Evidence map›Paper›PMID 26701911›Full record

ArticleeLife2015

Building accurate sequence-to-affinity models from high-throughput in vitro protein-DNA binding data using FeatureREDUCE.

Todd R Riley, Allan Lazarovici, Richard S Mann, Harmen J Bussemaker

Abstract read
In one paragraph

Article in eLife, 2015. 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. Article
  3. Article
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  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Diversification of transcription factor-DNA interactions and the evolution of gene regulatory networks.Wiley interdisciplinary reviews. Systems biology and medicine · 2018
    Review
  15. Article
  16. Article
  17. Accurate and sensitive quantification of protein-DNA binding affinity.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  18. Comprehensive, high-resolution binding energy landscapes reveal context dependencies of transcription factor binding.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  19. Article
  20. 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

4 authors.

Todd R RileyDepartment of Biological Sciences, Columbia University, New York, United States.
Allan LazaroviciDepartment of Biological Sciences, Columbia University, New York, United States.
Richard S MannDepartment of Systems Biology, Columbia University, New York, United States.
Harmen J BussemakerDepartment of Biological Sciences, Columbia University, New York, United States.

Funding

Nation Center: Multi-Scale Study- Cellular Networks(RMI)U54CA121852 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA · 2005 to 2015
$37.4M
Inferring regulatory circuitry from microarray dataR01HG003008 · NHGRI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI BUSSEMAKER, HARMEN J · 2004 to 2020
$7.0M
Proximo-distal Patterning inthe Drosophila appendegesR01GM058575 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MANN, RICHARD S · 1999 to 2016
$5.7M
Characterization of Hox transcription factor complexes using proteomicsF32GM099160 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ABE, NAMIKO · 2011 to 2013
$155k
Indentification of Hox target genes controlling tissue growthF32GM087047 · NIGMS · UNIVERSITY OF CHICAGO · PI SLATTERY, MATTHEW · 2009 to 2011
$151k
NCI NIH HHS U54 CA121852NHGRI NIH HHS R01 HG003008NHGRI NIH HHS R01HG003008NIGMS NIH HHS F32 GM087047NIGMS NIH HHS F32GM087047NIGMS NIH HHS F32 GM099160NIGMS NIH HHS F32GM099160NIGMS NIH HHS GM058575NIGMS NIH HHS R01 GM058575
6 · The paper itself

Abstract

Transcription factors are crucial regulators of gene expression. Accurate quantitative definition of their intrinsic DNA binding preferences is critical to understanding their biological function. High-throughput in vitro technology has recently been used to deeply probe the DNA binding specificity of hundreds of eukaryotic transcription factors, yet algorithms for analyzing such data have not yet fully matured. Here, we present a general framework (FeatureREDUCE) for building sequence-to-affinity models based on a biophysically interpretable and extensible model of protein-DNA interaction that can account for dependencies between nucleotides within the binding interface or multiple modes of binding. When training on protein binding microarray (PBM) data, we use robust regression and modeling of technology-specific biases to infer specificity models of unprecedented accuracy and precision. We provide quantitative validation of our results by comparing to gold-standard data when available.

Indexed as

Base SequenceBinding SitesBiophysical PhenomenaComputational BiologyDNAMicroarray AnalysisModels, TheoreticalProtein BindingSoftwareTranscription FactorsDNATranscription Factorsbiophysical modelcomputational biologyDNA binding specificitynoneprotein binding microarray technologysystems biologytranscription factor

Identifiers

PMID26701911
PMCPMC4758951

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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.