Evidence map›Paper›PMID 28111166›Full record

ArticleHuman immunology2017

High resolution HLA haplotyping by imputation for a British population bioresource.

Matt J Neville, Wanseon Lee, Peter Humburg, Daniel Wong, Martin Barnardo, Fredrik Karpe, Julian C Knight

Open access · hybridAbstract read
In one paragraph

Article in Human immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. HLA Genetics for the Human Diseases.Advances in experimental medicine and biology · 2024
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. No strong HLA association with MOG antibody disease in the UK population.Annals of clinical and translational neurology · 2021
    Article
  9. Article
  10. An immunogenetic view of COVID-19.Genetics and molecular biology · 2021
    Article
  11. Article
  12. Article
  13. Article
  14. Transgenic T-cell receptor immunotherapy for cancer: building on clinical success.Therapeutic advances in vaccines and immunotherapy · 2020
    Review
  15. Article
  16. 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

7 authors at 2 institutions in 2 countries.

Matt J NevilleOxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Churchill Hospital, Old Road, Oxford OX3 7LJ, UK; Oxford NIHR Biomedical Research Centre, Churchill Hospital, Oxford, UK.
Wanseon LeeWellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK.
Peter HumburgWellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK.
Daniel WongWellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK.
Martin BarnardoTransplant Immunology and Immunogenetics Laboratory, Oxford Transplant Centre, Churchill Hospital, Oxford OX3 7LJ, UK.
Fredrik KarpeOxford Centre for Diabetes, Endocrinology and Metabolism, University of Oxford, Churchill Hospital, Old Road, Oxford OX3 7LJ, UK; Oxford NIHR Biomedical Research Centre, Churchill Hospital, Oxford, UK.
Julian C KnightWellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK. Electronic address: julian@well.ox.ac.uk.
Centre for Human Genetics · GBChurchill Hospital · GB

Funding

European Research Council 281824Versus Arthritis 20773Wellcome Trust
6 · The paper itself

Abstract

This study aimed to establish the occurrence and frequency of HLA alleles and haplotypes for a healthy British Caucasian population bioresource from Oxfordshire. We present the results of imputation from HLA SNP genotyping data using SNP2HLA for 5553 individuals from Oxford Biobank, defining one- and two-field alleles together with amino acid polymorphisms. We show that this achieves a high level of accuracy with validation using sequence-specific primer amplification PCR. We define six- and eight-locus HLA haplotypes for this population by Bayesian methods implemented using PHASE. We determine patterns of linkage disequilibrium and recombination for these individuals involving classical HLA loci and show how analysis within a haplotype block structure may be more tractable for imputed data. Our findings contribute to knowledge of HLA diversity in healthy populations and further validate future large-scale use of HLA imputation as an informative approach in population bioresources.

Indexed as

HaplotypesPolymorphism, Single NucleotideAdultAllelesBayes TheoremEnglandFemaleGene FrequencyGenetics, PopulationGenotypeGenotyping TechniquesHLA AntigensHumansLinkage DisequilibriumMaleMiddle AgedHLA AntigensAlleleGenotypeHLAImputationSingle nucleotide polymorphism

Identifiers

PMID28111166
PMCPMC5367449
OpenAlexW2575786320

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.