TY - JOUR
T1 - An ontology-based approach to linking model organisms and resources to human diseases
AU - Mungall, Christopher J.
AU - Anderson, David
AU - Bandrowski, Anita
AU - Canada, Brian
AU - Chatyr-Aryamontri, Andrew
AU - Cheng, Keith
AU - Conn, P. Michael
AU - Dolinski, Kara
AU - Ellisman, Mark
AU - Eppig, Janan
AU - Grethe, Jeffrey S.
AU - Kemnitz, Joseph
AU - Iadonato, Shawn
AU - Larson, Stephen D.
AU - Magness, Charles
AU - Martone, Marvann E.
AU - Tyers, Mike
AU - Torniai, Carlo
AU - Troyanskaya, Olga G.
AU - Turner, Judith
AU - Westerfield, Monte
AU - Haendel, Melissa A.
PY - 2011
Y1 - 2011
N2 - The scientific community has invested heavily in the creation of genetically modified organisms, other model systems, and large genetic screens because they greatly inform our understanding of human disease. However, it remains difficult to identify organisms suitable for one's research because information about them is not readily accessible. The initiative to Link Animal Models to Human Disease (LAMHDI; http://lamhdi.org) was developed to allow users to search for a diverse set of models of disease using both curated disease-model links and inferred paths based on gene orthology and pathway membership. These inferences are made by traversing connections between records in publicly available data from resources such as the Online Mendelian Inheritance in Man (OMIM). Medical Subject Headings (MeSH), EntrezGene. Homologene. and WikiPathways. This allows researchers to rapidly explore and identify a wide range of model systems, visualizing the multi-step genetic relationship between disease and model. However, if LAMHDI were able to semantically link an organism's phenotypic attributes to diseases, genes, expression profiles, etc. their relevance and utility to a given line of research would be much more greatly illuminated and new novel insights between disease, genetics and phenotype discovered.
AB - The scientific community has invested heavily in the creation of genetically modified organisms, other model systems, and large genetic screens because they greatly inform our understanding of human disease. However, it remains difficult to identify organisms suitable for one's research because information about them is not readily accessible. The initiative to Link Animal Models to Human Disease (LAMHDI; http://lamhdi.org) was developed to allow users to search for a diverse set of models of disease using both curated disease-model links and inferred paths based on gene orthology and pathway membership. These inferences are made by traversing connections between records in publicly available data from resources such as the Online Mendelian Inheritance in Man (OMIM). Medical Subject Headings (MeSH), EntrezGene. Homologene. and WikiPathways. This allows researchers to rapidly explore and identify a wide range of model systems, visualizing the multi-step genetic relationship between disease and model. However, if LAMHDI were able to semantically link an organism's phenotypic attributes to diseases, genes, expression profiles, etc. their relevance and utility to a given line of research would be much more greatly illuminated and new novel insights between disease, genetics and phenotype discovered.
KW - Gene orthology
KW - Model organism
KW - Phenotype
KW - Similarity algorithm
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M3 - Conference article
AN - SCOPUS:84891955175
SN - 1613-0073
VL - 833
SP - 263
EP - 265
JO - CEUR Workshop Proceedings
JF - CEUR Workshop Proceedings
T2 - 2nd International Conference on Biomedical Ontology, ICBO 2011
Y2 - 26 July 2011 through 30 July 2011
ER -