Literature DB >> 26900164

Featured Article: Genotation: Actionable knowledge for the scientific reader.

Panduka Nagahawatte1, Ethan Willis2, Mark Sakauye2, Rony Jose2, Hao Chen3, Robert L Davis2.   

Abstract

We present an article viewer application that allows a scientific reader to easily discover and share knowledge by linking genomics-related concepts to knowledge of disparate biomedical databases. High-throughput data streams generated by technical advancements have contributed to scientific knowledge discovery at an unprecedented rate. Biomedical Informaticists have created a diverse set of databases to store and retrieve the discovered knowledge. The diversity and abundance of such resources present biomedical researchers a challenge with knowledge discovery. These challenges highlight a need for a better informatics solution. We use a text mining algorithm, Genomine, to identify gene symbols from the text of a journal article. The identified symbols are supplemented with information from the GenoDB knowledgebase. Self-updating GenoDB contains information from NCBI Gene, Clinvar, Medgen, dbSNP, KEGG, PharmGKB, Uniprot, and Hugo Gene databases. The journal viewer is a web application accessible via a web browser. The features described herein are accessible on www.genotation.org The Genomine algorithm identifies gene symbols with an accuracy shown by .65 F-Score. GenoDB currently contains information regarding 59,905 gene symbols, 5633 drug-gene relationships, 5981 gene-disease relationships, and 713 pathways. This application provides scientific readers with actionable knowledge related to concepts of a manuscript. The reader will be able to save and share supplements to be visualized in a graphical manner. This provides convenient access to details of complex biological phenomena, enabling biomedical researchers to generate novel hypothesis to further our knowledge in human health. This manuscript presents a novel application that integrates genomic, proteomic, and pharmacogenomic information to supplement content of a biomedical manuscript and enable readers to automatically discover actionable knowledge.
© 2016 by the Society for Experimental Biology and Medicine.

Entities:  

Keywords:  Genomic supplements; annotation gene; annotation protein; journal article viewer; pharmacogenomics

Mesh:

Year:  2016        PMID: 26900164      PMCID: PMC4950314          DOI: 10.1177/1535370216633795

Source DB:  PubMed          Journal:  Exp Biol Med (Maywood)        ISSN: 1535-3699


  17 in total

1.  KEGG: kyoto encyclopedia of genes and genomes.

Authors:  M Kanehisa; S Goto
Journal:  Nucleic Acids Res       Date:  2000-01-01       Impact factor: 16.971

2.  dbSNP: the NCBI database of genetic variation.

Authors:  S T Sherry; M H Ward; M Kholodov; J Baker; L Phan; E M Smigielski; K Sirotkin
Journal:  Nucleic Acids Res       Date:  2001-01-01       Impact factor: 16.971

3.  D³: Data-Driven Documents.

Authors:  Michael Bostock; Vadim Ogievetsky; Jeffrey Heer
Journal:  IEEE Trans Vis Comput Graph       Date:  2011-12       Impact factor: 4.579

4.  Declarative language design for interactive visualization.

Authors:  Jeffrey Heer; Michael Bostock
Journal:  IEEE Trans Vis Comput Graph       Date:  2010 Nov-Dec       Impact factor: 4.579

5.  PharmGKB: a logical home for knowledge relating genotype to drug response phenotype.

Authors:  Russ B Altman
Journal:  Nat Genet       Date:  2007-04       Impact factor: 38.330

6.  UniProt Knowledgebase: a hub of integrated protein data.

Authors:  Michele Magrane
Journal:  Database (Oxford)       Date:  2011-03-29       Impact factor: 3.451

7.  GoPubMed: exploring PubMed with the Gene Ontology.

Authors:  Andreas Doms; Michael Schroeder
Journal:  Nucleic Acids Res       Date:  2005-07-01       Impact factor: 16.971

8.  BioInfer: a corpus for information extraction in the biomedical domain.

Authors:  Sampo Pyysalo; Filip Ginter; Juho Heimonen; Jari Björne; Jorma Boberg; Jouni Järvinen; Tapio Salakoski
Journal:  BMC Bioinformatics       Date:  2007-02-09       Impact factor: 3.169

9.  Content-rich biological network constructed by mining PubMed abstracts.

Authors:  Hao Chen; Burt M Sharp
Journal:  BMC Bioinformatics       Date:  2004-10-08       Impact factor: 3.169

10.  ClinVar: public archive of relationships among sequence variation and human phenotype.

Authors:  Melissa J Landrum; Jennifer M Lee; George R Riley; Wonhee Jang; Wendy S Rubinstein; Deanna M Church; Donna R Maglott
Journal:  Nucleic Acids Res       Date:  2013-11-14       Impact factor: 16.971

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.