Ensembles of natural language processing systems for portable phenotyping solutions

[Display omitted] •Ensembles of natural language processing can improve phenotypic concept recognition.•A simple majority voting-based ensemble can increase the reproducibility.•An evaluation metric considering both concept relations and frequencies is useful. Manually curating standardized phenotyp...

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Veröffentlicht in:Journal of biomedical informatics 2019-12, Vol.100, p.103318-103318, Article 103318
Hauptverfasser: Liu, Cong, Ta, Casey N., Rogers, James R., Li, Ziran, Lee, Junghwan, Butler, Alex M., Shang, Ning, Kury, Fabricio Sampaio Peres, Wang, Liwei, Shen, Feichen, Liu, Hongfang, Ena, Lyudmila, Friedman, Carol, Weng, Chunhua
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container_title Journal of biomedical informatics
container_volume 100
creator Liu, Cong
Ta, Casey N.
Rogers, James R.
Li, Ziran
Lee, Junghwan
Butler, Alex M.
Shang, Ning
Kury, Fabricio Sampaio Peres
Wang, Liwei
Shen, Feichen
Liu, Hongfang
Ena, Lyudmila
Friedman, Carol
Weng, Chunhua
description [Display omitted] •Ensembles of natural language processing can improve phenotypic concept recognition.•A simple majority voting-based ensemble can increase the reproducibility.•An evaluation metric considering both concept relations and frequencies is useful. Manually curating standardized phenotypic concepts such as Human Phenotype Ontology (HPO) terms from narrative text in electronic health records (EHRs) is time consuming and error prone. Natural language processing (NLP) techniques can facilitate automated phenotype extraction and thus improve the efficiency of curating clinical phenotypes from clinical texts. While individual NLP systems can perform well for a single cohort, an ensemble-based method might shed light on increasing the portability of NLP pipelines across different cohorts. We compared four NLP systems, MetaMapLite, MedLEE, ClinPhen and cTAKES, and four ensemble techniques, including intersection, union, majority-voting and machine learning, for extracting generic phenotypic concepts. We addressed two important research questions regarding automated phenotype recognition. First, we evaluated the performance of different approaches in identifying generic phenotypic concepts. Second, we compared the performance of different methods to identify patient-specific phenotypic concepts. To better quantify the effects caused by concept granularity differences on performance, we developed a novel evaluation metric that considered concept hierarchies and frequencies. Each of the approaches was evaluated on a gold standard set of clinical documents annotated by clinical experts. One dataset containing 1,609 concepts derived from 50 clinical notes from two different institutions was used in both evaluations, and an additional dataset of 608 concepts derived from 50 case report abstracts obtained from PubMed was used for evaluation of identifying generic phenotypic concepts only. For generic phenotypic concept recognition, the top three performers in the NYP/CUIMC dataset are union ensemble (F1, 0.634), training-based ensemble (F1, 0.632), and majority vote-based ensemble (F1, 0.622). In the Mayo dataset, the top three are majority vote-based ensemble (F1, 0.642), cTAKES (F1, 0.615), and MedLEE (F1, 0.559). In the PubMed dataset, the top three are majority vote-based ensemble (F1, 0.719), training-based (F1, 0.696) and MetaMapLite (F1, 0.694). For identifying patient specific phenotypes, the top three performers in the NYP/CUIMC dataset are majority
