Evidence map›Paper›PMID 28717530›Full record

ArticleQuantitative biology (Beijing, China)2017

Comparative and integrative analysis of RNA structural profiling data: current practices and emerging questions.

Krishna Choudhary, Fei Deng, Sharon Aviran

Abstract read
In one paragraph

Article in Quantitative biology (Beijing, China), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Article
  2. Markov models of SHAPE data improve secondary structure prediction.bioRxiv : the preprint server for biology · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. RNA Structure Determination by High-Throughput Structural Analysis.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. ShaKer: RNA SHAPE prediction using graph kernel.Bioinformatics (Oxford, England) · 2019
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Detecting RNA G-Quadruplexes (rG4s) in the Transcriptome.Cold Spring Harbor perspectives in biology · 2018
    Review
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

3 authors.

Krishna ChoudharyDepartment of Biomedical Engineering and Genome Center, University of California at Davis, Davis, CA 95616, USA.
Fei DengDepartment of Biomedical Engineering and Genome Center, University of California at Davis, Davis, CA 95616, USA.
Sharon AviranDepartment of Biomedical Engineering and Genome Center, University of California at Davis, Davis, CA 95616, USA.

Funding

Methods for RNA structural analysis using computation and structure mapping experR00HG006860 · NHGRI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI AVIRAN, SHARON · 2014 to 2016
$725k
Methods for RNA structural analysis using computation and structure mapping experK99HG006860 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI AVIRAN, SHARON · 2012 to 2012
$103k
NHGRI NIH HHS K99 HG006860NHGRI NIH HHS R00 HG006860
6 · The paper itself

Abstract

backgroundStructure profiling experiments provide single-nucleotide information on RNA structure. Recent advances in chemistry combined with application of high-throughput sequencing have enabled structure profiling at transcriptome scale and in living cells, creating unprecedented opportunities for RNA biology. Propelled by these experimental advances, massive data with ever-increasing diversity and complexity have been generated, which give rise to new challenges in interpreting and analyzing these data.

resultsWe review current practices in analysis of structure profiling data with emphasis on comparative and integrative analysis as well as highlight emerging questions. Comparative analysis has revealed structural patterns across transcriptomes and has become an integral component of recent profiling studies. Additionally, profiling data can be integrated into traditional structure prediction algorithms to improve prediction accuracy.

conclusionsTo keep pace with experimental developments, methods to facilitate, enhance and refine such analyses are needed. Parallel advances in analysis methodology will complement profiling technologies and help them reach their full potential.

Indexed as

chemical structure probinghigh-throughput sequencingRNA secondary structure predictionRNA structure profilingSHAPE-Seq

Identifiers

PMID28717530
PMCPMC5510538

What Socratic holds

Textmetadata
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Registered trials

None linked

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 Socratic graph.