EBI Metagenomics - enabling the reconstruction of microbial populations
EBI 宏基因组学 - 实现微生物种群的重建
基本信息
- 批准号:BB/R015228/1
- 负责人:
- 金额:$ 113.62万
- 依托单位:
- 依托单位国家:英国
- 项目类别:Research Grant
- 财政年份:2018
- 资助国家:英国
- 起止时间:2018 至 无数据
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Microorganisms inhabit practically all environments on Earth. For example, there are more microbes in the ocean than stars in the known universe, with complex communities living in vastly different niches, from the tropics to the polar waters and from well-lit surface waters to the deep abyss. They harvest and transduce solar energy and is estimated that they contribute 50-90% to global primary production, turning light into biomass through photosynthesis, making them vital to the world's food chain. Microbes produce and consume most greenhouse gases (carbon dioxide, nitrous oxide and methane), which is of particular importance in relation to man-made climate change. They are also responsible for over half of all oxygen production on Earth. Within ecosystems, microbes catalyse the key bio-geochemical transformations of nutrients and trace elements that sustain organic productivity. Understanding these processes would bring many potential benefits. For example, working out the mechanisms by which microbes unlock organic phosphate to a soluble form that can be absorbed by plants could reduce the use of fertilizers and increase agricultural yields. Within each environment, the microbial population contains a vast and dynamic reservoir of genetic variability, much of which is yet to be studied. Current biological databases do not represent the vast majority of environmental organisms, as traditional genome sequencing approaches require isolation and culturing. Metagenomics, the sequencing of the entire collection of DNA found within an environmental sample, circumvents this need. As a result, we have begun to answer some of the key questions about which organisms are found in which environments. There has been a huge uptake of the approach across a broad range of disciplines. Nevertheless, the majority of metagenomics projects produced over the past decade have given only a fragmentary picture of underlying micro-organisms genomes, as larger volumes of sequencing are required to improve the level of genomic detail.In the era of data driven science, and with widespread access to sequencing technology and ever diminishing costs, huge volumes of sequence data present an amazing opportunity to understand the microbial world at a more detailed level. However, the field of metagenomics faces the following issues: 1) given the vast data volumes, specialist expert-built pipelines are required for efficient, high-throughput analysis; 2) bioinformatics analysis of results is costly to produce and requires expert knowledge; 3) to extract maximum knowledge from experiments, there is a need to systematically capture the associated experimental data along with the sequence data; 4) there is a lack of consistency between different analysis approaches, affecting comparability. The EBI Metagenomics (EMG) resource solves these issues by offering a free service for the analysis and archiving of all metagenomic data. With advances in algorithms and methods, it is now possible to piece together the fragments that make up an individual organism's genome. In this project, we will not only continue the provision of the EMG, but also develop the analysis, archiving, tools and data presentation frameworks required to generate genomes from metagenomes. Due to the unique position of EMG, we will be also able to combine data across different projects that contain similar microbial communities. This important data reuse will enable us to generate the highest quality genomes, allow us to detect different strains of bacteria and ensure that we capitalize on previous investments. Our genomes will enrich the current tree of life, and we will extend the EMG interfaces to accommodate the new data that we will produce. This will empower research and innovation in the environment, bioindustries, agriculture and medicine (human and livestock). We will work closely with biotechnological industries, to enable them to harness the huge potential for discovery.
微生物几乎栖息在地球上的所有环境中。例如,海洋中的微生物比已知宇宙中的恒星还要多,复杂的群落生活在截然不同的生态位中,从热带到极地水域,从光线充足的表层水域到深渊。它们收获并转换太阳能,估计对全球初级生产贡献了 50-90%,通过光合作用将光转化为生物质,使它们对世界食物链至关重要。微生物产生并消耗大部分温室气体(二氧化碳、一氧化二氮和甲烷),这对于人为气候变化尤为重要。它们还负责地球上一半以上的氧气生产。在生态系统内,微生物催化维持有机生产力的营养物质和微量元素的关键生物地球化学转化。了解这些过程将带来许多潜在的好处。例如,研究微生物将有机磷酸盐释放为可被植物吸收的可溶形式的机制可以减少肥料的使用并提高农业产量。在每个环境中,微生物种群都包含巨大且动态的遗传变异库,其中大部分仍有待研究。当前的生物数据库并不代表绝大多数环境生物,因为传统的基因组测序方法需要分离和培养。宏基因组学,即对环境样本中发现的整个 DNA 集合进行测序,就规避了这一需求。因此,我们已经开始回答一些关于在哪些环境中发现哪些生物体的关键问题。这种方法在广泛的学科中得到了广泛的采用。然而,过去十年中产生的大多数宏基因组学项目仅给出了底层微生物基因组的碎片图片,因为需要大量测序来提高基因组细节水平。随着测序技术的广泛使用和成本的不断降低,大量的序列数据为更详细地了解微生物世界提供了绝佳的机会。然而,宏基因组学领域面临以下问题:1)鉴于数据量巨大,需要专门构建的流程来进行高效、高通量的分析; 2)结果的生物信息学分析成本高昂,并且需要专业知识; 3)为了从实验中提取最大的知识,需要系统地捕获相关的实验数据以及序列数据; 4)不同分析方法之间缺乏一致性,影响可比性。 EBI 宏基因组学 (EMG) 资源通过提供所有宏基因组数据的分析和归档免费服务来解决这些问题。随着算法和方法的进步,现在可以将构成单个生物体基因组的片段拼凑在一起。在这个项目中,我们不仅将继续提供肌电图,还将开发从宏基因组生成基因组所需的分析、存档、工具和数据呈现框架。由于肌电图的独特地位,我们还能够将包含相似微生物群落的不同项目的数据结合起来。这种重要的数据重用将使我们能够生成最高质量的基因组,使我们能够检测不同的细菌菌株,并确保我们利用之前的投资。我们的基因组将丰富当前的生命树,我们将扩展肌电图接口以适应我们将产生的新数据。这将促进环境、生物工业、农业和医学(人类和牲畜)领域的研究和创新。我们将与生物技术行业密切合作,使他们能够利用巨大的发现潜力。
项目成果
期刊论文数量(10)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
The European Nucleotide Archive in 2020.
