• Overview

    Software tools and databases for metabolomics and lipidomics


    Universal software for untargeted metabolomics and lipidomics


    Searching spectra/structures for unknown metabolites


    Universal software for widely targeted metabolomics and lipidomics

  • Statistics in Microsoft Excel

    Graph analysis, T-test, PCA, PLS-DA, PLS-regression in Excel

New Features and Changes

New features:
1. One parameter 'gap filling by compulsion' is added: if unchecked, gap-filling is performed only when local maximum exists.
2. MS-DIAL now evaluates signal to noise (S/N) ratios to improve the peak picking results.
3. PLS-regression, PLS-DA, OPLS-regression, and OPLS-DA are now available at MS-DIAL.
4. Pathway mapping is executable in lipidomics project (please wait a bit for metabolomics project).
5. Rule-based lipid annotations are implemented in this program (e.g. SM d18:1/24:0 is abbrebated to SM d42:1 when the diagnostic ion is not detected.
(The rules are now implemented for PC, PE, PS, PI, PG, BMP, TAG, SM, LNAPS, and LNAPE. The others are also implemented when I have much time.)
6. New deconvolution algorighm (correlation-based deconvolution) is implemented for DIA-MS data, which is optimized for MSE, all-ions, and all ion fragmentation technologies.
7. Several lipid classes and adduct forms are also implemented especially in positive ion mode.
8. For the lipidomics library, the reference file of 'AritaM (Makoto Arita laboratory, Japan)' is now set as default (previously FiehnO was the default set).


MS-DIAL 3.30 new features:
1. MS-DIAL allows users to edit peaks in the result of peak alignment: check 'right click' feature on the 'aligned EIC' tab of the top panel of MS-DIAL.
2. New lipid theoretical MS/MS database (version 39) was released, which includes Ether LPC/LPE, sphingosine, SPLASH standards, LipidA etc.
3. Many bugs were fixed and many minor utility updates were performed for MS-DIAL lecture in Japan.
4. An option not to use the criteria of monotonically decreasing ions in isotope recognition process was created to deal with Br and Cl containing metabolites.
1. Bug fixed in parsing MSP and MAT files.

Change log
Software publications
  • Advances in computational metabolomics and databases deepen the understanding of metabolisms. Current Opinion in Biotechnology, 54, 10-17, 2018 [ScienceDirect link]
  • Identifying metabolites by integrating metabolome databases with mass spectrometry cheminformatics. Nature Methods, 15, 53-56, 2018 [NPG link]
  • Integrated strategy for unknown EI–MS identification using quality control calibration curve, multivariate analysis, EI–MS spectral database, and retention index prediction. Analytical Chemistry, 89, 6766-6773, 2017 [ACS link]
  • The importance of bioinformatics for connecting data-driven lipidomics and biological insights. BBA-Molecular and Cell Biology of Lipids, 8, 762-765, 2017 [ScienceDirect link]
  • Comprehensive identification of sphingolipid species by in silico retention time and tandem mass spectral library. Journal of Cheminformatics, 9:19, 2017 [Springer link]
  • Automation of chemical assignment for identifying molecular formula of S-containing metabolites by combining metabolomics and chemoinformatics with 34S labeling. Metabolomics, 12:168, 2016 [Springer link]
  • Hydrogen rearrangement rules: computational MS/MS fragmentation and structure elucidation using MS-FINDER software. Analytical Chemistry, 88, 7946-7958, 2016 [ACS page]
  • MS-DIAL: data independent MS/MS deconvolution for comprehensive metabolome analysis. Nature Methods, 12, 523-526, 2015 [PubMed]
  • MRM-DIFF: Data Processing Strategy for Differential Analysis in Large Scale MRM-based Lipidomics Studies. Frontiers in Genetics, 5:471, 2014 [PubMed]
  • MRMPROBS Suite for metablomics using large-scale MRM assays. Bioinformatics, 30, 2379-2380, 2014 [PubMed]
  • MRMPROBS: A Data Assessment and Metabolite Identification Tool for Large-Scale Multiple Reaction Monitoring Based Widely Targeted Metabolomics. Analytical Chemistry, 85, 5191-5199, 2013 [PubMed]
  • Practical non-targeted gas chromatography/mass spectrometry-based metabolomics platform for metabolic phenotype analysis. J. Biosci. Bioeng. 112, 292-298, 2011 [PubMed]
  • GC/MS based metabolomics: dvelopment of a data mining system for metabolite identification by using soft independent modeling of class analogy (SIMCA). BMC Bioinformatics 12: 131, 2011 [PubMed]
MS-DIAL 3.20, MS-FINDER 3.10 and MRMPROBS 2.46 were RELEASED.

