Literature DB >> 15180929

An entity tagger for recognizing acquired genomic variations in cancer literature.

Ryan T McDonald1, R Scott Winters, Mark Mandel, Yang Jin, Peter S White, Fernando Pereira.   

Abstract

VTag is an application for identifying the type, genomic location and genomic state-change of acquired genomic aberrations described in text. The application uses a machine learning technique called conditional random fields. VTag was tested with 345 training and 200 evaluation documents pertaining to cancer genetics. Our experiments resulted in 0.8541 precision, 0.7870 recall and 0.8192 F-measure on the evaluation set.

Entities:  

Mesh:

Year:  2004        PMID: 15180929     DOI: 10.1093/bioinformatics/bth350

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  12 in total

1.  tmVar: a text mining approach for extracting sequence variants in biomedical literature.

Authors:  Chih-Hsuan Wei; Bethany R Harris; Hung-Yu Kao; Zhiyong Lu
Journal:  Bioinformatics       Date:  2013-04-05       Impact factor: 6.937

2.  ResidueFinder: extracting individual residue mentions from protein literature.

Authors:  Ton E Becker; Eric Jakobsson
Journal:  J Biomed Semantics       Date:  2021-07-21

3.  Detection of IUPAC and IUPAC-like chemical names.

Authors:  Roman Klinger; Corinna Kolárik; Juliane Fluck; Martin Hofmann-Apitius; Christoph M Friedrich
Journal:  Bioinformatics       Date:  2008-07-01       Impact factor: 6.937

4.  Interpretation of the consequences of mutations in protein kinases: combined use of bioinformatics and text mining.

Authors:  Jose M G Izarzugaza; Martin Krallinger; Alfonso Valencia
Journal:  Front Physiol       Date:  2012-08-22       Impact factor: 4.566

5.  Challenges in the association of human single nucleotide polymorphism mentions with unique database identifiers.

Authors:  Philippe E Thomas; Roman Klinger; Laura I Furlong; Martin Hofmann-Apitius; Christoph M Friedrich
Journal:  BMC Bioinformatics       Date:  2011-07-05       Impact factor: 3.169

6.  Automated recognition of malignancy mentions in biomedical literature.

Authors:  Yang Jin; Ryan T McDonald; Kevin Lerman; Mark A Mandel; Steven Carroll; Mark Y Liberman; Fernando C Pereira; Raymond S Winters; Peter S White
Journal:  BMC Bioinformatics       Date:  2006-11-07       Impact factor: 3.169

7.  Extraction of pharmacokinetic evidence of drug-drug interactions from the literature.

Authors:  Artemy Kolchinsky; Anália Lourenço; Heng-Yi Wu; Lang Li; Luis M Rocha
Journal:  PLoS One       Date:  2015-05-11       Impact factor: 3.240

8.  Extraction of human kinase mutations from literature, databases and genotyping studies.

Authors:  Martin Krallinger; Jose M G Izarzugaza; Carlos Rodriguez-Penagos; Alfonso Valencia
Journal:  BMC Bioinformatics       Date:  2009-08-27       Impact factor: 3.169

9.  Getting more out of biomedical documents with GATE's full lifecycle open source text analytics.

Authors:  Hamish Cunningham; Valentin Tablan; Angus Roberts; Kalina Bontcheva
Journal:  PLoS Comput Biol       Date:  2013-02-07       Impact factor: 4.475

10.  OSIRISv1.2: a named entity recognition system for sequence variants of genes in biomedical literature.

Authors:  Laura I Furlong; Holger Dach; Martin Hofmann-Apitius; Ferran Sanz
Journal:  BMC Bioinformatics       Date:  2008-02-05       Impact factor: 3.169

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