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Manually curating standardized phenotypic concepts such as Human Phenotype Ontology (HPO) terms from narrative text in electronic health records (EHRs) is time consuming and error prone. Natural language processing (NLP) techniques can facilitate automated phenotype extraction and thus improve the efficiency of curating clinical phenotypes from clinical texts. While individual NLP systems can perform well for a single cohort, an ensemble-based method might shed light on increasing the portability of NLP pipelines across different cohorts. We compared four NLP systems, MetaMapLite, MedLEE, ClinPhen and cTAKES, and four ensemble techniques, including intersection, union, majority-voting and machine learning, for extracting generic phenotypic concepts. We addressed two important research questions regarding automated phenotype recognition. First, we evaluated the performance of different approaches in identifying generic phenotypic concepts. Second, we compared the performance of different methods to identify patient-specific phenotypic concepts. To better quantify the effects caused by concept granularity differences on performance, we developed a novel evaluation metric that considered concept hierarchies and frequencies. Each of the approaches was evaluated on a gold standard set of clinical documents annotated by clinical experts. One dataset containing 1,609 concepts derived from 50 clinical notes from two different institutions was used in both evaluations, and an additional dataset of 608 concepts derived from 50 case report abstracts obtained from PubMed was used for evaluation of identifying generic phenotypic concepts only. For generic phenotypic concept recognition, the top three performers in the NYP/CUIMC dataset are union ensemble (F1, 0.634), training-based ensemble (F1, 0.632), and majority vote-based ensemble (F1, 0.622). In the Mayo dataset, the top three are majority vote-based ensemble (F1, 0.642), cTAKES (F1, 0.615), and MedLEE (F1, 0.559). In the PubMed dataset, the top three are majority vote-based ensemble (F1, 0.719), training-based (F1, 0.696) and MetaMapLite (F1, 0.694). For identifying patient specific phenotypes, the top three performers in the NYP/CUIMC dataset are majority vote-based ensemble (F1, 0.610), MedLEE (F1, 0.609), and training-based ensemble (F1, 0.585). In the Mayo dataset, the top three are majority vote-based ensemble (F1, 0.604), cTAKES (F1, 0.531) and MedLEE (F1, 0.527). Our study demonstrates that ensembles of natural language processing can improve both generic phenotypic concept recognition and patient specific phenotypic concept identification over individual systems. Among the individual NLP systems, each individual system performed best when they were applied in the dataset that they were primary designed for. However, combining multiple NLP systems to create an ensemble can generally improve the performance. Specifically, the ensemble can increase the results reproducibility across different cohorts and tasks, and thus provide a more portable phenotyping solution compared to individual NLP systems.</description><identifier>ISSN: 1532-0464</identifier><identifier>EISSN: 1532-0480</identifier><identifier>DOI: 10.1016/j.jbi.2019.103318</identifier><identifier>PMID: 31655273</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Concept recognition ; Datasets as Topic ; Electronic Health Records ; Ensemble method ; Evaluation ; Human phenotype ontology ; Humans ; Natural Language Processing ; Phenotype ; Reproducibility ; Reproducibility of Results</subject><ispartof>Journal of biomedical informatics, 2019-12, Vol.100, p.103318-103318, Article 103318</ispartof><rights>2019 Elsevier Inc.</rights><rights>Copyright © 2019 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-e51fa729a16057cada1e2edba5821939b05236399b2f7b7bd01a753e8a54ad6b3</citedby><cites>FETCH-LOGICAL-c451t-e51fa729a16057cada1e2edba5821939b05236399b2f7b7bd01a753e8a54ad6b3</cites><orcidid>0000-0002-9624-0214 ; 0000-0002-7803-2331 ; 0000-0001-6024-3037</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1532046419302370$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31655273$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Cong</creatorcontrib><creatorcontrib>Ta, Casey N.</creatorcontrib><creatorcontrib>Rogers, James R.</creatorcontrib><creatorcontrib>Li, Ziran</creatorcontrib><creatorcontrib>Lee, Junghwan</creatorcontrib><creatorcontrib>Butler, Alex M.