Last updated: 2023-04-16
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Knit directory: Serreze-T1D_Workflow/
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Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-10_peak.marker-UNC18343990_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-11_peak.marker-UNC20070077_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-11_peak.marker-UNC20070077_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-12_peak.marker-UNC21652584_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-12_peak.marker-UNC21652584_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-13_peak.marker-UNCHS036579_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-13_peak.marker-UNCHS036579_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-14_peak.marker-UNCHS037782_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-14_peak.marker-UNCHS037782_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-15_peak.marker-UNC26069905_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-15_peak.marker-UNCHS041223_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-16_peak.marker-JAX00070117_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-16_peak.marker-JAX00070117_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-17_peak.marker-UNC28542319_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-17_peak.marker-UNCJPD006670_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-18_peak.marker-UNC28776739_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-18_peak.marker-UNCHS045594_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-19_peak.marker-UNC30414168_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-19_peak.marker-UNC30426276_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-1_peak.marker-UNC2031646_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-1_peak.marker-UNCHS003700_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-2_peak.marker-ICR5131_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-2_peak.marker-UNCHS006420_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-3_peak.marker-UNC5667757_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-3_peak.marker-UNC5667757_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-4_peak.marker-UNC6759992_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-4_peak.marker-UNC6765178_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-5_peak.marker-UNC9889957_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-5_peak.marker-UNC9900273_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-6_peak.marker-UNC10800126_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-6_peak.marker-UNC10832076_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-7_peak.marker-UNCHS020903_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-7_peak.marker-UNCHS021163_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-8_peak.marker-UNC15471847_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-8_peak.marker-UNC15548888_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-9_peak.marker-UNC16231874_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-9_peak.marker-UNC16231874_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-X_peak.marker-UNCHS049472_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_blup_sub_chr-X_peak.marker-UNCHS049472_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-10_peak.marker-UNC18343990_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-10_peak.marker-UNC18343990_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-11_peak.marker-UNC20070077_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-11_peak.marker-UNC20070077_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-12_peak.marker-UNC21652584_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-12_peak.marker-UNC21652584_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-13_peak.marker-UNCHS036579_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-13_peak.marker-UNCHS036579_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-14_peak.marker-UNCHS037782_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-14_peak.marker-UNCHS037782_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-15_peak.marker-UNC26069905_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-15_peak.marker-UNCHS041223_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-16_peak.marker-JAX00070117_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-16_peak.marker-JAX00070117_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-17_peak.marker-UNC28542319_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-17_peak.marker-UNCJPD006670_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-18_peak.marker-UNC28776739_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-18_peak.marker-UNCHS045594_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-19_peak.marker-UNC30414168_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-19_peak.marker-UNC30426276_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-1_peak.marker-UNC2031646_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-1_peak.marker-UNCHS003700_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-2_peak.marker-ICR5131_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-2_peak.marker-UNCHS006420_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-3_peak.marker-UNC5667757_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-3_peak.marker-UNC5667757_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-4_peak.marker-UNC6759992_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-4_peak.marker-UNC6765178_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-5_peak.marker-UNC9889957_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-5_peak.marker-UNC9900273_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-6_peak.marker-UNC10800126_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-6_peak.marker-UNC10832076_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-7_peak.marker-UNCHS020903_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-7_peak.marker-UNCHS021163_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-8_peak.marker-UNC15471847_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-8_peak.marker-UNC15548888_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-9_peak.marker-UNC16231874_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-9_peak.marker-UNC16231874_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-X_peak.marker-UNCHS049472_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_genes_chr-X_peak.marker-UNCHS049472_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_gm_qtl_snpsqc_dis_no-x_updated_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_gm_qtl_snpsqc_dis_no-x_updated_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_marker.freq_low.geno.freq.removed_geno.ratio_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_marker.freq_low.geno.freq.removed_geno.ratio_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_marker.freq_low.geno.freq.removed_sample.outliers.removed_geno.ratio_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_marker.freq_low.geno.freq.removed_sample.outliers.removed_geno.ratio_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_marker.freq_low.probs.freq.removed_geno.ratio_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_marker.freq_low.probs.freq.removed_geno.ratio_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_marker.freq_low.probs.freq.removed_sample.outliers.removed_geno.ratio_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_marker.freq_low.probs.freq.removed_sample.outliers.removed_geno.ratio_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_sample.genos_marker.freq_low.geno.freq.removed_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_sample.genos_marker.freq_low.geno.freq.removed_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_sample.genos_marker.freq_low.geno.freq.removed_sample.outliers.removed_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_sample.genos_marker.freq_low.geno.freq.removed_sample.outliers.removed_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_sample.genos_marker.freq_low.probs.freq.removed_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_sample.genos_marker.freq_low.probs.freq.removed_7.batches_myo_mis.csv
Untracked: data/ici-sick.vs.ici-eoi_sample.genos_marker.freq_low.probs.freq.removed_sample.outliers.removed_7.batches_myo.csv
Untracked: data/ici-sick.vs.ici-eoi_sample.genos_marker.freq_low.probs.freq.removed_sample.outliers.removed_7.batches_myo_mis.csv
Untracked: data/ici.vs.pbs_blup_sub_chr-7_peak.marker-UNCHS020711_lod.drop-1.5_snpsqc_dis_no-x_updated_7.batches_myo.csv
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Unstaged changes:
Modified: analysis/_site.yml
Modified: analysis/index.Rmd
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We will load the data and subset indivials out that are in the groups of interest.
