Knowledge Management Center for Illuminating the Druggable Genome
Knowledge Management Center for Illuminating the Druggable Genome
批准号:
10598542
负责人:
Jeremy S Edwards
金额:
$94.01万
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-01-03 至 2024-12-31
关键词:
AccelerationAddressAdoptionAgeAllelesArchivesArticulationBasic ScienceBiological SciencesBiologyBiomedical ResearchChemistryCodeCommunitiesCommunity OutreachComputer softwareCoupledDataData AnalyticsData ElementData SetDatabasesDependenceDiseaseDocumentationFAIR principlesFamilyFeedbackFundingFutureGenerationsGenesGenomeGenome ComponentsGenotypeGoalsGrantHealthcareHumanInformaticsInternationalInternetKnowledgeKnowledge ManagementKnowledge Management CenterLifeLinkMachine LearningManualsMapsMedicineMetadataMethodsModelingMutationNon-Human ProteinOntologyPathway interactionsPerformancePhasePhenotypeProcessProtein IsoformsProteinsProteomePublic DomainsPublicationsReagentResearch Domain CriteriaResourcesScientistSeriesServicesSourceStructureSystemTranslational ResearchTreesUnited States National Institutes of HealthUpdateWorkanalytical methodbasecomputer sciencedata ecosystemdata integrationdata resourcedesigndisease classificationexperiencegender differencegenome resourcehealth dataimprovedinterestknowledge baseknowledge graphknowledgebasemembernovelonline communityoutreachprogramspublic repositoryrepositorytherapeutic proteintoolweb site
中文摘要
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英文摘要
The main goal of the Knowledge Management Center (KMC) for the Illuminating the Druggable Genome (IDG)
program is to aggregate, update and articulate protein-centric data, information and knowledge for the entire
human proteome with emphasis on understudied proteins from the 3 families that are the focus of the IDG
(“IDG List”). The long-term objective of the KMC is to encourage and support biomedical research aimed at
understudied proteins by providing an extensive resource of data, information, knowledge, methods and
reagents for the entire human proteome, and to support the growing online community focused on
understudied proteins. With focus on the IDG List and human proteins, the KMC will enable support for
expanded coverage for non-human proteins of therapeutic interest and other associated human health data, in
order to catalyze novel biomedical discoveries. To support the overall IDG objective, and to maintain, update
and improve these integrated resources, the KMC draws upon expertise from multiple knowledge domains,
specifically biology, chemistry and medicine, as well as computer science, graphic design and web
programming. Specifically, for the Phase 2 of the IDG KMC we propose 4 Aims:1. Create an automated
workflow that captures relevant public data for the entire proteome and manual annotations for the IDG list.
The KMC knowledge management system will be built around knowledge graphs, focused on five major
branches of the target knowledge tree, tkt: Genotype, Phenotype, Expression, Structure & Function, and
Interactions & Pathways, respectively. Aim 2: Design, develop and implement a protein knowledgebase with
Data Analytics support. Our protein-centric biomedical knowledge base, TCKB (Target Central
Knowledgebase) will be comprised of the data, knowledge and information container, together with its
codebase and software pipelines. TCKB will be the repository for experimental, processed and computed data
and reagents originating from the IDG DRGCs (Data and Resource Generation Centers). We will provide
informatics and modeling support for DRGC activities. Aim 3: We will expand, improve and maintain Pharos.
Particularly “knowledge packages,” support automated data summaries for Protein Dossiers, and actively seek
feedback from our community. Aim 4. Outreach to scientific community. We will support a series of activities
that will leverage TCKB, Pharos and other IDG resources to increase adoption of IDG work, while observing
FAIR (findable, accessible, interoperable, reusable) principles for our knowledgebase, portal and pipelines.
The KMC will engage in community outreach by leading tutorials and feedback sessions and dissemination of
the Pharos system. To meet its goals, the KMC will coordinate all core activities in close coordination with the
IDG Steering Committee and IDG Project Scientists (PS), and include members of the IDG Consortium (IDG-
C), other NIH Common Fund programs, NIH Commons, as well as other initiatives.
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Molecular Complexity: You Know It When You See It.
