Evidence map›Paper›PMID 26130723›Full record

ArticleNucleic acids research2015

Identifying novel sequence variants of RNA 3D motifs.

Craig L Zirbel, James Roll, Blake A Sweeney, Anton I Petrov, Meg Pirrung, Neocles B Leontis

Abstract readValidation Study
In one paragraph

Article in Nucleic acids research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed.

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  18. Computational Methods for Modeling Aptamers and Designing Riboswitches.International journal of molecular sciences · 2017
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Craig L ZirbelDepartment of Mathematics and Statistics, Bowling Green State University, Bowling Green, OH 43403, USA zirbel@bgsu.edu.
James RollDepartment of Mathematics and Statistics, Bowling Green State University, Bowling Green, OH 43403, USA.
Blake A SweeneyDepartment of Biology, Bowling Green State University, Bowling Green, OH 43403, USA.
Anton I PetrovEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SD, UK.ORCID http://orcid.org/0000-0001-7279-2682
Meg PirrungDepartment of Pharmacology, University of Colorado Denver, Aurora, CO 80045, USA.
Neocles B LeontisDepartment of Chemistry, Bowling Green State University, Bowling Green, OH 43403, USA.

Funding

RNA 3D Motif Search, Atlas, and Prediction from SequenceR01GM085328 · NIGMS · BOWLING GREEN STATE UNIVERSITY · PI ZIRBEL, CRAIG L · 2010 to 2023
$4.0M
SELECTION AND ANALYSIS OF STABLE RNA 3 WAY JUNCTIONSR15GM055898 · NIGMS · BOWLING GREEN STATE UNIVERSITY · PI LEONTIS, NEOCLES B · 1997 to 2010
$680k
NIGMS NIH HHS GM055898NIGMS NIH HHS GM085328NIGMS NIH HHS R01 GM085328NIGMS NIH HHS R01GM085328
6 · The paper itself

Abstract

Predicting RNA 3D structure from sequence is a major challenge in biophysics. An important sub-goal is accurately identifying recurrent 3D motifs from RNA internal and hairpin loop sequences extracted from secondary structure (2D) diagrams. We have developed and validated new probabilistic models for 3D motif sequences based on hybrid Stochastic Context-Free Grammars and Markov Random Fields (SCFG/MRF). The SCFG/MRF models are constructed using atomic-resolution RNA 3D structures. To parameterize each model, we use all instances of each motif found in the RNA 3D Motif Atlas and annotations of pairwise nucleotide interactions generated by the FR3D software. Isostericity relations between non-Watson-Crick basepairs are used in scoring sequence variants. SCFG techniques model nested pairs and insertions, while MRF ideas handle crossing interactions and base triples. We use test sets of randomly-generated sequences to set acceptance and rejection thresholds for each motif group and thus control the false positive rate. Validation was carried out by comparing results for four motif groups to RMDetect. The software developed for sequence scoring (JAR3D) is structured to automatically incorporate new motifs as they accumulate in the RNA 3D Motif Atlas when new structures are solved and is available free for download.

Indexed as

Models, StatisticalBase SequenceGenetic VariationMarkov ChainsNucleotide MotifsRNASequence AlignmentSequence Analysis, RNASoftwareRNA

Identifiers

PMID26130723
PMCPMC4551918

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.