A New Method for Detecting Associations with Rare Copy-Number Variants

Jung-Ying Tzeng, Patrik K E Magnusson, Patrick F Sullivan, The Swedish Schizophrenia Consortium and Jin P Szatkiewicz

PLOS Genetics, 2015, vol. 11, issue 10, 1-24

Abstract: Copy number variants (CNVs) play an important role in the etiology of many diseases such as cancers and psychiatric disorders. Due to a modest marginal effect size or the rarity of the CNVs, collapsing rare CNVs together and collectively evaluating their effect serves as a key approach to evaluating the collective effect of rare CNVs on disease risk. While a plethora of powerful collapsing methods are available for sequence variants (e.g., SNPs) in association analysis, these methods cannot be directly applied to rare CNVs due to the CNV-specific challenges, i.e., the multi-faceted nature of CNV polymorphisms (e.g., CNVs vary in size, type, dosage, and details of gene disruption), and etiological heterogeneity (e.g., heterogeneous effects of duplications and deletions that occur within a locus or in different loci). Existing CNV collapsing analysis methods (a.k.a. the burden test) tend to have suboptimal performance due to the fact that these methods often ignore heterogeneity and evaluate only the marginal effects of a CNV feature. We introduce CCRET, a random effects test for collapsing rare CNVs when searching for disease associations. CCRET is applicable to variants measured on a multi-categorical scale, collectively modeling the effects of multiple CNV features, and is robust to etiological heterogeneity. Multiple confounders can be simultaneously corrected. To evaluate the performance of CCRET, we conducted extensive simulations and analyzed large-scale schizophrenia datasets. We show that CCRET has powerful and robust performance under multiple types of etiological heterogeneity, and has performance comparable to or better than existing methods when there is no heterogeneity.Author Summary: Copy number variants (CNVs) are the gain or loss of DNA segments in the genome that can vary in dosage, length and details of gene disruptions. Rare CNVs have been shown to be associated with neuropsychiatric disorders both collectively and at specific loci. To evaluate the collective effects of rare CNVs on disease risk, sophisticated association methods are needed to pool information across CNV loci while handling CNV-specific properties; however, such methods are under-developed. To address these challenges, we have developed a new collapsing method for rare CNVs named CCRET. CCRET is a random effects approach applicable to variants measured on a multi-categorical scale, collectively modeling the effects of multiple CNV features, and is robust to etiological heterogeneity. Multiple confounders can be simultaneously corrected. To evaluate the performance of CCRET, we conducted extensive simulation and analyzed large-scale schizophrenia datasets. We demonstrate the robustness, validity and utility of CCRET under a variety of scenarios.

Date: 2015
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Persistent link: https://EconPapers.repec.org/RePEc:plo:pgen00:1005403

DOI: 10.1371/journal.pgen.1005403

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