</creatorcontrib><creatorcontrib>Shang, Ning</creatorcontrib><creatorcontrib>Kury, Fabricio Sampaio Peres</creatorcontrib><creatorcontrib>Wang, Liwei</creatorcontrib><creatorcontrib>Shen, Feichen</creatorcontrib><creatorcontrib>Liu, Hongfang</creatorcontrib><creatorcontrib>Ena, Lyudmila</creatorcontrib><creatorcontrib>Friedman, Carol</creatorcontrib><creatorcontrib>Weng, Chunhua</creatorcontrib><title>Ensembles of natural language processing systems for portable phenotyping solutions</title><title>Journal of biomedical informatics</title><addtitle>J Biomed Inform</addtitle><description>[Display omitted] •Ensembles of natural language processing can improve phenotypic concept recognition.•A simple majority voting-based ensemble can increase the reproducibility.•An evaluation metric considering both concept relations and frequencies is useful. Manually curating standardized phenotypic concepts such as Human Phenotype Ontology (HPO) terms from narrative text in electronic health records (EHRs) is time consuming and error prone. Natural language processing (NLP) techniques can facilitate automated phenotype extraction and thus improve the efficiency of curating clinical phenotypes from clinical texts. While individual NLP systems can perform well for a single cohort, an ensemble-based method might shed light on increasing the portability of NLP pipelines across different cohorts. We compared four NLP systems, MetaMapLite, MedLEE, ClinPhen and cTAKES, and four ensemble techniques, including intersection, union, majority-voting and machine learning, for extracting generic phenotypic concepts. We addressed two important research questions regarding automated phenotype recognition. First, we evaluated the performance of different approaches in identifying generic phenotypic concepts. Second, we compared the performance of different methods to identify patient-specific phenotypic concepts. To better quantify the effects caused by concept granularity differences on performance, we developed a novel evaluation metric that considered concept hierarchies and frequencies. Each of the approaches was evaluated on a gold standard set of clinical documents annotated by clinical experts. One dataset containing 1,609 concepts derived from 50 clinical notes from two different institutions was used in both evaluations, and an additional dataset of 608 concepts derived from 50 case report abstracts obtained from PubMed was used for evaluation of identifying generic phenotypic concepts only. For generic phenotypic concept recognition, the top three performers in the NYP/CUIMC dataset are union ensemble (F1, 0.634), training-based ensemble (F1, 0.632), and majority vote-based ensemble (F1, 0.622). In the Mayo dataset, the top three are majority vote-based ensemble (F1, 0.642), cTAKES (F1, 0.615), and MedLEE (F1, 0.559). In the PubMed dataset, the top three are majority vote-based ensemble (F1, 0.719), training-based (F1, 0.696) and MetaMapLite (F1, 0.694). For identifying patient specific phenotypes, the top three performers in the NYP/CUIMC dataset are majority vote-based ensemble (F1, 0.610), MedLEE (F1, 0.609), and training-based ensemble (F1, 0.585). In the Mayo dataset, the top three are majority vote-based ensemble (F1, 0.604), cTAKES (F1, 0.531) and MedLEE (F1, 0.527). Our study demonstrates that ensembles of natural language processing can improve both generic phenotypic concept recognition and patient specific phenotypic concept identification over individual systems. Among the individual NLP systems, each individual system performed best when they were applied in the dataset that they were primary designed for. However, combining multiple NLP systems to create an ensemble can generally improve the performance. Specifically, the ensemble can increase the results reproducibility across different cohorts and tasks, and thus provide a more portable phenotyping solution compared to individual NLP systems.