Abstract
The Matchmaker Exchange application programming interface (API) allows searching a patient's genotypic or phenotypic profiles across clinical sites, for the purposes of cohort discovery and variant disease causal validation. This API can be used not only to search for matching patients, but also to match against public disease and model organism data. This public disease data enable matching known diseases and variant-phenotype associations using phenotype semantic similarity algorithms developed by the Monarch Initiative. The model data can provide additional evidence to aid diagnosis, suggest relevant models for disease mechanism and treatment exploration, and identify collaborators across the translational divide. The Monarch Initiative provides an implementation of this API for searching multiple integrated sources of data that contextualize the knowledge about any given patient or patient family into the greater biomedical knowledge landscape. While this corpus of data can aid diagnosis, it is also the beginning of research to improve understanding of rare human diseases.
Keywords
Matchmaker Exchange
informatics
model systems
ontology
phenotype
rare disease
MeSH Terms
Animals
Databases, Genetic
Disease/genetics
Disease Models, Animal
Genetic Predisposition to Disease/genetics
Genetic Variation
Humans
Information Dissemination
Phenotype
User-Computer Interface
Authors & Affiliations
12 authors, click to expand affiliations / ORCID
Mungall Christopher J
Genomics Division, Lawrence Berkeley National Laboratory, Berkeley, California.
Washington Nicole L
Genomics Division, Lawrence Berkeley National Laboratory, Berkeley, California.
Nguyen-Xuan Jeremy
Genomics Division, Lawrence Berkeley National Laboratory, Berkeley, California.
Condit Christopher
San Diego Supercomputing Center, UC San Diego, La Jolla, California.
Smedley Damian
Wellcome Trust Sanger Institute, Mouse Informatics group, Hinxton, UK.
Köhler Sebastian
Charité - Universitätsmedizin Berlin, Institute for Medical and Human Genetics, Berlin, Germany.
Groza Tudor
Kinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Sydney, Australia.
Shefchek Kent
Department of Biomedical Informatics and Clinical Epidemiology, Oregon Health and Science University, Portland, Oregon.
Hochheiser Harry
Department of Biomedical Informatics, University of Pittsburgh, Pittsburgh, Pennsylvania.
Robinson Peter N
Charité - Universitätsmedizin Berlin, Institute for Medical and Human Genetics, Berlin, Germany.
Lewis Suzanna E
Genomics Division, Lawrence Berkeley National Laboratory, Berkeley, California.
Haendel Melissa A
Department of Biomedical Informatics and Clinical Epidemiology, Oregon Health and Science University, Portland, Oregon.
References (27)
27 references, click to expand
-
The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease.
Am J Hum Genet. 2008 Nov;83(5):610-5
PMID: 18950739
-
York platelet syndrome is a CRAC channelopathy due to gain-of-function mutations in STIM1.
Mol Genet Metab. 2015 Mar;114(3):474-82
PMID: 25577287
-
The zebrafish anatomy and stage ontologies: representing the anatomy and development of Danio rerio.
J Biomed Semantics. 2014 Feb 25;5(1):12
PMID: 24568621
-
Improved exome prioritization of disease genes through cross-species phenotype comparison.
Genome Res. 2014 Feb;24(2):340-8
PMID: 24162188
-
The Matchmaker Exchange: a platform for rare disease gene discovery.
Hum Mutat. 2015 Oct;36(10):915-21
PMID: 26295439
-
The Matchmaker Exchange API: automating patient matching through the exchange of structured phenotypic and genotypic profiles.
Hum Mutat. 2015 Oct;36(10):922-7
PMID: 26255989
-
Unification of multi-species vertebrate anatomy ontologies for comparative biology in Uberon.
J Biomed Semantics. 2014 May 19;5:21
PMID: 25009735
-
Uberon, an integrative multi-species anatomy ontology.
Genome Biol. 2012 Jan 31;13(1):R5
PMID: 22293552
-
The International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping data.
Nucleic Acids Res. 2014 Jan;42(Database issue):D802-9
PMID: 24194600
-
PhenoDigm: analyzing curated annotations to associate animal models with human diseases.
Database (Oxford). 2013 May 09;2013:bat025
PMID: 23660285
-
A systematic survey of loss-of-function variants in human protein-coding genes.
Science. 2012 Feb 17;335(6070):823-8
PMID: 22344438
-
The Cancer Genome Atlas Pan-Cancer analysis project.
Nat Genet. 2013 Oct;45(10):1113-20
PMID: 24071849
-
GeneMatcher: a matching tool for connecting investigators with an interest in the same gene.
Hum Mutat. 2015 Oct;36(10):928-30
PMID: 26220891
-
Construction and accessibility of a cross-species phenotype ontology along with gene annotations for biomedical research.
F1000Res. 2013 Feb 01;2:30
PMID: 24358873
-
Rare-disease genetics in the era of next-generation sequencing: discovery to translation.
Nat Rev Genet. 2013 Oct;14(10):681-91
PMID: 23999272
-
Expanding the mammalian phenotype ontology to support automated exchange of high throughput mouse phenotyping data generated by large-scale mouse knockout screens.
J Biomed Semantics. 2015 Mar 25;6:11
PMID: 25825651
-
A systematic genome-wide analysis of zebrafish protein-coding gene function.
Nature. 2013 Apr 25;496(7446):494-7
PMID: 23594742
-
Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome.
Sci Transl Med. 2014 Sep 3;6(252):252ra123
PMID: 25186178
-
The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data.
Nucleic Acids Res. 2014 Jan;42(Database issue):D966-74
PMID: 24217912
-
ZFIN, the Zebrafish Model Organism Database: increased support for mutants and transgenics.
Nucleic Acids Res. 2013 Jan;41(Database issue):D854-60
PMID: 23074187
-
Linking human diseases to animal models using ontology-based phenotype annotation.
PLoS Biol. 2009 Nov;7(11):e1000247
PMID: 19956802
-
OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders.
Nucleic Acids Res. 2015 Jan;43(Database issue):D789-98
PMID: 25428349
-
Phenotype ontologies and cross-species analysis for translational research.
PLoS Genet. 2014 Apr 03;10(4):e1004268
PMID: 24699242
-
Representation of rare diseases in health information systems: the Orphanet approach to serve a wide range of end users.
Hum Mutat. 2012 May;33(5):803-8
PMID: 22422702
-
ClinVar: public archive of relationships among sequence variation and human phenotype.
Nucleic Acids Res. 2014 Jan;42(Database issue):D980-5
PMID: 24234437
-
Integrating phenotype ontologies across multiple species.
Genome Biol. 2010 Jan 08;11(1):R2
PMID: 20064205
-
The Mouse Genome Database: integration of and access to knowledge about the laboratory mouse.
Nucleic Acids Res. 2014 Jan;42(Database issue):D810-7
PMID: 24285300