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Paterson, A. D.

Publications and source records attributed to Paterson, A. D..

10 recordsLinked to original sources

A General Statistical Framework for Hardy-Weinberg Equilibrium Inference on the X Chromosome

Testing for Hardy-Weinberg equilibrium (HWE) is a fundamental component of genetic data analysis, widely used for quality control and model validation. Although HWE testing is well established for autosomal loci, inference on the X chromosome is more complex due to sex-specific genotype structures and potential sex differences in minor allele frequency (sdMAF). Existing tests differ in their assumptions about sdMAF and male sample inclusion, often leading to distinct but poorly characterized null hypotheses. We develop a general statistical framework for HWE inference using the robust allele-based regression model. By formulating HWE testing as an assessment of allele-level dependence, the framework directly parameterizes Hardy-Weinberg disequilibrium, unifies existing Pearson{chi} 2-based tests under explicit modeling assumptions, and clarifies their null hypotheses, degrees of freedom, and sensitivity to sdMAF. The framework also accommodates covariate and population-structure adjustment within a unified regression-based formulation. The proposed framework provides robust, interpretable, and flexible inference, establishing a unified statistical foundation for HWE testing across autosomal and X-chromosomal regions. Simulation studies and analysis of high-coverage 1000 Genomes Project data demonstrate that commonly used X-chromosome tests can exhibit inflated type I error or misleading inference when sdMAF is present.

genetics↗

Assessing Hardy-Weinberg Equilibrium in T2T-aligned 1000 Genomes Project

Quality control of markers in genome-wide association studies often includes testing for Hardy-Weinberg equilibrium (HWE). However, this is usually implemented in a homogeneous population without stratifying by sex. Previous work indicates sex-based selection at numerous autosomal loci in cohorts with active recruitment. Sex chromosome sequences can also interfere with autosomal SNPs. We examined genome-wide sex-specific HWE deviations across populations in the telomere-to-telomere (T2Tv2)-aligned high-coverage whole genome sequence of the 1000 Genomes Project data of 2,490 individuals. Our analysis was restricted to bi-allelic SNPs with non-missing genotypes and MAF>=5% in both sexes of the five super-populations. We employed a robust allele-based approach for HWE testing, which enabled the quantification of directional deviations from HWE. A second-order omnibus meta-analysis combining results from the five super-populations and both sexes revealed that 0.9% autosomal SNPs exhibited a significant deviation from HWE at p<5e-8. Most of these deviations were found to be associated with genomic features relating to poor sequence quality. Filtering results to reliable genomic regions yielded 255 autosomal and 1 NPR X chromosomal SNPs, of which 140 autosomal SNPs also showed significant heterogeneity across populations but not across sexes. 8 SNPs in a 15-bp region on chr14 showed excess heterozygosity in both sexes of the AFR (African) super-population. We also generated a well-performing multivariate predictor of HWD (deviation from HWE) using multiple sequence features, which could be combined with HWD estimates in future studies to select SNPs that deviate from HWE due to technical rather than biological reasons. Author SummaryWe conducted a specific quality control test, which compares the observed and expected genotype counts, on an updated version of the 1000 Genomes Project whole genome sequence data generated on [~]2500 individuals. We first performed this analysis by grouping the data by ancestry and sex. We then combined and contrasted the group results. We found that most regions that differed between observed and expected counts overlapped regions of the genome which are difficult to sequence using current short read technology. In the remaining regions we found an interesting cluster of SNPs in a single ancestry, where there is a gross excess of heterozygous genotypes. GWASes typically use a standard strict threshold for this quality control test for genotyping arrays to remove SNPs. Here we suggest a more nuanced approach that is applicable to whole genome sequence data.

genomics↗

Detecting latent gene-environment interaction when analyzing binary traits

In genome-wide association studies (GWAS), it is desirable to test for interactions (GxE) between single-nucleotide polymorphisms (SNPs,Gs) and environmental variables (Es). However, directly accounting for interaction is often infeasible, because E is latent. For quantitative traits (Y) that are approximately normally distributed, it has been shown that indirect testing on GxE can be done by testing for heteroskedasticity of Y between genotypes. However, when traits are binary, the existing methodology based on testing the heteroskedasticity of the trait across genotypes cannot be generalized. In this paper, we propose an approach to indirectly test GxE for binary traits based on the non-additive effect G, and subsequently propose a joint test that accounts for the main and interaction effects of each SNP during GWAS. We illustrate the statistical features including type-I-error control and power of the proposed method through extensive numerical studies. Applying our method to the UK Biobank dataset, we showcase the practical utility of the proposed method, revealing SNPs and genes with strong potential for latent interaction effects.