</description><subject>Concept recognition</subject><subject>Datasets as Topic</subject><subject>Electronic Health Records</subject><subject>Ensemble method</subject><subject>Evaluation</subject><subject>Human phenotype ontology</subject><subject>Humans</subject><subject>Natural Language Processing</subject><subject>Phenotype</subject><subject>Reproducibility</subject><subject>Reproducibility of Results</subject><issn>1532-0464</issn><issn>1532-0480</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9v3CAQxVGVqPnTfoBeKh9z2Q0DxjaKVKmK0iZSpB7SnhHg8YaVDQ7gSPvtQ7rpqr30NIz4vccwj5BPQNdAobncrrfGrRkFWXrOoXtHTkFwtqJ1R48O56Y-IWcpbSkFEKJ5T044NEKwlp-ShxufcDIjpioMldd5iXqsRu03i95gNcdgMSXnN1XapYxTqoYQqznErIuomh_Rh7ybfwNhXLILPn0gx4MeE358q-fk17ebn9e3q_sf3--uv96vbC0gr1DAoFsmNTRUtFb3GpBhb7ToGEguDRWMN1xKw4bWtKanoFvBsdOi1n1j-Dn5svedFzNhb9HnMryao5t03Kmgnfr3xrtHtQnPqumkBFkXg4s3gxieFkxZTS5ZHMv3MSxJMU5l3daStgWFPWpjSCnicHgGqHoNQ21VCUO9hqH2YRTN57_nOyj-bL8AV3sAy5aeHUaVrENvsXcRbVZ9cP-xfwFSPJzn</recordid><startdate>20191201</startdate><enddate>20191201</enddate><creator>Liu, Cong</creator><creator>Ta, Casey N.</creator><creator>Rogers, James R.</creator><creator>Li, Ziran</creator><creator>Lee, Junghwan</creator><creator>Butler, Alex M.</creator><creator>Shang, Ning</creator><creator>Kury, Fabricio Sampaio Peres</creator><creator>Wang, Liwei</creator><creator>Shen, Feichen</creator><creator>Liu, Hongfang</creator><creator>Ena, Lyudmila</creator><creator>Friedman, Carol</creator><creator>Weng, Chunhua</creator><general>Elsevier Inc</general><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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9624-0214</orcidid><orcidid>https://orcid.org/0000-0002-7803-2331</orcidid><orcidid>https://orcid.org/0000-0001-6024-3037</orcidid></search><sort><creationdate>20191201</creationdate><title>Ensembles of natural language processing systems for portable phenotyping solutions</title><author>Liu, Cong ; Ta, Casey N. ; Rogers, James R. ; Li, Ziran ; Lee, Junghwan ; Butler, Alex M. ; Shang, Ning ; Kury, Fabricio Sampaio Peres ; Wang, Liwei ; Shen, Feichen ; Liu, Hongfang ; Ena, Lyudmila ; Friedman, Carol ; Weng, Chunhua</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-e51fa729a16057cada1e2edba5821939b05236399b2f7b7bd01a753e8a54ad6b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Concept recognition</topic><topic>Datasets as Topic</topic><topic>Electronic Health Records</topic><topic>Ensemble method</topic><topic>Evaluation</topic><topic>Human phenotype ontology</topic><topic>Humans</topic><topic>Natural Language Processing</topic><topic>Phenotype</topic><topic>Reproducibility</topic><topic>Reproducibility of Results</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Cong</creatorcontrib><creatorcontrib>Ta, Casey N.</creatorcontrib><creatorcontrib>Rogers, James R.</creatorcontrib><creatorcontrib>Li, Ziran</creatorcontrib><creatorcontrib>Lee, Junghwan</creatorcontrib><creatorcontrib>Butler, Alex M.</creatorcontrib><creatorcontrib>Shang, Ning</creatorcontrib><creatorcontrib>Kury, Fabricio Sampaio Peres</creatorcontrib><creatorcontrib>Wang, Liwei</creatorcontrib><creatorcontrib>Shen, Feichen</creatorcontrib><creatorcontrib>Liu, Hongfang</creatorcontrib><creatorcontrib>Ena, Lyudmila</creatorcontrib><creatorcontrib>Friedman, Carol</creatorcontrib><creatorcontrib>Weng, Chunhua</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of biomedical informatics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Cong</au><au>Ta, Casey N.</au><au>Rogers, James R.</au><au>Li, Ziran</au><au>Lee, Junghwan</au><au>Butler, Alex M.</au><au>Shang, Ning</au><au>Kury, Fabricio Sampaio Peres</au><au>Wang, Liwei</au><au>Shen, Feichen</au><au>Liu, Hongfang</au><au>Ena, Lyudmila</au><au>Friedman, Carol</au><au>Weng, Chunhua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ensembles of natural language processing systems for portable phenotyping solutions</atitle><jtitle>Journal of biomedical informatics</jtitle><addtitle>J Biomed Inform</addtitle><date>2019-12-01</date><risdate>2019</risdate><volume>100</volume><spage>103318</spage><epage>103318</epage><pages>103318-103318</pages><artnum>103318</artnum><issn>1532-0464</issn><eissn>1532-0480</eissn><abstract>[Display omitted] •Ensembles of natural language processing can improve phenotypic concept recognition.