Skip to content
2000
Volume 17, Issue 5
  • ISSN: 1389-2029
  • E-ISSN: 1875-5488

Abstract

Analytical models usually assume an additive sex effect by treating it as a covariate to identify genetic associations with sex-influenced traits. Their underlying assumptions are violated by ignoring interactions of sex with genetic factors and heterogeneous genetic effects by sex. Methods to deal with the problems are compared and discussed in this article. Especially, heterogeneity of genetic variance by sex can be assessed employing a mixed model with genetic relationship matrix constructed from genome-wide nucleotide variant information. Estimating genetic architecture of each sex would help understand different prevalence, course, and severity of complex diseases between women and men in the era of personalized medicine.

Loading

Article metrics loading...

/content/journals/cg/10.2174/1389202917666160420142601
2016-10-01
2025-05-31
Loading full text...

Full text loading...

/content/journals/cg/10.2174/1389202917666160420142601
Loading
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test