2012
DOI: 10.1007/978-3-642-31040-9_8
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Validating Candidate Gene-Mutation Relations in MEDLINE Abstracts via Crowdsourcing

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Cited by 8 publications
(18 citation statements)
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“…The average F score of workers that completed a hundred or more abstracts was 0.791 with a standard deviation of 0.066. This result generally reiterates the findings in [10], which observed a clear increase in performance for workers that completed more than 100 of their gene-mutation validation tasks. However, the correlation between the number of tasks performed and the average quality of the work was not statistically significant in this experiment.…”
Section: Resultssupporting
confidence: 89%
See 1 more Smart Citation
“…The average F score of workers that completed a hundred or more abstracts was 0.791 with a standard deviation of 0.066. This result generally reiterates the findings in [10], which observed a clear increase in performance for workers that completed more than 100 of their gene-mutation validation tasks. However, the correlation between the number of tasks performed and the average quality of the work was not statistically significant in this experiment.…”
Section: Resultssupporting
confidence: 89%
“…Two early studies demonstrated that a gold standard corpus of annotated clinical trials documents could be assembled through microtask crowdsourcing [8, 9]. Recently, others have successfully applied microtasking to validate predicted gene-mutation relations in PubMed abstracts [10] and for medical relation extraction [11]. Here we extend these efforts by implementing and testing a disease mention annotation task on PubMed abstracts using the AMT platform.…”
Section: Introductionmentioning
confidence: 94%
“…However, in contrast to the general NLP domain, there are only a few studies involving crowdsourcing in biomedical NLP and almost none for clinical NLP. Most recently, Burger et al [19] performed a task of extracting the gene-mutation relations in Medical Literature Analysis and Retrieval System Online (MEDLINE) abstracts on AMT. In their work, candidate mutations were extracted from 250 MEDLINE abstracts using the Extractor of Mutations (EMU) presented together with the curated gene lists from the National Center for Biotechnology Information (NCBI).…”
Section: Introductionmentioning
confidence: 99%
“…Building on results from an earlier experiment (22), we refined the framework and enriched the gold standard for easier evaluation.…”
Section: Methodsmentioning
confidence: 99%