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A Statistical Procedure to Selectively Detect Metabolite Signals in LC-MS Data Based on Using Variable Isotope Ratios
The tracing of metabolite signals in LC-MS data using stable isotope-labeled compounds has been described in the literature. However, the filtering efficiency and confidence when mining metabolite signals in complex LC-MS datasets can be improved. Here, we propose an additional statistical procedure...
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Published in: | Journal of the American Society for Mass Spectrometry 2010-02, Vol.21 (2), p.232-241 |
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creator | Lin, Lung-Cheng Wu, Hsin-Yi Tseng, Vincent Shin-Mu Chen, Lien-Chin Chang, Yu-Chen Liao, Pao-Chi |
description | The tracing of metabolite signals in LC-MS data using stable isotope-labeled compounds has been described in the literature. However, the filtering efficiency and confidence when mining metabolite signals in complex LC-MS datasets can be improved. Here, we propose an additional statistical procedure to increase the compound-derived signal mining efficiency. This method also provides a highly confident approach to screen out metabolite signals because the correlation of varying concentration ratios of native/stable isotope-labeled compounds and their instrumental response ratio is used. An in-house computational program [signal mining algorithm with isotope tracing (SMAIT)] was developed to perform the statistical procedure. To illustrate the SMAIT concept and its effectiveness for mining metabolite signals in LC-MS data, the plasticizer, di-(2-ethylhexyl) phthalate (DEHP), was used as an example. The statistical procedure effectively filtered 15 probable metabolite signals from 3617 peaks in the LC-MS data. These probable metabolite signals were considered structurally related to DEHP. Results obtained here suggest that the statistical procedure could be used to confidently facilitate the detection of probable metabolites from a compound-derived precursor presented in a complex LC-MS dataset.
A statistical procedure was proposed and developed to selectively detect metabolite signals in LC-MS data based on using variable isotope ratios. |
doi_str_mv | 10.1016/j.jasms.2009.10.002 |
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A statistical procedure was proposed and developed to selectively detect metabolite signals in LC-MS data based on using variable isotope ratios.</description><identifier>ISSN: 1044-0305</identifier><identifier>EISSN: 1879-1123</identifier><identifier>DOI: 10.1016/j.jasms.2009.10.002</identifier><identifier>PMID: 19892567</identifier><language>eng</language><publisher>New York: Elsevier Inc</publisher><subject>Algorithms ; Analytical Chemistry ; Animals ; Bioinformatics ; Biotechnology ; Chemistry ; Chemistry and Materials Science ; Chromatographic methods and physical methods associated with chromatography ; Chromatography, Liquid - methods ; Computational Biology - methods ; Confidence ; Confidence intervals ; Data mining ; Diethylhexyl Phthalate - chemistry ; Exact sciences and technology ; Filtering ; Filtration ; Isotope ratios ; Isotopes - chemistry ; Liver - metabolism ; Male ; Mass spectrometry ; Mass Spectrometry - methods ; Metabolites ; Mining ; Models, Statistical ; Organic Chemistry ; Other chromatographic methods ; Precursors ; Proteomics ; Rats ; Rats, Wistar ; Solid Phase Extraction</subject><ispartof>Journal of the American Society for Mass Spectrometry, 2010-02, Vol.21 (2), p.232-241</ispartof><rights>2010 American Society for Mass Spectrometry</rights><rights>American Society for Mass Spectrometry 2010</rights><rights>2015 INIST-CNRS</rights><rights>2010 American Society for Mass Spectrometry. Published by Elsevier Inc. All rights reserved.</rights><rights>Journal of The American Society for Mass Spectrometry is a copyright of Springer, 2010.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c560t-c4ef36813a3a9d387f69e345f9b1bc05c8f652ce631f483bd9cfdd1bddeebeb3</citedby><cites>FETCH-LOGICAL-c560t-c4ef36813a3a9d387f69e345f9b1bc05c8f652ce631f483bd9cfdd1bddeebeb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22453245$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19892567$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lin, Lung-Cheng</creatorcontrib><creatorcontrib>Wu, Hsin-Yi</creatorcontrib><creatorcontrib>Tseng, Vincent Shin-Mu</creatorcontrib><creatorcontrib>Chen, Lien-Chin</creatorcontrib><creatorcontrib>Chang, Yu-Chen</creatorcontrib><creatorcontrib>Liao, Pao-Chi</creatorcontrib><title>A Statistical Procedure to Selectively Detect Metabolite Signals in LC-MS Data Based on Using Variable Isotope Ratios</title><title>Journal of the American Society for Mass Spectrometry</title><addtitle>J Am Soc Mass Spectrom</addtitle><addtitle>J Am Soc Mass Spectrom</addtitle><description>The tracing of metabolite signals in LC-MS data using stable isotope-labeled compounds has been described in the literature. However, the filtering efficiency and confidence when mining metabolite signals in complex LC-MS datasets can be improved. Here, we propose an additional statistical procedure to increase the compound-derived signal mining efficiency. This method also provides a highly confident approach to screen out metabolite signals because the correlation of varying concentration ratios of native/stable isotope-labeled compounds and their instrumental response ratio is used. An in-house computational program [signal mining algorithm with isotope tracing (SMAIT)] was developed to perform the statistical procedure. To illustrate the SMAIT concept and its effectiveness for mining metabolite signals in LC-MS data, the plasticizer, di-(2-ethylhexyl) phthalate (DEHP), was used as an example. The statistical procedure effectively filtered 15 probable metabolite signals from 3617 peaks in the LC-MS data. These probable metabolite signals were considered structurally related to DEHP. Results obtained here suggest that the statistical procedure could be used to confidently facilitate the detection of probable metabolites from a compound-derived precursor presented in a complex LC-MS dataset.
