Single-Cell and Spatial Transcriptomics Core
单细胞和空间转录组学核心
基本信息
- 批准号:10714238
- 负责人:
- 金额:$ 9.2万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2018
- 资助国家:美国
- 起止时间:2018-03-16 至 2028-06-30
- 项目状态:未结题
- 来源:
- 关键词:ATAC-seqAddressAreaBackBiologicalCell NucleusCell surfaceCellsCommunitiesComplexComputational BiologyComputer AnalysisComputer softwareConsultConsultationsCore FacilityDataData AnalysesData SetDetectionDevelopmentDiseaseDrug TargetingEffectivenessEnsureEquipmentFacility AccessesFaculty RecruitmentFundingFutureGene ExpressionGenesGoalsGrantGreat PlainsHeterogeneityIndividualInvestmentsLegal patentLettersLibrariesLocationMachine LearningMapsMeasuresMentorsMessenger RNAMethodsMicroscopyMissionMolecular ProfilingMolecular TargetNebraskaPhasePositioning AttributePostdoctoral FellowPreparationPrincipal InvestigatorProceduresProtein SecretionPublicationsQuality ControlReagentResearchResearch PersonnelResolutionResourcesStudentsSuspensionsSystemTechnologyTissuesTrainingTranscriptTranslatingTumor SubtypeUniversitiesValidationWorkanalysis pipelineanalytical toolbiomedical informaticschromatin immunoprecipitationcomplex datacomputerized toolscostcost comparisoncyber infrastructuredifferential expressiongenomic platformhigh throughput analysisimplementation toolimprovedinnovationinsightinstrumentationmembermolecular subtypesmultiple omicsnew technologyprogramsreference genomesingle cell sequencingsingle-cell RNA sequencingskills trainingtooltranscriptomicsuser-friendly
项目摘要
Project Summary: Single-Cell and Spatial Transcriptomics (SCST) Core
Single cell transcriptomics permits researchers to analyze tissue heterogeneity and complexity in disease states.
These technologies add enormous value to research strategies aimed at discovering new disease-specific cell
surface markers, drug targets, molecular subtypes of tumors, etc. However, common single cell-omics platforms
are limited by high cost and access to robust computational analysis. The goals of the Single-Cell and Spatial
Transcriptomics (SCST) Core are to lower barriers of entry to single cell and spatial transcriptomics technologies
for CMTDD investigators and the broader UNMC community at a reasonable cost, offer consultations and
technical assistance for training new users, enable users to analyze complex datasets, and remain adaptable to
increase capacity and tools as needed from the UNMC community. The working hypothesis is that increased
access to these emergent and powerful technologies will pay dividends on the back end in the form of more
impactful publications and a higher rate of grant funding. To achieve these goals, we will provide users with
sufficient low-cost equipment, consultations, and computational tools to analyze single cell and spatial
transcriptomics data. Pioneering work in the Shalek group identified a lower cost solution to droplet based
scRNA-seq called Seq-Well to generate high quality libraries. We have successfully implemented Seq-Well at
UNMC and generated hiqh quality data with unique biological insights. Our core also will provide subsidized
access to spatial transcriptomics (MERSCOPE). Thus, the SCST core will provide low-cost access to Seq-Well
and MERSCOPE, allowing for a range of options for high resolution molecular profiling of tissue and cellular
heterogeneity in complex systems. Implementation of these tools at UNMC will enable investigators to develop
innovative new research areas. The SCST will ensure that cutting edge computational tools are available to
users who want to conduct their own rigorous data analysis and anticipate and develop new low-cost “omics”
technologies. By lowering the financial bar of access to these technologies, research program competitiveness
will increase, enhancing publication impact factors, grant funding, patents, and faculty recruitment to UNMC.
项目概述:单细胞和空间转录组学(SCST)核心
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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Kyle J Hewitt其他文献
Anemia-Activated Cis Regulatory Requirements for Erythroid Regeneration
- DOI:
10.1182/blood-2022-167544 - 发表时间:
2022-11-15 - 期刊:
- 影响因子:
- 作者:
Yichao Zhou;Linda Chee;Suhita Ray;Meg Schaefer;Venkatasai Rahul Dogiparthi;Jordan Rowley;Kyle J Hewitt - 通讯作者:
Kyle J Hewitt
Transcriptional Control of Erythropoiesis Via a Kit-Response Cistrome
- DOI:
10.1182/blood-2024-208254 - 发表时间:
2024-11-05 - 期刊:
- 影响因子:
- 作者:
Venkatasai Rahul Dogiparthi;Linda Chee;Jordan Rowley;Kyle J Hewitt - 通讯作者:
Kyle J Hewitt
Lipid-Dependent Roles for SAMD14 in Stress Erythropoiesis
- DOI:
10.1182/blood-2024-207597 - 发表时间:
2024-11-05 - 期刊:
- 影响因子:
- 作者:
Pooja Roy;Suhita Ray;Suyong Choi;Nicholas Woods;Kyle J Hewitt - 通讯作者:
Kyle J Hewitt
Early Response Transcription Factors in Erythroid Regeneration
- DOI:
10.1182/blood-2023-189994 - 发表时间:
2023-11-02 - 期刊:
- 影响因子:
- 作者:
Yichao Zhou;Kyle J Hewitt - 通讯作者:
Kyle J Hewitt
The Sterile Alpha Motif Protein-1 Transcription Factor Controls Hematopoiesis through Modulation of H3K4 Methylation
- DOI:
10.1182/blood-2024-209230 - 发表时间:
2024-11-05 - 期刊:
- 影响因子:
- 作者:
Meg Schaefer;Venkatasai Rahul Dogiparthi;Yichao Zhou;Kyle J Hewitt - 通讯作者:
Kyle J Hewitt
Kyle J Hewitt的其他文献
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{{ truncateString('Kyle J Hewitt', 18)}}的其他基金
Hematopoietic Signaling Pathway Mechanism in a GATA Factor-Dependent Network
GATA 因子依赖性网络中的造血信号通路机制
- 批准号:
10672858 - 财政年份:2022
- 资助金额:
$ 9.2万 - 项目类别:
GATA Factor Mechanisms in Erythroid Regeneration
红细胞再生中的 GATA 因子机制
- 批准号:
10322093 - 财政年份:2021
- 资助金额:
$ 9.2万 - 项目类别:
GATA Factor Mechanisms in Erythroid Regeneration
红细胞再生中的 GATA 因子机制
- 批准号:
10097331 - 财政年份:2021
- 资助金额:
$ 9.2万 - 项目类别:
GATA Factor Mechanisms in Erythroid Regeneration
红细胞再生中的 GATA 因子机制
- 批准号:
10538585 - 财政年份:2021
- 资助金额:
$ 9.2万 - 项目类别:
Hematopoietic Signaling Pathway Mechanism in a GATA Factor-Dependent Network
GATA 因子依赖性网络中的造血信号通路机制
- 批准号:
10117106 - 财政年份:2018
- 资助金额:
$ 9.2万 - 项目类别:
Mechanisms of a GATA Factor-Dependent Hematopoietic Signaling Pathway
GATA 因子依赖性造血信号通路的机制
- 批准号:
9295276 - 财政年份:2017
- 资助金额:
$ 9.2万 - 项目类别:
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