Last updated: 2022-05-17
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Knit directory: Serreze-T1D_Workflow/
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Unstaged changes:
Modified: analysis/4.1.1_qtl.analysis_binary_ici-early.vs.pbs_5.batches.Rmd
Modified: analysis/4.1.1_qtl.analysis_binary_ici-early.vs.pbs_5.batches_mis.Rmd
Modified: analysis/4.1.1_qtl.analysis_binary_ici-early.vs.pbs_snpsqc_5.batches.Rmd
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Modified: analysis/4.1.1_qtl.analysis_binary_ici-early.vs.pbs_snpsqc_dis_no-x_updated_5.batches_mis.Rmd
Modified: analysis/4.1.1_qtl.analysis_binary_ici.vs.eoi_snpsqc_dis_no-x_updated.Rmd
Modified: analysis/4.1.1_qtl.analysis_binary_ici.vs.pbs_snpsqc_dis_no-x_updated.Rmd
Modified: analysis/4.1.2_qtl.analysis_cont_age_ici-early.vs.pbs_pheno.corrected.cleaned_5.batches.Rmd
Modified: analysis/4.1.2_qtl.analysis_cont_age_ici-early.vs.pbs_pheno.corrected.cleaned_5.batches_mis.Rmd
Modified: analysis/4.1.2_qtl.analysis_cont_age_ici-early.vs.pbs_snpsqc_pheno.corrected.cleaned_5.batches.Rmd
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Modified: analysis/4.1.2_qtl.analysis_cont_age_ici-early.vs.pbs_snpsqc_pheno.corrected.cleaned_dis_no-xk_5.batches_mis.Rmd
Modified: analysis/4.1.2_qtl.analysis_cont_age_ici.vs.eoi_pheno.corrected.cleaned_5.batches.Rmd
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Modified: analysis/4.1.2_qtl.analysis_cont_age_ici.vs.pbs_pheno.corrected.cleaned_5.batches.Rmd
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Note that any generated files, e.g. HTML, png, CSS, etc., are not included in this status report because it is ok for generated content to have uncommitted changes.
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load("data/gm_allqc_5.batches.RData")
#gm_allqc
gm=gm_allqc
gm
Object of class cross2 (crosstype "bc")
Total individuals 308
No. genotyped individuals 308
No. phenotyped individuals 308
No. with both geno & pheno 308
No. phenotypes 1
No. covariates 6
No. phenotype covariates 0
No. chromosomes 20
Total markers 34537
No. markers by chr:
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16
2643 2629 1857 1890 1774 1941 1672 1627 1878 1176 1871 1300 1549 1578 1257 935
17 18 19 X
501 913 1014 4532
#pr <- readRDS("data/serreze_probs_allqc.rds")
#pr <- readRDS("data/serreze_probs.rds")
##extracting animals with ici and pbs group status
miceinfo <- gm$covar[gm$covar$group == "PBS" | gm$covar$group == "ICI",]
table(miceinfo$group)
ICI PBS
104 34
mice.ids <- rownames(miceinfo)
gm <- gm[mice.ids]
gm
Object of class cross2 (crosstype "bc")
Total individuals 138
No. genotyped individuals 138
No. phenotyped individuals 138
No. with both geno & pheno 138
No. phenotypes 1
No. covariates 6
No. phenotype covariates 0
No. chromosomes 20
Total markers 34537
No. markers by chr:
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16
2643 2629 1857 1890 1774 1941 1672 1627 1878 1176 1871 1300 1549 1578 1257 935
17 18 19 X
501 913 1014 4532
table(gm$covar$group)
ICI PBS
104 34
##loading genotypes
genos.1 <- read.csv("data/ici.vs.pbs_sample.genos_marker.freq_low.geno.freq.removed_5.batches.csv")
dim(genos.1)
[1] 26548 149
genos.1 <- genos.1[genos.1$Include,]
dim(genos.1)
[1] 6556 149
#dis.genos.1 <- read.csv("data/ici.vs.pbs_marker.freq_low.geno.freq.removed_geno.ratio_5.batches_mis.csv")
#dim(dis.genos.1)
