Evidence map›Paper›PMID 27798116›Full record

ArticleHuman molecular genetics2017

Most brain disease-associated and eQTL haplotypes are not located within transcription factor DNase-seq footprints in brain.

Adam E Handel, Giuseppe Gallone, M Zameel Cader, Chris P Ponting

Open access · bronzeAbstract read
In one paragraph

Article in Human molecular genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. 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 at 1 institution in 1 country.

Adam E HandelMRC Functional Genomics Unit, Department of Physiology, Anatomy and Genetics.
Giuseppe GalloneMRC Functional Genomics Unit, Department of Physiology, Anatomy and Genetics.
M Zameel CaderWeatherall Institute of Molecular Medicine, University of Oxford, Oxford, Oxfordshire, UK.
Chris P PontingMRC Functional Genomics Unit, Department of Physiology, Anatomy and Genetics.
MRC Weatherall Institute of Molecular Medicine · GB

Funding

Medical Research Council MC_PC_15075Medical Research Council MC_PC_16034Medical Research Council MC_UU_12021/1Wellcome TrustWellcome Trust 100643/Z/12/Z
6 · The paper itself

Abstract

Dense genotyping approaches have revealed much about the genetic architecture both of gene expression and disease susceptibility. However, assigning causality to genetic variants associated with a transcriptomic or phenotypic trait presents a far greater challenge. The development of epigenomic resources by ENCODE, the Epigenomic Roadmap and others has led to strategies that seek to infer the likely functional variants underlying these genome-wide association signals. It is known, for example, that such variants tend to be located within areas of open chromatin, as detected by techniques such as DNase-seq and FAIRE-seq. We aimed to assess what proportion of variants associated with phenotypic or transcriptomic traits in the human brain are located within transcription factor binding sites. The bioinformatic tools, Wellington and HINT, were used to infer transcription factor footprints from existing DNase-seq data derived from central nervous system tissues with high spatial resolution. This dataset was then employed to assess the likely contribution of altered transcription factor binding to both expression quantitative trait loci (eQTL) and genome-wide association study (GWAS) signals. Surprisingly, we show that most haplotypes associated with GWAS or eQTL phenotypes are located outside of DNase-seq footprints. This could imply that DNase-seq footprinting is too insensitive an approach to identify a large proportion of true transcription factor binding sites. Importantly, this suggests that prioritising variants for genome engineering studies to establish causality will continue to be frustrated by an inability of footprinting to identify the causative variant within a haplotype.

Indexed as

Binding SitesBrainBrain DiseasesChromatinChromatin ImmunoprecipitationComputational BiologyDatabases, FactualDeoxyribonuclease IDNA FootprintingGene Expression RegulationGenetic VariationGenome, HumanGenome-Wide Association StudyGenotypeHaplotypesHigh-Throughput Nucleotide SequencingChromatinDeoxyribonuclease ITranscription Factors

Identifiers

PMID27798116
PMCPMC5351933
OpenAlexW2544335650

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.