Name: 분석 방법의 구조 검색 가능한 데이터베이스를 개발하기 위한 화학정보학 적용 (동영상) | JoVE Journal
Uploaded: 2025-06-06T15:15:00.000+00:00
Duration: 5 min 34 s
Description: 학습하세요 화학정보학을 활용하여 분석 방법과 스펙트럼 데이터베이스인 AMOS를 개발하는 방법을. 이 웹 기반 플랫폼은 연구자들이 분석 방법과 스펙트럼 데이터에 쉽게 접근하고 공유할 수 있도록 지원합니다.

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The authors thank the curation team for all their work curating chemicals for the database, and Joshua Powell, Asif Rashid, and Freddie Valone for technical support in the construction and deployment of AMOS. We also thank Charles Lowe for his review of the manuscript.

<ol><li>Kim, S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((PubChem+substance+and+compound+databases%5BTitle%5D)+AND+%22Nucleic+Acids+Res%22%5BJournal%5D)">PubChem substance and compound databases.</a> Nucleic Acids Res. 44 (D1), D1202-D1213 (2016).</li>
<li>Pence, H. E., Williams, A. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((ChemSpider%3A+An+online+chemical+information+resource%5BTitle%5D)+AND+%22J+Chem+Educ%22%5BJournal%5D)">ChemSpider: An online chemical information resource.</a> J Chem Educ. 87 (11), 1123-1124 (2010).</li>
<li>Williams, A. J., Grulke, C. M., Edwards, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+CompTox+chemistry+dashboard%3A+A+community+data+resource+for+environmental+chemistry%5BTitle%5D)+AND+%22J+Cheminform%22%5BJournal%5D)">The CompTox chemistry dashboard: A community data resource for environmental chemistry.</a> J Cheminform. 9, 61(2017).</li>
<li>Grulke, C. M., Williams, A. J., Thillanadarajah, I., Richard, A. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((EPA%27s+DSSTox+database%3A+History+of+development+of+a+curated+chemistry+resource+supporting+computational+toxicology+research%5BTitle%5D)+AND+%22Comput+Toxicol%22%5BJournal%5D)">EPA's DSSTox database: History of development of a curated chemistry resource supporting computational toxicology research.</a> Comput Toxicol. 12, 100096(2019).</li>
<li>Tickner, J. A., Schifano, J. N., Blake, A., Rudisill, C., Mulvihill, M. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Advancing+safer+alternatives+through+functional+substitution%5BTitle%5D)+AND+%22Environ+Sci+Technol%22%5BJournal%5D)">Advancing safer alternatives through functional substitution.</a> Environ Sci Technol. 49 (2), 742-749 (2015).</li>
<li>Phillips, K. A., Wambaugh, J. F., Grulke, C. M., Dionisio, K. L., Isaacs, K. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((High-throughput+screening+of+chemicals+as+functional+substitutes+using+structure-based+classification+models%5BTitle%5D)+AND+%22Green+Chem%22%5BJournal%5D)">High-throughput screening of chemicals as functional substitutes using structure-based classification models.</a> Green Chem. 19 (4), 1063-1074 (2017).</li>
<li>Isaacs, K. K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((A+harmonized+chemical+monitoring+database+for+support+of+exposure+assessments%5BTitle%5D)+AND+%22Sci+Data%22%5BJournal%5D)">A harmonized chemical monitoring database for support of exposure assessments.</a> Sci Data. 9, 314(2022).</li>
<li>SpectraBase. , 
 <a target="_blank" href="https://spectrabase.com/">https://spectrabase.com/</a> (2025).</li>
<li>Djoumbou Feunang, Y., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((ClassyFire%3A+Automated+chemical+classification+with+a+comprehensive%2C+computable+taxonomy%5BTitle%5D)+AND+%22J+Cheminform%22%5BJournal%5D)">ClassyFire: Automated chemical classification with a comprehensive, computable taxonomy.</a> J Cheminform. 8, 61(2016).</li>
<li>Ulrich, E. M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((EPA%27s+non-targeted+analysis+collaborative+trial+%28ENTACT%29%3A+Genesis%2C+design%2C+and+initial+findings%5BTitle%5D)+AND+%22Anal+Bioanal+Chem%22%5BJournal%5D)">EPA's non-targeted analysis collaborative trial (ENTACT): Genesis, design, and initial findings.</a> Anal Bioanal Chem. 411 (4), 853-866 (2019).</li>
<li>Sobus, J. R., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Using+prepared+mixtures+of+ToxCast+chemicals+to+evaluate+non-targeted+analysis+%28NTA%29+method+performance%5BTitle%5D)+AND+%22Anal+Bioanal+Chem%22%5BJournal%5D)">Using prepared mixtures of ToxCast chemicals to evaluate non-targeted analysis (NTA) method performance.</a> Anal Bioanal Chem. 411 (4), 835-851 (2019).</li>
<li>Chao, A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((In+silico+MS%2FMS+spectra+for+identifying+unknowns%3A+A+critical+examination+using+CFM-ID+algorithms+and+ENTACT+mixture+samples%5BTitle%5D)+AND+%22Anal+Bioanal+Chem%22%5BJournal%5D)">In silico MS/MS spectra for identifying unknowns: A critical examination using CFM-ID algorithms and ENTACT mixture samples.</a> Anal Bioanal Chem. 412 (6), 1303-1315 (2020).</li>
<li>McEachran, A. D., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Revisiting+five+years+of+CASMI+contests+with+EPA+identification+tools%5BTitle%5D)+AND+%22Metabolites%22%5BJournal%5D)">Revisiting five years of CASMI contests with EPA identification tools.</a> Metabolites. 10 (6), 260(2020).</li>
<li>Charest, N., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Improving+predictions+of+compound+amenability+for+liquid+chromatography-mass+spectrometry+to+enhance+non-targeted+analysis%5BTitle%5D)+AND+%22Anal+Bioanal+Chem%22%5BJournal%5D)">Improving predictions of compound amenability for liquid chromatography-mass spectrometry to enhance non-targeted analysis.</a> Anal Bioanal Chem. 416 (10), 2565-2579 (2024).</li>
</ol>

