Construction of A Reference Sequence Data Set For The Human Microbiome Project
Construction of A Reference Sequence Data Set For The Human Microbiome Project
批准号:
8310922
负责人:
Karen E. Nelson
金额:
$86.92万
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:
2009-05-22 至 2014-08-31
关键词:
ArchaeaArtsAutomated AnnotationBacteriaBacteriophagesCell SeparationComplementConsentDNADataData SetDiseaseEducation and OutreachFlow CytometryFoundationsFungal GenomeFutureGenesGenomeGenomicsHealthHumanHuman MicrobiomeHuman bodyHybridsIndividualInstitutesKineticsKnowledgeLabelLaboratoriesLibrariesMapsMeasuresMessenger RNAMetagenomicsMicrobeMinorPhylogenetic AnalysisPhysiologyProcessProkaryotic CellsRNARNA markerReadingResearchSamplingShotgun SequencingSiteSourceSurveysTechniquesTechnologyTranscriptUncertaintyViralViral GenomeVirusfungusgenome sequencingimprovedmembermetagenomic sequencingmicrobialmicrobial genomemicroorganismnext generationnovelrRNA Genestool
中文摘要
人体生理和健康高度依赖于数十亿微生物的活动,这些微生物栖息在人体内和人体上的多个小生境中。这些微生物中很少有被鉴定的,很大程度上是因为大多数还没有被培养。因此,这一数量庞大的物种对人类健康的影响仍有待阐明。该提案提出了J.克雷格文特尔研究所的方法,以产生大量参考物种的基因组序列,包括与人体相关的细菌、真菌、病毒和噬菌体。我们还描述了如何从多个个体的不同身体部位收集的DNA样本中生成宏基因组序列。
具体目标包括对400个微生物基因组进行测序、组装和注释(其中60个将关闭),为宏基因组数据提供参考基因组;通过对这些样本进行鸟枪测序,对来自多个身体部位的微生物群进行表征,并使用我们最先进的组装和分析工具进一步解释这些数据。我们还将研究微真核生物的多样性,重点是28 S rRNA基因和内部转录间隔区。将采用细胞分选与全基因组扩增相结合的方法从先前未培养的原核生物中获得基因组DNA。最后,通过宏基因组分析鉴定的标记基因的表达RNA的动态范围将使用新的mRNA转录本捕获和扩增方法进行询问。
这项研究将使用尖端技术进行,包括下一代测序方法。我们将继续对临床研究人员进行宣传和教育,并将随时提供所有数据。毫无疑问,拟议研究的结果将增加目前对与人体相关的微生物多样性以及这些物种对健康和疾病的影响的了解。
英文摘要
Human physiology and health is highly dependent on the activities of billions of microorganisms that inhabit multiple niches within and on the human body. Few of these microorganisms have been characterized, in large part because the majority are yet to be cultivated. As such, the impact this vast number of species has on human health remains to be elucidated. This proposal presents the J. Craig Venter Institute's approach to generating the genomic sequences of a significant number of reference species including bacteria, fungi, viruses and phage that are associated with the human body. We also describe how we will generate metagenomic sequences from DNA samples collected from various body sites of multiple individuals.
The specific aims include the sequencing, assembly and annotation of 400 microbial genomes (60 of which will be closed) to provide reference genomes for metagenomic data; characterization of the microbiota from multiple body sites via shotgun sequencing of these samples, and the use of our state-of-the-art assembly and analysis tools to further interpret this data. We will also investigate microeukaryotic diversity, focusing on the 28S rRNA gene and internal transcribed spacer regions. Cell sorting, combined with whole genome amplification will be employed to obtain genomic DNA from previously uncultured prokaryotes. Finally, the dynamic range of expressed RNA from marker genes identified through metagenomic analyses will be interrogated using a novel mRNA transcript capture and amplification approach.
This study will be conducted using cutting edge technologies including next generation approaches to sequencing. We will continue outreach and education to research clinicians, and will make all data readily available. Without a doubt, the findings from the proposed study will increase current understanding of the microbial diversity associated with the human body and the impact of these species on health and disease.
期刊论文(14)
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DOI:
10.1128/genomea.00234-13
发表时间:
2013
期刊:
Genome announcements
影响因子:
--
作者:
[Shkoporov,AN, Efimov,BA, Khokhlova,EV, Chaplin,AV, Kafarskaya,LI, Durkin,AS, McCorrison,J, Torralba,M, Gillis,M, Sutton,G, Weibel,DB, Nelson,KE, Smeianov,VV]
通讯作者:
Smeianov,VV
DOI:
10.1099/ijs.0.060988-0
发表时间:
2014-08
期刊:
International journal of systematic and evolutionary microbiology
影响因子:
2.8
作者:
[M. Sizova;Paul A. Muller;David Stancyk;N. Panikov;M. Mandalakis;Amanda Hazen;Tine Hohmann;Sebastian N. Doerfert;W. Fowle;A. Earl;K. Nelson;S. Epstein]
通讯作者:
M. Sizova;Paul A. Muller;David Stancyk;N. Panikov;M. Mandalakis;Amanda Hazen;Tine Hohmann;Sebastian N. Doerfert;W. Fowle;A. Earl;K. Nelson;S. Epstein
DOI:
10.1371/journal.pone.0032118
发表时间:
2012
期刊:
PloS one
影响因子:
3.7
作者:
[Li K, Bihan M, Yooseph S, Methé BA]
通讯作者:
Methé BA
HSV-1 clinical isolates with unique in vivo and in vitro phenotypes and insight into genomic differences.
HSV-1 临床分离株具有独特的体内和体外表型以及对基因组差异的洞察。
DOI:
10.1007/s13365-016-0485-9
发表时间:
2017
期刊:
Journal of neurovirology
影响因子:
3.2
作者:
[Danaher,RobertJ, Fouts,DerrickE, Chan,AgnesP, Choi,Yongwook, DePew,Jessica, McCorrison,JamisonM, Nelson,KarenE, Wang,Chunmei, Miller,CraigS]
通讯作者:
Miller,CraigS
DOI:
10.4056/sigs.651139
发表时间:
2010-03-30
期刊:
Standards in genomic sciences
影响因子:
--
作者:
[Tanenbaum DM, Goll J, Murphy S, Kumar P, Zafar N, Thiagarajan M, Madupu R, Davidsen T, Kagan L, Kravitz S, Rusch DB, Yooseph S]
通讯作者:
Yooseph S
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