Evidence map›Paper›PMID 26608661›Full record

ArticleBMC genomics2015

Wellington-bootstrap: differential DNase-seq footprinting identifies cell-type determining transcription factors.

Jason Piper, Salam A Assi, Pierre Cauchy, Christophe Ladroue, Peter N Cockerill, Constanze Bonifer, Sascha Ott

Open access · goldAbstract 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. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

22 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. CScience advances · 2023
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  9. Analytical Approaches for ATAC-seq Data Analysis.Current protocols in human genetics · 2020
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  10. Review
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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

7 authors at 2 institutions in 1 country.

Jason PiperWarwick Systems Biology Centre, University of Warwick, Coventry, CV4 7AL, UK.
Salam A AssiInstitute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, Institute of Biomedical Research, University of Birmingham, Birmingham, B15 2TT, UK.
Pierre CauchyInstitute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, Institute of Biomedical Research, University of Birmingham, Birmingham, B15 2TT, UK.
Christophe LadroueDepartment of Computer Science, University of Warwick, Coventry, CV4 7AL, UK.
Peter N CockerillInstitute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, Institute of Biomedical Research, University of Birmingham, Birmingham, B15 2TT, UK. P.N.Cockerill@bham.ac.uk.
Constanze BoniferInstitute of Cancer and Genomic Sciences, College of Medical and Dental Sciences, Institute of Biomedical Research, University of Birmingham, Birmingham, B15 2TT, UK. C.Bonifer@bham.ac.uk.
Sascha OttWarwick Systems Biology Centre, University of Warwick, Coventry, CV4 7AL, UK. s.ott@warwick.ac.uk.
University of Birmingham · GBUniversity of Warwick · GB

Funding

Medical Research Council MR/M009157/1
6 · The paper itself

Abstract

backgroundThe analysis of differential gene expression is a fundamental tool to relate gene regulation with specific biological processes. Differential binding of transcription factors (TFs) can drive differential gene expression. While DNase-seq data can provide global snapshots of TF binding, tools for detecting differential binding from pairs of DNase-seq data sets are lacking.

resultsIn order to link expression changes with changes in TF binding we introduce the concept of differential footprinting alongside a computational tool. We demonstrate that differential footprinting is associated with differential gene expression and can be used to define cell types by their specific TF occupancy patterns.

conclusionsOur new tool, Wellington-bootstrap, will enable the detection of differential TF binding facilitating the study of gene regulatory systems.

Indexed as

Binding SitesDNA FootprintingHigh-Throughput Nucleotide SequencingAntigens, CD19B-Lymphocyte SubsetsCD8-Positive T-LymphocytesCluster AnalysisComputational BiologyDeoxyribonucleasesGene Expression RegulationHumansOrgan SpecificityProtein BindingTranscription FactorsAntigens, CD19DeoxyribonucleasesTranscription Factors

Identifiers

PMID26608661
PMCPMC4658755
OpenAlexW2175955375

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.