rownames(genos.1) <- genos.1$marker
genos.1 <- t(genos.1[3:(ncol(genos.1)-9)])
rownames(genos.1) <- gsub("\\.","-",rownames(genos.1))
genos.2<- read.csv("data/ici.vs.pbs_sample.genos_marker.freq_low.geno.freq.removed_sample.outliers.removed_5.batches.csv")
dim(genos.2)
[1] 26548 149
genos.2 <- genos.2[genos.2$Include,]
dim(genos.2)
[1] 6556 149
#dis.genos.2 <- read.csv("data/ici.vs.pbs_marker.freq_low.geno.freq.removed_sample.outliers.removed_geno.ratio_5.batches_mis.csv")
rownames(genos.2) <- genos.2$marker
genos.2 <- t(genos.2[3:(ncol(genos.2)-9)])
rownames(genos.2) <- gsub("\\.","-",rownames(genos.2))
##merge with phenotypes (age.of.onset & binary)
names(gm$covar)[3] <- c("age.of.onset")
gm$covar[gm$covar$id=="NG00453",]$age.of.onset = 13.7
gm$covar[gm$covar$age.of.onset=='',] <- 0
gm$covar$age.of.onset <- as.numeric(gm$covar$age.of.onset)
geno.pheno.1 <- merge(data.frame(genos.1), gm$covar, by="row.names", all.x=T, sort=F)
aov.1 <- stats::aov(age.of.onset ~ group, geno.pheno.1)
mse.1 <- mean(aov.1$residuals^2)
geno.pheno.2 <- merge(data.frame(genos.2), gm$covar, by="row.names", all.x=T, sort=F)
aov.2 <- stats::aov(age.of.onset ~ group, geno.pheno.2)
mse.2 <- mean(aov.2$residuals^2)
## calculating effect (age.of.onset)
age.marker.sum.1 <- list()
geno.pheno.1a <- geno.pheno.1[-1]
for(i in 1:(ncol(geno.pheno.1a)-7)){
#geno.pheno.1$snp=geno.pheno.1[i]
age.marker.1 <- geno.pheno.1a %>%
group_by(geno.pheno.1a[i]) %>%
summarize(mean_age.of.onset = mean(as.numeric(age.of.onset), na.rm =T))
names(age.marker.1) <- c("genotypes", paste0(names(geno.pheno.1a[i]),"_age.of.onset"))
genotypes <- as.data.frame(c("-","AA","AB"))
names(genotypes) <- c("genotypes")
age.marker.1 <- merge(genotypes, age.marker.1, by=c("genotypes"), all=T, sort=T)
#print(age.marker.1)
age.marker.sum.1[[i]] <- as.data.frame(age.marker.1)
}
age.marker.sum.1.all <- Reduce(function(x, y) merge(x, y, by=c("genotypes"),all=TRUE),age.marker.sum.1)
rownames(age.marker.sum.1.all) <- age.marker.sum.1.all$genotypes
age.marker.sum.1.all.t <- t(age.marker.sum.1.all[-1])
rownames(age.marker.sum.1.all.t) <- gsub("_age.of.onset","",rownames(age.marker.sum.1.all.t))
age.marker.sum.1.all.t <- as.data.frame(age.marker.sum.1.all.t)
age.marker.sum.1.all.t$diffhethom <- age.marker.sum.1.all.t$AB - age.marker.sum.1.all.t$AA
max.1 <- max(age.marker.sum.1.all.t$diffhethom)
min.1 <- min(age.marker.sum.1.all.t$diffhethom)
write.csv(age.marker.sum.1.all.t,"data/mean.differences_age.of.onset_ici.vs.pbs_sample.genos_marker.freq_low.geno.freq.removed_5.batches.csv")
age.marker.sum.2 <- list()
geno.pheno.2a <- geno.pheno.2[-1]
for(i in 1:(ncol(geno.pheno.2a)-7)){
#geno.pheno.2$snp=geno.pheno.2[i]
age.marker.2 <- geno.pheno.2a %>%
group_by(geno.pheno.2a[i]) %>%
summarize(mean_age.of.onset = mean(as.numeric(age.of.onset), na.rm =T))
names(age.marker.2) <- c("genotypes", paste0(names(geno.pheno.2a[i]),"_age.of.onset"))
genotypes <- as.data.frame(c("-","AA","AB"))
names(genotypes) <- c("genotypes")
age.marker.2 <- merge(genotypes, age.marker.2, by=c("genotypes"), all=T, sort=T)
#print(age.marker.2)
age.marker.sum.2[[i]] <- as.data.frame(age.marker.2)
}
age.marker.sum.2.all <- Reduce(function(x, y) merge(x, y, by=c("genotypes"),all=TRUE),age.marker.sum.2)
rownames(age.marker.sum.2.all) <- age.marker.sum.2.all$genotypes
age.marker.sum.2.all.t <- t(age.marker.sum.2.all[-1])
