Genomics Core
基因组学核心
基本信息
- 批准号:10490401
- 负责人:
- 金额:$ 13.19万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2010
- 资助国家:美国
- 起止时间:2010-09-28 至 2026-08-31
- 项目状态:未结题
- 来源:
- 关键词:AddressAfrican AmericanAfrican ancestryAndrogen ReceptorBRCA2 geneBioinformaticsBiomedical ResearchBiostatistical MethodsBostonCHD1 geneCancer BiologyCancer CenterCodeDNA SequenceDana-Farber Cancer InstituteDataData AnalysesEducation and OutreachEducational workshopFeesFrequenciesGenomic approachGenomicsGoalsInfrastructureInstitutionInstructionLeadLearningMalignant neoplasm of prostateMassachusettsMinority-Serving InstitutionModelingOutcomePopulationProstatic NeoplasmsRNAReceptor SignalingResearchResearch DesignResearch PersonnelResearch TrainingResourcesReverse Transcriptase Polymerase Chain ReactionRiskSNP genotypingStructureStudentsTechnologyTrainingUnderrepresented PopulationsUnderrepresented StudentsUniversitiesUntranslated RNAanticancer researchbasecancer health disparitycancer initiationcancer riskcostdesigneducation researchexperiencegenomic datahealth disparity populationsinnovationinstrumentationmennano-stringnext generation sequencingnovelpersonalized cancer therapyprogramssingle cell sequencingtherapy resistanttooltumor progression
项目摘要
SUMMARY
A critical gap often exists at institutions serving underserved health disparity populations and underrepresented
students (ISUPS) between access to Genomics technologies and the high costs associated with the required
instrumentation, technical proficiency, and analytical expertise. The Genomics Core (GC) addresses this gap
by providing expert and affordable access to high-throughput genomics technologies on a reduced fee basis
for all Partnership investigators. The GC benefits the entire Partnership by providing innovative approaches to
explore early project ideas, and by working with Partnership investigators and their trainees to facilitate the use
of genomics technologies to build sustainable cancer biology and cancer disparities research. To accomplish
these goals, the GC (through the auspices of the Center for Personalized Cancer Therapy, CPCT) provides
front-line genomics-related technologies, as well as bioinformatics support for data analysis, to Partnership
investigators through an affordable reimbursement model. The GC proposes to accomplish these goals
through the pursuit of four specific aims designed to build capacity for biomedical and cancer research and
training at UMass Boston by bridging a gap in the availability of cutting-edge genomics-based tools; support
Partnership investigators who wish to pursue early project ideas, especially those that require innovative
and/or technically challenging genomics approaches; bridge a training gap between students and high-level
genomics-based technologies, and provide bioinformatics analysis of data generated in the core. In this
application, the GC specifically supports FP2: Targeting androgen receptor signaling in prostate cancer in men
with African Ancestry – Steven Balk (DF/HCC - BIDMC) and Changmeng Cai (UMass Boston) and PP2: High
frequency of CHD1 loss in BRCA2-deficient African American prostate tumors drives treatment resistance –
Zoltan Szallasi (DF/HCC - BCH) and Shailja Pathania (UMass Boston).
总结
在为服务不足的健康差距人口和代表性不足的人口提供服务的机构中,
学生(IUPS)之间的访问基因组学技术和所需的高成本
仪器、技术熟练程度和分析专业知识。基因组学核心(GC)解决了这一差距
通过以较低的费用提供专家和负担得起的高通量基因组学技术
所有合伙人调查员GC通过提供创新的方法来使整个伙伴关系受益,
探索早期项目想法,并与合作伙伴调查人员及其学员合作以促进使用
基因组学技术,以建立可持续的癌症生物学和癌症差异研究。完成
为了实现这些目标,GC(通过个性化癌症治疗中心,CPCT)提供
前沿基因组学相关技术以及对数据分析的生物信息学支持,
调查人员通过负担得起的报销模式。GC建议实现这些目标
通过追求旨在建设生物医学和癌症研究能力的四个具体目标,
在马萨诸塞大学波士顿分校的培训,弥合了尖端基因组学为基础的工具的可用性的差距;支持
希望追求早期项目想法的合作伙伴关系调查人员,特别是那些需要创新的项目。
和/或技术上具有挑战性的基因组学方法;弥合学生和高水平
基因组学为基础的技术,并提供生物信息学分析产生的数据的核心。在这
GC特别支持FP 2:靶向男性前列腺癌中的雄激素受体信号传导
与非洲制药公司- Steven Balk(DF/HCC - BIDMC)和Changmeng Cai(马萨诸塞大学波士顿分校)和PP 2:高
BRCA 2缺陷型非裔美国人前列腺肿瘤中CHD 1丢失的频率导致治疗耐药性-
Zoltan Szallasi(DF/HCC-BCH)和Shailja Pathania(马萨诸塞大学波士顿分校)。
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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Jill A. Macoska其他文献
Fluorescence In Situ Hybridization (FISH) to Metaphase and Interphase Chromosomes.
中期和间期染色体荧光原位杂交 (FISH)。
- DOI:
10.1385/1-59259-144-2:101 - 发表时间:
2001 - 期刊:
- 影响因子:0
- 作者:
Jill A. Macoska - 通讯作者:
Jill A. Macoska
Jill A. Macoska的其他文献
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{{ truncateString('Jill A. Macoska', 18)}}的其他基金
Persistence of an IL-4/IL-13 autocrine loop promotes fibrosis-mediated urinary voiding dysfunction
IL-4/IL-13 自分泌环的持续存在促进纤维化介导的尿排尿功能障碍
- 批准号:
10022319 - 财政年份:2014
- 资助金额:
$ 13.19万 - 项目类别:
Persistence of an IL-4/IL-13 autocrine loop promotes fibrosis-mediated urinary voiding dysfunction
IL-4/IL-13 自分泌环的持续存在促进纤维化介导的尿排尿功能障碍
- 批准号:
10700930 - 财政年份:2014
- 资助金额:
$ 13.19万 - 项目类别:
Persistence of an IL-4/IL-13 autocrine loop promotes fibrosis-mediated urinary voiding dysfunction
IL-4/IL-13 自分泌环的持续存在促进纤维化介导的尿排尿功能障碍
- 批准号:
10264807 - 财政年份:2014
- 资助金额:
$ 13.19万 - 项目类别:
Fibrosis-Associated Urinary Gene Transcripts for LUTS Detection and Treatment
用于 LUTS 检测和治疗的纤维化相关尿液基因转录
- 批准号:
8738645 - 财政年份:2013
- 资助金额:
$ 13.19万 - 项目类别:
Fibrosis-Associated Urinary Gene Transcripts for LUTS Detection and Treatment
用于 LUTS 检测和治疗的纤维化相关尿液基因转录
- 批准号:
8486921 - 财政年份:2013
- 资助金额:
$ 13.19万 - 项目类别:
Society for Basic Urologic Research Fall Symposium 2012
基础泌尿学研究学会 2012 年秋季研讨会
- 批准号:
8453755 - 财政年份:2012
- 资助金额:
$ 13.19万 - 项目类别:
Role of Prostatic Fibrosis in BPH/LUTS Development & Symptomology
前列腺纤维化在 BPH/LUTS 发展中的作用
- 批准号:
8150959 - 财政年份:2010
- 资助金额:
$ 13.19万 - 项目类别:
Role of Prostatic Fibrosis in BPH/LUTS Development & Symptomology
前列腺纤维化在 BPH/LUTS 发展中的作用
- 批准号:
8049846 - 财政年份:2010
- 资助金额:
$ 13.19万 - 项目类别:
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