Evidence map›Paper›PMID 26608597›Full record

ArticleBMC genomics2015

MicroRNA target prediction using thermodynamic and sequence curves.

Asish Ghoshal, Raghavendran Shankar, Saurabh Bagchi, Ananth Grama, Somali Chaterji

Erratum issuedAbstract read
In one paragraph

Article in BMC genomics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. MicroRNA Targeting.Methods in molecular biology (Clifton, N.J.) · 2022
    Review
  7. Article
  8. Article
  9. Review
  10. The Role of MicroRNA in the Airway Surface Liquid Homeostasis.International journal of molecular sciences · 2020
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Asish GhoshalDepartment of Computer Science, Purdue University, West Lafayette, IN, 47907, USA. aghoshal@purdue.edu.
Raghavendran ShankarDepartment of Computer Science, Purdue University, West Lafayette, IN, 47907, USA. rshankar@purdue.edu.
Saurabh BagchiSchool of Electrical and Computer Engineering, Purdue University, West Lafayette, IN, 47907, USA. sbagchi@purdue.edu.
Ananth GramaDepartment of Computer Science, Purdue University, West Lafayette, IN, 47907, USA. ayg@purdue.edu.
Somali ChaterjiDepartment of Computer Science, Purdue University, West Lafayette, IN, 47907, USA. schaterj@purdue.edu.

Funding

Theoretical Foundations and Software Infrastructure for Biological Network DatabasesU01CA198941 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI KOYUTURK, MEHMET · 2015 to 2017
$1.4M
NCI NIH HHS U01 CA198941
6 · The paper itself

Abstract

backgroundMicroRNAs (miRNAs) are small regulatory RNA that mediate RNA interference by binding to various mRNA target regions. There have been several computational methods for the identification of target mRNAs for miRNAs. However, these have considered all contributory features as scalar representations, primarily, as thermodynamic or sequence-based features. Further, a majority of these methods solely target canonical sites, which are sites with "seed" complementarity. Here, we present a machine-learning classification scheme, titled Avishkar, which captures the spatial profile of miRNA-mRNA interactions via smooth B-spline curves, separately for various input features, such as thermodynamic and sequence features. Further, we use a principled approach to uniformly model canonical and non-canonical seed matches, using a novel seed enrichment metric.

resultsWe demonstrate that large number of seed-match patterns have high enrichment values, conserved across species, and that majority of miRNA binding sites involve non-canonical matches, corroborating recent findings. Using spatial curves and popular categorical features, such as target site length and location, we train a linear SVM model, utilizing experimental CLIP-seq data. Our model significantly outperforms all established methods, for both canonical and non-canonical sites. We achieve this while using a much larger candidate miRNA-mRNA interaction set than prior work.

conclusionsWe have developed an efficient SVM-based model for miRNA target prediction using recent CLIP-seq data, demonstrating superior performance, evaluated using ROC curves, specifically about 20% better than the state-of-the-art, for different species (human or mouse), or different target types (canonical or non-canonical). To the best of our knowledge we provide the first distributed framework for microRNA target prediction based on Apache Hadoop and Spark. AVAILABILITY: All source code and data is publicly available at https://bitbucket.org/cellsandmachines/avishkar.

Indexed as

Binding SitesRNA InterferenceThermodynamics3' Untranslated Regions5' Untranslated RegionsAnimalsComputational BiologyHumansMiceMicroRNAsReproducibility of ResultsRNA, MessengerROC CurveSequence Analysis, RNASupport Vector Machine3' Untranslated Regions5' Untranslated RegionsMicroRNAsRNA, Messenger

Identifiers

PMID26608597
PMCPMC4658802

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.