In addition, EI-MS and MS/MS spectral databases were also updated to define the metabolite ontology for metabolites.

MS-DIAL 3.20 new features:
1. The quant mass manager for GC-MS based metabolomics was created where users can quantify the targeted metabolite by the defined m/z value.
2. The function for retention time correction by using diagnostic marker ions (basically authentic standard ions) was created.
3. The function linked to MRMPROBS was improved for DIA-MRM based metabolomics approach.

MS-FINDER 3.10 new features (in the command line application):
1. The 'annotate' function was added where users can assign ion substructures to mass spectra by importing the metabolite Formula and SMILES code and spectral information.
2. The 'generate' function was created, which provide all of possible substructure fragments as the neutralized form by importing SMILES code.
The 'generate' function was made for an education purpose.

MRMPROBS 2.46 new features:
The clash bug in analyzing 'empty' chroatogram was fixed.

MS-DIAL 3.12 and MRMPROBS 2.44 were RELEASED.
MS-DIAL 3.12 new features (the bug in importing the previous project at 3.10 was fixed):
1. The mzML parser was fixed to correctly import the mzML format from Shimadzu QTOFMS.
2. The isotope tracking function was improved by considering users feedback.
3. The functions for adduct picking, gap-filling, and duplicate peak recognition were improved.

MRMPROBS 2.44 new features:
The bug not matching the result in chromatogram viewers with the raw data matrix was fixed.

MS-DIAL 3.08 and MS-FINDER 3.04 were RELEASED.
Bug fixed:
The export function for isotope labeled tracking result in MS-DIAL was fixed.
GUIs of MS-DIAL and MS-FINDER were fixed.
BinVestigate searcher was fixed.

Bug fixed:
Several bugs in MS-DIAL graphical user interface for GC-MS and LC-MS projects were fixed.
The report function of identification process in GC-MS project with "after peak alignment" option was fixed. (The metabolite name was actually wrong although the other metadata such as InChIKey was correct.)

Blank filtering is now available.
If users have a suitable procedure 'blank' sample, MS-DIAL can consider the ion features of blank samples to remove the redundant ions.
Note that users have to set the analysis type as 'Blank' in file setting window to use this function.

MS-DIAL parameters are divided into 'basic' and 'advanced' sections.

We released version 3 series of MS-DIAL and MS-FINDER.
Many functions were updated or newly created, and the upgrades will provide more accurate data analysis in addition to faster data processing speed.
We hope that our tools are furthor contributed to mass spectrometry-based metabolomics and lipidomics.
Importantly, we no longer support the Windows XP OS, and the programs require .Net Framework 4.5 or later.
(The .NET framework should have been installed in Windows 7, 8, and 10.)
Below is the release note.

(3.00 & 3.02 were replaced by 3.04 for minor revision.)
Major upgrades compared to the previously reported MS-DIAL version 2 series are summarized.

The extensions (*.mtd, *.med, *.pai, *.arf) created in MS-DIAL project are changed to *.*2 (*.mtd2, *.med2, *.pai2, *.arf2).
There is the compatibility for the previous projects, and all of storages will automatically be reorganized with new formats when you import a previous project.