load("data/gm_allqc_7.batches_myo.RData")
#gm_allqc
gm=gm_allqc
gm
Object of class cross2 (crosstype "bc")
Total individuals 357
No. genotyped individuals 357
No. phenotyped individuals 357
No. with both geno & pheno 357
No. phenotypes 1
No. covariates 11
No. phenotype covariates 0
No. chromosomes 20
Total markers 32660
No. markers by chr:
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16
2482 2412 1742 1772 1648 1842 1541 1517 1769 1092 1754 1230 1441 1505 1128 842
17 18 19 X
655 820 945 4523
#pr <- readRDS("data/serreze_probs_allqc.rds")
#pr <- readRDS("data/serreze_probs.rds")
##extracting animals with ici and pbs group status
#miceinfo <- covars[gm$covar$group == "PBS" | gm$covar$group == "ICI",]
#table(miceinfo$group)
#mice.ids <- rownames(miceinfo)
#gm <- gm[mice.ids]
#gm
#table(gm$covar$group)
#gm$covar$myo.yes_vs_myo.no <- ifelse(gm$covar$group == "PBS", 0, 1)
#gm.full <- gm
covars <- read_csv("data/covar_corrected_myo-yes.vs.myo-no_7.batches_myo.csv")
#removing any missing info
#covars <- subset(covars, covars$myo.yes_vs_myo.no!='')
nrow(covars)
[1] 241
table(covars$"Myocarditis Status")
NO YES
29 212
table(covars$"Murine MHC KO Status")
HOM
241
table(covars$"Drug Treatment")
ICI PBS
145 96
table(covars$"clinical pheno")
EOI SICK
95 146
#keeping only informative mice
gm <- gm[covars$Mouse.ID]
gm
Object of class cross2 (crosstype "bc")
Total individuals 241
No. genotyped individuals 241
No. phenotyped individuals 241
No. with both geno & pheno 241
No. phenotypes 1
No. covariates 11
No. phenotype covariates 0
No. chromosomes 20
Total markers 32660
No. markers by chr:
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16
2482 2412 1742 1772 1648 1842 1541 1517 1769 1092 1754 1230 1441 1505 1128 842
17 18 19 X
655 820 945 4523
table(gm$covar$"Myocarditis Status")
NO YES
29 212
table(gm$covar$"Murine MHC KO Status")
HOM
241
table(gm$covar$"Drug Treatment")
ICI PBS
145 96
table(gm$covar$"clinical pheno")
EOI SICK
95 146
#pr.qc.ids <- pr
#for (i in 1:20){pr.qc.ids[[i]] = pr.qc.ids[[i]][covars$Mouse.ID,,]}
##removing problmetic marker
#gm <- drop_markers(gm, "UNCHS013106")
##dropping monomorphic markers within the dataset
g <- do.call("cbind", gm$geno)
gf_mar <- t(apply(g, 2, function(a) table(factor(a, 1:2))/sum(a != 0)))
#gn_mar <- t(apply(g, 2, function(a) table(factor(a, 1:2))))
gf_mar <- gf_mar[gf_mar[,2] != "NaN",]
count <- rowSums(gf_mar <=0.05)
low_freq_df <- merge(as.data.frame(gf_mar),as.data.frame(count), by="row.names",all=T)
low_freq_df[is.na(low_freq_df)] <- ''
low_freq_df <- low_freq_df[low_freq_df$count == 1,]
rownames(low_freq_df) <- low_freq_df$Row.names
low_freq <- find_markerpos(gm, rownames(low_freq_df))
low_freq$id <- rownames(low_freq)
nrow(low_freq)
[1] 6169
low_freq_bad <- merge(low_freq,low_freq_df, by="row.names",all=T)
names(low_freq_bad)[1] <- c("marker")
gf_mar <- gf_mar[gf_mar[,2] != "NaN",]
MAF <- apply(gf_mar, 1, function(x) min(x))
