Functional Genomics
功能基因组学
基本信息
- 批准号:10174821
- 负责人:
- 金额:$ 30.6万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1997
- 资助国家:美国
- 起止时间:1997-05-01 至 2025-04-30
- 项目状态:未结题
- 来源:
- 关键词:AdenovirusesAdoptedAutomationBioinformatics Shared ResourceBiological AssayCRISPR libraryCRISPR screenCRISPR/Cas technologyCancer CenterCancer Center Support GrantCell LineCellsClustered Regularly Interspaced Short Palindromic RepeatsCollaborationsCommunicationComputer softwareContract ServicesCore FacilityCultured CellsCustomDataData AnalysesDoctor of PhilosophyEmployeeEngineeringEquipmentExperimental DesignsFacultyFeedbackGene ActivationGene FamilyGeneticGenetic ScreeningGenomics Shared ResourceGoalsGrantGuide RNAImageLabelLaboratoriesLeadershipLibrariesMaintenanceMalignant NeoplasmsMethodsMicroRNAsMicroscopyMiniaturizationMutationPatientsPreparationPublicationsRNA InterferenceReagentResearchResearch PersonnelResource SharingScienceScientistServicesSmall Interfering RNAStatistical Data InterpretationSupporting CellSurveysSystemTechnologyTimeViralViral VectorWorkassay developmentbasecost effectivenessdesignexomefunctional genomicsgene repressiongenome-widehigh throughput screeninginhibitor/antagonistmeetingsmembernucleic acid deliveryprogramsrepairedrepositoryscreeningsmall hairpin RNAsmall molecule librariestoolvectorwhole genome
项目摘要
ABSTRACT – FUNCTIONAL GENOMICS SHARED RESOURCE
The central goal of the Functional Genomics Shared Resource, which is managed by the Cancer Center, is to
provide services and tools for Center members to perform RNAi and CRISPR-CAS9 genetic screens in cultured
cells. Core staff interact with Center faculty members throughout their projects, starting with project
conceptualization and feasibility assessment through to the final verification of targets identified in the screens.
The Core utilizes the extensive amount of HTS equipment available in the Prebys Center and the Chemical
Library Screening Core. In addition to the wealth of expertise brought by the staff, the Core serves as a repository
for reagents, assays, and technical information, which are shared with Cancer Center researchers. The Core
provides a variety of libraries for functional genomics analysis, including a genome-wide siRNA library, and
comprehensive miRNA activator and inhibitor libraries, broad shRNA libraries, as well as targeted arrayed and
genome-wide pooled CRISPR libraries. The Core's primary effort is dedicated to genetic screening via RNAi and
CRISPR-Cas9, although significant time is also currently dedicated to engineering of cell lines. Within the Core,
the main laboratory focuses on cellular genetics, while the viral vector laboratory specializes in high-quality vector
preparation in a centralized facility with expert staff, and produces an array of sophisticated viral systems to
enable nucleic acid delivery. Both laboratories are also actively involved in developing tools tailored to the
specific needs of Center researchers. Functional Genomics operates in close connection with other Shared
Resources at SBP. Thus, the Core utilizes automation and high-throughput imaging support from the adjacent
Chemical Library Screening Shared Resource; interacts with the Bioinformatics Shared Resource to perform
statistical analysis of the raw data and design custom CRISPR libraries; and uses the sequencing services of
the Genomics Shared Resource to execute CRISPR-Cas9 screens. Overall, the Functional Genomics Core has
strived to maintain its place at the forefront of cellular genetics and nucleic acid delivery by adopting state-of-
the-art technologies, implementing methods to fill technology gaps, and adapting methods to fulfill the specific
needs of the Cancer Center. In the past 5 years, the Core was used by a total of 45 Center members representing
all three programs, and it supported at least 29 cancer-related publications by Cancer Center members.
摘要-功能基因组学共享资源
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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Aniruddha J. Deshpande其他文献
with deregulated HOX gene expression in human acute myeloid leukemia progenitors depending on its N-terminal domain and is closely correlated Overexpression of CDX2 perturbs HOX gene expression in murine
人急性髓性白血病祖细胞中 HOX 基因表达失调,取决于其 N 末端结构域,并且与 CDX2 过度表达扰乱小鼠 HOX 基因表达密切相关
- DOI:
- 发表时间:
2013 - 期刊:
- 影响因子:0
- 作者:
K. Spiekermann;W. Hiddemann;M. Feuring‐Buske;C. Buske;Konstantin Petropoulos;Aniruddha J. Deshpande;L. Quintanilla‐Martinez;S. Bohlander;V. P. Rawat;S. Thoene;V. Naidu;Natalia Arseni;B. Heilmeier;K. Metzeler - 通讯作者:
K. Metzeler
AML1-ETO Collaborates with the Homeobox Gene Meis1 in Inducing Acute Leukemia in the Mouse Bone Marrow Transplantation Model.
