Evidence map›Paper›PMID 27406314›Full record

ArticleHuman mutation2016

Regulatory Single-Nucleotide Variant Predictor Increases Predictive Performance of Functional Regulatory Variants.

Thomas A Peterson, Matthew Mort, David N Cooper, Predrag Radivojac, Maricel G Kann, Sean D Mooney

Abstract read
In one paragraph

Article in Human mutation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Using GWAS to identify novel therapeutic targets for osteoporosis.Translational research : the journal of laboratory and clinical medicine · 2017
    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

6 authors.

Thomas A PetersonDepartment of Biological Sciences, University of Maryland, Baltimore County, Baltimore, Maryland.
Matthew MortInstitute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, CF14 4XN, United Kingdom.
David N CooperInstitute of Medical Genetics, School of Medicine, Cardiff University, Cardiff, CF14 4XN, United Kingdom.
Predrag RadivojacDepartment of Computer Science and Informatics, Indiana University, Bloomington, Indiana.
Maricel G KannDepartment of Biological Sciences, University of Maryland, Baltimore County, Baltimore, Maryland.
Sean D MooneyDepartment of Biomedical Informatics and Medical Education, University of Washington, Seattle, Washington. sdmooney@uw.edu.

Funding

Informatic Profiling of Clinically Relevant MutationR01LM009722 · NLM · UNIVERSITY OF WASHINGTON · PI MOONEY, SEAN DAVID · 2007 to 2014
$3.5M
A computational framework for predicting the impact of mutations in autismR01MH105524 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI IAKOUCHEVA, LILIA M, RADIVOJAC, PREDRAG · 2014 to 2016
$1.4M
Protein domains as molecular units to unravel functional pathways of cancer genesK22CA143148 · NCI · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI KANN, MARICEL G. · 2009 to 2011
$490k
NCI NIH HHS K22 CA143148NIMH NIH HHS R01 MH105524NLM NIH HHS R01 LM009722
6 · The paper itself

Abstract

In silico methods for detecting functionally relevant genetic variants are important for identifying genetic markers of human inherited disease. Much research has focused on protein-coding variants since coding regions have well-defined physicochemical and functional properties. However, many bioinformatics tools are not applicable to variants outside coding regions. Here, we increase the classification performance of our regulatory single-nucleotide variant predictor (RSVP) for variants that cause regulatory abnormalities from an AUC of 0.90-0.97 by incorporating genomic regions identified by the ENCODE project into RSVP. RSVP is comparable to a recently published tool, Genome-Wide Annotation of Variants (GWAVA); both RSVP and GWAVA perform better on regulatory variants than a traditional variant predictor, combined annotation-dependent depletion (CADD). However, our method outperforms GWAVA on variants located at similar distances to the transcription start site as the positive set (AUC: 0.96) as compared with GWAVA (AUC: 0.71). Much of this disparity is due to RSVP's incorporation of features pertaining to the nearest gene (expression, GO terms, etc.), which are not included in GWAVA. Our findings hold out the promise of a framework for the assessment of all functional regulatory variants, providing a means to predict which rare or de novo variants are of pathogenic significance.

Indexed as

Polymorphism, Single NucleotideComputational BiologyComputer SimulationGenetic Predisposition to DiseaseGenome, HumanGenomicsHumansMachine LearningENCODEintergenicregulatory variantRSVPvariant predictionvariant predictor

Identifiers

PMID27406314
PMCPMC6192032

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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.