2020 年欧洲核苷酸档案。
- DOI:http://dx.10.1093/nar/gkaa1028
- 发表时间:2021
- 期刊:
- 影响因子:14.9
- 作者:Harrison PW
- 通讯作者:Harrison PW
MGnify Genomes: A Resource for Biome-specific Microbial Genome Catalogues.
MGnify Genomes:生物群系特定微生物基因组目录的资源。
- DOI:http://dx.10.1016/j.jmb.2023.168016
- 发表时间:2023
- 期刊:
- 影响因子:5.6
- 作者:Gurbich TA
- 通讯作者:Gurbich TA
The European Nucleotide Archive in 2019.
2019 年欧洲核苷酸档案。
- DOI:http://dx.10.1093/nar/gkz1063
- 发表时间:2020
- 期刊:
- 影响因子:14.9
- 作者:Amid C
- 通讯作者:Amid C
The European Nucleotide Archive in 2022.
2022 年欧洲核苷酸档案。
- DOI:http://dx.10.1093/nar/gkac1051
- 发表时间:2023
- 期刊:
- 影响因子:14.9
- 作者:Burgin J
- 通讯作者:Burgin J
A unified catalog of 204,938 reference genomes from the human gut microbiome.
来自人类肠道微生物组的 204,938 个参考基因组的统一目录。
- DOI:http://dx.10.1038/s41587-020-0603-3
- 发表时间:2021
- 期刊:
- 影响因子:46.9
- 作者:Almeida A
- 通讯作者:Almeida A
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Robert Finn其他文献
2-BLOCKS WITH MINIMAL NONABELIAN DEFECT GROUPS
具有最小非纳贝尔缺陷组的 2 块
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
B. E. S. Ambale;F. A. M. Athematik;Paul Balmer;Robert Finn;Sorin Popa;Vyjayanthi Chari;Kefeng Liu;Jie Qing;Daryl Cooper;Jiang;Paul Yang;Silvio Levy - 通讯作者:
Silvio Levy
The small GTPase Rab4A interacts with the central region of cytoplasmic dynein light intermediate chain-1.
