ABI Innovation: Towards Recovery of Biological Information

ABI Innovation:迈向生物信息恢复

基本信息

  • 批准号:
    1356569
  • 负责人:
  • 金额:
    $ 121.68万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
    Continuing Grant
  • 财政年份:
    2014
  • 资助国家:
    美国
  • 起止时间:
    2014-09-01 至 2017-08-31
  • 项目状态:
    已结题

项目摘要

Baylor College of Medicine is awarded a grant to develop novel techniques of network analysis, rooted on the evolutionary principle of continuity, to tackle the fundamental problems of biological data integration and analysis. A problem in biology is that experimental information accumulates far faster than it can be analyzed. These data are complicated, incomplete, and noisy, slowing down their interpretation, but a major difficulty is that because they arise from different experiments they are analyzed separately, or in small groups. This project aims instead to tie all biological data into one network so that each bit of information is understood in light of all other data. To make this approach feasible we propose a new, efficient use of evolutionary relationships to coalesce experimental results arising from hundreds of species into a single network that, although massive, is still easy to compute over. Another insight is that neighboring regions of the network are likely to carry out related biological functions. This hypothesis translates into precise mathematical rules to spread information across the entire network and, as much as possible, resolve contradictions. In practice, these network and computational tools will predict various aspects of protein function that will then be tested experimentally across a broad range of applications (p53, a central gene in animal biology; in proteins that regulate stress adaptation in bacteria; and in malarial proteins). Together computation and experiments will assess the value and limitations of this novel and versatile network approach to discover the molecular origin of function in any organism. The project will fulfill many goals of broader societal significance. First, it will validate novel techniques of biological network analysis that can be used in any area touched by research in molecular biology; this includes biotechnology, bioengineering, nanotechnology, agriculture, renewable energy production, and synthetic biology applications for industrial processes. Second, it is also important to note that the scientific results fall in the area of BIG DATA analytics, which cuts across science, finance, social and national defense areas of interest. In that light, third, we note that the projects will train both postdoctoral scientists, graduate students, and offer summer internships to undergraduate students, including some from programs supporting minority education and research, who will therefore be able later to contribute their skills in Big Data analytics to many fields of national interest.
贝勒医学院获得一笔拨款,用于开发基于连续性进化原理的网络分析新技术,以解决生物数据集成和分析的基本问题。生物学中的一个问题是实验信息的积累速度远远快于分析速度。这些数据复杂、不完整且嘈杂,减慢了它们的解释速度,但一个主要困难是,因为它们来自不同的实验,所以需要单独或小组进行分析。该项目的目标是将所有生物数据连接到一个网络中,以便根据所有其他数据来理解每一位信息。为了使这种方法可行,我们提出了一种新的、有效的利用进化关系的方法,将数百个物种的实验结果合并到一个网络中,该网络虽然庞大,但仍然很容易计算。另一个见解是网络的邻近区域可能执行相关的生物功能。这一假设转化为精确的数学规则,以在整个网络中传播信息,并尽可能地解决矛盾。在实践中,这些网络和计算工具将预测蛋白质功能的各个方面,然后在广泛的应用中进行实验测试(p53,动物生物学的中心基因;调节细菌应激适应的蛋白质;以及疟疾蛋白质)。计算和实验将共同评估这种新颖且多功能的网络方法的价值和局限性,以发现任何生物体中功能的分子起源。该项目将实现许多具有更广泛社会意义的目标。首先,它将验证生物网络分析的新技术,该技术可用于分子生物学研究涉及的任何领域;这包括生物技术、生物工程、纳米技术、农业、可再生能源生产以及工业过程中的合成生物学应用。其次,还需要注意的是,科学成果属于大数据分析领域,涉及科学、金融、社会和国防等感兴趣的领域。第三,我们注意到这些项目将培训博士后科学家和研究生,并为本科生提供暑期实习机会,其中包括一些来自支持少数族裔教育和研究项目的实习机会,因此他们以后将能够将大数据分析方面的技能贡献给国家利益的许多领域。

项目成果

期刊论文数量(0)
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Olivier Lichtarge其他文献