This paper does not necessarily represent the views or policies of the U.S. Environmental Protection Agency.

While many projects and applications focus on collecting and standardizing information from a single type of record, such as methods, fact sheets, or a specific kind of spectra, AMOS is the first tool identified that compiles and integrates large volumes of information across multiple record types. The unification, harmonization, and structuring of data from these diverse sources result in a database that can be more readily incorporated into workflows requiring access to analytical chemistry methodologies. The ability to search the database in several complementary ways enables efficient retrieval of information that might otherwise require extensive manual effort across multiple websites or tools.
Before public release, the utility of AMOS was demonstrated through its use by EPA staff to support a wide range of projects. The EPA has a sustained interest in the application of mass spectrometry for non-targeted analysis10,11, and multiple initiatives have leveraged the experimental mass spectra in AMOS to enhance searches against a large in silico spectral library generated from DSSTox chemicals12,13. Other projects have used structural similarity searching to identify starting points for developing new methods, examined existing methods to assess detection and quantitation limits, and analyzed collections of chemicals linked to methods to evaluate the extent of chemical space coverage.
AMOS' aggregation of potential training data further supports the development of quantitative models of amenability for analytical methods14, a core need for advancing non-targeted analysis (NTA) workflows. The curation efforts within AMOS also facilitate initiatives to model, explore, and visualize chemical spaces associated with methodological coverage14.
While the core functionality of AMOS is mature, ongoing development is guided by user feedback. Current tasks include the incorporation of additional data, curation of further metadata for enhanced filtering, and expansion of search capabilities. In collaboration with EPA stakeholders, application programming interfaces (APIs) are under development to enable programmatic access, addressing use cases where the graphical user interface (GUI) may be inefficient. A release notes page has been integrated into the application to track and communicate code updates over time.
New data records and chemicals are currently added on a weekly basis; however, a slower release schedule is anticipated following the public launch. While significant effort is made to ensure the accuracy of records and associated metadata, much of the data originates from public databases. As such, complete verification of every record is not feasible, and users should be aware that absolute data accuracy cannot be guaranteed.

