Accelerated BAC Library Construction And Analysis
Accelerated BAC Library Construction And Analysis
批准号:
6549184
负责人:
DAVID Alan MEAD
金额:
$10.0万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-08-14 至 2004-02-13
中文摘要
描述(由申请人提供):大型插入DNA文库对于人类基因组和其他对我们的健康很重要的基因组的分子分析至关重要。比较基因组学揭示了代谢途径,癌症,水平基因转移,进化,蛋白质家族和许多物种的遗传库的新信息。这也大大增加了对额外基因组BAC文库的需求。这些图书馆的建设既费时又费钱,而且具有挑战性。该提案的长期目标是促进克隆人类基因组中目前的缺口,并将构建大型BAC文库所需的时间从几个月缩短到几周。这些文库的质量将超过当前的标准,包括偏倚、随机性、保真度和低污染。具体目标包括开发新的BAC克隆工具、菌株和方法,这些工具、菌株和方法绕过传统瓶颈,并大大提高高分子量基因组DNA的分子克隆和转化效率。一个新的E. coli转化系统可使大片段DNA的摄取提高100倍,平均插入片段大小可达300 kb以上。其他技术创新包括随机剪切高分子量DNA的简单方法,零背景克隆系统和消除几种形式克隆偏差的无转录克隆系统。
拟议的商业应用:
商业产品和服务包括:一个新的E。该系统包括具有极高DNA摄取效率的大肠杆菌转化系统、用于无偏克隆嵌合基因和gneomes的零背景无转录载体、BAC文库构建kt、BAC DNA亲和纯化试剂盒、减少质粒骨架重新测序的载体弹出以及经济的BAC文库构建服务。
英文摘要
DESCRIPTION (provided by applicant): Large insert DNA libraries are essential for the molecular analysis of the human genome and other genomes important to our well-being. Comparative genomics reveals new information about metabolic pathways, cancer, horizontal gene transfer, evolution, protein families, and the genetic repertoire of numerous species. It has also greatly increased the demand for additional genomic BAC libraries. Construction of these libraries is time consuming, costly and challenging. The long-term objectives of this proposal are to facilitate cloning the current gaps in the human genome and reduce the time required for constructing large BAC libraries to a few weeks from several months. The quality of these libraries will surpass current standards for bias, randomness, fidelity, and low contamination. Specific aims include the development of new BAC cloning tools, strains, and methods that circumvent traditional bottlenecks and substantially improve the molecular cloning and transformation efficiency of high molecular weight genomic DNA. A new E. coli transformation system could improve large DNA uptake 100-fold and increase average insert size to above 300 kb. Other technical innovations include a simple method for randomly shearing high molecular weight DNA, a zero background cloning system, and a transcription-free cloning system that eliminates several forms of cloning bias.
PROPOSED COMMERCIAL APPLICATIONS:
Commercial products and services include: a new E. coli transformation system with exceptionally high DNA uptake efficiency, a zero background, transcription-free vector for unbiased cloning of recalcitrant genes and gneomes, a BAC library construction kt, a BAC DNA affinity purification kit, a vector pop-out to reduce re-sequencing of the plasmid backbone, and an economical BAC library construction service.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
6-{[(Benz-yloxy)carbon-yl]-oxy}-2-methyl-hexa-hydro-pyrano[3,2-d][1,3]dioxin-7,8-diyl bis-(chloro-acetate).
6-{[(苯甲氧基)碳基]-氧基}-2-甲基-六氢-吡喃并[3,2-d][1,3]二恶英-7,8-二基双-(氯-
DOI:
10.1107/s1600536810004356
发表时间:
2010
期刊:
Acta crystallographica. Section E, Structure reports online
影响因子:
--
作者:
[Jasinski,JerryP, Butcher,RayJ, Swamy,MT, Yathirajan,HS, Narayana,B]
通讯作者:
Narayana,B
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项目类别:
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依托单位:
Enabling Technologies for Low Resource Molecular Diagnostics
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资助金额:$20.0万
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财政年份:2010
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依托单位:
NOVEL SOLUBILITY-ENHANCING PROTEIN EXPRESSION TECHNOLOGY
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批准号:8501542
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财政年份:2009
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NOVEL SOLUBILITY-ENHANCING PROTEIN EXPRESSION TECHNOLOGY
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财政年份:2009
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Massively Parallel Single Cell Genomics of the Human Microbiome
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资助金额:$12.44万
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财政年份:2008
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HIGH THROUGHPUT CLONING OVEREXPRESSION AND PURIFICATION OF ACTIVE MEMBRANE PROT
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项目类别:
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财政年份:2006
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依托单位:
Ex Cyto DNA Sequencing from Single Bacterial Colonies
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项目类别:
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资助金额:$13.72万
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财政年份:2006
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依托单位:
Accelerated BAC Library Construction And Analysis
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财政年份:2002
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依托单位:
PENTAPLEX CLONING VECTOR FOR DECAPLEX DNA SEQUENCING
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批准号:2902430
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资助金额:$5.07万
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财政年份:1998
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负责人:DAVID Alan MEAD
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依托单位:
AN INTEGRATED MULTIPLEX CLONING AND SEQUENCING SYSTEM
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依托单位:
PENTAPLEX CLONING VECTOR FOR DECAPLEX DNA SEQUENCING
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AN INTEGRATED MULTIPLEX CLONING AND SEQUENCING SYSTEM
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海外基金