•A simple majority voting-based ensemble can increase the reproducibility.•An evaluation metric considering both concept relations and frequencies is useful. Manually curating standardized phenotypic concepts such as Human Phenotype Ontology (HPO) terms from narrative text in electronic health records (EHRs) is time consuming and error prone. Natural language processing (NLP) techniques can facilitate automated phenotype extraction and thus improve the efficiency of curating clinical phenotypes from clinical texts. While individual NLP systems can perform well for a single cohort, an ensemble-based method might shed light on increasing the portability of NLP pipelines across different cohorts. We compared four NLP systems, MetaMapLite, MedLEE, ClinPhen and cTAKES, and four ensemble techniques, including intersection, union, majority-voting and machine learning, for extracting generic phenotypic concepts. We addressed two important research questions regarding automated phenotype recognition. First, we evaluated the performance of different approaches in identifying generic phenotypic concepts. Second, we compared the performance of different methods to identify patient-specific phenotypic concepts. To better quantify the effects caused by concept granularity differences on performance, we developed a novel evaluation metric that considered concept hierarchies and frequencies. Each of the approaches was evaluated on a gold standard set of clinical documents annotated by clinical experts. One dataset containing 1,609 concepts derived from 50 clinical notes from two different institutions was used in both evaluations, and an additional dataset of 608 concepts derived from 50 case report abstracts obtained from PubMed was used for evaluation of identifying generic phenotypic concepts only. For generic phenotypic concept recognition, the top three performers in the NYP/CUIMC dataset are union ensemble (F1, 0.634), training-based ensemble (F1, 0.632), and majority vote-based ensemble (F1, 0.622). In the Mayo dataset, the top three are majority vote-based ensemble (F1, 0.642), cTAKES (F1, 0.615), and MedLEE (F1, 0.559). In the PubMed dataset, the top three are majority vote-based ensemble (F1, 0.719), training-based (F1, 0.696) and MetaMapLite (F1, 0.694). For identifying patient specific phenotypes, the top three performers in the NYP/CUIMC dataset are majority vote-based ensemble (F1, 0.610), MedLEE (F1, 0.609), and training-based ensemble (F1, 0.585). In the Mayo dataset, the top three are majority vote-based ensemble (F1, 0.604), cTAKES (F1, 0.531) and MedLEE (F1, 0.527). Our study demonstrates that ensembles of natural language processing can improve both generic phenotypic concept recognition and patient specific phenotypic concept identification over individual systems. Among the individual NLP systems, each individual system performed best when they were applied in the dataset that they were primary designed for. However, combining multiple NLP systems to create an ensemble can generally improve the performance. Specifically, the ensemble can increase the results reproducibility across different cohorts and tasks, and thus provide a more portable phenotyping solution compared to individual NLP systems.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>31655273</pmid><doi>10.1016/j.jbi.2019.103318</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-9624-0214</orcidid><orcidid>https://orcid.org/0000-0002-7803-2331</orcidid><orcidid>https://orcid.org/0000-0001-6024-3037</orcidid><oa>free_for_read</oa></addata></record>
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subjects Concept recognition
Datasets as Topic
Electronic Health Records
Ensemble method
Evaluation
Human phenotype ontology
Humans
Natural Language Processing
Phenotype
Reproducibility
Reproducibility of Results
title Ensembles of natural language processing systems for portable phenotyping solutions
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