Web-based delivery of chemistry data to the community is exemplified by applications such as PubChem1, ChemSpider2, and the CompTox Chemicals Dashboard (CCD)3. Efforts have been made to circulate analytical method details published in journal articles, released by instrument vendors as technical application notes, provided by government agencies as standard operating procedures or regulatory methods, and issued by standards organizations such as the International Organization for Standardization (ISO). Tens of thousands of chemicals have been studied by these sources under a wide range of conditions and analytical techniques. This extensive body of sources covers diverse substances and includes scenarios ranging from the quantification of a single chemical in a specific matrix (e.g., blood), to mixtures of pesticides and their residues in specific crops, to hundreds of chemicals identified in drinking water. While many analytical methods can be discovered via public search engines, not all are freely available or open-access.
Locating specific information of interest can be challenging. General-purpose search engines are not optimized for chemistry data, and their ranking algorithms may obscure high-quality content intended for narrow audiences. Searches across journal websites can yield more targeted results, but access is often restricted, with only abstracts publicly available, making it difficult to assess a method&#39;s usefulness. Furthermore, critical parameters-such as sample matrices, limits of detection, and quantitation-are often not stored in a structured format. Another significant challenge lies in the variation and inconsistency of chemical identifiers, names, and synonyms associated with a single chemical. The lack of structured methods data limits the development of software tools that could leverage decades of accumulated analytical chemistry knowledge and related publications.
As a result of these challenges and limitations, there is a need for a curated, chemistry-oriented application for harmonizing and searching analytical methods-one that was not identified elsewhere. To address this gap, the U.S. Environmental Protection Agency developed AMOS, the Analytical Methods and Open Spectra database and web-based application. AMOS currently collects and organizes three types of data records: analytical methods, various analytical spectra, and a broad category of supplemental documents collectively referred to as fact sheets. Each record is linked to the method&#39;s target chemical analytes and reagents. The data are searchable in multiple ways, including by text queries, chemical structure, and structural or spectral similarity.
The AMOS application primarily focuses on delivering open access and open data records. Where possible, records in the database are hyperlinked to their original sources. Records not under open licensing and therefore not stored directly in the database can still be integrated and accessed via URL, provided they are otherwise available. This applies to two types of records: analytical methods that are behind paywalls, typically from journals or standards organizations to which the EPA has access, and spectra that are available but require login access.
Data sources vary in how records are structured, necessitating substantial effort in extraction and curation to assemble and harmonize the content. Most records provide substance identifiers (e.g., CASRN, DTXSID, InChIKey, common names), and in many cases, extraction is straightforward. However, matching these identifiers to chemical structures and substance details can be complex. Some identifiers can be directly matched to entries in the EPA&#39;s Distributed Structure-Searchable Toxicity (DSSTox) database4; when matches are not found, identifiers are linked to existing substances, or new substances are registered. The AMOS initiative has consequently led to the expansion of the DSSTox database, improving the foundational data supporting other EPA databases and applications, such as the CompTox Chemicals Dashboard3.
Manual curation is required for certain valuable additional information. For analytical methods, experimental parameters such as limits of detection and quantitation, sample matrix, and analytical methodology are not organized in a standardized way, and automated tools cannot identify this information due to its inconsistent storage.
Two elements of record information, the media associated with the sample and the functional use of the analyte, are highly relevant to ongoing efforts to monitor hazard and exposure concerns from contaminants. As such, considerable attention was given to structuring these attributes within the record data. An ontology of functional use classifications was developed for this project. This ontology organizes the functional uses of substances into a hierarchical structure, ranging from more general &#39;parent&#39; uses to more specific &#39;child&#39; uses. The ontology facilitates the exploration of substances from an application perspective, supporting research initiatives that emphasize functional uses as a means to assess exposure and hazard5,6. Additionally, methods were labeled according to their samples&#39; harmonized media category, as specified in the EPA&#39;s multimedia monitoring database (MMDB)7. This categorization enables the search for chemicals based on their occurrence in specific media, streamlining the development of solutions focused on detecting chemicals in specific environmental or biological samples. These annotations enhance the integration of AMOS into exposure- and hazard-oriented workflows under development within the EPA.
In assembling the spectra, the challenge of processing various file formats-some of which are only nominally standardized-and parsing accompanying metadata often requires custom handling. In cases where spectral collections are linked to a publication, details documented within the publication may need to be manually extracted for data loading. This effort has resulted in a database that integrates and structures these disparate spectra, allowing researchers to avoid the need for laborious curation in future endeavors.
As of March 2025, the database contains approximately 935,000 spectra, with nearly 99% being mass spectra and smaller collections of NMR (~2,000) and IR (~400). Additionally, there are approximately 770,000 externally linked spectra (connected to the SpectraBase database8), ~36,000 fact sheets, and ~7,400 analytical methods. The substances integrated into the application are a subset of those from the DSSTox database, which is incorporated into the CompTox Chemicals Dashboard (CCD) and contains over 1.2 million substances.

