Manhattan++: displaying genome-wide association summary statistics with multiple annotation layers.


Journal

BMC bioinformatics
ISSN: 1471-2105
Titre abrégé: BMC Bioinformatics
Pays: England
ID NLM: 100965194

Informations de publication

Date de publication:
27 Nov 2019
Historique:
received: 11 06 2019
accepted: 08 11 2019
entrez: 29 11 2019
pubmed: 30 11 2019
medline: 6 2 2020
Statut: epublish

Résumé

Over the last 10 years, there have been over 3300 genome-wide association studies (GWAS). Almost every GWAS study provides a Manhattan plot either as a main figure or in the supplement. Several software packages can generate a Manhattan plot, but they are all limited in the extent to which they can annotate gene-names, allele frequencies, and variants having high impact on gene function or provide any other added information or flexibility. Furthermore, in a conventional Manhattan plot, there is no way of distinguishing a locus identified due to a single variant with very significant p-value from a locus with multiple variants which appear to be in a haplotype block having very similar p-values. Here we present a software tool written in R, which generates a transposed Manhattan plot along with additional features like variant consequence and minor allele frequency to annotate the plot and addresses these limitations. The software also gives flexibility on how and where the user wants to display the annotations. The software can be downloaded from CRAN repository and also from the GitHub project page. We present a major step up to the existing conventional Manhattan plot generation tools. We hope this form of display along with the added annotations will bring more insight to the reader from this new Manhattan++ plot.

Sections du résumé

BACKGROUND BACKGROUND
Over the last 10 years, there have been over 3300 genome-wide association studies (GWAS). Almost every GWAS study provides a Manhattan plot either as a main figure or in the supplement. Several software packages can generate a Manhattan plot, but they are all limited in the extent to which they can annotate gene-names, allele frequencies, and variants having high impact on gene function or provide any other added information or flexibility. Furthermore, in a conventional Manhattan plot, there is no way of distinguishing a locus identified due to a single variant with very significant p-value from a locus with multiple variants which appear to be in a haplotype block having very similar p-values.
RESULTS RESULTS
Here we present a software tool written in R, which generates a transposed Manhattan plot along with additional features like variant consequence and minor allele frequency to annotate the plot and addresses these limitations. The software also gives flexibility on how and where the user wants to display the annotations. The software can be downloaded from CRAN repository and also from the GitHub project page.
CONCLUSIONS CONCLUSIONS
We present a major step up to the existing conventional Manhattan plot generation tools. We hope this form of display along with the added annotations will bring more insight to the reader from this new Manhattan++ plot.

Identifiants

pubmed: 31775616
doi: 10.1186/s12859-019-3201-y
pii: 10.1186/s12859-019-3201-y
pmc: PMC6882345
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

610

Références

Sci Adv. 2016 Jun 17;2(6):e1501678
pubmed: 27386562
Nature. 2011 Aug 10;476(7359):214-9
pubmed: 21833088
Hum Mol Genet. 2012 Jun 15;21(12):2825-35
pubmed: 22407130
J Am Coll Cardiol. 2016 Sep 27;68(13):1435-1448
pubmed: 27659466
Nat Genet. 2017 Sep;49(9):1385-1391
pubmed: 28714975
BMC Bioinformatics. 2010 May 28;11:288
pubmed: 20509871
BMC Bioinformatics. 2012 Nov 30;13:319
pubmed: 23199373
Brief Bioinform. 2013 Mar;14(2):178-92
pubmed: 22517427

Auteurs

Christopher Grace (C)

Division of Cardiovascular Medicine, Radcliffe Department of Medicine, John Radcliffe Hospital, University of Oxford, Oxford, OX3 9DU, UK.
Wellcome Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.

Martin Farrall (M)

Division of Cardiovascular Medicine, Radcliffe Department of Medicine, John Radcliffe Hospital, University of Oxford, Oxford, OX3 9DU, UK.
Wellcome Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.

Hugh Watkins (H)

Division of Cardiovascular Medicine, Radcliffe Department of Medicine, John Radcliffe Hospital, University of Oxford, Oxford, OX3 9DU, UK.
Wellcome Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK.

Anuj Goel (A)

Division of Cardiovascular Medicine, Radcliffe Department of Medicine, John Radcliffe Hospital, University of Oxford, Oxford, OX3 9DU, UK. anuj.goel@well.ox.ac.uk.
Wellcome Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK. anuj.goel@well.ox.ac.uk.

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Classifications MeSH