Peak character evaluatior: it concatenates the different ion types of one metabolite such as isotope, adduct, and in source fragment ions by the deisotoping, the adduct-ion picking, the chromatogram correlation, and the partial MS1 and MS/MS spectral comparison techniques.
Ion feature amalgamator: for example, the list of retention time and m/z for monoisotopic ions detected in negative ion mode can be imported to the project of positive ion mode, which is useful for curating the adduct type.
Labeled metabolite tracking: the function is designed to group the same metabolite ions from partially labelled, fully-labelled, and time-course labeling experiments using carbon (13C), deuterium (D), nitrogen (15N), oxygen (18O), sulfur (34S), or combinations thereof.
Molecular spectrum network: the known- and unknown metabolite features are mapped to the network based on the spectrum similarity (as used in GNPS and MS2LDA) and/or ion abundance correlation among samples.
Searching unique product ions and neutral losses: the precursor ions containing user-defined product ions and/or neutral losses can be queried easily.

MS-DIAL package contains the spectra of MassBank, MassBankEU, GNPS, ReSpect, MetaboBASE, FiehnHILIC, CASMI2016, RIKEN oxidized phospholipids, and RIKEN PlaSMA standard compounds.
It can be used as the "start-up kit" for untargeted metabolomics.
Moreover, we also manage the "bio mass spectral database" from plant extracts. (see the detail at PlaSMA website)
Now, a total of 29,269 and 17,810 spectral records can be used for positive- and negative ion mode data, respectively.
For lipidomics, MS-DIAL package contains the theoretical tandem mass spectra for a total of 56 lipid classes (197,527 lipid molecules).
Dr. Tomas Cajka and Dr. Jeremy Koelmel always help the curations for lipid theoretical mass spectra.
No update for EI-MS database (yet).

Creating a graphical user interface is an important part of science at least I think.
A part of GUI was optimized to check the result of isotope tracking function.
Moreover, the peak table- and alignment table viewers were developed for the rapid data curation.
The parallell processing is available, resulting in faster data processing especially for large-scale dataset.

(3.00 was replaced by 3.02 for minor revision.)
Major upgrades compared to the previously reported MS-FINDER version 2 series are summarized.

It accepts two formats, *.msp and *.mat (to import both MS1 and MSMS data).
All of queries should be recorded in the separated files, and therefore, we created an easy converter "MspToSeparatedMsps" and "MgfToSeparatedMsps" for users.

Molecular formula calculator: there was a critical issue in the previous versions where some of formula were not computationally generated. The current program will provide all of putative candidates with parallel computing.
Metabolite class recommendation (FSEA): new function, fragment set enrichment analysis (FSEA) is officially released to recommend the metabolite classes (ontologies) for unknown spectra. This method does not require any structure databases.
New ranking method for structure candidates: In addition to the previously reported method including the approval of hydrogen rearrangement rules and reference count, it incorporates the Jaccard index (similarity) between new molecular fingerprint and MS/MS spectra. Both molecular fingerprint and MS/MS spectra is adjusted to a total of 459 binary vector of fragment ontologies.
Integrated molecular spectrum network: the unknown query is further inspected in the network analysis using the modified Bonanza spectral clustering score (for MS/MS similarity), the Levenshtein distance score (for metabolite ontology similarity), and formula based bioreaction linkage as performed in this papar .

MS-FINDER 3.0 encompasses KNApSAcK (45,852), UNPD (166,995), FooDB (21,943), NANPDB (3,882), STOFF-IDENT (10,231), PlantCyc (3,817), LipidMAPS (34,466), ChEBI (53,746), PubChem biosynthetic pathway (8,285), DrugBank (6,273), SMPDB (1,490), YMDB (1,840), ECMDB (1,342), T3DB (2,499), BMDB (7,232), and the HMDB family including HMDB (95,924), Urine (3,929), Saliva (1,129), Fecal (1,073), CSF (360), and Serum (23,138). The count of structure records is cited in parentheses. Now, the total count of structures is 321,616. An enzymatically expanded in silico structure database MINE (643,307) is also incorporated. We also use the direct parent term of ClassyFire as the name of metabolite ontology for each structure. Note that the name of metabolite class used in FSEA is not assigned by ClassyFire, but determined manually by our curation team that took into account the MS resolution for structure characterization.

