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Transcriptome & Networks Analysis Core

Transcriptome & Networks Analysis Core
转录组
批准号:
10593070
负责人:
Jose Luis Gonzalez Hernandez
金额:
$38.92万
依托单位国家:
美国
项目类别:
财政年份:
2022
资助国家:
美国
项目状态:
未结题
起止时间:
2022-03-20 至 2027-01-31

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中文摘要
翻译
项目摘要-核心B:转录组和网络分析核心 高通量组学技术的出现使得对细胞转录的强大分析成为可能 项目、基因-功能关系和全基因组调查,其细节前所未有。个体 调查人员在实施这些新技术并有效地将这些大型 将数据集转化为对分子途径的机械性理解。译本与网络的目标 分析核心(TNAC)是为了促进组学技术人员的有效利用和下游 生物信息学分析。这一核心利用了SDSU主任冈萨雷斯·埃尔南德斯博士的专业知识 基因组测序设施,具有遗传学和基因组分析专业知识,葛锡进博士, 经验丰富的生物信息学家和生物医学研究员。具体地说,这一核心将使项目领导 使用以下技术研究炎症:RNA测序(rna-seq)、CRISPR全基因组 筛选、空间分辨rna-seq和蛋白质组学。TNAC有三个具体目标:1)译本 用常规RNA-Seq和深度测序分析CRISPR插入;2)使用 空间分辨和单细胞rna-seq技术和相关的生物信息学工作流程;以及3)数据 使用和调整生物信息学工具和资源进行整合和广泛的途径分析,包括 由葛锡进博士开发的那些,用来构建潜在炎症的基因调控网络,整合 蛋白质组学数据,并对这三个项目生成的数据与 公有领域。这一核心具有创新性,因为它将尖端的实验技术与 最新的生物信息学工具和方法。与四个项目负责人密切合作,这一核心将成为 跨学科协作,并显著促进尖端技术在 该地区的生物医学研究人员。
英文摘要
Project Summary – Core B: TRANSCRIPTOME AND NETWORK ANALYSIS CORE The advent of high-throughput omics technologies enables powerful analyses of cellular transcriptional programs, gene-function relationships and genome-wide surveys at unprecedented detail. Individual investigators face many hurdles in implementing these new technologies and effectively translating these large datasets into mechanistic understanding of molecular pathways. The goal of the Transcriptome and Network Analysis Core (TNAC) is to facilitate the effective use of omics technologists and the downstream bioinformatics analyses. This core leverages the expertise of Dr. Gonzalez Hernandez, Director of the SDSU Genomics Sequencing Facility, with expertise in genetics and genomics analysis, and Dr. Xijin Ge, experienced bioinformatician and biomedical researcher. Specifically, this core will enable the project leads to use the following technology to study inflammation: RNA sequencing (RNA-seq), CRISPR whole genome screening, spatially resolved RNA-seq, and proteomics. The TNAC has 3 specific aims: 1) Transcriptomic analyses by conventional RNA-Seq and deep sequencing for analysis of CRISPR insertions; 2) The use of spatially resolved and single cell RNA-seq technology and associated bioinformatics workflows; and 3) Data integration and extensive pathway analysis using and adapting bioinformatics tools and resources, including those developed by Dr. Xijin Ge, to construct gene regulatory networks underlying inflammation, integrate proteomics data, and conduct meta-analysis of data generated by the three projects alongside data in the public domain. This core is innovative in that it brings together cutting-edge experimental technology with the latest bioinformatics tools and approaches. Working closely with the four project leads, this core will exemplify interdisciplinary collaboration, and significantly promote the adoption of cutting-edge technologies among biomedical researchers in the region.
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