|
Post by mmagoo6 on Sept 1, 2016 22:34:08 GMT
Hello All, I am trying to estimate the phenotypic variance explained by SNPs using GCTA. I have a sample of 1903 with 400 events. I was concerned from this paper and the FAQs that this might be too small of a sample, but from the output, I'm not sure that is the case. I would have expected an error ("Error: the variance-covaraince matrix V is not positive definite" or ""Log-likelihood not converged”) if the sample size were too small, or a non-zero estimate with a large standard error. Instead, I get an estimate of exactly zero with a regular-sized standard error: Source Variance SE V(G) 0.000000 0.017752 V(e) 0.166104 0.018566 Vp 0.166104 0.005386 V(G)/Vp 0.000001 0.106875 The estimate of variance explained on the observed scale is transformed to that on the underlying scale: (Proportion of cases in the sample = 0.210194; User-specified disease prevalence = 0.210000) V(G)/Vp_L 0.000002 0.213321 logL 752.426 logL0 752.426 LRT 0.000 df 1 Pval 0.5 n 1903
The zero value makes me particularly suspicious. I have re-checked my inputs, and they seem right. This analysis was is also a subset of a larger sample of 3000 people, and when I run the analysis on the larger sample, I get heritability estimates that are in line with what I expect.
Can anyone comment on how to think of a V(G) that is exactly zero? Does it suggest that the sample size is too small, or some error on my end? Thank you!
|
|
|
Post by Jian Yang on Sept 8, 2016 5:20:10 GMT
|
|