分子复杂性:当你看到它时你就知道它。
DOI:
10.1021/acs.jmedchem.3c01507
发表时间:
2023
期刊:
Journal of medicinal chemistry
影响因子:
7.3
作者:
[Oprea,TudorI, Bologa,Cristian]
通讯作者:
Bologa,Cristian
DOI:
10.1093/nar/gkaa997
发表时间:
2021-01-08
期刊:
Nucleic acids research
影响因子:
14.9
作者:
[Avram S, Bologa CG, Holmes J, Bocci G, Wilson TB, Nguyen DT, Curpan R, Halip L, Bora A, Yang JJ, Knockel J, Sirimulla S, Ursu O, Oprea TI]
通讯作者:
Oprea TI
DOI:
10.1016/j.sbi.2022.102372
发表时间:
2022-06
期刊:
CURRENT OPINION IN STRUCTURAL BIOLOGY
影响因子:
6.8
作者:
[Binder, Jessica L., Berendzen, Joel, Stevens, Amy O., He, Yi, Wang, Jian, Dokholyan, Nikolay, V, Oprea, Tudor, I]
通讯作者:
Oprea, Tudor, I
DOI:
10.1093/nar/gkac1085
发表时间:
2023-01-06
期刊:
NUCLEIC ACIDS RESEARCH
影响因子:
14.9
作者:
[Avram, Sorin, Wilson, Thomas B., Curpan, Ramona, Halip, Liliana, Borota, Ana, Bora, Alina, Bologa, Cristian G., Holmes, Jayme, Knockel, Jeffrey, Yang, Jeremy J., Oprea, Tudor, I]
通讯作者:
Oprea, Tudor, I
DOI:
10.1021/acsptsci.0c00131
发表时间:
2020-12-11
期刊:
ACS pharmacology & translational science
影响因子:
--
作者:
[Bocci G, Bradfute SB, Ye C, Garcia MJ, Parvathareddy J, Reichard W, Surendranathan S, Bansal S, Bologa CG, Perkins DJ, Jonsson CB, Sklar LA, Oprea TI]
通讯作者:
Oprea TI
共 8 条
Haplotype Resolved Sequencing Technology
-
批准号:8728983
-
项目类别:
-
资助金额:$44.1万
-
财政年份:2013
-
负责人:Jeremy S Edwards
-
依托单位:
Haplotype Resolved Sequencing Technology
-
批准号:8568163
-
项目类别:
-
资助金额:$45.0万
-
财政年份:2013
-
负责人:Jeremy S Edwards
-
依托单位:
A Spatially coarse-grained, rule-based frame work for modeling large molecular
-
批准号:8446651
-
项目类别:
-
资助金额:$33.79万
-
财政年份:2012
-
负责人:Jeremy S Edwards
-
依托单位:
A Spatially coarse-grained, rule-based frame work for modeling large molecular
-
批准号:8503615
-
项目类别:
-
资助金额:$32.54万
-
财政年份:2012
-
负责人:Jeremy S Edwards
-
依托单位:
A Spatially coarse-grained, rule-based frame work for modeling large molecular
-
批准号:8892207
-
项目类别:
-
资助金额:$31.19万
-
财政年份:2012
-
负责人:Jeremy S Edwards
-
依托单位:
A Spatially coarse-grained, rule-based frame work for modeling large molecular
-
批准号:8656139
-
项目类别:
-
资助金额:$33.46万
-
财政年份:2012
-
负责人:Jeremy S Edwards
-
依托单位:
Polony Sequencing and the $1000 Genome
-
批准号:7976897
-
项目类别:
-
资助金额:$104.78万
-
财政年份:2010
-
负责人:Jeremy S Edwards
-
依托单位:
Polony Sequencing and the $1000 Genome
-
批准号:8324730
-
项目类别:
-
资助金额:$84.32万
-
财政年份:2010
-
负责人:Jeremy S Edwards
-
依托单位:
Polony Sequencing and the $1000 Genome
-
批准号:8134450
-
项目类别:
-
资助金额:$83.92万
-
财政年份:2010
-
负责人:Jeremy S Edwards
-
依托单位:
UNM MODELING
-
批准号:7905561
-
项目类别:
-
资助金额:$16.35万
-
财政年份:2009
-
负责人:Jeremy S Edwards
-
依托单位:
Modeling and Bioinformatics Core
-
批准号:8919395
-
项目类别:
-
资助金额:$44.34万
-
财政年份:2009
-
负责人:Jeremy S Edwards
-
依托单位:
Modeling and Bioinformatics Core
-
批准号:8873025
-
项目类别:
-
资助金额:$52.54万
-
财政年份:2009
-
负责人:Jeremy S Edwards
-
依托单位:
Sequencing Chr. 6 in Melanoma Patients
-
批准号:7501225
-
项目类别:
-
资助金额:$20.25万
-
财政年份:2008
-
负责人:Jeremy S Edwards
-
依托单位:
Sequencing Chr. 6 in Melanoma Patients
-
批准号:7683895
-
项目类别:
-
资助金额:$16.88万
-
财政年份:2008
-
负责人:Jeremy S Edwards
-
依托单位:
Polony Sequencing the Human Genome
-
批准号:7477273
-
项目类别:
-
资助金额:$30.0万
-
财政年份:2007
-
负责人:Jeremy S Edwards
-
依托单位:
Polony Sequencing the Human Genome
-
批准号:7320995
-
项目类别:
-
资助金额:$30.0万
-
财政年份:2007
-
负责人:Jeremy S Edwards
-
依托单位:
Polony Sequencing the Human Genome
-
批准号:7665566
-
项目类别:
-
资助金额:$30.0万
-
财政年份:2007
-
负责人:Jeremy S Edwards
-
依托单位:
COBRE:UDE CHEM ENG: ASSAYS & MODELING PROTEIN SEQUENCE
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批准号:7170349
-
项目类别:
-
资助金额:$15.81万
-
财政年份:2005
-
负责人:Jeremy S Edwards
-
依托单位:
COBRE:UDE CHEM ENG: ASSAYS & MODELING TO ID PROTEIN
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批准号:7011794
-
项目类别:
-
资助金额:$19.16万
-
财政年份:2004
-
负责人:Jeremy S Edwards
-
依托单位:
UNM MODELING
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批准号:8309118
-
项目类别:
-
资助金额:$15.07万
-
财政年份:--
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负责人:Jeremy S Edwards
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依托单位:
海外基金