EDAC: ENCODE Data Analysis Center
EDAC: ENCODE Data Analysis Center
批准号:
8494858
负责人:
Ewan Birney
金额:
$37.11万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-05-15 至 2012-12-31
关键词:
AddressAlgorithmsAreaBehaviorBerylliumBioinformaticsBiologicalBiological SciencesCollaborationsComplexComputational TechniqueComputing MethodologiesCoupledDataData AnalysesData CollectionData SetDevelopmentEducational workshopEngineeringEquipment and supply inventoriesFreezingGene Expression RegulationGenomeGenomicsGoalsHeterogeneityHuman GenomeHypersensitivityIndiumLinkMachine LearningManuscriptsMapsMethodsMetricNaturePhasePilot ProjectsPublicationsRNARecordsReportingResearch PersonnelResourcesScientistSourceStatistical ModelsStructureTechniquesTelephoneTranscriptVertebral columnWorkbasecomputer sciencedata integrationexperienceexperimental analysisflexibilityfootgenome-wideinsightmeetingsmembernovelquality assurancescale upsymposiumtheoriestoolworking group
中文摘要
描述(由申请人提供): ENCODE数据分析中心(EDAC)的建议旨在为ENCODE项目提供灵活的分析资源。ENCODE项目是一个大型多中心项目,旨在定义人类基因组中的所有功能元件。这将使用许多不同的实验技术与众多的计算技术相结合来实现。交付这组功能元素的一个关键部分是集成来自多个源的数据。艾德AC提案旨在提供这种整合。正如RFA在本提案中所规定的那样,EDAC工作的确切优先顺序将由一个外部小组,即分析工作组(AWG)确定。根据以往的经验,这些分析方法将需要各种技术。我们预计必须应用复杂的统计模型来整合数据,特别是减轻人类基因组变量的广泛异质性和相关性问题。我们有统计学专家,他们可以利用人类基因组的巨大规模,加上有限数量的合理假设,来产生对这种相当大的异质性具有鲁棒性的统计技术。我们还希望应用机器学习技术来构建结合数据集的集成方法。其中包括基于贝叶斯的推理方法和强大的计算机科学技术支持向量机。这些方法中的每一种都在ENCODE试点项目中表现良好,我们希望它们在完整的ENCODE项目中更加有用。我们还将提供全基因组多重比对的质量保证和汇总指标。这个领域有许多复杂的统计,算法和工程问题,我们将使用最先进的技术来解决。总体而言,我们的目标是在AWG的指导下,并与ENCODE联盟的其他成员密切合作,提供ENCODE数据的深度集成。
英文摘要
DESCRIPTION (provided by applicant): The ENCODE Data Analysis Center (EDAC) proposal aims to provide a flexible analysis resource for the ENCODE project. The ENCODE project is a large multi center project which aims to define all the functional elements in the human genome. This will be achieved using many different experimental techniques coupled with numerous computational techniques. A critical part in delivering this set of functional elements is the integration of data from multiple sources. The ED AC proposal aims to provide this integration. As proscribed by the RFA for this proposal, the precise prioritization for the EDAC's work will be set by an external group, the Analysis Working Group (AWG). Based on previous experience, these analysis methods will require a variety of techniques. We expect to have to apply sophisticated statistical models to the integration of the data, in particular mitigating the problems of the extensive heterogeneity and correlation of variables on the human genome. We have statistical experts who can use the large size of the human genome, coupled with a limited number of sensible assumptions to produce statistical techniques which are robust to this considerable heterogeneity. We also expect to apply machine learning techniques to build integration methods combining datasets. These included Bayesian based inference methods and the robust computer science technique of Support Vector Machines. Each of these methods have performed well in the ENCODE pilot project and we expect them to be even more useful in the full ENCODE project. We will also provide quality assurance and summary metrics of genome-wide multiple alignments. This area has a number of complex statistical, algorithmic and engineering issues, which we will solve using state of the art techniques. Overall we aim to provide deep integration of the ENCODE data, under the direction of the AWG and in tight collaboration with the other members of the ENCODE consortium.
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DOI:
10.1093/nar/gks1236
发表时间:
2013-01
期刊:
Nucleic acids research
影响因子:
14.9
作者:
[Flicek P, Ahmed I, Amode MR, Barrell D, Beal K, Brent S, Carvalho-Silva D, Clapham P, Coates G, Fairley S, Fitzgerald S, Gil L, García-Girón C, Gordon L, Hourlier T, Hunt S, Juettemann T, Kähäri AK, Keenan S, Komorowska M, Kulesha E, Longden I, Maurel T, McLaren WM, Muffato M, Nag R, Overduin B, Pignatelli M, Pritchard B, Pritchard E, Riat HS, Ritchie GR, Ruffier M, Schuster M, Sheppard D, Sobral D, Taylor K, Thormann A, Trevanion S, White S, Wilder SP, Aken BL, Birney E, Cunningham F, Dunham I, Harrow J, Herrero J, Hubbard TJ, Johnson N, Kinsella R, Parker A, Spudich G, Yates A, Zadissa A, Searle SM]
通讯作者:
Searle SM
DOI:
10.1093/bioinformatics/btq164
发表时间:
2010-06-01
期刊:
Bioinformatics (Oxford, England)
影响因子:
--
作者:
[Hoffman MM, Buske OJ, Noble WS]
通讯作者:
Noble WS
DOI:
10.1371/journal.pone.0043128
发表时间:
2012
期刊:
PloS one
影响因子:
3.7
作者:
[Lowe CB, Haussler D]
通讯作者:
Haussler D
DOI:
10.1093/nar/gkr991
发表时间:
2012-01
期刊:
Nucleic acids research
影响因子:
14.9
作者:
[Flicek P, Amode MR, Barrell D, Beal K, Brent S, Carvalho-Silva D, Clapham P, Coates G, Fairley S, Fitzgerald S, Gil L, Gordon L, Hendrix M, Hourlier T, Johnson N, Kähäri AK, Keefe D, Keenan S, Kinsella R, Komorowska M, Koscielny G, Kulesha E, Larsson P, Longden I, McLaren W, Muffato M, Overduin B, Pignatelli M, Pritchard B, Riat HS, Ritchie GR, Ruffier M, Schuster M, Sobral D, Tang YA, Taylor K, Trevanion S, Vandrovcova J, White S, Wilson M, Wilder SP, Aken BL, Birney E, Cunningham F, Dunham I, Durbin R, Fernández-Suarez XM, Harrow J, Herrero J, Hubbard TJ, Parker A, Proctor G, Spudich G, Vogel J, Yates A, Zadissa A, Searle SM]
通讯作者:
Searle SM
DOI:
10.1101/gr.127712.111
发表时间:
2012-09
期刊:
Genome research
影响因子:
7
作者:
[Arvey A, Agius P, Noble WS, Leslie C]
通讯作者:
Leslie C
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