A single cell spatial genomics platform for multi-modal characterization of tissue organization
A single cell spatial genomics platform for multi-modal characterization of tissue organization
批准号:
10408000
负责人:
Fei Chen
金额:
$94.64万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-08-08 至 2023-05-31
关键词:
ATAC-seqAdoptedAdoptionAgingAlgorithmsBar CodesBiological AssayBrainCellsChromatinChromosomesComplexDNADataData AnalysesData CollectionData SetDevelopmentDiseaseEnsureEpigenetic ProcessGene Expression ProfileGenerationsGenesGenomic approachHealthIndividualJointsLibrariesLocationMeasurementMeasuresMessenger RNAMiniaturizationMolecularMolecular BiologyOrganPathologicProcessProteinsProtocols documentationRNARegulatory ElementResearch PersonnelResolutionSlideStructureTechnologyTestingTissuesTransposaseValidationWorkantibody librariescell typecomputerized toolsdata integrationdevelopmental diseaseexperimental studygenomic platformgenomic toolshigh throughput technologyindexingmultimodal datamultimodalitynew technologynext generationnoveloligo (dT)protein expressionsingle cell sequencingsingle-cell RNA sequencingtissue resourcetooltranscriptometranscriptome sequencingtranscriptomics
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Project Summary/Abstract
Cells are the unit building blocks of tissues and organs, thus, to understand how tissues
function, it is important to understand where different types of cells reside in health and disease.
In this proposal, we propose to develop a novel spatial genomics platform that will enable
multi-modal characterization of tissue structure at the single cell level. This will be
revolutionary for the study of tissue organization in development and pathological changes
in aging and disease. Our tools will enable us to look at RNA, proteins and regulatory elements
in DNA all within the tissue context. We will ensure these novel genomic tools are easy to use
and adopt, which will be especially powerful for pathological settings, where tissue resources
are precious, and adoption of tools is limited by ease of use. The successful completion of
this work will lead to a comprehensive toolset for understanding tissue structure from
the perspective of single cell organization.
期刊论文(1)
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科研奖励(0)
会议论文
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MicroRNA-190 and Oxidative Stress in Arsenic carcinogenesis
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MicroRNA-190 and Oxidative Stress in Arsenic carcinogenesis
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