rownames(age.marker.sum.2.all.t) <- gsub("_age.of.onset","",rownames(age.marker.sum.2.all.t))
age.marker.sum.2.all.t <- as.data.frame(age.marker.sum.2.all.t)
age.marker.sum.2.all.t$diffhethom <- age.marker.sum.2.all.t$AB - age.marker.sum.2.all.t$AA
max.2 <- max(age.marker.sum.2.all.t$diffhethom)
min.2 <- min(age.marker.sum.2.all.t$diffhethom)
write.csv(age.marker.sum.2.all.t,"data/mean.differences_age.of.onset_ici.vs.pbs_sample.genos_marker.freq_low.geno.freq.removed_sample.outliers.removed_5.batches.csv")
max.a <- max(max.1, max.2)
print(max.a)
[1] 3.343679
min.a <- min(min.1, min.2)
print(min.a)
[1] -3.122579
mse.a <- (mse.1 + mse.2)/2
print(mse.a)
[1] 27.12483
## calculating effect (group)
age.marker.sum.1 <- list()
geno.pheno.1a <- geno.pheno.1[-1]
for(i in 1:(ncol(geno.pheno.1a)-7)){
#geno.pheno.1$snp=geno.pheno.1[i]
age.marker.1 <- geno.pheno.1a %>%
group_by(geno.pheno.1a[i]) %>%
summarize(mean_group = mean(as.numeric(group), na.rm =T))
names(age.marker.1) <- c("genotypes", paste0(names(geno.pheno.1a[i]),"_group"))
genotypes <- as.data.frame(c("-","AA","AB"))
names(genotypes) <- c("genotypes")
age.marker.1 <- merge(genotypes, age.marker.1, by=c("genotypes"), all=T, sort=T)
#print(age.marker.1)
age.marker.sum.1[[i]] <- as.data.frame(age.marker.1)
}
age.marker.sum.1.all <- Reduce(function(x, y) merge(x, y, by=c("genotypes"),all=TRUE),age.marker.sum.1)
rownames(age.marker.sum.1.all) <- age.marker.sum.1.all$genotypes
age.marker.sum.1.all.t <- t(age.marker.sum.1.all[-1])
rownames(age.marker.sum.1.all.t) <- gsub("_group","",rownames(age.marker.sum.1.all.t))
age.marker.sum.1.all.t <- as.data.frame(age.marker.sum.1.all.t)
age.marker.sum.1.all.t$diffhethom <- age.marker.sum.1.all.t$AB - age.marker.sum.1.all.t$AA
write.csv(age.marker.sum.1.all.t,"data/mean.differences_group_ici.vs.pbs_sample.genos_marker.freq_low.geno.freq.removed_5.batches.csv")
age.marker.sum.2 <- list()
geno.pheno.2a <- geno.pheno.2[-1]
for(i in 1:(ncol(geno.pheno.2a)-7)){
#geno.pheno.2$snp=geno.pheno.2[i]
age.marker.2 <- geno.pheno.2a %>%
group_by(geno.pheno.2a[i]) %>%
summarize(mean_group = mean(as.numeric(group), na.rm =T))
names(age.marker.2) <- c("genotypes", paste0(names(geno.pheno.2a[i]),"_group"))
genotypes <- as.data.frame(c("-","AA","AB"))
names(genotypes) <- c("genotypes")
age.marker.2 <- merge(genotypes, age.marker.2, by=c("genotypes"), all=T, sort=T)
#print(age.marker.2)
age.marker.sum.2[[i]] <- as.data.frame(age.marker.2)
}
age.marker.sum.2.all <- Reduce(function(x, y) merge(x, y, by=c("genotypes"),all=TRUE),age.marker.sum.2)
rownames(age.marker.sum.2.all) <- age.marker.sum.2.all$genotypes
age.marker.sum.2.all.t <- t(age.marker.sum.2.all[-1])
rownames(age.marker.sum.2.all.t) <- gsub("_group","",rownames(age.marker.sum.2.all.t))
age.marker.sum.2.all.t <- as.data.frame(age.marker.sum.2.all.t)
age.marker.sum.2.all.t$diffhethom <- age.marker.sum.2.all.t$AB - age.marker.sum.2.all.t$AA
write.csv(age.marker.sum.2.all.t,"data/mean.differences_group_ici.vs.pbs_sample.genos_marker.freq_low.geno.freq.removed_sample.outliers.removed_5.batches.csv")
max.g <- max(max.1, max.2)
print(max.g)
[1] 3.343679
min.g <- min(min.1, min.2)
print(min.g)
[1] -3.122579
mse.g <- (mse.1 + mse.2)/2
print(mse.g)
[1] 27.12483
For powercalc the power is returned, along with the proportion of variance explained. LOD threshold set to 3 (which is roughly what is seen for suggestive significance)
