scholarly journals Imputation aware tag SNP selection to improve power for multi-ethnic association studies

2017 ◽  
Author(s):  
Genevieve L. Wojcik ◽  
Christian Fuchsberger ◽  
Daniel Taliun ◽  
Ryan Welch ◽  
Alicia R Martin ◽  
...  

AbstractThe emergence of very large cohorts in genomic research has facilitated a focus on genotype-imputation strategies to power rare variant association. Consequently, a new generation of genotyping arrays are being developed designed with tag single nucleotide polymorphisms (SNPs) to improve rare variant imputation. Selection of these tag SNPs poses several challenges as rare variants tend to be continentally-or even population-specific and reflect fine-scale linkage disequilibrium (LD) structure impacted by recent demographic events. To explore the landscape of tag-able variation and guide design considerations for large-cohort and biobank arrays, we developed a novel pipeline to select tag SNPs using the 26 population reference panel from Phase of the 1000 Genomes Project. We evaluate our approach using leave-one-out internal validation via standard imputation methods that allows the direct comparison of tag SNP performance by estimating the correlation of the imputed and real genotypes for each iteration of potential array sites. We show how this approach allows for an assessment of array design and performance that can take advantage of the development of deeper and more diverse sequenced reference panels. We quantify the impact of demography on tag SNP performance across populations and provide population-specific guidelines for tag SNP selection. We also examine array design strategies that target single populations versus multi-ethnic cohorts, and demonstrate a boost in performance for the latter can be obtained by prioritizing tag SNPs that contribute information across multiple populations simultaneously. Finally, we demonstrate the utility of improved array design to provide meaningful improvements in power, particularly in trans-ethnic studies. The unified framework presented will enable investigators to make informed decisions for the design of new arrays, and help empower the next phase of rare variant association for global health.

2005 ◽  
Vol 03 (05) ◽  
pp. 1089-1106 ◽  
Author(s):  
TIE-FEI LIU ◽  
WING-KIN SUNG ◽  
YI LI ◽  
JIAN-JUN LIU ◽  
ANKUSH MITTAL ◽  
...  

Single nucleotide polymorphisms (SNPs), due to their abundance and low mutation rate, are very useful genetic markers for genetic association studies. However, the current genotyping technology cannot afford to genotype all common SNPs in all the genes. By making use of linkage disequilibrium, we can reduce the experiment cost by genotyping a subset of SNPs, called Tag SNPs, which have a strong association with the ungenotyped SNPs, while are as independent from each other as possible. The problem of selecting Tag SNPs is NP-complete; when there are large number of SNPs, in order to avoid extremely long computational time, most of the existing Tag SNP selection methods first partition the SNPs into blocks based on certain block definitions, then Tag SNPs are selected in each block by brute-force search. The size of the Tag SNP set obtained in this way may usually be reduced further due to the inter-dependency among blocks. This paper proposes two algorithms, TSSA and TSSD, to tackle the block-independent Tag SNP selection problem. TSSA is based on A* search algorithm, and TSSD is a heuristic algorithm. Experiments show that TSSA can find the optimal solutions for medium-sized problems in reasonable time, while TSSD can handle very large problems and report approximate solutions very close to the optimal ones.


2018 ◽  
Vol 8 (10) ◽  
pp. 3255-3267 ◽  
Author(s):  
Genevieve L. Wojcik ◽  
Christian Fuchsberger ◽  
Daniel Taliun ◽  
Ryan Welch ◽  
Alicia R Martin ◽  
...  

2009 ◽  
Vol 9 (3) ◽  
pp. 269-282 ◽  
Author(s):  
Ofir Davidovich ◽  
Eran Halperin ◽  
Gad Kimmel ◽  
Ron Shamir

2016 ◽  
Vol 10 (S7) ◽  
Author(s):  
Huanhuan Zhu ◽  
Zhenchuan Wang ◽  
Xuexia Wang ◽  
Qiuying Sha

2015 ◽  
pp. btv457
Author(s):  
Na Zhu ◽  
Verena Heinrich ◽  
Thorsten Dickhaus ◽  
Jochen Hecht ◽  
Peter N. Robinson ◽  
...  

2019 ◽  
Vol 44 (1) ◽  
pp. 104-116
Author(s):  
Tianzhong Yang ◽  
Junghi Kim ◽  
Chong Wu ◽  
Yiding Ma ◽  
Peng Wei ◽  
...  

2020 ◽  
Vol 19 (7) ◽  
pp. 1132-1144
Author(s):  
Nora Linscheid ◽  
Pi Camilla Poulsen ◽  
Ida Dalgaard Pedersen ◽  
Emilie Gregers ◽  
Jesper Hastrup Svendsen ◽  
...  

Genetic and genomic research has greatly advanced our understanding of heart disease. Yet, comprehensive, in-depth, quantitative maps of protein expression in hearts of living humans are still lacking. Using samples obtained during valve replacement surgery in patients with mitral valve prolapse (MVP), we set out to define inter-chamber differences, the intersect of proteomic data with genetic or genomic datasets, and the impact of left atrial dilation on the proteome of patients with no history of atrial fibrillation (AF).We collected biopsies from right atria (RA), left atria (LA) and left ventricle (LV) of seven male patients with mitral valve regurgitation with dilated LA but no history of AF. Biopsy samples were analyzed by high-resolution mass spectrometry (MS), where peptides were pre-fractionated by reverse phase high-pressure liquid chromatography prior to MS measurement on a Q-Exactive-HF Orbitrap instrument. We identified 7,314 proteins based on 130,728 peptides. Results were confirmed in an independent set of biopsies collected from three additional individuals. Comparative analysis against data from post-mortem samples showed enhanced quantitative power and confidence level in samples collected from living hearts. Our analysis, combined with data from genome wide association studies suggested candidate gene associations to MVP, identified higher abundance in ventricle for proteins associated with cardiomyopathies and revealed the dilated LA proteome, demonstrating differential representation of molecules previously associated with AF, in non-AF hearts.This is the largest dataset of cardiac protein expression from human samples collected in vivo. It provides a comprehensive resource that allows insight into molecular fingerprints of MVP and facilitates novel inferences between genomic data and disease mechanisms. We propose that over-representation of proteins in ventricle is consequent not to redundancy but to functional need, and conclude that changes in abundance of proteins known to associate with AF are not sufficient for arrhythmogenesis.


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