peaks from spectra in
aggregatedRcSpecs are reanalyzed, allowing \(N_2O\) as additional elements (to account for oxidation products and \(N_2\) adducts). The results are stored in
reanalyzedRcSpecs. A backup copy of all present results is saved as
* Step 8: The function
filterMultiplicity is applied to the peaks: Peaks which occur only once in all analyzed spectra of a compound are eliminated. The filtered list is stored under
refilteredSpecs, and a final version of all results is saved as
filterMultiplicity creates a CSV file with a list of (relatively) high-intensity unassigned peaks with the name
archivename``_Failpeaks.csv, which should be manually checked. Peaks to include must be marked with OK = 1.
The steps can be called individually using the
steps parameter of
newRecalibration parameter, one can specify if RMassBank should do a new
TRUE) or use the recalibration curve stored in
FALSE). This is useful for re-using a recalibration curve in the reanalysis of the same
data in another mode: After the detection and processing of all [M+H]+ spectra, which will be
present for a large number of compounds, one can rerun the workflow with
newRecalibration = F, mode="pNa"
and reuse the same calibration curve for Na adduct spectra (which on their own would be too few
for a sufficiently good recalibration curve.) The
useRtLimit parameter activates or
deactivates the usage of retention time constraints when searching for spectra with
It is useful to perform the workflow in two blocks, the first being step 1-4 and
the second being 5-8. After step 4, a graph is displayed which allows the user
to visually evaluate the performance of the recalibration. The top graphs show
the distribution of the mass deviation of MS/MS fragments from the predicted
mass and the recalibration curve calculated from them; the bottom graphs show
the mass deviation of MS precursor ions. The graph to the left is a complete xy
plot while the graph to the right is a 2D histogram (if the package
installed on the user’s computer).
TODO: Workflow execution in Chunk 10 is currently disabled, I execute Chunk 11 instead for steps that are already done.
w <- msmsWorkflow(w, mode="pH", steps=c(1:4), archivename = "pH_narcotics")
## msmsWorkflow: Step 1. Acquire all MSMS spectra from files
## msmsWorkflow: Step 2. First analysis pre recalibration
## msmsWorkflow: Step 3. Aggregate all spectra
## msmsWorkflow: Step 4. Recalibrate m/z values in raw spectra
## msmsWorkflow: Done.