genetics↗

Dimension Reduction using Local Principal Components for Regression-based Multi-SNP Analysis in 1000 Genomes and the Canadian Longitudinal Study on Aging (CLSA)

For genetic association analysis based on multiple SNP regression of genotypes obtained by dense DNA sequencing or array data imputation, multi-collinearity can be a severe issue causing failure to fit the regression model. In this study, we proposed a method of Dimension Reduction using Local Principal Components (DRLPC) which aims to resolve multi-collinearity by removing SNPs under the assumption that the remaining SNPs can capture the effect of a removed SNP due to high linear dependency. This approach to dimension reduction is expected to improve the power of regression-based statistical tests. We apply DRLPC to chromosome 22 SNPs of two data sets, the 1000 Genomes Project (phase 3) and Canadian Longitudinal Study on Aging (CLSA), and calculated Variance Inflation Factors (VIF) in various SNP-sets before and after implementing DRLPC as a metric of collinearity. Notably, DRLPC addresses multi-collinearity by excluding variables with a VIF exceeding a predetermined threshold (VIF=20), thereby improving applicability for subsequent regression analyses. The number of variables in a final set for regression analysis is reduced to around 20% on average for larger-sized genes, whereas for smaller ones, the proportion is around 48%; suggesting that DRLPC is more effective for larger genes. We also compare the power of several multi-SNP statistics constructed for gene-specific analysis to evaluate power gains achieved by DRLPC. In simulation studies based on 100 genes with [&le;]500 SNPs per gene, DRLPC effectively increased the power of the multiple regression Wald test from 60% to around 80%.

genetics↗

RegionScan: A comprehensive R package for region-level genome-wide association testing with integration and visualization of multiple-variant and single-variant hypothesis testing

SummaryRegionScan is an R package for comprehensive and scalable genome-wide association testing of region-level multiple-variant and single-variant statistics and visualization of the results. It implements various state-of-the-art region-level tests to improve signal detection under heterogeneous genetic architectures and facilitates comparison of multiple-variant region-level and single-variant test results. It exploits local linkage disequilibrium (LD) structure for genomic partitioning and LD-adaptive region definition. RegionScan is compatible with VCF input file formats for genotyped and imputed variants, and options are available for analysis of multi-allelic variants and unbalanced binary phenotypes. It accommodates parallel region-level processing and analysis to improve computational time and memory efficiency and provides detailed outputs and utility functions to assist results comparison, visualization, and interpretation. Availability and implementationRegionScan is freely available for download on GitHub (https://github.com/brossardMyriam/RegionScan). Contactbull@lunenfeld.ca, brossard@lunenfeld.ca. Supplementary informationSupplementary data are available at Bioinformatics online.

genetics↗

The effect of ascertainment on penetrance estimates for rare variants: implications for establishing pathogenicity and for genetic counselling

Next-generation sequencing has led to an explosion of genetic findings for many rare diseases. However, most of the variants identified are very rare and were identified in small pedigrees, which creates challenges in terms of penetrance estimation and translation into genetic counselling in the setting of cascade testing. We use simulations to show that for a rare (dominant) disorder where a variant is identified in a small number of small pedigrees, the penetrance estimate can both have large uncertainty and be drastically inflated, due to underlying ascertainment bias. We have developed PenEst, an app that allows users to investigate the phenomenon across ranges of parameter settings. We also illustrate robust ascertainment corrections via the LOD score, and recommend a LOD-based approach to assessing pathogenicity of rare variants in the presence of reduced penetrance.

genetics↗

eXclusionarY: Ten years later, where are the sex chromosomes in GWAS?

Ten years ago, a detailed analysis of genome-wide association studies showed that only 33% of the studies included the X chromosome. Multiple recommendations were made to combat eXclusion. Here we re-surveyed the research landscape to determine if these earlier recommendations had been translated. Unfortunately, among the summary statistics reported in 2021 in the NHGRI-EBI GWAS catalog, only 25% provided results for the X chromosome and 3% for the Y chromosome, suggesting that the eXclusion phenomenon documented earlier not only persists but has also expanded into an eXclusionarY problem. Normalizing by physical length of the chromosome, the average number of studies published until 11/29/22 with genome-wide significant findings on the X chromosome is ~1 study/Mb. In contrast, it ranges from ~6 to ~16 studies/Mb for chromosomes 4 and 19, respectively. Compared with the autosomal growth rate of ~0.086 studies/Mb/year over the last decade, studies of the X chromosome grew at less than one-seventh that rate, only ~0.012 studies/Mb/year. Among the studies that reported significant association on the X chromosome, there were extreme heterogeneities in how they analyzed the data and documented the results, suggesting the need for guidelines. Not surprisingly, among the 430 scores sampled from the PolyGenic Score catalog, 0% contained weights for sex chromosomal SNPs. To overcome the dearth of sex chromosome analyses, we provide five sets of recommendations and future directions. Finally, until the sex chromosomes are included in a whole-genome study, instead of GWAS, we propose they be more properly referred to as "AWAS" for "autosome-wide scan".

