| Anthro_LDSC | R Documentation |
A dataset containing the genetic covariance structure from LD score regression (LDSC)
for 9 anthropometric phenotypes: BMI, WHR, CO, Waist, Hip, Height, IHC, BL, and BW.
Same list layout as Psych_LDSC - pass the object as covstruc to umxGSEM() or
umxGSEM_GWAS().
data(Anthro_LDSC)
A list with elements S, V, I, N, and m (see Details).
LDSC list fields (same S/V/I/N/m layout as GenomicSEM ldsc; V names are OpenMx residual labels):
S: 9 x 9 genetic covariance matrix among the phenotypes
(diagonals are SNP heritabilities on the LDSC scale).
V: 45 x 45 sampling covariance of the unique elements of S
(OpenMx vech order; dimnames like var_BMI, poly_WHR_BMI). Used as asymptotic covariance for WLS/DWLS. Not GenomicSEM BMI_BMI / WHR_BMI.
I: 9 x 9 LDSC intercept matrix. Diagonal = per-trait LDSC intercepts
(expected near 1 without confounding; elevations can flag stratification).
Off-diagonal = cross-trait intercepts reflecting sample overlap. Used for genomic
control when expanding SNPs in umxGSEM_GWAS().
N: 1 x 45 effective sample sizes for each unique S element.
m: Number of SNPs used in LDSC (here 1,173,569).
Psych_LDSC, umxGSEM(), umxGSEM_GWAS(), umxGSEM_ldsc()
Other GSEM:
Psych_LDSC,
plot.umx_GWAS(),
umxGSEM(),
umxGSEM_GWAS(),
umxGSEM_dl_tutorial_files(),
umxGSEM_label_ldsc(),
umxGSEM_ldsc(),
umxGSEM_munge(),
umxGSEM_std(),
umxGSEM_sumstats(),
umxSummary.MxDataStatic(),
umxSummary.list()
Other datasets:
Fischbein_wt,
GFF,
HSwls,
Psych_LDSC,
docData,
iqdat,
umx,
us_skinfold_data
## Not run:
data(Anthro_LDSC)
str(Anthro_LDSC, max.level = 1)
names(Anthro_LDSC) # S, V, I, N, m
# I = LDSC intercepts (diag) and cross-trait intercepts (off-diag)
Anthro_LDSC$I[1:3, 1:3]
## End(Not run)
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