Core C: Developmental Genomics-Epigenetics Core
核心C:发育基因组学-表观遗传学核心
基本信息
- 批准号:10451567
- 负责人:
- 金额:$ 24.01万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2021
- 资助国家:美国
- 起止时间:2021-07-16 至 2026-05-31
- 项目状态:未结题
- 来源:
- 关键词:AdoptedAdultAgingAnimal ModelAnimalsAreaBackBasic ScienceBioinformaticsBiologicalBiological AssayBiological ModelsCell NucleusCellsCertificationChIP-seqChromiumClinicalClinical ResearchCodeCollectionCommunitiesComplementComplexComputer AnalysisComputer softwareConceptionsCountryDNA MethylationDNA methylation profilingDataData AnalysesData PoolingData SetDevelopmentDiagnosisEducationEducational workshopEnsureEpigenetic ProcessEquipmentExonsFoundationsFundingGeneticGenomeGenomicsGenotypeHawksHigh-Throughput Nucleotide SequencingHumanHuman GeneticsInstitutesIntellectual and Developmental Disabilities Research CentersIntellectual functioning disabilityIowaLaboratoriesLeadershipLongevityMachine LearningManualsMeta-AnalysisMethodologyMethylationMicroarray AnalysisMusOrganization administrative structuresPersonsPharmaceutical PreparationsPreventionProtein IsoformsQuality ControlRattusReproducibilityResearchResearch PersonnelResearch Project GrantsResourcesRibosomesRiskRural PopulationSalivaSamplingServicesSmall Nuclear RNASourceStandardizationSystems DevelopmentTechnologyTissuesTrainingUnited States National Institutes of HealthUniversitiesVariantZebrafishanalysis pipelineanalytical methodbasebioinformatics resourcecognitive functioncomputing resourcescost effectivenessdata formatdifferential expressionepigenomicsexome sequencingexperienceexperimental studygenome sequencinggenome-widegenomic datahuman modelhuman tissueinnovationinsightmethylomeneurodevelopmentnovelpolygenic risk scoreprogramsrecruitresearch studyservice utilizationsingle cell sequencingsingle-cell RNA sequencingtooltraining opportunitytranscriptometranscriptome sequencingwhole genome
项目摘要
PROJECT SUMMARY: DEVELOPMENTAL GENOMICS/EPIGENETICS CORE (DGC)
The primary objective of the Developmental Genomics/Epigenetics core (DGC) is to support innovative and
cutting-edge genome-scale research of intellectual and developmental disabilities (IDDs) across the lifespan—
from conception to adulthood, tailored to a rural population. Under the leadership of co-directors Dr. Richard
Smith and Dr. Jake Michaelson, who together have substantial, NIH-backed experience in experimental
(Smith) and computational (Michaelson) genomics, the DGC will provide broad expertise that encompasses
model system development, high-throughput sequencing technologies (e.g., genome and exome sequencing,
RNA sequencing, chromatin immunoprecipitation sequencing, methylation sequencing, and ribosome
sequencing), and bioinformatics and computational analysis of the results. Each of these foundational services
is housed within its own organizational unit: 1) the Genomics Division provides high-throughput sequencing
and array services including exome and genome sequencing, RNA-sequencing (including 10X Chromium
single-cell sequencing), and array-based genotyping and methylation services under the direction of Dr.
Richard Smith, an accomplished genomics investigator; and 2) the Bioinformatics Division provides services
for quality control, basic processing (e.g., alignment, variant calling, and expression quantification), and
pipelines for calculating polygenic risk scores from data produced by array or sequencing services generated
by the genomics division, and is led by Dr. Jake Michaelson, an experienced computational genomics
investigator. The DGC will utilize existing resources within the Iowa Institute for Human Genetics (led by co-
director Dr. Richard Smith), which has a strong track record in education and dissemination, with regularly
occurring workshops, tutorials, videos, and online certification opportunities. Since its inception, the DGC has
been calibrated to the overall theme of the Hawk-IDDRC: IDD research across the lifespan. In particular,
epigenetic signatures specific to development and aging are accessible through the Core's epigenetic array-
and sequencing-based assays. The DGC also interrogates intrinsic and extrinsic sources of risk by offering
genomic (intrinsic) and epigenetic (extrinsic) assay options. Finally, a focus on rural populations is achieved
through the extensive experience of both Drs. Smith and Michaelson in collecting samples from sparsely
populated areas, both in person and through mail recruitment campaigns (e.g., using saliva collection kits or
Guthrie cards). Services from the DGC will complement and synergize with those of the other Cores in the
Center, such as with the Clinical Translational Core in recruitment efforts to obtain biosamples, and will
support 17 federally funded projects ($4.8 million per year). Collectively, the available expertise and cutting-
edge services provided by the DGC will catalyze IDD research by minimizing barriers for entry into genome-
scale studies of neurodevelopment and cognitive function.
项目概述:发育基因组学/表观遗传学核心(dgc)
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Richard J.H. Smith其他文献
Standards for ethical publication.
