rboAnalyzer: A Software to Improve Characterization of Non-coding RNAs From Sequence Database Search Output

. 2020 ; 11 () : 675. [epub] 20200728

Status PubMed-not-MEDLINE Jazyk angličtina Země Švýcarsko Médium electronic-ecollection

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid32849767

Searching for similar sequences in a database via BLAST or a similar tool is one of the most common bioinformatics tasks applied in general, and to non-coding RNAs in particular. However, the results of the search might be difficult to interpret due to the presence of partial matches to the database subject sequences. Here, we present rboAnalyzer - a tool that helps with interpreting sequence search result by (1) extending partial matches into plausible full-length subject sequences, (2) predicting homology of RNAs represented by full-length subject sequences to the query RNA, (3) pooling information across homologous RNAs found in the search results and public databases such as Rfam to predict more reliable secondary structures for all matches, and (4) contextualizing the matches by providing the prediction results and other relevant information in a rich graphical output. Using predicted full-length matches improves secondary structure prediction and makes rboAnalyzer robust with regards to identification of homology. The output of the tool should help the user to reliably characterize non-coding RNAs in BLAST output. The usefulness of the rboAnalyzer and its ability to correctly extend partial matches to full-length is demonstrated on known homologous RNAs. To allow the user to use custom databases and search options, rboAnalyzer accepts any search results as a text file in the BLAST format. The main output is an interactive HTML page displaying the computed characteristics and other context of the matches. The output can also be exported in an appropriate sequence and/or secondary structure formats.

Zobrazit více v PubMed

Bernhart S. H., Hofacker I. L., Will S., Gruber A. R., Stadler P. F. (2008). RNAalifold: improved consensus structure prediction for RNA alignments. PubMed DOI PMC

Camacho C., Coulouris G., Avagyan V., Ma N., Papadopoulos J., Bealer K., et al. (2009). BLAST plus: architecture and applications. PubMed DOI PMC

Cock P. J. A., Antao T., Chang J. T., Chapman B. A., Cox C. J., Dalke A., et al. (2009). Biopython: freely available Python tools for computational molecular biology and bioinformatics. PubMed DOI PMC

Edgar R. C. (2004). MUSCLE: multiple sequence alignment with high accuracy and high throughput. PubMed DOI PMC

Hamada M., Sato K., Kiryu H., Mituyama T., Asai K. (2009). Predictions of RNA secondary structure by combining homologous sequence information. PubMed DOI PMC

Hunter J. D. (2007). Matplotlib: a 2D graphics environment. DOI

Jelínek J., Hoksza D., Hajiè J., Pešek J., Drozen J., Hladík T., et al. (2019). rPredictorDB: a predictive database of individual secondary structures of RNAs and their formatted plots. PubMed DOI PMC

Klein R. J., Eddy S. R. (2003). RSEARCH: finding homologs of single structured RNA sequences. PubMed DOI PMC

Lorenz R., Hofacker I. L., Stadler P. F. (2016). RNA folding with hard and soft constraints. PubMed DOI PMC

Markham N. R., Zuker M. (2008). UNAFold: software for nucleic acid folding and hybridization. PubMed

McKinney W. (2010). “Data structures for statistical computing in python,” in

Nawrocki E. P., Burge S. W., Bateman A., Daub J., Eberhardt R. Y., Eddy S. R., et al. (2015). Rfam 12.0: updates to the RNA families database. PubMed DOI PMC

Nawrocki E. P., Eddy S. R. (2013). Infernal 1.1: 100-fold faster RNA homology searches. PubMed DOI PMC

Oliphant T. E. (2006).

Pánek J., Krásnı L., Bobek J., Ježková E., Korelusová J., Vohradskı J. (2010). The suboptimal structures find the optimal RNAs: homology search for bacterial non-coding RNAs using suboptimal RNA structures. PubMed DOI PMC

Puton T., Kozlowski L. P., Rother K. M., Bujnicki J. M. (2013). CompaRNA: a server for continuous benchmarking of automated methods for RNA secondary structure prediction. PubMed DOI PMC

Sievers F., Wilm A., Dineen D., Gibson T. J., Karplus K., Li W., et al. (2011). Fast, scalable generation of high-quality protein multiple sequence alignments using Clustal Omega. PubMed DOI PMC

Tafer H., Höner zu Siederdissen C., Stadler P. F., Bernhart S. H., Hofacker I. L., Lorenz R., et al. (2011). ViennaRNA Package 2.0. PubMed DOI PMC

Tan Z., Fu Y., Sharma G., Mathews D. H. (2017). TurboFold II: RNA structural alignment and secondary structure prediction informed by multiple homologs. PubMed DOI PMC

Will S., Joshi T., Hofacker I. L., Stadler P. F., Backofen R. (2012). LocARNA-P: accurate boundary prediction and improved detection of structural RNAs. PubMed DOI PMC

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...