Some model experiments in hemodynamics: VI. Two-body collisions between blood cells.
血流动力学的一些模型实验:VI.
  • DOI:
  • 发表时间:
    1981
  • 期刊:
  • 影响因子:
    1.1
  • 作者:
    Harry L. Goldsmith;Olivier Lichtarge;M. Tessier;S. Spain
  • 通讯作者:
    S. Spain
Evaluating predictors of kinase activity of STK11 variants identified in primary human non-small cell lung cancers
  • DOI:
    10.1007/s00439-025-02726-0
  • 发表时间:
    2025-02-12
  • 期刊:
  • 影响因子:
    3.600
  • 作者:
    Yile Chen;Kyoungyeul Lee;Junwoo Woo;Dong-wook Kim;Changwon Keum;Giulia Babbi;Rita Casadio;Pier Luigi Martelli;Castrense Savojardo;Matteo Manfredi;Yang Shen;Yuanfei Sun;Panagiotis Katsonis;Olivier Lichtarge;Vikas Pejaver;David J. Seward;Akash Kamandula;Constantina Bakolitsa;Steven E. Brenner;Predrag Radivojac;Anne O’Donnell-Luria;Sean D. Mooney;Shantanu Jain
  • 通讯作者:
    Shantanu Jain
114 Expanding clinical spectrum of RRM2B mutations to include MNGIE
  • DOI:
    10.1016/j.mito.2009.12.106
  • 发表时间:
    2010-03-01
  • 期刊:
  • 影响因子:
  • 作者:
    Lee-Jun Wong;Aziz Shaibani;Oleg A. Shchelochkov;Shulin Zhang;Panagiotis Katsonis;Olivier Lichtarge;Marwan Shinawi
  • 通讯作者:
    Marwan Shinawi
Assessing the predicted impact of single amino acid substitutions in calmodulin for CAGI6 challenges
  • DOI:
    10.1007/s00439-024-02720-y
  • 发表时间:
    2024-12-23
  • 期刊:
  • 影响因子:
    3.600
  • 作者:
    Paola Turina;Giuditta Dal Cortivo;Carlos A. Enriquez Sandoval;Emil Alexov;David B. Ascher;Giulia Babbi;Constantina Bakolitsa;Rita Casadio;Piero Fariselli;Lukas Folkman;Akash Kamandula;Panagiotis Katsonis;Dong Li;Olivier Lichtarge;Pier Luigi Martelli;Shailesh Kumar Panday;Douglas E. V. Pires;Stephanie Portelli;Fabrizio Pucci;Carlos H. M. Rodrigues;Marianne Rooman;Castrense Savojardo;Martin Schwersensky;Yang Shen;Alexey V. Strokach;Yuanfei Sun;Junwoo Woo;Predrag Radivojac;Steven E. Brenner;Daniele Dell’Orco;Emidio Capriotti
  • 通讯作者:
    Emidio Capriotti
CAGI6 ID panel challenge: assessment of phenotype and variant predictions in 415 children with neurodevelopmental disorders (NDDs)
  • DOI:
    10.1007/s00439-024-02722-w
  • 发表时间:
    2025-01-09
  • 期刊:
  • 影响因子:
    3.600
  • 作者:
    Maria Cristina Aspromonte;Alessio Del Conte;Shaowen Zhu;Wuwei Tan;Yang Shen;Yexian Zhang;Qi Li;Maggie Haitian Wang;Giulia Babbi;Samuele Bovo;Pier Luigi Martelli;Rita Casadio;Azza Althagafi;Sumyyah Toonsi;Maxat Kulmanov;Robert Hoehndorf;Panagiotis Katsonis;Amanda Williams;Olivier Lichtarge;Su Xian;Wesley Surento;Vikas Pejaver;Sean D. Mooney;Uma Sunderam;Rajgopal Srinivasan;Alessandra Murgia;Damiano Piovesan;Silvio C. E. Tosatto;Emanuela Leonardi
  • 通讯作者:
    Emanuela Leonardi

Olivier Lichtarge的其他文献

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{{ truncateString('Olivier Lichtarge', 18)}}的其他基金

RAPID - COVID-19 target epitopes and human genetic factors of virulence
RAPID - COVID-19 靶标表位和人类遗传毒力因素
  • 批准号:
    2032904
  • 财政年份:
    2020
  • 资助金额:
    $ 121.68万
  • 项目类别:
    Standard Grant
ABI Innovation: Tunable Perturbation of Proteins and Pathways
ABI 创新:蛋白质和通路的可调节扰动
  • 批准号:
    1062455
  • 财政年份:
    2011
  • 资助金额:
    $ 121.68万
  • 项目类别:
    Continuing Grant
Data Flow across Heterogenous and Frustrated Protein Networks
跨异质和受挫蛋白质网络的数据流
  • 批准号:
    0905536
  • 财政年份:
    2009
  • 资助金额:
    $ 121.68万
  • 项目类别:
    Standard Grant
Automated Annotation of Function in Protein Structures from Evolutionary-based 3D-Templates
根据基于进化的 3D 模板自动注释蛋白质结构中的功能
  • 批准号:
    0547695
  • 财政年份:
    2006
  • 资助金额:
    $ 121.68万
  • 项目类别:
    Continuing Grant
MRI: Acquisition of a Cluster Computer for Digital Biology
MRI:购买用于数字生物学的集群计算机
  • 批准号:
    0420984
  • 财政年份:
    2004
  • 资助金额:
    $ 121.68万
  • 项目类别:
    Standard Grant
Algorithms for the Discovery and Geometric-Matching of Hierarchical 3-D Templates of Functional Sites in Protein Structures
蛋白质结构中功能位点分层 3D 模板的发现和几何匹配算法
  • 批准号:
    0318415
  • 财政年份:
    2003
  • 资助金额:
    $ 121.68万
  • 项目类别:
    Continuing Grant
Development of a Database for the Discovery and Annotation of Functional Sites in Protein Structures
开发用于发现和注释蛋白质结构中功能位点的数据库
  • 批准号:
    0114796
  • 财政年份:
    2001
  • 资助金额:
    $ 121.68万
  • 项目类别:
    Continuing Grant

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