<table><tbody><tr><td>Git</td><td>N/A</td><td>https://git-scm.com/</td><td>Open-source version control system.</td></tr><tr><td>JavaScript</td><td>N/A</td><td>https://ecma-international.org/publications-and-standards/standards/ecma-262/</td><td>Programming language.&amp;nbsp; Defined by ECMA International standards.</td></tr><tr><td>PostgreSQL</td><td>PostgreSQL Global Development Group</td><td>https://postgresql.org/about/licence</td><td>Open-source database management system.</td></tr><tr><td>Python</td><td>Python Software Foundation</td><td>https://www.python.org/</td><td>Open-source programming language.</td></tr></tbody></table>

applying cheminformatics to develop a structure searchable database of analytical methods

Applying Cheminformatics to Develop a Structure Searchable Database of Analytical Methods

Analytical methods can range from detailed regulatory documents to simpler summaries. Regulatory methods may include information on amenable analytes, supported matrices, required reagents, statistical performance, interlaboratory validation, and other specifics. Summaries typically provide a general overview of reagents, instrumentation, and often a short list of analytes. Analytical methods from U.S. government bodies, including the U.S. Environmental Protection Agency (USEPA), U.S. Geological Survey (USGS), U.S. Department of Agriculture (USDA), the Food and Drug Administration (FDA), and others, offer detailed procedural information. Instrument vendors such as Agilent, Shimadzu, Thermo Fisher Scientific, Sciex, and others also provide access to hundreds of application notes, which may be considered summary methods. This study has developed a cheminformatics-enabled database of methods in which chemicals are extracted from method documents, with identifiers (names and/or Chemical Abstracts Service registry numbers (CASRN)) mapped to chemical structures. The resulting database, containing approximately 7,000 methods, is searchable by identifier, chemical structure, and structural similarity, and is supplemented by approximately one million public domain spectra (LC/MS, GC/MS, NMR, and IR). The application supports searching of analytical methods and filtering based on analytes, functional usage, method sources, and other related metadata.

The screenshots of AMOS shown above show typical outcomes from the individual searches in the application, including both searches for substances of interest and among spectra, fact sheets, and methods. The variety of ways of interrogating the database is intended to cover the most likely and most useful kinds of searches in ways that allow for deeper investigation into the data and the substances that they relate to.
To assist a user's searching, much of the functionality is interconnected in ways intended to support deeper examination of the available data. As an example workflow, the functional use classification visualization links to views of the methods and fact sheets that are related to that functional class, from which lists of substances can be extracted and fed into the batch search, or individual documents can be examined, and individual substances in those documents can be investigated further. Since many substances in methods also have experimental mass spectra in the database, this can allow a researcher to quickly go from a category of substances to a set of methods and spectra that can test for the presence of a specific substance (see Figure 9).
Since the results will depend heavily on what is being searched for and which search or searches are run, representative results for the entire application are difficult to define. Overall, it may be more accurate to describe a "success" in terms of user experience; in that case, it is hoped that the following will generally hold true: That the methods of searching and filtering (and the ability to move between different searches and filters) are effective at identifying which subsets of information a user wants; that the results that the user finds are accurate and useful. Figure 10 depicts an example workflow demonstrating AMOS functionalities.
<img alt="Functional use classification network diagram; methods database filtering; toxicological analysis results." class="xfigimg" src="/files/ftp_upload/68194/68194fig10.jpg" data-altupdatedat="1788840098000" data-alt="Figure 10"> 
Figure 10: Example workflow demonstrating AMOS functionalities. The workflow begins with a functional use classification (respiratory drugs), filters methods related to respiratory drugs in blood, examines one specific method, and identifies spectra for a substance included in that method. <a href="https://www.jove.com/files/ftp_upload/68194/68194fig10large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

This article describes AMOS, the web-based Analytical Methods and Open Spectra database, a cheminformatics application designed to provide researchers with easy access to analytical methods and spectral data.