Unique product ions (PIs) and neutral losses (NLs) for a certain metabolite class have been used for metabolite annotations. For instance, (1) m/z 78.9585 and m/z 96.9595 are used for searching phosphate (PO3-)- and sulfate (HSO4-)-containing metabolites, respectively; (2) neutral losses of 146.0579 (C6H10O4), 162.05282 (C6H10O5), and 176.0321 (C6H8O6) are used for searching metabolites that contain deoxyhexose (dHex), hexose (Hex), and uronic acid (HexA) moieties; (3) aglycones of the flavonol class, e.g. kaempferol, quercetin, and isorhamnetin can be searched by their specific m/z values, e.g. 285.0405 (C15H9O6-), 301.0354 (C15H9O7-), and 315.051 (C16H11O7-).
By means of our computational and manual curations, MS-FINDER 3.0 contains 1,352- and 1,643 product ion queries for positive and negative spectra, respectively. Moreover, 729- and 914 neutral loss queries are also registered. The m/z and neutral loss query contains the information of mass, formula candidates, ontology candidates, and (substructure) InChIKey candidates.

--Opinions for computational mass spectrometry was published in SCIENCE TRENDS.

--MS-DIAL version 2.92 was released.
(1) Molecular-spectrum networking approach by means of spectrum similarity and ion abundance similarity among samples is now available directly.
* please set 'FireFox' as the default html viewer for the quick visualization of networking.
(2) The nodes and edges for local cytoscape program can also be generated from alignment result export.
(3) Alignment table viewer provides ANOVA-P and fold change values.
(4) Lipid MS/MS library version 36 was released: SHexCer and GM3 are now in the scope of MS-DIAL lipidomics.
(5) Several peak picking and alignment functions were improved.
--MS-FINDER version 2.42 was released.
(1) The utility to generate separated msp format files from combined msp or mgf is now available.
(2) Several bugs were fixed.

--MS-DIAL version 2.90 was released.
(1) Deisotoping function, which was not performed well in version 2.82, was fixed.
(2) New project for DIA-MS with 'multiple CEs (like 0V, 10V, and 30V)' is newly opened. (see the updated tutorial as well)
(3) Peak- or alignment table viewers were improved.
(4) Export function for molecular spectrum netwokring was added (edge file is created for cytoscape).
(5) Lipid MS/MS library version 35 was released.
(6) Several crashed problems were solved.

--MS-FINDER version 2.40 was released.
(1) The function for de novo formula calculation was improved. Although the computational time has become a little bit longer than that of previous versions, it works well to calculate all of formula combinations.
(2) Export layout was a little bit modified.
(3) Several bugs were fixed.

--MS-DIAL version 2.84 was released.
(1) Feature detection (peak spotting), spectral matching, and alignment functions were improved.
(2) Overlaid chromatograms of multiple sample data, termed as 'aligned EICs' can be seen in the MS-DIAL GUI.
(3) 'Show ion table' is created to look at the overview of peak detection and peak alignment result.
(4) The searce space of MS-DIAL lipid profiling was expanded.
(5) Multithreading for a large scale MS data is supported.
(6) Nomenclature in MS-DIAL lipidomics was described here
(7) The tutorial was updated. See the details in the tutorial.

--MS-FINDER version 2.30 was released.
(1) In silico fragmenter was improved.
(2) The following metabolome structure databases were supported. KNApSAcK, UNPD, PlantCyc, FooDB, NANPDB, STOFF-IDENT, LipidMAPS, ChEBI, PubChem biosynthetic pathway, DrugBank, SMPDB, YMDB, ECMDB, T3DB, BMDB, MINE, and HMDB family including HMDB4.0, Urine, Saliva, Fecal, CSF, and Serum
(3) The tutorial was updated.

