Quantifying the unobserved protein-coding variants in human populations provides a roadmap for large-scale sequencing projects

BioRxiv : the Preprint Server for Biology
James ZouDaniel G MacArthur

Abstract

As new proposals aim to sequence ever larger collection of humans, it is critical to have a quantitative framework to evaluate the statistical power of these projects. We developed a new algorithm, UnseenEst, and applied it to the exomes of 60,706 individuals to estimate the frequency distribution of all protein-coding variants, including rare variants that have not been observed yet in the current cohorts. Our results quantified the number of new variants that we expect to identify as sequencing cohorts reach hundreds of thousands of individuals. With 500K individuals, we find that we expect to capture 7.5% of all possible loss-of-function variants and 12% of all possible missense variants. We also estimate that 2,900 genes have loss-of-function frequency of less than 10-5 in healthy humans, consistent with very strong intolerance to gene inactivation.

Related Concepts

Genes
Research Project
Intolerance Function
Nucleic Acid Sequencing
Sequencing
NIH Roadmap Initiative Tag
Large-Scale Sequencing
Exome
Gene Silencing
Cohort

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