## age.of onset
powercalc(cross = "bc",n=length(mice.ids),effect=min.a,sigma2=mse.a,thresh=3,sel.frac=1,theta=0,bio.reps=1)
power percent.var.explained
[1,] 0.4225683 8.245675
powercalc(cross = "bc",n=length(mice.ids),effect=max.a,sigma2=mse.a,thresh=3,sel.frac=1,theta=0,bio.reps=1)
power percent.var.explained
[1,] 0.5215428 9.341773
#powercalc("bc",100,31,sigma2=1,sel.frac=1,theta=0)
## group (binary)
powercalc(cross = "bc",n=length(mice.ids),effect=min.g,sigma2=mse.g,thresh=3,sel.frac=1,theta=0,bio.reps=1)
power percent.var.explained
[1,] 0.4225683 8.245675
powercalc(cross = "bc",n=length(mice.ids),effect=max.g,sigma2=mse.g,thresh=3,sel.frac=1,theta=0,bio.reps=1)
power percent.var.explained
[1,] 0.5215428 9.341773
## graph
For samplesize the sample size (rounded up to the nearest integer) is returned along with the proportion of variance explained. LOD threshold set to 3 (which is roughly what is seen for suggestive significance) and 80% power
## age.of onset
samplesize(cross = "bc",effect=min.a,sigma2=mse.a,thresh=3,sel.frac=1,theta=0,bio.reps=1)
sample.size percent.var.explained
[1,] 232 8.245675
samplesize(cross = "bc",effect=max.a,sigma2=mse.a,thresh=3,sel.frac=1,theta=0,bio.reps=1)
sample.size percent.var.explained
[1,] 202 9.341773
## group (binary)
samplesize(cross = "bc",effect=min.g,sigma2=mse.g,thresh=3,sel.frac=1,theta=0,bio.reps=1)
sample.size percent.var.explained
[1,] 232 8.245675
samplesize(cross = "bc",effect=max.g,sigma2=mse.g,thresh=3,sel.frac=1,theta=0,bio.reps=1)
sample.size percent.var.explained
[1,] 202 9.341773
## graph
R version 3.6.2 (2019-12-12)
Platform: x86_64-apple-darwin15.6.0 (64-bit)
Running under: macOS Catalina 10.15.7
Matrix products: default
BLAS: /Library/Frameworks/R.framework/Versions/3.6/Resources/lib/libRblas.0.dylib
LAPACK: /Library/Frameworks/R.framework/Versions/3.6/Resources/lib/libRlapack.dylib
locale:
[1] en_AU.UTF-8/en_AU.UTF-8/en_AU.UTF-8/C/en_AU.UTF-8/en_AU.UTF-8
attached base packages:
[1] stats graphics grDevices utils datasets methods base
other attached packages:
[1] qtlDesign_0.941 abind_1.4-5 qtl2_0.28 reshape2_1.4.4
[5] ggplot2_3.3.6 tibble_3.1.7 psych_2.0.7 readxl_1.4.0
[9] cluster_2.1.0 dplyr_1.0.9 optparse_1.6.6 rhdf5_2.28.1
[13] mclust_5.4.6 tidyr_1.2.0 data.table_1.14.2 knitr_1.39
[17] kableExtra_1.1.0 workflowr_1.6.2
loaded via a namespace (and not attached):
[1] httr_1.4.3 sass_0.4.1 bit64_4.0.5 jsonlite_1.8.0
[5] viridisLite_0.4.0 bslib_0.3.1 assertthat_0.2.1 highr_0.9
[9] blob_1.2.3 cellranger_1.1.0 yaml_2.3.5 pillar_1.7.0
[13] RSQLite_2.2.14 lattice_0.20-38 glue_1.6.2 digest_0.6.29
[17] promises_1.1.0 rvest_1.0.2 colorspace_2.0-3 htmltools_0.5.2
[21] httpuv_1.5.2 plyr_1.8.7 pkgconfig_2.0.3 purrr_0.3.4
[25] scales_1.2.0 webshot_0.5.2 getopt_1.20.3 later_1.0.0
[29] tzdb_0.3.0 git2r_0.26.1 generics_0.1.2 ellipsis_0.3.2
[33] cachem_1.0.6 withr_2.5.0 cli_3.3.0 mnormt_1.5-7
[37] magrittr_2.0.3 crayon_1.5.1 memoise_2.0.1 evaluate_0.15
[41] fs_1.5.2 fansi_1.0.3 nlme_3.1-142 xml2_1.3.3
[45] tools_3.6.2 hms_1.1.1 lifecycle_1.0.1 stringr_1.4.0
[49] Rhdf5lib_1.6.3 munsell_0.5.0 compiler_3.6.2 jquerylib_0.1.4
[53] rlang_1.0.2 grid_3.6.2 rstudioapi_0.13 rmarkdown_2.14
[57] gtable_0.3.0 DBI_1.1.2 R6_2.5.1 fastmap_1.1.0
[61] bit_4.0.4 utf8_1.2.2 rprojroot_2.0.3 readr_2.1.2
[65] stringi_1.7.6 parallel_3.6.2 Rcpp_1.0.8.3 vctrs_0.4.1
[69] tidyselect_1.1.2 xfun_0.31