--MS-DIAL version 2.82 was released.
Function updated:
(1) New function 'MS/MS fragment searcher' was implemented.
(2) Lipid in silico MS/MS spectra were further curated.
(3) The reference RI and RT in GC-MS project can be exported in the alignment result.

--MRMPROBS version 2.42 was released.
(1) In the previous version, the program was clashed if parenthesis '( )' is used as metabolite name. Now, MRMPROBS will accept the use.

--MRMPROBS version 2.40 was released.
(1) The issue (fatal) that scan-type MS data by negative ion mode could not be imported correctly was fixed.

--MRMPROBS version 2.40 was released.
(1) The issue (fatal) that scan-type MS data by negative ion mode could not be imported correctly was fixed.

--MS-DIAL version 2.80 was released.
Function updated:
(1) Scoring method for MS/MS matching for lipids was modified.
(2) Some utilities in MS-DIAL GUI were improved.
(3) The theoretical MS/MS spectra for EtherPC and EtherPE (formerly named as plasmenyl-PC and plasmenyl-PE) were improved.
(4) Naming of lipid classes was organized (see the detail in MS-DIAL web page).

--MS-FINDER version 2.28 was released.
(1) The link between MS-DIAL and MS-FINDER was fixed.

--MS-DIAL version 2.78 was released.
Function updated:
(1) The function for de-isotoping was improved to deal with multiple charged ions especially targeted in Proteomics and small RNA assays.
(2) The peak detection algorithm was modified so that the user defined parameter like minimum peak width can be reflected in the result.
(3) MoNA export function was modified.
(4) The theoretical MS/MS spectrum for Cardiolipin and HemiBMP was included in lipidomics project.
(5) The function for peak identification in GC-MS project was modified to correctly reflect the RT/RI tolerance that users defined.
(6) The MS2Dec function was modified to keep the precursor's isotopic ions in DIA-MS deconvoluted result.
(7) The export function to MS-FINDER was improved.

--MS-FINDER version 2.26 was released.
Function updated:
(1) The function for computational fragmentation was improved to deal with complecated- and cleaved aromatic bonds.
(2) The chemical ontologies for all of structures included in MS-FINDER metabolome structure database were assigned.
(3) The function of fragment set enrichment analysis (FSEA) was improved.

--Our latest achievement related to MS-DIAL and MS-FINDER was published in Nature Methods. [NPG link]

--MS-DIAL version 2.76 was released.
Function updated:
(1) A filtering option of 'at least N% in one sample group' was added in LC-MS aligner.
(2) An option to keep isotope ions of precursors in DIA-MS is added in LC-MS project.

(1) The format bug of peak list's export function in GC-MS project was fixed.
(2) The mis-labeling problem for post identification in LC-MS project was fixed.

--MS-FINDER version 2.24 was released.
Function updated:
(1) The scoring system of MS-FINDER structure elucidation was improved.

--MS-DIAL version 2.74 was released.
Function updated:
(1) The isotope ions are also exported by the export functions.
(2) The clean-up efficiency for reducing duplicate alignment spots is improved.
(3) The MoNA uploader was improved.

--MS-FINDER version 2.22 was released.
Function updated:
(1) The retention time prediction was now available by a simple regression model based on XLogP.
(2) The retention time/index can be used as the diagnostic criteria for spectral searching.
(3) Structure ontologies by means of ClassyFire are constructed.
(4) Fragment set enrichment analysis (FSEA) is now available for ontology prediction. (contact me for the trial)

--MS-DIAL version 2.72 was released.
(1) some bugs in alignment results were fixed.
(2) the criterion of fragment percentage in the MS/MS matching calculations was fixed.

Function updated:
(1) the peak alignment function for LC-MS data was improved.
(2) the gap filling method in GC-MS project was improved.

--MRMPROBS version 2.38/MRMDIFF version 2.13 were released.
The bug where the left panel in MRM-DIFF function was sometimes empty was fixed.

--MS-FINDER console application was released.