出版道德标准。
- DOI:
10.1001/archotol.133.1.7 - 发表时间:
2006 - 期刊:
- 影响因子:0
- 作者:
Jonas T. Johnson;J. Niparko;Paul A. Levine;D. Kennedy;S. Rudy;P. Weber;R. Weber;M. Benninger;R. Rosenfeld;R. Ruben;Richard J.H. Smith;R. Sataloff;N. Weir - 通讯作者:
N. Weir
COL11A2 is associated with dominantly inherited hearing loss
- DOI:
10.1016/s0194-5998(99)80054-0 - 发表时间:
1999-08-01 - 期刊:
- 影响因子:
- 作者:
Wyman T McGuirt;Sai D Prasad;Glenn E Green;Richard J.H. Smith - 通讯作者:
Richard J.H. Smith
Localization of a gene for otosclerosis to chromosome 15q25-q26.
耳硬化症基因定位于染色体 15q25-q26。
- DOI:
- 发表时间:
1998 - 期刊:
- 影响因子:3.5
- 作者:
Michael S. Tomek;Matthew R. Brown;Sabitha R. Mani;A. Ramesh;C. Srisailapathy;Paul J. Coucke;Ross I. S. Zbar;Adam M. Bell;W. McGuirt;Kunihiro Fukushima;Kunihiro Fukushima;Patrick J. Willems;G. V. Camp;Richard J.H. Smith - 通讯作者:
Richard J.H. Smith
The value of resident presentations at scientific meetings
科学会议上驻场演讲的价值
- DOI:
10.1002/lary.23859 - 发表时间:
2013 - 期刊:
- 影响因子:0
- 作者:
M. Stewart;R. Chandra;Alexander Chiu;Ehab Y. Hanna;D. Kennedy;D. Kraus;M. Gleeson;Paul A. Levine;J. Niparko;B. O’Malley;R. Rosenfeld;R. Ruben;R. Sataloff;Richard J.H. Smith;P. Weber - 通讯作者:
P. Weber
Surgical management of laryngomalacia
- DOI:
10.1016/s1043-1810(99)80003-7 - 发表时间:
1999-12-01 - 期刊:
- 影响因子:
- 作者:
Nancy M. Bauman;Richard J.H. Smith - 通讯作者:
Richard J.H. Smith
Richard J.H. Smith的其他文献
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{{ truncateString('Richard J.H. Smith', 18)}}的其他基金
Core C: Developmental Genomics-Epigenetics Core
核心C:发育基因组学-表观遗传学核心
- 批准号:
10669145 - 财政年份:2021
- 资助金额:
$ 24.01万 - 项目类别:
Autosomal Dominant Non-Syndromic Hearing Loss - Its Genetic Diagnosis and Treatment
常染色体显性遗传性非综合征性听力损失 - 其遗传诊断和治疗
- 批准号:
10461782 - 财政年份:2019
- 资助金额:
$ 24.01万 - 项目类别:
Autosomal Dominant Non-Syndromic Hearing Loss - Its Genetic Diagnosis and Treatment
常染色体显性遗传性非综合征性听力损失 - 其遗传诊断和治疗
- 批准号:
10200758 - 财政年份:2019
- 资助金额:
$ 24.01万 - 项目类别:
Autosomal Dominant Non-Syndromic Hearing Loss - Its Genetic Diagnosis and Treatment
常染色体显性遗传性非综合征性听力损失 - 其遗传诊断和治疗
- 批准号:
9793612 - 财政年份:2019
- 资助金额:
$ 24.01万 - 项目类别:
Autosomal Dominant Non-Syndromic Hearing Loss - Its Genetic Diagnosis and Treatment
常染色体显性遗传性非综合征性听力损失 - 其遗传诊断和治疗
- 批准号:
10655597 - 财政年份:2019
- 资助金额:
$ 24.01万 - 项目类别:
Fourth Dense Deposit Disease Focus Group Meeting
第四次密集沉积病焦点小组会议
- 批准号:
8203263 - 财政年份:2011
- 资助金额:
$ 24.01万 - 项目类别:
Optimizing Genetic Testing for Deafness for Clinical Diagnostics
优化耳聋基因检测以进行临床诊断
- 批准号:
8224101 - 财政年份:2011
- 资助金额:
$ 24.01万 - 项目类别:
Optimizing Genetic Testing for Deafness for Clinical Diagnostics
优化耳聋基因检测以进行临床诊断
- 批准号:
8712451 - 财政年份:2011
- 资助金额:
$ 24.01万 - 项目类别:
Optimizing Genetic Testing for Deafness for Clinical Diagnostics
优化耳聋基因检测以进行临床诊断
- 批准号:
8336850 - 财政年份:2011
- 资助金额:
$ 24.01万 - 项目类别:
Optimizing Genetic Testing for Deafness for Clinical Diagnostics
优化耳聋基因检测以进行临床诊断
- 批准号:
8514562 - 财政年份:2011
- 资助金额:
$ 24.01万 - 项目类别:
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