Evidence map›Paper›PMID 31114870›Full record

ArticleNucleic acids research2019

QBiC-Pred: quantitative predictions of transcription factor binding changes due to sequence variants.

Vincentius Martin, Jingkang Zhao, Ariel Afek, Zachery Mielko, Raluca Gordân

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.2field-weighted citation impact, top 11% of its field
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

19 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
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  7. UV irradiation remodels the specificity landscape of transcription factors.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  8. Article
  9. Transcription Factor-Centric Approach to Identify Non-Recurring Putative Regulatory Drivers in Cancer.Research in computational molecular biology : ... Annual International Conference, RECOMB ... : proceedings. RECOMB (Conference : 2005- ) · 2022
    Article
  10. Article
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  17. Learning the Regulatory Code of Gene Expression.Frontiers in molecular biosciences · 2021
    Review
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  19. Article
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

5 authors at 1 institution in 1 country.

Vincentius MartinDepartment of Computer Science, Duke University, Durham, NC 27708, USA.
Jingkang ZhaoCenter for Genomic and Computational Biology, Duke University, Durham, NC 27708, USA.
Ariel AfekCenter for Genomic and Computational Biology, Duke University, Durham, NC 27708, USA.
Zachery MielkoCenter for Genomic and Computational Biology, Duke University, Durham, NC 27708, USA.
Raluca GordânDepartment of Computer Science, Duke University, Durham, NC 27708, USA.
Duke University · US

Funding

Computational Biology and Bioinformatics Training ProgramT32GM071340 · NIGMS · DUKE UNIVERSITY · PI MAGWENE, PAUL MITAARI · 2005 to 2020
$3.3M
New methods for quantitative modeling of protein-DNA interactionsR01GM117106 · NIGMS · DUKE UNIVERSITY · PI GORDAN, RALUCA · 2015 to 2019
$1.8M
Data commons for 'omic, microscopy and analysis core facilitiesS10OD018164 · OD · DUKE UNIVERSITY · PI WRAY, GREGORY A. · 2014 to 2014
$598k
NIGMS NIH HHS R01 GM117106NIGMS NIH HHS T32 GM071340NIH HHS S10 OD018164
6 · The paper itself

Abstract

Non-coding genetic variants/mutations can play functional roles in the cell by disrupting regulatory interactions between transcription factors (TFs) and their genomic target sites. For most human TFs, a myriad of DNA-binding models are available and could be used to predict the effects of DNA mutations on TF binding. However, information on the quality of these models is scarce, making it hard to evaluate the statistical significance of predicted binding changes. Here, we present QBiC-Pred, a web server for predicting quantitative TF binding changes due to nucleotide variants. QBiC-Pred uses regression models of TF binding specificity trained on high-throughput in vitro data. The training is done using ordinary least squares (OLS), and we leverage distributional results associated with OLS estimation to compute, for each predicted change in TF binding, a P-value reflecting our confidence in the predicted effect. We show that OLS models are accurate in predicting the effects of mutations on TF binding in vitro and in vivo, outperforming widely-used PWM models as well as recently developed deep learning models of specificity. QBiC-Pred takes as input mutation datasets in several formats, and it allows post-processing of the results through a user-friendly web interface. QBiC-Pred is freely available at http://qbic.genome.duke.edu.

Indexed as

SoftwareAlgorithmsBinding SitesComputational BiologyDNAGenomicsHumansProtein BindingTranscription FactorsDNATranscription Factors

Identifiers

PMID31114870
PMCPMC6602471
OpenAlexW2945144872

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 OpenQuestion graph.