--MS-DIAL version 2.70 was released.
(1) some bugs in LC-MS alignment function was fixed.
(2) wrong precursor m/z information of sphingomyelin lipid species in in silico MS/MS version 24 was fixed.
Function updated:
(1) an option "-p" was prepared to provide "MTD" format file in console app to be used in MS-DIAL GUI application.
(2) parallel source code was improved in MS-DIAL GC-MS spectral searching.

--MS-FINDER version 2.20 was released.
Function updated:
(1) the function of molecular formula prediction was drastically improved.
(2) the function for in silico fragment annotation was totally improved. All of the source codes was changed.
(3) MS-FINDER scoring method in searching structures now uses "fragment fingerprints", which can be monitored in CID-MS/MS, for the calculation of substructure similarities.
(4) One natural product database, NANPDB, was imported in MS-FINDER.

--MRMPROBS version 2.36 was released.
(1) The library import method was fixed.

--MS/MS spectra library of oxidized lipids analyzed in RIKEN IMS was uploaded in MS-DIAL section.

--MS-DIAL console application was released

--MS-DIAL version 2.68 was released
Function updated:
(1) identification for GC-MS data is now performed by parallel processing.
(2) isotope labeled tracking is improved.
(3) An option where RT information is not used for identification scoring is prepared.
(4) GNPS export function was prepared.
GUI updated:
text boxes on the botom of MSDIAL main window were prepared to easily access the targeted spot that you want to find.

--MS-DIAL version 2.66 was released: new lipid classes GlcADG and AcylGlcADG were added for lipid profiling. Also, the functions for isotope labeled tracking, adduct feature detection, and spectrum similarity calculation were improved. The use of version 2.64 is not recommended for GCMS project, where there was not efficient source codes for EI-MS spectrum matching.

--MRMPROBS version 2.34 was released: bug fixed in MRM-DIFF function.
--MS-DIAL version 2.62 was released: 1) Make sure that a lot of functions (peak spotting, deisotoping, adduct finder, and peak alignment) are improved, so the MS-DIAL result will be drastically changed from the result of previous MS-DIALs. 2) PeakSpoting function was improved to reduce the duplicate peak spots, 3) deisotoping, adduct finding, and isotope tracking functions were improved with the considerations from user's comments, 4) peak alignment function was also improved so that in source fragment spots can be found by the correlation score between spots having similar RTs.
--LOWESS normalization tool version 1.1 was released: Fixed a bug related to only zero values of QC samples.

--MS-DIAL version 2.62 was released: There was a fatal problem in version 2.58 and 2.60 of MS-DIAL. So, please replace them by version 2.62 or former version from MS-DIAL 2.56.

--MS-DIAL version 2.60 was released: Major updates: (1) Improved the function for MRMPROBS reference format export. (2) Prepared the 'project' property setting window to register users metadata like instrument, license, authors, comment etc to be uploaded to MoNA or MassBank. (3) Bug fixed for MSP library setting in FAMES method.

--MS-FINDER version 2.14 was released: The function of neutral loss and product ion assignments was improved.

--MS-DIAL version 2.58 was released: BinVestigate API is now available at MS-DIAL GCMS project. MSP export function was improved to correctly export their meta data.

--MS-FINDER version 2.12 was released: A bug in the result export was fixed.

--MRMPROBS version 2.32 was released: The program now accepts all of scan type data like survey scan MS only, and data dependent MS/MS acquisition.

--MassBank and MoNA EI-MS and 'predicted' retention index library was uploaded in MS-DIAL section.

--MS-DIAL version 2.56 was released: Bug fixed: MS/MS and EI-MS export function. Some crash problems were fixed. LipidBlast version 23 was imported in MS-DIAL.

--LipidBlast ceramides fork version 3 was updated: fixed the specific ion (m/z 184) of Sphingomyelin (SM) in positive ion mode.

--MS-DIAL version 2.54 was released: 1) improved peak detection methods to deal with co-eluting chromatographic peaks; 2) bug fixed in peak alignment function to determine the representative spectra for aligned spots; and 3) improved spectral similarity calculation methods for EI-MS data.