genetics↗

Statistical learning of large-scale genetic data: How to run a genome-wide association study of gene-expression data using the 1000 GenomesProject data

Teaching statistics through engaging applications to contemporary large-scale datasets is essential to attracting students to the field. To this end, we developed a hands-on, week-long workshop for senior high-school or junior undergraduate students, without prior knowledge in statistical genetics but with some basic knowledge in data science, to conduct their own genome-wide association studies (GWAS). The GWAS was performed for open source gene expression data, using publicly-available human genetics data. Assisted by a detailed instruction manual, students were able to obtain [~]1.4 million p-values from a real scientific study, within several days. This early motivation kept students engaged in learning the theories that support their results, including regression, data visualization, results interpretation, and large-scale multiple hypothesis testing. To further their learning motivation by emphasizing the personal connection to this type of data analysis, students were encouraged to make short presentations about how GWAS has provided insights into the genetic basis of diseases that are present in their friends and/or families. The appended open source, step-by-step instruction manual includes descriptions of the datasets used, the software needed, and results from the workshop. Additionally, scripts used in the workshop are archived on Zenodo to further enhance reproducible research and training.

scientific communication and education↗

Major sex differences in allele frequencies for X chromosome variants in the 1000 Genomes Project data

An unexpectedly high proportion of SNPs on the X chromosome in the 1000 Genomes Project phase 3 data were identified with significant sex differences in minor allele frequencies (sdMAF). sdMAF persisted for many of these SNPs in the recently released high coverage whole genome sequence, and it was consistent between the five super-populations. Among the 245,825 common biallelic SNPs in phase 3 data presumed to be high quality, 2,039 have genome-wide significant sdMAF (p-value <5e-8). sdMAF varied by location: (NPR)=0.83%, pseudo-autosomal region (PAR1)=0.29%, PAR2=13.1%, and PAR3=0.85% of SNPs had sdMAF, and they were clustered at the NPR-PAR boundaries, among others. sdMAF at the NPR-PAR boundaries are biologically expected due to sex-linkage, but have generally been ignored in association studies. For comparison, similar analyses found only 6, 1 and 0 SNPs with significant sdMAF on chromosomes 1, 7 and 22, respectively. Future X chromosome analyses need to take sdMAF into account.

genetics↗

Genome-wide Association Study of Pediatric Obsessive-Compulsive Traits: Shared Genetic Risk between Traits and Disorder

ObjectiveTo identify genetic variants associated with obsessive-compulsive (OC) traits and test for sharing of genetic risks between OC traits and obsessive-compulsive disorder (OCD). MethodsWe conducted a genome-wide association analysis of OC traits using the Toronto Obsessive-Compulsive Scale (TOCS) in 5018 unrelated Caucasian children and adolescents from the community (Spit for Science sample). We tested the hypothesis that genetic variants associated with OC traits from the community would be associated with clinical OCD using a meta-analysis of three OCD case-controls samples (cases=3384, controls=8363). Shared genetic risk was examined between OC traits and OCD in the respective samples using polygenic risk score and genetic correlation analyses. ResultsA locus tagged by rs7856850 in an intron of PTPRD (protein tyrosine phosphatase {delta}) was significantly associated with OC traits at the genome-wide significance level (p=2.48x10-8). The rs7856850 locus was also associated with OCD in a meta-analysis of three independent OCD case/control genome-wide datasets (p=0.0069). Polygenic risk scores derived from OC traits were significantly associated with OCD in a sample of childhood-onset OCD and vice versa (ps<0.01). OC traits were highly but not significantly genetically correlated with OCD (rg=0.83, p=0.07). ConclusionsWe report the first validated genome-wide significant variant for OC traits. OC traits measured in the community sample shared genetic risk with OCD case/control status. Our results demonstrate the importance of the type of measure used to measure traits as well as the feasibility and power of using trait-based approaches in community samples for genetic discovery.

genomics↗