The American Journal of Human GeneticsGeneticsPeer-reviewed journal article
RAREsim: A simulation method for very rare genetic variants
Megan Null, Josée DupuisiD, Pezhman SheinidashtegoliD, Ryan M. LayeriD, Christopher R. GignouxiD, Audrey E. HendricksiD
- Citations
- 8
- FWCI
- 0.90
- Field percentile
- top 30%
Abstract
Identification of rare variant associations is crucial to fully characterize the genetic architecture of complex traits and diseases. Essential in this process is the evaluation of novel methods in simulated data that mirrors the distribution of rare variants and haplotype structure in real data. Additionally, importing real variant annotation enables in silico comparison of methods that focus on putative causal variants, such as rare variant association tests, and polygenic scoring methods. Existing simulation methods are either unable to employ real variant annotation or severely under- or over-estimate the number of singletons and doubletons reducing the ability to generalize simulation results to real studies. We present RAREsim, a flexible and accurate rare variant simulation algorithm. Using parameters and haplotypes derived from real sequencing data, RAREsim efficiently simulates the expected variant distribution and enables real variant annotations. We highlight RAREsims utility across various genetic regions, sample sizes, ancestries, and variant classes.
- assay: whole-exome sequencing
- assay: whole-genome sequencing
- research focus: benchmarking
- research focus: variant effect prediction
- research focus: variant calling
- approach: simulation
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