小 GTP 酶 Rab4A 与细胞质动力蛋白轻中间链 1 的中心区域相互作用。
- DOI:
10.1006/bbrc.2001.4468 - 发表时间:
2001-03-16 - 期刊:
- 影响因子:3.1
- 作者:
A. Bielli;Per;Alan G. Hendrick;Robert Finn;Kathleen Fitzgerald;M. Mccaffrey - 通讯作者:
M. Mccaffrey
Atomistic study of Urbach tail energies in (Al,Ga)N quantum well systems
(Al,Ga)N 量子阱系统中乌尔巴赫尾能的原子研究
- DOI:
- 发表时间:
2023 - 期刊:
- 影响因子:0
- 作者:
M. O’Donovan;Robert Finn;S. Schulz;T. Koprucki - 通讯作者:
T. Koprucki
Petersberg Papers on Afghanistan and the Region
关于阿富汗和该地区的彼得斯堡文件
- DOI:
- 发表时间:
2009 - 期刊:
- 影响因子:0
- 作者:
Wolfgang F. Danspeckgruber;Rangin Dadfar Spanta;Volker Stanzel;Rita Kieber;W. Maley;A. Wardak;A. Tarzi;Leanne Smith;A. Saikal;Susanne Schmeidl;M. Jansen;T. Ruttig;N. Banerjee;N. Bizhan;Zahir Tanin;Mahmoud Saikal;R. D. Mullen;V. Sahni;Carol Wang;Robert Finn - 通讯作者:
Robert Finn
The shape of a pendant liquid drop
悬垂液滴的形状
- DOI:
10.1098/rsta.1979.0064 - 发表时间:
1979 - 期刊:
- 影响因子:0
- 作者:
P. Concus;Robert Finn - 通讯作者:
Robert Finn
Robert Finn的其他文献
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{{ truncateString('Robert Finn', 18)}}的其他基金
Enriching MGnify Genomes to capture the full spectrum of the microbiota and bolster taxonomic classifications
丰富 MGnify 基因组以捕获微生物群的全谱并支持分类学分类
- 批准号:
BB/V01868X/1 - 财政年份:2022
- 资助金额:
$ 113.62万 - 项目类别:
Research Grant
2020BBSRC-NSF/BIO: REDEFINE - Development of efficient, large-scale metagenomics sequence comparison algorithms to facilitate novel genomic insights
2020BBSRC-NSF/BIO:REDEFINE - 开发高效、大规模的宏基因组序列比较算法,以促进新的基因组见解
- 批准号:
BB/W002965/1 - 财政年份:2022
- 资助金额:
$ 113.62万 - 项目类别:
Research Grant
SENSE - Screening of ENvironmental SEquences to discover novel protein functions using informatics target selection and high-throughput validation
SENSE - 使用信息学目标选择和高通量验证筛选环境序列以发现新的蛋白质功能
- 批准号:
BB/T000902/1 - 财政年份:2020
- 资助金额:
$ 113.62万 - 项目类别:
Research Grant
EMERALD - Enriching MEtagenomics Results using Artificial intelligence and Literature Data
EMERALD - 使用人工智能和文献数据丰富宏基因组学结果
- 批准号:
BB/S009043/1 - 财政年份:2019
- 资助金额:
$ 113.62万 - 项目类别:
Research Grant
Bilateral NSF/BIO-BBSRC:A Metagenomics Exchange - enriching analysis by synergistic harmonisation of MG-RAST and the EBI Metagenomics Portal
双边 NSF/BIO-BBSRC:宏基因组学交流 - 通过 MG-RAST 和 EBI 宏基因组学门户的协同协调丰富分析
- 批准号:
BB/N018354/1 - 财政年份:2017
- 资助金额:
$ 113.62万 - 项目类别:
Research Grant
Expanding Genome3D and disseminating the structural annotations via InterPro and PDBe
通过 InterPro 和 PDBe 扩展 Genome3D 并传播结构注释
- 批准号:
BB/N019172/1 - 财政年份:2016
- 资助金额:
$ 113.62万 - 项目类别:
Research Grant
EBI Metagenomics Portal - Towards a better understanding of community metabolism
EBI 宏基因组学门户 - 更好地了解群落代谢
- 批准号:
BB/M011755/1 - 财政年份:2015
- 资助金额:
$ 113.62万 - 项目类别:
Research Grant
14 NSFBIO:Towards detailed and consistent function prediction from protein family databases
14 NSFBIO:从蛋白质家族数据库进行详细且一致的功能预测
- 批准号:
BB/N00521X/1 - 财政年份:2015
- 资助金额:
$ 113.62万 - 项目类别:
Research Grant
Collaborative Research: Capillary Interfaces
合作研究:毛细管接口
- 批准号:
0103954 - 财政年份:2001
- 资助金额:
$ 113.62万 - 项目类别:
Standard Grant
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相似海外基金
Enabling synthetic biology through single cell functional genomics
通过单细胞功能基因组学实现合成生物学
- 批准号:
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Enabling comprehensive diagnosis of sub-acute infection in chronic respiratory disease via high sensitivity next generation sequencing
通过高灵敏度下一代测序实现慢性呼吸道疾病亚急性感染的全面诊断
- 批准号:
10325843 - 财政年份:2020
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EBI Metagenomics - enabling the reconstruction of microbial populations
EBI 宏基因组学 - 实现微生物种群的重建
- 批准号:
BB/R015171/2 - 财政年份:2020
- 资助金额:
$ 113.62万 - 项目类别:
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Enabling comprehensive diagnosis of sub-acute infection in chronic respiratory disease via high sensitivity next generation sequencing
通过高灵敏度下一代测序实现慢性呼吸道疾病亚急性感染的全面诊断
- 批准号:
10460284 - 财政年份:2020
- 资助金额:
$ 113.62万 - 项目类别:
Enabling comprehensive diagnosis of sub-acute infection in chronic respiratory disease via high sensitivity next generation sequencing
通过高灵敏度下一代测序实现慢性呼吸道疾病亚急性感染的全面诊断
- 批准号:
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