--LipidBlast glycerolipids fork version 7 was updated: it newly contains LysoPA as deprotonated ions ([M-H]-).

--LipidBlast glycerolipids fork version 7 was updated: it newly contains LysoPS, LysoPG, and LysoPI classes as deprotonated ions ([M-H]-).

--LipidBlast glycerolipids fork version 7 was released: it newly contains PG [M+NH4]+, BMP (Bis(Monoacylglycero)Phosphate) [M+NH4]+, and FAHFA (Fatty Acid ester of Hydroxyl Fatty Acid) molecules.

--MS-DIAL 2.52 was released: Isotope recognition is now applied to double chaged ions as well. Bug fixed: GUI problems.
--MS-FINDER 2.10 was released: New existing structure database (.ESD file) was released to find structure data correctly. Bug fixed: user-defined adduct ion is now available correctly.

--MS-DIAL 2.50 was released: Improved peak alignment function, and modified the source code to reduce computational time. Bug fixed: GUI and normalization problems.

--LOWESS normalization tool was modified: Modified the source code to deal with "all zero" array.

--MetaboloDerivatizer section was opened: for getting the TMS- and MeOX structures from the original structure input.

--MS-DIAL 2.48 was released: improved peak alignment functions for both GC/MS and LCMS, and improved GUI for MS/MS check.

--MRMPROBS and MS-DIAL tutorial were updated.

--MRMPROBS 2.30 was released, and it was launched as a universal program for targeted metabolomics.

--MS-DIAL 2.46 was released. Bug fixed.

--MS-DIAL for GC/MS was released.

--MS-FINDER 2.08 was launced as a universal program for compound ‘annotation’ that supports EI-MS (GC/MS) and MS/MS spectral mining.
The tutorial was also updated.

--MS-DIAL 2.44 was released. The function of peak alignment was improved. Bug fixed.

--MS-DIAL 2.42 was released. Major update 1) RI based peak alignment in GC/MS is now available. 2) Parameter file can be exported in each alignment result. 3) some bugs were fixed.

--MS-FINDER 2.06 was released: Added spectral search function.

--MS-DIAL 2.40 was released: bug fixed.

--MS-DIAL 2.0 and MS-FINDER 2.0 were updated (private).

--Curated EI-MS and MS/MS library (as MSP format) was updated.

--MS-DIAL tutorial was updated.

--The SmetSearch page was opened.

--The MS-DIAL section was improved especially for MSP databases. And it also includes the update of MS-DIAL's LipidBlast to deal with Ceramide species.

--Hydrogen rearrangement rules (MS-FINDER) paper was formally published.

--New curated MS/MS spectra (from MassBank, GNPS, ReSpect) were uploaded in MS-DIAL section.

--MS-DIAL ver. 2.24 and MS-FINDER ver. 1.76 were released. The current MS-DIAL program accepts all of MS vendor formats and all method types (normal LC/MS, data dependent MS/MS, and data independent MS/MS).

--MS-FINDER ver. 1.70 was released. Bug fixed.

--MS-FINDER ver. 1.68 was released. And opened the MS-FINDER page.

--MS-DIAL ver. 2.06 was released. Debug for export functions and identifications.

--SmetSearch ver. 1.01 was newly released.

--MS-DIAL ver. 2.02 was released.

--Curated MassBank MS/MS page was opened.

--MS-FINDER ver. 1.54 was released. Improved the function of MS/MS spectral peaks.

--MRMPROBS ver. 2.22 was released. Improved the peak detection program.

--MassBankToMsp ver. 1.02 was released. Improved the retrieve program for GC/MS.

--MSDIAL ver. 1.98 was released. Improved the MS2Dec program.

--MRMPROBS ver. 2.19 was released.

--MS-DIAL ver. 1.96 was released. Improved the export function.

--MS-FINDER ver. 1.44 was released. Bug fixed.

--Novel program, MS-FINDER ver. 1.40 was released. Also, the web page was opened.

