Evidence map›Paper›PMID 28753602›Full record

ArticlePLoS computational biology2017

Automated incorporation of pairwise dependency in transcription factor binding site prediction using dinucleotide weight tensors.

Saeed Omidi, Mihaela Zavolan, Mikhail Pachkov, Jeremie Breda, Severin Berger, Erik van Nimwegen

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Article in PLoS computational biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Saeed OmidiBiozentrum, University of Basel, Basel, Switzerland.
Mihaela ZavolanBiozentrum, University of Basel, Basel, Switzerland.
Mikhail PachkovBiozentrum, University of Basel, Basel, Switzerland.
Jeremie BredaBiozentrum, University of Basel, Basel, Switzerland.
Severin BergerBiozentrum, University of Basel, Basel, Switzerland.
Erik van NimwegenBiozentrum, University of Basel, Basel, Switzerland.ORCID http://orcid.org/0000-0001-6338-1312

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene regulatory networks are ultimately encoded by the sequence-specific binding of (TFs) to short DNA segments. Although it is customary to represent the binding specificity of a TF by a position-specific weight matrix (PSWM), which assumes each position within a site contributes independently to the overall binding affinity, evidence has been accumulating that there can be significant dependencies between positions. Unfortunately, methodological challenges have so far hindered the development of a practical and generally-accepted extension of the PSWM model. On the one hand, simple models that only consider dependencies between nearest-neighbor positions are easy to use in practice, but fail to account for the distal dependencies that are observed in the data. On the other hand, models that allow for arbitrary dependencies are prone to overfitting, requiring regularization schemes that are difficult to use in practice for non-experts. Here we present a new regulatory motif model, called dinucleotide weight tensor (DWT), that incorporates arbitrary pairwise dependencies between positions in binding sites, rigorously from first principles, and free from tunable parameters. We demonstrate the power of the method on a large set of ChIP-seq data-sets, showing that DWTs outperform both PSWMs and motif models that only incorporate nearest-neighbor dependencies. We also demonstrate that DWTs outperform two previously proposed methods. Finally, we show that DWTs inferred from ChIP-seq data also outperform PSWMs on HT-SELEX data for the same TF, suggesting that DWTs capture inherent biophysical properties of the interactions between the DNA binding domains of TFs and their binding sites. We make a suite of DWT tools available at dwt.unibas.ch, that allow users to automatically perform 'motif finding', i.e. the inference of DWT motifs from a set of sequences, binding site prediction with DWTs, and visualization of DWT 'dilogo' motifs.

Indexed as

DNATranscription FactorsBinding SitesComputational BiologyModels, StatisticalNucleotide MotifsRNASequence Analysis, DNADNARNATranscription Factors

Identifiers

PMID28753602
PMCPMC5550003

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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.