An all-in-one web server for RNA structure prediction using evolutionary information
An all-in-one web server for RNA structure prediction using evolutionary information
批准号:
10574944
负责人:
Elena Rivas
金额:
$24.99万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2023
资助国家:
美国
项目状态:
已结题
起止时间:
2023-01-01 至 2024-12-31
关键词:
AdoptedAdoptionAlgorithmsBiologicalBiologyCellsCommunitiesComputational BiologyComputer softwareComputing MethodologiesDevelopmentEvaluationEvolutionExperimental DesignsFamilyFree EnergyGenomeGoalsHomologous GeneKnowledgeLinkMapsMethodsModelingOrganismOutcomeOutputPhylogenetic AnalysisRNARNA SequencesResearchRetrievalRunningScienceSequence AlignmentSequence HomologsSite-Directed MutagenesisSortingStructureTechniquesTechnologyTimeValidationVariantWorkcomparativecomputerized toolscostimprovedinterestnovelprediction algorithmpredictive toolsprogramsprotein structure predictionstructural biologytherapeutic RNAtooltranscriptomewastingweb platformweb server
中文摘要
项目摘要
RNA的结构和功能是紧密相连的。为了弄清楚转录本中的无数RNA是什么
要做到这一点,我们需要严格的方法来推断结构。许多预测算法已经存在,但它们
任何序列的输出模型,不同的方法通常输出不同的模型
相同的序列。这导致了渗透到该领域的次优模型,并将结构归因于RNA
它们实际上没有任何保守的结构。RNA研究领域现在需要的是一种
一种计算工具,它将评估某个RNA序列具有生物结构的可能性,以及
提出精度最高的结构。长期以来,解决这个问题的最佳方法是
不同生物体的同源序列的比较。这种相同的方法实际上是基于
最成功的蛋白质结构预测工具。但广泛采用这种方法的障碍
对于预测RNA结构来说,序列比较需要计算方面的知识和专业知识
和结构生物学,以及使用非主流工具。这项建议是关于
开发一种可免费获得的网络服务器,用于可靠地预测RNA二级和最终三级
使用进化信息的结构。此Web服务器将在后台作为一套工具(
其输出将可供感兴趣的用户使用),从同源序列检索到对
生成的模型。首先,这个工具将自动检索和比对同源序列,使用
现有的和新的算法。该目标将搜索与输入的任何单个序列相关的同源序列
输入,这对大多数当前的计划来说是一个尚未满足的挑战。第二,应用程序使用
协变分析将解决输入RNA序列具有保守结构的可能性,
因此,并不是每个用作输入的序列都一定会输出结构模型。中的后续模块
在线工具将评估对齐的质量,并可能改进这种对齐,以便模型
可以提出一个有置信度的分数。无论结果如何,用户都将得到一个需要
考虑到进化和最新的RNA结构信息,所以它不会因为使用
一组参数,就像现有预测方法经常出现的情况一样。更具整体性和
利用进化信息的简单计算工具将有助于传播这些信息的使用
方法到更大的RNA生物学社区,以最大限度地影响RNA研究中的实验设计。
英文摘要
Project Abstract
RNA structure and function are intimately linked. To sort out what the myriad RNAs in transcriptomes are
doing, we need rigorous approaches that also infer structure. Many predictive algorithms already exist, but they
output models for any and every sequence, and different approaches often output different models for the
same sequence. This results in suboptimal models that permeate the field, and in ascribing structure to RNAs
that don't in fact have any conserved structure. What the field of RNA research needs now to go forward is a
computational tool that will evaluate the likelihood that a certain RNA sequence has a biological structure, and
propose that structure with the highest accuracy. The best approach to this issue has been for a long time the
comparison of homologous sequences from diverse organisms. This same approach is actually at the basis of
the most successful protein structure prediction tools. But a hindrance in the wide adoption of such approaches
for predicting RNA structure is that sequence comparison requires knowledge and expertise in computational
and structural biology as well as access to tools that are not mainstream. This proposal is about the
development of a freely available webserver for reliably predicting RNA secondary and eventually tertiary
structures using evolutionary information. This webserver will operate behind the scenes as a suite of tools (the
outputs of which will be available for interested users), from homologous sequences retrieval to evaluation of
the resulting model. First, this tool will automatically retrieve and align homologous sequences using
existing and novel algorithms. This aim will search for relevant homologs to any single sequence entered as
input, which represents an unmet challenge for most current programs. Second, the application using
covariation analysis will address the likeliness that the input RNA sequence has a conserved structure,
so not every sequence used as input will necessarily output a structure model. Subsequent modules in
the online tool will evaluate the quality of the alignment, and possibly improve this alignment, so that a model
with a confidence score could be proposed. Regardless of the outcome, the user will have a result that will take
into account evolutionary as well as up-to-date RNA structural information, so it will not be biased by the use of
a single set of parameters, as is often the case with existing predictive methods. A more holistic and
straightforward computational tool harnessing evolutionary information will help disseminate the use of those
methods to the larger RNA biology community, for maximum impact on experimental design in RNA research.
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科研奖励(0)
会议论文
Discovery of structural RNAs involved in human health and disease
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批准号:10704745
-
项目类别:
-
资助金额:$34.86万
-
财政年份:2022
-
负责人:Elena Rivas
-
依托单位:
Computational approaches to noncoding RNAs
-
批准号:7059274
-
项目类别:
-
资助金额:$2.0万
-
财政年份:2006
-
负责人:Elena Rivas
-
依托单位:
Computational methods to identify noncoding RNA genes
-
批准号:6869927
-
项目类别:
-
资助金额:$15.75万
-
财政年份:2005
-
负责人:Elena Rivas
-
依托单位:
Computational methods to identify noncoding RNA genes
-
批准号:7025050
-
项目类别:
-
资助金额:$15.38万
-
财政年份:2005
-
负责人:Elena Rivas
-
依托单位:
Regulatory and functional RNAs: computational approaches
-
批准号:6687991
-
项目类别:
-
资助金额:$4.18万
-
财政年份:2003
-
负责人:Elena Rivas
-
依托单位:
Probabilistic methods to identify noncoding RNA genes
-
批准号:6536488
-
项目类别:
-
资助金额:$9.51万
-
财政年份:2001
-
负责人:Elena Rivas
-
依托单位:
Probabilistic methods to identify noncoding RNA genes
-
批准号:6321572
-
项目类别:
-
资助金额:$9.24万
-
财政年份:2001
-
负责人:Elena Rivas
-
依托单位:
Probabilistic methods to identify noncoding RNA genes
-
批准号:6638074
-
项目类别:
-
资助金额:$9.8万
-
财政年份:2001
-
负责人:Elena Rivas
-
依托单位:
海外基金