MAF <- as.data.frame(MAF)
MAF$index <- 1:nrow(gf_mar)
gf_mar_maf <- merge(gf_mar,as.data.frame(MAF), by="row.names")
gf_mar_maf <- gf_mar_maf[order(gf_mar_maf$index),]
gfmar <- NULL
gfmar$gfmar_mar_0 <- sum(gf_mar_maf$MAF==0)
gfmar$gfmar_mar_1 <- sum(gf_mar_maf$MAF< 0.01)
gfmar$gfmar_mar_5 <- sum(gf_mar_maf$MAF< 0.05)
gfmar$gfmar_mar_10 <- sum(gf_mar_maf$MAF< 0.10)
gfmar$gfmar_mar_15 <- sum(gf_mar_maf$MAF< 0.15)
gfmar$gfmar_mar_25 <- sum(gf_mar_maf$MAF< 0.25)
gfmar$gfmar_mar_50 <- sum(gf_mar_maf$MAF< 0.50)
gfmar$total_snps <- nrow(as.data.frame(gf_mar_maf))
gfmar <- t(as.data.frame(gfmar))
gfmar <- as.data.frame(gfmar)
gfmar$count <- gfmar$V1
gfmar[c(2)] %>%
kable(escape = F,align = c("ccccccccc"),linesep ="\\hline") %>%
kable_styling(full_width = F) %>%
kable_styling("striped", full_width = F) %>%
row_spec(8 ,bold=T,color= "white",background = "black")
count | |
---|---|
gfmar_mar_0 | 3929 |
gfmar_mar_1 | 4156 |
gfmar_mar_5 | 6167 |
gfmar_mar_10 | 6516 |
gfmar_mar_15 | 6544 |
gfmar_mar_25 | 6625 |
gfmar_mar_50 | 32274 |
total_snps | 32660 |
gm_qc <- drop_markers(gm, low_freq_bad$marker)
gm_qc <- drop_nullmarkers(gm_qc)
gm = gm_qc
gm
Object of class cross2 (crosstype "bc")
Total individuals 241
No. genotyped individuals 241
No. phenotyped individuals 241
No. with both geno & pheno 241
No. phenotypes 1
No. covariates 11
No. phenotype covariates 0
No. chromosomes 20
Total markers 26491
No. markers by chr:
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16
2326 2278 1598 1656 1520 1685 1453 1443 1665 958 1657 1120 1366 1408 1036 745
17 18 19 X
565 742 897 373
## dropping disproportionate markers
#dismark <- read.csv("data/myo-yes.vs.myo-no_marker.freq_low.geno.freq.removed_geno.ratio_7.batches_myo.csv")
#nrow(dismark)
#ames(dismark)[1] <- c("marker")
#dismark <- dismark[!dismark$Include,]
#nrow(dismark)
#gm_qc_dis <- drop_markers(gm_qc, dismark$marker)
#gm_qc_dis <- drop_nullmarkers(gm_qc_dis)
#gm = gm_qc_dis
#gm
markers <- marker_names(gm)
gmapdf <- read.csv("data/genetic_map_7.batches_myo.csv")
pmapdf <- read.csv("data/physical_map_7.batches_myo.csv")
#mapdf <- merge(gmapdf,pmapdf, by=c("marker","chr"), all=T)
#rownames(mapdf) <- mapdf$marker
#mapdf <- mapdf[markers,]
#names(mapdf) <- c('marker','chr','gmapdf','pmapdf')
#mapdfnd <- mapdf[!duplicated(mapdf[c(2:3)]),]
pr.qc <- calc_genoprob(gm)
colnames(covars) <- gsub(" ", ".", colnames(covars))
For each of the phenotype analyzed, permutations were used for each model to obtain genome-wide LOD significance threshold for p < 0.01, p < 0.05, p < 0.10, respectively, separately for X and automsomes (A).
The table shows the estimated significance thresholds from permutation test.
We also looked at the kinship to see how correlated each sample is. Kinship values between pairs of samples range between 0 (no relationship) and 1.0 (completely identical). The darker the colour the more indentical the pairs are.
