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Construct a tool for thermodynamic controlled prediction of conserved secondary structure
A tool for prediction of conserved secondary structure of a set of homologous single-stranded RNAs is presented. For each RNA of the set the structure distribution is calculated and stored in a base pair probability matrix. Gaps, resulting from a multiple sequence alignment of the RNA set, are intro...
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Published in: | Nucleic acids research 1999-11, Vol.27 (21), p.4208-4217 |
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creator | Rupert, Luck Stefan, Graf Gerhard, Steger |
description | A tool for prediction of conserved secondary structure of a set of homologous single-stranded RNAs is presented. For each RNA of the set the structure distribution is calculated and stored in a base pair probability matrix. Gaps, resulting from a multiple sequence alignment of the RNA set, are introduced into the individual probability matrices. These ‘aligned’ probability matrices are summed up to give a consensus probability matrix emphasizing the conserved structural elements of the RNA set. Because the multiple sequence alignment is independent of any structural constraints, such an alignment may result in introduction of gaps into the homologous probability matrices that disrupt a common consensus structure. By use of its graphical user interface the presented tool allows the removal of such misalignments, which are easily recognized, from the individual probability matrices by optimizing the sequence alignment with respect to a structural alignment. From the consensus probability matrix a consensus structure is extracted, which is viewable in three different graphical representations. The functionality of the tool is demonstrated using a small set of U7 RNAs, which are involved in 3′ -end processing of histone mRNA precursors. Supplementary Material lists further results obtained. Advantages and drawbacks of the tool are discussed in comparison to several other algorithms. |
doi_str_mv | 10.1093/nar/27.21.4208 |
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For each RNA of the set the structure distribution is calculated and stored in a base pair probability matrix. Gaps, resulting from a multiple sequence alignment of the RNA set, are introduced into the individual probability matrices. These ‘aligned’ probability matrices are summed up to give a consensus probability matrix emphasizing the conserved structural elements of the RNA set. Because the multiple sequence alignment is independent of any structural constraints, such an alignment may result in introduction of gaps into the homologous probability matrices that disrupt a common consensus structure. By use of its graphical user interface the presented tool allows the removal of such misalignments, which are easily recognized, from the individual probability matrices by optimizing the sequence alignment with respect to a structural alignment. From the consensus probability matrix a consensus structure is extracted, which is viewable in three different graphical representations. 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Advantages and drawbacks of the tool are discussed in comparison to several other algorithms.</description><subject>Algorithms</subject><subject>Animals</subject><subject>Base Pair Mismatch</subject><subject>Base Pairing</subject><subject>Base Sequence</subject><subject>Consensus Sequence - genetics</subject><subject>Conserved Sequence - genetics</subject><subject>Databases, Factual</subject><subject>histones</subject><subject>Humans</subject><subject>Mutation - genetics</subject><subject>Nucleic Acid Conformation</subject><subject>RNA - chemistry</subject><subject>RNA - genetics</subject><subject>RNA - metabolism</subject><subject>RNA, Small Nuclear - genetics</subject><subject>Sequence Alignment</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>snRNA U7</subject><subject>Software</subject><subject>Thermodynamics</subject><subject>User-Computer Interface</subject><issn>0305-1048</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkc1v1DAUxC1ERZfClSOKOHDL1t-ODxzoAtuKSgiplaAXy3GeaUoSL7ZT0f8er1JVhQunZ3l-8zT2IPSK4DXBmh1PNh5TtaZkzSlunqAVYZLWXEv6FK0ww6ImmDeH6HlKNxgTTgR_hg4JFqSRhK7Q902YUo6zy5WtcghD5UOs8jXEMXR3kx17V7kw5RiGAbpqF6HrXe7DVAW_FxLE23KfoJw7G--qZdkc4QU68HZI8PJ-HqHLTx8vNqf1-Zft2eb9ee2EkrnWHHPAWjGrW8yI8N5SBo63jLVlKqmE9q12WrLGddJ5B9p23jUgibKkZUfo3bJ3N7cjdA5KWDuYXezHkscE25u_lam_Nj_CrSG8kVoU_9t7fwy_ZkjZjH1yMAx2gjAno3BDleb6vyBRHGvBVQHf_APehDlO5RMMxVhyRiQr0HqBXAwpRfAPiQk2-2pNqdZQZSgx-2qL4fXjdz7Cly4LUC9AnzL8ftBt_GmkYkqY029XZnvy4SveXmnzmf0BkWKx3g</recordid><startdate>19991101</startdate><enddate>19991101</enddate><creator>Rupert, Luck</creator><creator>Stefan, Graf</creator><creator>Gerhard, Steger</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7SS</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19991101</creationdate><title>Construct a tool for thermodynamic controlled prediction of conserved secondary structure</title><author>Rupert, Luck ; 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For each RNA of the set the structure distribution is calculated and stored in a base pair probability matrix. Gaps, resulting from a multiple sequence alignment of the RNA set, are introduced into the individual probability matrices. These ‘aligned’ probability matrices are summed up to give a consensus probability matrix emphasizing the conserved structural elements of the RNA set. Because the multiple sequence alignment is independent of any structural constraints, such an alignment may result in introduction of gaps into the homologous probability matrices that disrupt a common consensus structure. By use of its graphical user interface the presented tool allows the removal of such misalignments, which are easily recognized, from the individual probability matrices by optimizing the sequence alignment with respect to a structural alignment. From the consensus probability matrix a consensus structure is extracted, which is viewable in three different graphical representations. 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subjects | Algorithms Animals Base Pair Mismatch Base Pairing Base Sequence Consensus Sequence - genetics Conserved Sequence - genetics Databases, Factual histones Humans Mutation - genetics Nucleic Acid Conformation RNA - chemistry RNA - genetics RNA - metabolism RNA, Small Nuclear - genetics Sequence Alignment Sequence Homology, Nucleic Acid snRNA U7 Software Thermodynamics User-Computer Interface |
title | Construct a tool for thermodynamic controlled prediction of conserved secondary structure |
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