A statistical procedure was proposed and developed to selectively detect metabolite signals in LC-MS data based on using variable isotope ratios.</description><subject>Algorithms</subject><subject>Analytical Chemistry</subject><subject>Animals</subject><subject>Bioinformatics</subject><subject>Biotechnology</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chromatographic methods and physical methods associated with chromatography</subject><subject>Chromatography, Liquid - methods</subject><subject>Computational Biology - methods</subject><subject>Confidence</subject><subject>Confidence intervals</subject><subject>Data mining</subject><subject>Diethylhexyl Phthalate - chemistry</subject><subject>Exact sciences and technology</subject><subject>Filtering</subject><subject>Filtration</subject><subject>Isotope ratios</subject><subject>Isotopes - chemistry</subject><subject>Liver - metabolism</subject><subject>Male</subject><subject>Mass spectrometry</subject><subject>Mass Spectrometry - methods</subject><subject>Metabolites</subject><subject>Mining</subject><subject>Models, Statistical</subject><subject>Organic Chemistry</subject><subject>Other chromatographic methods</subject><subject>Precursors</subject><subject>Proteomics</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Solid Phase Extraction</subject><issn>1044-0305</issn><issn>1879-1123</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp9kV2L1DAUhoMo7jr6CwQJiOBNx5ymaZsLL9ZZPxZmUZzV25Amp0OGTjObpAv7702dQcWLvQg5nLzv-chDyEtgS2BQv9stdzru47JkTObMkrHyETmHtpEFQMkf55hVVcE4E2fkWYw7xqBhsnlKzkC2shR1c06mC7pJOrmYnNED_Ra8QTsFpMnTDQ5okrvD4Z5eYsoxvcakOz-4hHTjtqMeInUjXa-K6w291EnTDzqipX6kP6Ibt_SnDk53A9Kr6JM_IP2ee_n4nDzpsxdfnO4Fufn08Wb1pVh__Xy1ulgXRtQsFabCntctcM21tLxt-loir0QvO-gME6bta1EarDn0Vcs7K01vLXTWInbY8QV5eyx7CP52wpjU3kWDw6BH9FNUUDfASyagydLX_0l3fgrzggqkAFEyyHMsCD-qTPAxBuzVIbi9DvcKmJqhqJ36DUXNUOZkhpJdr061p26P9q_nRCEL3pwEOmYKfdCjcfGPriwrweezINVRF_PTuMXwz5AP9n9_tGH-6juXbdE4HDNoFzJUZb170P8LbsO87g</recordid><startdate>20100201</startdate><enddate>20100201</enddate><creator>Lin, Lung-Cheng</creator><creator>Wu, Hsin-Yi</creator><creator>Tseng, Vincent Shin-Mu</creator><creator>Chen, Lien-Chin</creator><creator>Chang, Yu-Chen</creator><creator>Liao, Pao-Chi</creator><general>Elsevier Inc</general><general>Springer-Verlag</general><general>Elsevier</general><general>Springer Nature B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FG</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>P5Z</scope><scope>P62</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20100201</creationdate><title>A Statistical Procedure to Selectively Detect Metabolite Signals in LC-MS Data Based on Using Variable Isotope Ratios</title><author>Lin, Lung-Cheng ; Wu, Hsin-Yi ; Tseng, Vincent Shin-Mu ; Chen, Lien-Chin ; Chang, Yu-Chen ; Liao, Pao-Chi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c560t-c4ef36813a3a9d387f69e345f9b1bc05c8f652ce631f483bd9cfdd1bddeebeb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Algorithms</topic><topic>Analytical Chemistry</topic><topic>Animals</topic><topic>Bioinformatics</topic><topic>Biotechnology</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chromatographic methods and physical methods associated with chromatography</topic><topic>Chromatography, Liquid - methods</topic><topic>Computational Biology - methods</topic><topic>Confidence</topic><topic>Confidence intervals</topic><topic>Data mining</topic><topic>Diethylhexyl Phthalate - chemistry</topic><topic>Exact sciences and technology</topic><topic>Filtering</topic><topic>Filtration</topic><topic>Isotope ratios</topic><topic>Isotopes - chemistry</topic><topic>Liver - metabolism</topic><topic>Male</topic><topic>Mass spectrometry</topic><topic>Mass Spectrometry - methods</topic><topic>Metabolites</topic><topic>Mining</topic><topic>Models, Statistical</topic><topic>Organic Chemistry</topic><topic>Other chromatographic methods</topic><topic>Precursors</topic><topic>Proteomics</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Solid Phase Extraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lin, Lung-Cheng</creatorcontrib><creatorcontrib>Wu, Hsin-Yi</creatorcontrib><creatorcontrib>Tseng, Vincent Shin-Mu</creatorcontrib><creatorcontrib>Chen, Lien-Chin</creatorcontrib><creatorcontrib>Chang, Yu-Chen</creatorcontrib><creatorcontrib>Liao, Pao-Chi</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of the American Society for Mass Spectrometry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lin, Lung-Cheng</au><au>Wu, Hsin-Yi</au><au>Tseng, Vincent Shin-Mu</au><au>Chen, Lien-Chin</au><au>Chang, Yu-Chen</au><au>Liao, Pao-Chi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Statistical Procedure to Selectively Detect Metabolite Signals in LC-MS Data Based on Using Variable Isotope Ratios</atitle><jtitle>Journal of the American Society for Mass Spectrometry</jtitle><stitle>J Am Soc Mass Spectrom</stitle><addtitle>J Am Soc Mass Spectrom</addtitle><date>2010-02-01</date><risdate>2010</risdate><volume>21</volume><issue>2</issue><spage>232</spage><epage>241</epage><pages>232-241</pages><issn>1044-0305</issn><eissn>1879-1123</eissn><abstract>The tracing of metabolite signals in LC-MS data using stable isotope-labeled compounds has been described in the literature. However, the filtering efficiency and confidence when mining metabolite signals in complex LC-MS datasets can be improved. Here, we propose an additional statistical procedure to increase the compound-derived signal mining efficiency. This method also provides a highly confident approach to screen out metabolite signals because the correlation of varying concentration ratios of native/stable isotope-labeled compounds and their instrumental response ratio is used. An in-house computational program [signal mining algorithm with isotope tracing (SMAIT)] was developed to perform the statistical procedure. To illustrate the SMAIT concept and its effectiveness for mining metabolite signals in LC-MS data, the plasticizer, di-(2-ethylhexyl) phthalate (DEHP), was used as an example. The statistical procedure effectively filtered 15 probable metabolite signals from 3617 peaks in the LC-MS data. These probable metabolite signals were considered structurally related to DEHP. Results obtained here suggest that the statistical procedure could be used to confidently facilitate the detection of probable metabolites from a compound-derived precursor presented in a complex LC-MS dataset.
A statistical procedure was proposed and developed to selectively detect metabolite signals in LC-MS data based on using variable isotope ratios.</abstract><cop>New York</cop><pub>Elsevier Inc</pub><pmid>19892567</pmid><doi>10.1016/j.jasms.2009.10.002</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Algorithms Analytical Chemistry Animals Bioinformatics Biotechnology Chemistry Chemistry and Materials Science Chromatographic methods and physical methods associated with chromatography Chromatography, Liquid - methods Computational Biology - methods Confidence Confidence intervals Data mining Diethylhexyl Phthalate - chemistry Exact sciences and technology Filtering Filtration Isotope ratios Isotopes - chemistry Liver - metabolism Male Mass spectrometry Mass Spectrometry - methods Metabolites Mining Models, Statistical Organic Chemistry Other chromatographic methods Precursors Proteomics Rats Rats, Wistar Solid Phase Extraction |
title | A Statistical Procedure to Selectively Detect Metabolite Signals in LC-MS Data Based on Using Variable Isotope Ratios |
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