AML1-ETO 与同源盒基因 Meis1 合作在小鼠骨髓移植模型中诱导急性白血病。
- DOI:
- 发表时间:
2008 - 期刊:
- 影响因子:0
- 作者:
V. Naidu;V. P. Rawat;Christina Schessl;Konstantin Petropoulus;M. Cusan;Aniruddha J. Deshpande;Leticia Quintanilla Martinez;W. Hiddemann;M. Buske;C. Buske - 通讯作者:
C. Buske
RETRACTED ARTICLE: Tumor necrosis factor overcomes immune evasion in p53-mutant medulloblastoma
撤回文章:肿瘤坏死因子克服 p53 突变型髓母细胞瘤中的免疫逃避
- DOI:
10.1038/s41593-020-0628-4 - 发表时间:
2020-05-18 - 期刊:
- 影响因子:20.000
- 作者:
Alexandra Garancher;Hiromichi Suzuki;Svasti Haricharan;Lianne Q. Chau;Meher Beigi Masihi;Jessica M. Rusert;Paula S. Norris;Florent Carrette;Megan M. Romero;Sorana A. Morrissy;Patryk Skowron;Florence M. G. Cavalli;Hamza Farooq;Vijay Ramaswamy;Steven J. M. Jones;Richard A. Moore;Andrew J. Mungall;Yussanne Ma;Nina Thiessen;Yisu Li;Alaide Morcavallo;Lin Qi;Mari Kogiso;Yuchen Du;Patricia Baxter;Jacob J. Henderson;John R. Crawford;Michael L. Levy;James M. Olson;Yoon-Jae Cho;Aniruddha J. Deshpande;Xiao-Nan Li;Louis Chesler;Marco A. Marra;Harald Wajant;Oren J. Becher;Linda M. Bradley;Carl F. Ware;Michael D. Taylor;Robert J. Wechsler-Reya - 通讯作者:
Robert J. Wechsler-Reya
High Density Domain-Focused CRISPR Screens Reveal Novel Epigenetic Regulators of HOX/MEIS Activation in Acute Myeloid Leukemia
高密度域聚焦 CRISPR 筛选揭示了急性髓系白血病 HOX/MEIS 激活的新型表观遗传调节因子
- DOI:
- 发表时间:
2023 - 期刊:
- 影响因子:0
- 作者:
Karina Barbosa;Anagha Deshpande;M. Perales;P. Xiang;Rabi Murad;A. Minkina;N. Robertson;Fiorella Schischlik;Xue Lei;Younguk Sun;Adam Brown;D. Amend;I. Jeremias;John G Doench;R. Humphries;E. Ruppin;J. Shendure;P. Mali;P. Adams;Aniruddha J. Deshpande - 通讯作者:
Aniruddha J. Deshpande
AMultiscaleMap of the StemCell State in Pancreatic Adenocarcinoma Graphical Abstract Highlights
胰腺癌干细胞状态的多尺度图图形摘要亮点
- DOI:
- 发表时间:
2019 - 期刊:
- 影响因子:0
- 作者:
Nikki K. Lytle;L. P. Ferguson;Nirakar Rajbhandari;K. Gilroy;R. Fox;Anagha Deshpande;C. Schürch;Michael Hamilton;N. Robertson;Wei Lin;Pawan Noel;Martin Wartenberg;I. Zlobec;Micha Eichmann;J. Galván;E. Karamitopoulou;Tami Gilderman;L. Esparza;Y. Shima;Philipp N Spahn;R. French;N. Lewis;K. Fisch;R. Sásik;S. Rosenthal;M. Kritzik;D. Hoff;Haiyong Han;T. Ideker;Aniruddha J. Deshpande;A. Lowy;P. Adams;T. Reya - 通讯作者:
T. Reya
Aniruddha J. Deshpande的其他文献
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{{ truncateString('Aniruddha J. Deshpande', 18)}}的其他基金
Molecular Pathogenesis of AF10-Rearranged Leukemias
AF10 重排白血病的分子发病机制
- 批准号:
10609055 - 财政年份:2022
- 资助金额:
$ 30.6万 - 项目类别:
Molecular Pathogenesis of AF10-Rearranged Leukemias
AF10 重排白血病的分子发病机制
- 批准号:
10454043 - 财政年份:2022
- 资助金额:
$ 30.6万 - 项目类别:
The role of AF10 in normal and leukemic hematopoiesis
AF10 在正常和白血病造血中的作用
- 批准号:
8601977 - 财政年份:2012
- 资助金额:
$ 30.6万 - 项目类别:
The role of AF10 in normal and leukemic hematopoiesis
AF10 在正常和白血病造血中的作用
- 批准号:
8190104 - 财政年份:2011
- 资助金额:
$ 30.6万 - 项目类别:
The role of AF10 in normal and leukemic hematopoiesis
AF10 在正常和白血病造血中的作用
- 批准号:
9178059 - 财政年份:2011
- 资助金额:
$ 30.6万 - 项目类别:
The role of AF10 in normal and leukemic hematopoiesis
AF10 在正常和白血病造血中的作用
- 批准号:
8302260 - 财政年份:2011
- 资助金额:
$ 30.6万 - 项目类别:
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