Because of the staggering complexity of biological systems, biomedical research is becoming increasingly dependent on knowledge stored in a computable form. The Gene Ontology (GO) is by far the largest knowledgebase of how genes function, and has become a critical component of the computational infrastructure enabling the genomic revolution. It has become nearly indispensible in the interpretation of large- scale molecular measurements in biological research. Crucially, for human health research, GO is also one of a suite of complementary ontologies constructed in such as way to maximally promote interoperability and comparability of data sets. It represents the gene functions and biological processes that are perturbed in human disease, e.g. via the links from Human Phenotype Ontology (HPO) class abnormality of lipid metabolism, defined in relation to the GO class lipid metabolic process (GO_0006629), researchers or clinicians can find the set of genes that are known to be involved in this process. GO is a knowledge resource that can be statistically mined, either standalone or in combination with data from other knowledge resources, which enables experts to discover connections and form new hypotheses from the biological networks GO represents. All knowledge in GO is represented using semantic web technologies and so is amenable to computational integration and consistency checking. The proposed GO knowledge environment will enable a wider community of scientists to contribute to, and to utilize, a common, computable representation of biology. To ensure the knowledge environment meets the requirements of biomedical researchers, we will: a) deliver a comprehensive, detailed, computable knowledgebase of gene function, encoded in the Gene Ontology and annotations (computer-readable statements about the how specific genes function), focusing on human biology; b) provide a ?hub? for a broad community of scientists to collaboratively extend, correct and improve the knowledgebase; c) ensure the GO knowledge resource is of the highest quality with regards to depth, breadth and accuracy; d) facilitate the transfer of insights obtained from studies of non-human organisms, such as the mouse and zebrafish, to human biology; and e) enable the scientific community to use the knowledgebase in analyses of large-scale genetic and -omics data.
Our aims reflect the essential requirements for realizing the overarching objectives for a biomedical data resource: efficiently capturing and integrating biological knowledge and adhering to the highest possible standard for accuracy and detail; constructing and providing a robust, flexible, powerful, and extensible technological infrastructure available not only for internal use but just as easily by the wider community; and lastly, leveraging state-of-the-art social media, web services and other technologies to disseminate the GO resource to the entire biomedical research community.

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Biotechnology Resource Cooperative Agreements (U41)
Project #
2U41HG002273-17
Application #
9209991
Study Section
Genome Research Review Committee (GNOM-G)
Project Start
Project End
Budget Start
2017-03-01
Budget End
2018-02-28
Support Year
17
Fiscal Year
2017
Total Cost
$1,002,376
Indirect Cost
$139,869
Name
University of Southern California
Department
Type
Domestic Higher Education
DUNS #
072933393
City
Los Angeles
State
CA
Country
United States
Zip Code
90032
Christie, Karen R; Blake, Judith A (2018) Sensing the cilium, digital capture of ciliary data for comparative genomics investigations. Cilia 7:3
Müller, H-M; Van Auken, K M; Li, Y et al. (2018) Textpresso Central: a customizable platform for searching, text mining, viewing, and curating biomedical literature. BMC Bioinformatics 19:94
Pichler, Klemens; Warner, Kate; Magrane, Michele et al. (2018) SPIN: Submitting Sequences Determined at Protein Level to UniProt. Curr Protoc Bioinformatics 62:e52
The UniProt Consortium (2017) UniProt: the universal protein knowledgebase. Nucleic Acids Res 45:D158-D169
Gaudet, Pascale; Dessimoz, Christophe (2017) Gene Ontology: Pitfalls, Biases, and Remedies. Methods Mol Biol 1446:189-205
Kramer, Michael H; Farré, Jean-Claude; Mitra, Koyel et al. (2017) Active Interaction Mapping Reveals the Hierarchical Organization of Autophagy. Mol Cell 65:761-774.e5
Hastings, Janna (2017) Primer on Ontologies. Methods Mol Biol 1446:3-13
Zaru, Rossana; Magrane, Michele; O'Donovan, Claire et al. (2017) From the research laboratory to the database: the Caenorhabditis elegans kinome in UniProtKB. Biochem J 474:493-515
Tkavc, Rok; Matrosova, Vera Y; Grichenko, Olga E et al. (2017) Prospects for Fungal Bioremediation of Acidic Radioactive Waste Sites: Characterization and Genome Sequence of Rhodotorula taiwanensis MD1149. Front Microbiol 8:2528
Lewis, Suzanna E (2017) The Vision and Challenges of the Gene Ontology. Methods Mol Biol 1446:291-302

Showing the most recent 10 out of 88 publications