Dynamically scalable accessible analysis for next generation sequence data
Dynamically scalable accessible analysis for next generation sequence data
批准号:
7937844
负责人:
ANTON NEKRUTENKO
金额:
$73.49万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-25 至 2012-07-31
关键词:
AccountingAddressBase SequenceBiological AssayBiological SciencesBiomedical ResearchChromatin StructureComplexComputer AnalysisComputer SimulationComputer softwareCore FacilityCustomDNA SequenceDataData AnalysesData SetData Storage and RetrievalDependencyEngineeringGalaxyGene Expression RegulationHereditary DiseaseHumanHuman GeneticsIndividualInformaticsInternetLarge-Scale SequencingLibrariesMalignant NeoplasmsMapsModelingMutationOccupationsPatternResearch InfrastructureResearch PersonnelResourcesRunningScheduleSequence AnalysisSolutionsSystemTechniquesTechnologyTestingTimeUpdateVariantWorkcomputer infrastructurecomputing resourcescostimprovedinstrumentmeetingsnext generationnovelprogramspublic health relevancesoftware systemstoolvirtualweb based interface
中文摘要
描述(由申请人提供):项目概述“下一代”测序(NGS)仪器的广泛可用性使任何研究者能够以适度的成本产生大量的DNA序列数据。然而,处理这些原始序列对个人调查人员、小型实验室或核心设施提出了重大问题。对于一个没有计算专业知识的实验组来说,仅仅运行一个数据分析程序是一个障碍,更不用说建立一个能够处理NGS数据的计算和数据存储基础设施了。幸运的是,最近出现了一种计算模型——“云计算”,它非常适合分析大规模序列数据。在该模型中,计算和存储作为虚拟资源存在,可以根据需要动态分配和释放。重要的是,对于某些用例,云资源可以以比专用资源低得多的成本提供存储和计算。然而,要使这些资源提供给个别调查人员,还需要解决一些艰巨的挑战。具体来说,尽管云计算提供了一种按需获取计算资源的方法,但所提供的资源要么是Internet上的虚拟机,要么是特定的编程库,这对于实验人员来说是不可用的。因此,一个可行的分析解决方案需要在没有信息学专业知识的情况下易于访问和部署;它必须在考虑时间和成本的同时,有效地、自动地使用动态可扩展的资源;它必须包含适当的分析工具,并在新工具出现时方便地支持添加新工具。我们以前开发了一个软件系统——Galaxy (http://galaxyproject.org)——它为满足这些需求提供了一个健壮的框架。在这里,我们建议大大扩展这个框架,以允许任何实验家利用云计算基础设施的力量进行大规模的NGS分析。特别是,我们将修改现有的Galaxy框架,使其完全在云中运行。我们将调整Galaxy调度和执行任务的方式,以有效地利用云风格。我们将为个人用户提供一种机制,通过完全基于web的界面在云上创建和部署自定义Galaxy实例。最后,我们将通过将开发的设备应用于现有的人类重测序数据来测试我们的方法,以便在非常大的范围内发现导致人类遗传疾病的隐藏突变模式。
英文摘要
DESCRIPTION (provided by applicant): Project Summary Wide availability of "next-generation" sequencing (NGS) instruments has enabled any investigator, for a modest cost, to produce enormous amounts of DNA sequence data. However, working with these raw sequences presents significant problems for individual investigators, small labs, or core facilities. For an experimental group with no computational expertise, simply running a data analysis program is a barrier, let alone building a compute and data storage infrastructure capable of dealing with NGS data. Fortunately, a computational model - "Cloud computing" - has recently emerged and is ideally suited to the analysis of large- scale sequence data. In this model, computation and storage exist as virtual resources, which can be dynamically allocated and released as needed. Importantly, cloud resources can provide storage and computation at far less cost than dedicated resources for certain use cases. However, formidable challenges need to be addressed to make these resources available to individual investigators. Specifically, although cloud computing provides a way to acquire computational resources on demand, the resources provided are either virtual machines on the Internet or specific programming libraries, which are unusable for experimentalists. Thus, a viable analysis solution needs to be accessible and deployable without informatics expertise; it must efficiently and automatically use dynamically scalable resources, while taking into account time and cost; it must include appropriate analysis tools and easily support addition of new tools as they emerge. We have previously developed a software system - Galaxy (http://galaxyproject.org) - that provides a robust framework for addressing these needs. Here we propose to significantly extend this framework to allow any experimentalist to perform large-scale NGS analyses utilizing the power of cloud computing infrastructure. In particular, we will modify the existing Galaxy framework to run entirely within the cloud. We will adapt the way Galaxy schedules and executes jobs to make effective use of cloud-style. We will provide a mechanism for individual users to create and deploy custom Galaxy instances on a cloud through an entirely web-based interface. Finally, we will test our approach by applying the developed facilities to the existing human re- sequencing data in order to uncover hidden patters of mutations causing human genetic disease on a very large scale.
PUBLIC HEALTH RELEVANCE: Project Narrative Increasingly available and inexpensive high-throughput DNA sequencing holds great promise for biomedical research, but informatics challenge block the full realization of the potential of this transformative technology. In particular progress is limited by the informatics and engineering expertise of biomedical researchers, and the availability of sufficient computational infrastructure to analyze these enormous datasets. This project will address these problems by bringing together Galaxy, a system for making complex computational analysis accessible and reproducible, with "cloud computing", an infrastructure model where computing resources are purchased on demand as needed, making it possible for investigators with no informatics expertise to perform data-intensive analysis using cloud resources.
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