--MS-DIAL ver. 1.94 was released. Connection service to MS-FIDNER program is now available.

--MS-DIAL ver. 1.92 was released. The peak detection method was improved to remove peaks from spike noise.

--MS-DIAL ver. 1.90 was released. The layout of data matrix exported from the program was modified.

-A quick tool to normalize the data matrix by means of QC samples and LOWESS/Spline method was released.

-MS-DIAL ver. 1.88 was released. Add the cross validation program to optimize the span of LOWESS-normalization. Bug fixed for alignment results.

-InertCap 5MS library for AIoutput was updated.

-MS-DIAL ver. 1.82 was released. Bug fixed for export options.

-The explanation PDF of MS-DIAL mathematics was uploaded in MS-DIAL section.

-MS-DIAL ver. 1.80 was released. MS2Dec method was fixed for all ion fragmentation (AIF, Thermo).

-MS-DIAL ver. 1.78 was released. Bug fixed for peak alignment.

-MS-DIAL ver. 1.76 was released. Bug fixed for data access API and LipidBlast internal Database.

-MRMPROBS ver. 2.17 was released. Update the export functions. Bug fixed for MRM-DIFF.

-MS-DIAL ver. 1.72 was released.

-MRMPROBS ver. 2.14 was released. Update the export functions.

-MRMPROBS ver. 2.13 was released. Bug fixes for peak area calculations and LOWESS normalization.

-MS-DIAL ver. 1.65 was released. Bug fixes of MSP file parcer.

-MassBankToNIST converter was released. This program helps us to convert the download folder including MassBank records to NIST Search MSP format library.

-AIoutput recommended for Shimadzu GC-MS was released.

-MS-DIAL ver. 1.64 was released. Add new normalizations (by TIC or mTIC), add the GUI for lowess parameter setting, and update the copy and paste functions. Bug fixes for loess normalization. Fix adduct ion parser. Add the user-defined adduct ion option.

-MS-DIAL ver. 1.63 was released. Modified: Error handling.

-MS-DIAL ver. 1.61 was released. Modified: Add sorting functions in GUI.

-MS-DIAL ver. 1.59 was released. Modified: See the updated tutorial.

-MS-DIAL ver. 1.54 was released. Modified: Adduct ion handling. Error handling.

-The link of MRM database section was repaired.

-MRM-DIFF page was opened.

-MRMPROBS ver. 2.11 was released. Error handling.

-MS-DIAL ver. 1.43 was released. Error handling.

-MRMPROBS ver. 2.10 was released. Error handling and MRM-DIFF algorithm was implemented.

-MS-DIAL ver. 1.42 was released.

-MRMPROBS ver. 2.08 was released. Error handling.

-MS-DIAL ver. 1.38 was released.

-AIoutput2 ver. 1.30 was released. Modified: Error handling.

-Some bugs of excel macro based statistical analysis tool were fixed.

-New MRMPROBS ver. 2.08 was released. Error handling.

-New MRMPROBS ver. 2.01 was released. Modified: mzML data format is now available. Error handling. Manual is also updated.

-New MRMPROBS ver. 1.21 was released. Modified: Error handling.

-MRM database section was opened.

-New database for AIoutput was released !!

-New MRMPROBS was released !! The GUI and implemented algorithm were innovatively improved.
File conversion of Shimadzu, Agilent Technologies, AB Sciex, and Thermo Fisher Scientific became applicable!!

-MRMPROBS ver. 1.06 was released. Modified: Error handling. GUI improvement.

-Agilent data format is now accepted by the Reifycs file converter for MRMPROBS software.

-MRMPROBS ver. 1.04 was released. Modified: Error handling
-The manual containing the required conditions in LabSolutions software (Shimadzu Inc.) handling LCMS-8030, LCMS-8040 and so on was now prepared.

-Tool for statistical analyses on Microsoft Excel was released.

-MRMPROBS ver. 1.03 was released. Modified: Area calculation method; Error handling; User interface.

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