Gene-Based Methods for Estimating the Degree of the Skewness of X Chromosome Inactivation.

Genes (Basel)

Department of Biostatistics, State Key Laboratory of Organ Failure Research, Ministry of Education, and Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou 510515, China.

Published: May 2022

AI Article Synopsis

  • The paper discusses the issue of skewed X chromosome inactivation (XCI-S) related to certain X-linked diseases and introduces new methods for estimating the degree of XCI-S in genes, referred to as γ.
  • It proposes point estimates and confidence intervals for γ using Fieller's methods and explores Bayesian approaches (GBN and GBU) to improve estimation accuracy.
  • Simulation results show that the GBN method is superior for estimating γ without producing extreme or non-informative results, and it is applied to real-world data from the Minnesota Center for Twin and Family Research.

Article Abstract

Skewed X chromosome inactivation (XCI-S) has been reported to be associated with some X-linked diseases, and currently several methods have been proposed to estimate the degree of the XCI-S (denoted as γ) for a single locus. However, no method has been available to estimate γ for genes. Therefore, in this paper, we first propose the point estimate and the penalized point estimate of γ for genes, and then derive its confidence intervals based on the Fieller’s and penalized Fieller’s methods, respectively. Further, we consider the constraint condition of γ∈[0, 2] and propose the Bayesian methods to obtain the point estimates and the credible intervals of γ, where a truncated normal prior and a uniform prior are respectively used (denoted as GBN and GBU). The simulation results show that the Bayesian methods can avoid the extreme point estimates (0 or 2), the empty sets, the noninformative intervals ([0, 2]) and the discontinuous intervals to occur. GBN performs best in both the point estimation and the interval estimation. Finally, we apply the proposed methods to the Minnesota Center for Twin and Family Research data for their practical use. In summary, in practical applications, we recommend using GBN to estimate γ of genes.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140558PMC
http://dx.doi.org/10.3390/genes13050827DOI Listing

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