Cancer Genomics
Cancer Genomics
批准号:
8378884
负责人:
Paolo M Fortina
金额:
$22.53万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
AccountingBasic ScienceBiological AssayBiostatistics Shared ResourceCancer CenterChemistryChromatinCitiesClinical ResearchCommunitiesCopy Number PolymorphismCustomDNA SequenceDNA Sequence AnalysisDataDevelopmentEpigenetic ProcessFosteringGene ChipsGene ExpressionGene TargetingGenesGenetic Predisposition to DiseaseGenomeGenomicsGenomics Shared ResourceGenotypeGoalsHousingInformaticsLinkMalignant NeoplasmsMicroRNAsMicroarray AnalysisMissionMolecularMolecular ProfilingMonitorNucleic AcidsOligonucleotidesOnline SystemsPathogenesisPharmaceutical PreparationsPrintingProteinsQuality ControlResearch PersonnelResource SharingResourcesReverse Transcriptase Polymerase Chain ReactionSNP genotypingServicesSingle Nucleotide Polymorphism MapSlideSusceptibility GeneTechnologyTherapeuticTimeTranscriptTranslational Researchanticancer researchaustinbasecancer genomicscostflexibilitygene discoverygenetic linkage analysisgenome wide association studygenome-widegenome-wide analysisinstrumentationmRNA Expressionmeetingsmembernew technologyprogramsresponseuser-friendly
中文摘要
点击翻译按钮获取中文摘要
英文摘要
CANCER GENOMICS SHARED RESOURCE
In July 2006, to better meet the needs of Kimmel Cancer Center investigators, the former Nucleic Acid and
Custom Microarray Facilities were restructured into the Cancer Genomics Shared Resource. The center
hired a new director, manager and senior technician. This new resource provides state-of-the-art molecular
assays and expertise to facilitate projects in basic, translational and clinical research. By serving as a
centralized resource with a variety of platforms for genome-wide and gene-targeted services, it offers a
wide spectrum of services, high quality control and low costs to investigators. This shared resource was
established in response to technological advances in gene arrays and demand for high-throughput
expression analysis and genome-wide analyses to investigate pathogenesis, therapeutics, genetic
susceptibility and gene discovery in cancer research. For gene expression, this facility offers in-house
printed slides for microRNA analysis as well as commercial arrays using the Affymetrix GeneChip platform.
Differentially expressed transcripts defined by microarray-based mRNA expression profiling are confirmed
by real-time RT-PCR. Since informatics is of paramount importance, the Cancer Genomics Shared
Resource operates seamlessly linked to the new Biostatistic Shared Resource and has close links to the
protein facility. In addition, it provides service for DNA sequence analysis, with increased throughput of
DNA sequencing submission through development of a web-based program for ordering oligonucleotides,
retrieving sequencing results and accounting for Shared Resource usage. Service is provided for Taqmanbased
SNP typing, multiplex SNP genotyping using single-base extension (SBE) and pyrosequencing
chemistry on ABI 3730, Beckman Coulter GenomeLab SNPstream and Pyrosequencing PSQ HS 96A
platforms, respectively, and Affymetrix SNP Mapping GeneChips for use in genome-wide association
studies, linkage analysis and copy number variation. It supports DNA sequence-based and genotyping
projects ranging from single SNPs through custom multiplex to whole-genome panels. The shared resource
has the flexibility to adapt, as the field of array technology changes. This shared resource will expand its
services to include chromatin occupancy and epigenetic studies associated with differentiation, delineation
of differences between normal and diseased states, and monitoring response to drugs. Regular microarray
and novel technology seminars are provided bimonthly by major companies such as Affymetrix, Inc. (Santa
Clara, CA), Agilent Technologies, Inc. (Santa Clara, CA), Luminex Corp. (Austin, TX), Beckman Coulter,
Inc. (Fullerton, CA) and Applied Biosystems (Foster City, CA). In addition, presentations from users are
arranged on a monthly basis for all center members and the TJU community.
期刊论文(0)
专著(0)
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会议论文
Single cell analysis of healthy and diseased temporomandibular joint synovial fluid
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批准号:10524512
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项目类别:
-
资助金额:$32.63万
-
财政年份:2022
-
负责人:Paolo M Fortina
-
依托单位:
Automated Liquid Handler
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批准号:10424767
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项目类别:
-
资助金额:$24.72万
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财政年份:2022
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负责人:Paolo M Fortina
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依托单位:
Cancer Genomics
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批准号:8302949
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项目类别:
-
资助金额:$23.1万
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财政年份:2011
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负责人:Paolo M Fortina
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依托单位:
Cancer Genomics
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批准号:8084104
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项目类别:
-
资助金额:$24.47万
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财政年份:2010
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负责人:Paolo M Fortina
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依托单位:
FOUR COLOR ARRAY BOUND SNP/MUTATION DETECTION IN CANCER
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批准号:6704389
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项目类别:
-
资助金额:$38.88万
-
财政年份:2000
-
负责人:Paolo M Fortina
-
依托单位:
FOUR COLOR ARRAY BOUND SNP/MUTATION DETECTION IN CANCER
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批准号:6744321
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项目类别:
-
资助金额:$61.75万
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财政年份:2000
-
负责人:Paolo M Fortina
-
依托单位:
FOUR COLOR ARRAY BOUND SNP/MUTATION DETECTION IN CANCER
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批准号:6682787
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项目类别:
-
资助金额:$58.96万
-
财政年份:2000
-
负责人:Paolo M Fortina
-
依托单位:
FOUR COLOR ARRAY BOUND SNP/MUTATION DETECTION IN CANCER
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批准号:6583709
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项目类别:
-
资助金额:$21.61万
-
财政年份:2000
-
负责人:Paolo M Fortina
-
依托单位:
DNA DIAGNOSIS OF HEMOGLOBINOPATHIES USING MICROFABRICATED SILICON CHIPS
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批准号:6325926
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项目类别:
-
资助金额:$17.18万
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财政年份:2000
-
负责人:Paolo M Fortina
-
依托单位:
FOUR COLOR ARRAY BOUND SNP/MUTATION DETECTION IN CANCER
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批准号:6198876
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项目类别:
-
资助金额:$15.0万
-
财政年份:2000
-
负责人:Paolo M Fortina
-
依托单位:
DNA DIAGNOSIS OF HEMOGLOBINOPATHIES USING MICROFABRICATED SILICON CHIPS
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批准号:6109858
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项目类别:
-
资助金额:$17.18万
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财政年份:1999
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负责人:Paolo M Fortina
-
依托单位:
DNA DIAGNOSIS OF HEMOGLOBINOPATHIES USING MICROFABRICATED SILICON CHIPS
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批准号:6272787
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项目类别:
-
资助金额:$17.38万
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财政年份:1998
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负责人:Paolo M Fortina
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依托单位:
SPECIFIC DIAGNOSIS OF HEMOGLOBINOPATHIES
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批准号:6241955
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项目类别:
-
资助金额:$12.53万
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财政年份:1997
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负责人:Paolo M Fortina
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依托单位:
MetaOmics
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批准号:10447608
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项目类别:
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资助金额:$43.89万
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财政年份:1995
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负责人:Paolo M Fortina
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依托单位:
SPECIFIC DIAGNOSIS OF HEMOGLOBINOPATHIES
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批准号:5213649
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项目类别:
-
资助金额:$0.0万
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财政年份:--
-
负责人:Paolo M Fortina
-
依托单位:--
海外基金