Analytical methods can range from detailed regulatory documents to simpler summaries. Regulatory methods may include information on amenable analytes, ...

We wanna create an easy way for EPA scientists to find analytical methods from across distributed resources so that our scientists can spend less time scouring the internet, and instead have a curated resource integrated into our existing chemical informatics system. What we've built is essentially a lightweight document management system that maps those documents to extracted chemical substances. As a result, thousands of analytical methods can be searched using different chemical identifiers to find methods already applied to detect those chemicals. There is no other free online database of analytical methods for the community to search to obtain either an existing reference analytical method for a chemical, or a good set of starting conditions for a particular method. This protocol teaches the reader how to use AMOS to harvest useful data to support their method development work. We have learned a lot about how to harvest and integrate analytical methods data into our database and application. By aggregating these thousands of documents and mapping to their associated chemical substances, we now have an excellent data set to explore the use of these documents and augmenting a large language AI model the scientists can query.[Narrator] To begin, go to the text field at the top left of the navigation bar or the search field on the front page and input a Substance Name, CAS Registry Number, InChIKey, or DSSTox Substance Identifier. Press Enter or click on Search to execute the search. Select a row in the resulting table to display the associated record on the right side of the page. To perform a batch search, enter a list of DSSTox Substance Identifiers in the input data field, placing one identifier per line. Use the check boxes under Search options to filter results or add additional information to the records. Click on search at the bottom of the page to generate and download a spreadsheet file that lists information on all records in the database that are associated with a given list of substances. Once the search is complete, click on Additional Searches, followed by Similarity Structure Search. Input the Substance Identifier, set filter minimum substance similarity to 0.8, and click on Search to obtain a tab table. Then, select a row in the table to display a structural comparison between the searched substance and the one selected from the table. To perform a classifier search, select the first classification level using the field at the top of the page. Then, click the button below the field to display the list of classifications for the next level. Repeat this process for the second and third levels, each time selecting a classification and clicking the button to continue. After selecting the fourth level, click the button below to run the search and list all substances that belong to the selected four levels of the classifier classification. Search the database for all fact sheets and methods by performing a method list and fact sheet search. Once the results table loads, use the input fields at the top of each column to filter the data by specific fields. To perform a mass spectrum search, enter a mass range for the target substance in Daltons, along with a margin of error in either Daltons or parts per million. Set the value for window for peak similarity to 0.05 Dalton. Select a methodology, either gas chromatography-mass spectrometry or liquid chromatography-mass spectrometry. Input the mass spectrum as a list of mass-to-charge and intensity pairs. After completing all fields, click the Search button to retrieve a list of mass spectrum matches from the database based on the user-supplied spectrum. Select a row in the resulting table for the spectral display. Now, to visualize the functional use classification, use the Search Classes field to search the list of functional use classes. Hover over a class name in the list to highlight the corresponding node in the graph. If exploring the graph directly, hover over a node to display a short description of the class and highlight any direct parent or child classes for that node. A soil ternary plot classifying texture types based on clay, silt, and sand proportions with labeled zones, such as clay, loam, and sandy loam, is presented here. This classification tool enabled AMOS users to link soil texture types to relevant fact sheets, analytical methods, and experimental spectra, facilitating efficient workflows from compositional data to targeted substance searches based on functional classifications.

applying-cheminformatics-to-develop-structure-searchable-database

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학습하세요 화학정보학을 활용하여 분석 방법과 스펙트럼 데이터베이스인 AMOS를 개발하는 방법을. 이 웹 기반 플랫폼은 연구자들이 분석 방법과 스펙트럼 데이터에 쉽게 접근하고 공유할 수 있도록 지원합니다.

Applying Cheminformatics to Develop a Structure Searchable Database of Analytical Methods

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