• No results found

University of Groningen Development of bioinformatic tools and application of novel statistical methods in genome- wide analysis van der Most, Peter Johannes

N/A
N/A
Protected

Academic year: 2021

Share "University of Groningen Development of bioinformatic tools and application of novel statistical methods in genome- wide analysis van der Most, Peter Johannes"

Copied!
7
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

University of Groningen

Development of bioinformatic tools and application of novel statistical methods in

genome-wide analysis

van der Most, Peter Johannes

IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from it. Please check the document version below.

Document Version

Publisher's PDF, also known as Version of record

Publication date: 2017

Link to publication in University of Groningen/UMCG research database

Citation for published version (APA):

van der Most, P. J. (2017). Development of bioinformatic tools and application of novel statistical methods in genome-wide analysis. University of Groningen.

Copyright

Other than for strictly personal use, it is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license (like Creative Commons).

Take-down policy

If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim.

Downloaded from the University of Groningen/UMCG research database (Pure): http://www.rug.nl/research/portal. For technical reasons the number of authors shown on this cover page is limited to 10 maximum.

(2)

Development of bioinformatic tools and

application of novel statistical methods in

genome-wide analysis

(3)

The research reported in this thesis has been performed at the Department of Epidemiology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

The printing of this thesis was financially supported by the University of Groningen, the University Medical Center Groningen and the research institute Science in Healthy Ageing and healthcaRE (SHARE).

ISBN: 978-94-034-0148-5 (printed version) ISBN: 978-94-034-0147-8 (electronic version) Cover and layout design: Iliana Boshoven-Gkini http://www.AgileColor.com

Printed by: Ridderprint https://www.ridderprint.nl

Copyright © 2017 by Peter Johannes van der Most. All rights reserved. No part of this thesis may be reproduced, stored in a retrieval system, or transmitted in any form or by any means without permission of the author and when appropriate, the publisher holding the copyrights of the published articles.

(4)

Development of bioinformatic tools and

application of novel statistical methods in

genome-wide analysis

PhD thesis

to obtain the degree of PhD at the

University of Groningen

on the authority of the

Rector Magnificus Prof. E. Sterken

and in accordance with

the decision by the College of Deans.

This thesis will be defended in public on

Wednesday 8 November 2017 at 12.45 hours

by

Peter Johannes van der Most

born on 26 July 1984

in Amsterdam

(5)

Supervisors

Prof. H. Snieder

Prof. P. van der Harst

Co-supervisor

Dr. I.M. Nolte

Assessment Committee

Prof. S.J.L. Bakker

Prof. E.C. Wit

Prof. A. Realo

(6)

Contents

Chapter 1 Introduction 7

Chapter 2 QCGWAS: a flexible R package for automated quality control of genome-wide

association results

15

Chapter 3 QCEWAS: automated quality control of results of epigenome-wide association

studies

21

Chapter 4 lodGWAS: a software package for genome-wide association analysis of biomarkers

with a limit of detection

27

Chapter 5 Missing heritability: is the gap closing? An analysis of 32 complex traits in the

Lifelines Cohort Study.

33

Chapter 6 SNP-based heritability estimates of common and specific variance in self- and

informant-reported neuroticism scales

53

Chapter 7 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function 73

Chapter 8 Genome-wide survival meta-analysis of age at first cannabis use 91

Chapter 9 Discussion and future perspectives 171

Summary 187

Samenvatting 189

Acknowledgements 193

Curriculum vitae 195

Research output 196

(7)

Referenties

GERELATEERDE DOCUMENTEN

We developed ‘lodGWAS’, a flexible, easy-to-use software package that is capable of performing GWAS analysis of biomarkers while accommodating the problem of LOD by applying survival

Despite the recent explosive rise in number of genetic markers for complex disease traits identified in genome-wide association studies, there is still a large gap between the

The SNP-based heritability estimates in the EGCUT sample for self-reported residual facet scales – from which the common variance of Neuroticism had been statistically removed –

We undertook a meta-analysis of GWAS from 33 studies that imputed genotypes from The 1000 Genomes reference panel, hypothesizing that this would uncover novel common

Results from the GWAS discovery meta-analysis were used to create PRS in an independent sample from the Netherlands (the combined sample of NTR2- RADAR; information about the

We approached this from four different angles: QC of GWAS and EWAS results, use of survival analysis in GWAS, estimation of common-SNP heritability of complex traits, and the use of

In chapter 5 we used genetic risk scores (GRS) and genomic restricted maximum likelihood (GREML) methods to estimate the amount of common SNP heritability accounted for by the

In hoofdstuk 5 gebruikten we genetische risico scores (GRS) en genomic restricted maximum likelihood (GREML) methodes om te schatten welke proportie van de totale erfelijkheid