Bioinformatics Core
Bioinformatics Core
批准号:
8895849
负责人:
Xiaole Shirley Liu
金额:
$8.09万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-09-18 至 2016-06-30
关键词:
Acute T Cell LeukemiaAreaBioinformaticsBiomedical ResearchCellsChIP-seqCommunitiesComplexComputational BiologyComputer AnalysisDataData SetDatabasesEpigenetic ProcessGene ExpressionGene Expression ProfilingGene Expression RegulationGenesGoalsGrowthHeadHumanHuman Cell LineInformaticsInstructionMalignant - descriptorMalignant NeoplasmsModelingMolecular ProfilingMusOncogenicProcessResearch DesignResource SharingResourcesServicesSignal TransductionT cell differentiationT-Lymphocytebasecancer cellcomputerized toolscost effectiveexperienceinnovationmeetingsnotch proteinprogenitorprogramssuccessthymocytetooltranscription factor
中文摘要
核心B(生物信息学)的主要目标是为该计划提供计算工具,
处理、分析、整合和解释复杂ChIP-Seq和基因表达所需的专业知识
分析从正常和恶性T细胞祖细胞获得的数据集。迄今为止,
这些地方是临时提供的。创建此核心将为该计划提供
专门的纵向信息学和生物统计学支持,这对该计划的整体
成功该机构由X博士领导。Shirley Liu,一位经验丰富、高效的计算专家
生物学家和生物统计学家,在癌细胞计算分析方面有创新记录
表观遗传学和基因调控。其主要职责将包括分析获得的ChIP-Seq数据
来自人和鼠T-ALL细胞系、人和鼠原发性T-ALL以及正常人和
分析从这些细胞获得的基因表达谱和/或RNASeq;
以及这些ChIP-Seq和基因表达数据集的综合建模。
核心B在下一个项目期间的具体目标如下:
目标1.为了处理、分析和整合来自正常和非正常组织的ChIP-Seq和基因表达数据集,
恶性T细胞祖细胞
目标二。表征和量化与T细胞分化或扰动相关的表观遗传变化
转录因子在T-ALL细胞中的表达
目标3.就研究设计和计算/技术进步向计划PIS提供建议
目标4。作为项目和生物医学研究的数据库和资源中心
整个社会
英文摘要
The major goals ofthe Core B (Bioinformatics) are to provide the Program with the computational tools and
expertise needed to process, analyze, integrate and interpret complex ChlP-Seq and gene expression
profiling datasets obtained from normal and malignant T cell progenitors. To date, programmatic needs in
these areas have been provided on an ad hoc basis. Creating this Core will provide the Program with
dedicated longitudinal informatics and biostatistical support, which is important for the Program's overall
success. The facility is headed by Dr. X. Shirley Liu, an experienced, highly productive computational
biologist and biostatistician with a track record of innovation in computational analysis of cancer cell
epigenetics and gene regulation. Its principle responsibilities will include analysis of ChlP-Seq data obtained
from human and murine T-ALL cell lines, human and murine pnmary T-ALLs, and nonnal human and
murine thymocyte subsets; analysis of gene expression profiles and/or RNASeq obtained from these cells;
and integrative modeling ofthese ChlP-Seq and gene expression datasets.
The specific aims of Core B in the next project period are as follows:
Aim 1. To process, analyze, and integrate ChlP-Seq and gene expression datasets from normal and
malignant T cell progenitors
Aim 2. To characterize and quantify epigenetic changes associated with T cell differentiation or perturbation
of transcription factors in T-ALL cells
Aim 3. To advise Program Pis on study design and computational/technological advances
Aim 4. To serve as a data repository and resource center for the program and the biomedical research
community as a whole
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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