Literature DB >> 18172928

Application of automatic mutation-gene pair extraction to diseases.

Muge Erdogmus1, Osman Ugur Sezerman.   

Abstract

To have a better understanding of the mechanisms of disease development, knowledge of mutations and the genes on which the mutations occur is of crucial importance. Information on disease-related mutations can be accessed through public databases or biomedical literature sources. However, information retrieval from such resources can be problematic because of two reasons: manually created databases are usually incomplete and not up to date, and reading through a vast amount of publicly available biomedical documents is very time-consuming. In this paper, we describe an automated system, MuGeX (Mutation Gene eXtractor), that automatically extracts mutation-gene pairs from Medline abstracts for a disease query. Our system is tested on a corpus that consists of 231 Medline abstracts. While recall for mutation detection alone is 85.9%, precision is 95.9%. For extraction of mutation-gene pairs, we focus on Alzheimer's disease. The recall for mutation-gene pair identification is estimated at 91.3%, and precision is estimated at 88.9%. With automatic extraction techniques, MuGeX overcomes the problems of information retrieval from public resources and reduces the time required to access relevant information, while preserving the accuracy of retrieved information.

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Year:  2007        PMID: 18172928     DOI: 10.1142/s021972000700317x

Source DB:  PubMed          Journal:  J Bioinform Comput Biol        ISSN: 0219-7200            Impact factor:   1.122


  20 in total

1.  Toward an automatic method for extracting cancer- and other disease-related point mutations from the biomedical literature.

Authors:  Emily Doughty; Attila Kertesz-Farkas; Olivier Bodenreider; Gary Thompson; Asa Adadey; Thomas Peterson; Maricel G Kann
Journal:  Bioinformatics       Date:  2010-12-07       Impact factor: 6.937

2.  A literature search tool for intelligent extraction of disease-associated genes.

Authors:  Jae-Yoon Jung; Todd F DeLuca; Tristan H Nelson; Dennis P Wall
Journal:  J Am Med Inform Assoc       Date:  2013-09-02       Impact factor: 4.497

3.  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

4.  Text mining for precision medicine: automating disease-mutation relationship extraction from biomedical literature.

Authors:  Ayush Singhal; Michael Simmons; Zhiyong Lu
Journal:  J Am Med Inform Assoc       Date:  2016-04-27       Impact factor: 4.497

5.  Improved mutation tagging with gene identifiers applied to membrane protein stability prediction.

Authors:  Rainer Winnenburg; Conrad Plake; Michael Schroeder
Journal:  BMC Bioinformatics       Date:  2009-08-27       Impact factor: 3.169

Review 6.  Towards precision medicine: advances in computational approaches for the analysis of human variants.

Authors:  Thomas A Peterson; Emily Doughty; Maricel G Kann
Journal:  J Mol Biol       Date:  2013-08-17       Impact factor: 5.469

7.  Prospects for the automated extraction of mutation data from the scientific literature.

Authors:  Peter D Stenson; David N Cooper
Journal:  Hum Genomics       Date:  2010-10       Impact factor: 4.639

8.  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

9.  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

10.  EnzyMiner: automatic identification of protein level mutations and their impact on target enzymes from PubMed abstracts.

Authors:  Süveyda Yeniterzi; Ugur Sezerman
Journal:  BMC Bioinformatics       Date:  2009-08-27       Impact factor: 3.169

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