#Xcovar <- get_x_covar(gm)
addcovar = model.matrix(~sex+Histology.Score, data = covars)[,-1]
covars$myo.yes_vs_myo.no= as.numeric(covars$myo.yes_vs_myo.no)
kinship <- calc_kinship(pr.qc)
heatmap(kinship)
operm <- scan1perm(pr.qc, covars["myo.yes_vs_myo.no"], model="binary", addcovar=addcovar, n_perm=1000, perm_Xsp=TRUE, chr_lengths=chr_lengths(gm$gmap))
summary_table<-data.frame(unclass(summary(operm, alpha=c(0.01, 0.05, 0.1))))
names(summary_table) <- c("autosomes","X")
summary_table$significance.level <- rownames(summary_table)
rownames(summary_table) <- NULL
summary_table[c(3,1:2)] %>%
kable(escape = F,align = c("ccc")) %>%
kable_styling("striped", full_width = T) %>%
column_spec(1, bold=TRUE)
significance.level | autosomes | X |
---|---|---|
0.01 | 0 | 0 |
0.05 | 0 | 0 |
0.1 | 0 | 0 |
The figures below show QTL maps for each phenotype
#out <- scan1(pr.qc, covars["myo.yes_vs_myo.no"], Xcovar=Xcovar, model="binary")
out <- scan1(pr.qc, covars["myo.yes_vs_myo.no"], model="binary",addcovar=addcovar)
summary_table<-data.frame(unclass(summary(operm, alpha=c(0.01, 0.05, 0.1))))
plot_lod<-function(out,map){
for (i in 1:dim(out)[2]){
#png(filename=paste0("/Users/chenm/Documents/qtl/Jai/",colnames(out)[i], "_lod.png"))
ymx <- maxlod(out) # overall maximum LOD score
plot(out, map, lodcolumn=i, col="slateblue", ylim=c(0, ymx+0.5))
#legend("topright", lwd=2, colnames(out)[i], bg="gray90")
title(main = paste0(colnames(out)[i], " [positions in cM]"))
add_threshold(map, summary(operm,alpha=0.1), col = 'purple')
add_threshold(map, summary(operm, alpha=0.05), col = 'red')
add_threshold(map, summary(operm, alpha=0.01), col = 'blue')
##par(mar=c(5.1, 6.1, 1.1, 1.1))
#ymx <- 11 # overall maximum LOD score
#plot(out, map, lodcolumn=i, col="slateblue", ylim=c(0, ymx+0.5))
##legend("topright", lwd=2, colnames(out)[i], bg="gray90")
#title(main = paste0(colnames(out)[i], " [positions in cM] \n(using same scale as eoi vs ici for easier comparison)"))
#add_threshold(map, summary(operm, alpha=0.1), col = 'purple')
#add_threshold(map, summary(operm, alpha=0.05), col = 'red')
#add_threshold(map, summary(operm, alpha=0.01), col = 'blue')
##for (j in 1: dim(summary_table)[1]){
## abline(h=summary_table[j, i],col="red")
## text(x=400, y =summary_table[j, i]+0.12, labels = paste("p=", row.names(summary_table)[j]))
##}
##dev.off()
}
}
plot_lod(out,gm$gmap)
The table below shows QTL peaks associated with the phenotype. We use the 95% threshold from the permutations to find peaks.
peaks <- find_peaks(out, gm$gmap, threshold=summary(operm,alpha=0.05)$A, thresholdX = summary(operm,alpha=0.05)$X, peakdrop=3, drop=1.5)
if(nrow(peaks) >0){
peaks$marker <- find_marker(gm$gmap, chr=peaks$chr,pos=peaks$pos)
names(peaks)[2] <- c("phenotype")
peaks <- peaks[-1]
rownames(peaks) <- NULL
print(kable(peaks, escape = F, align = c("cccccccc"), "html")
%>% kable_styling("striped", full_width = T)%>%
column_spec(1, bold=TRUE)
)
#plot only peak chromosomes
plot_lod_chr<-function(out,map,chrom){
for (i in 1:dim(out)[2]){
#png(filename=paste0("/Users/chenm/Documents/qtl/Jai/",colnames(out)[i], "_lod.png"))
#par(mar=c(5.1, 6.1, 1.1, 1.1))
ymx <- maxlod(out) # overall maximum LOD score
plot(out, map, chr = chrom, lodcolumn=i, col="slateblue", ylim=c(0, ymx+0.5))
#legend("topright", lwd=2, colnames(out)[i], bg="gray90")
title(main = paste0(colnames(out)[i], " - chr", chrom, " [positions in cM]"))
add_threshold(map, summary(operm,alpha=0.1), col = 'purple')
add_threshold(map, summary(operm, alpha=0.05), col = 'red')
add_threshold(map, summary(operm, alpha=0.01), col = 'blue')
#for (j in 1: dim(summary_table)[1]){
# abline(h=summary_table[j, i],col="red")
# text(x=400, y =summary_table[j, i]+0.12, labels = paste("p=", row.names(summary_table)[j]))
#}
#dev.off()
#ymx <- 11
#plot(out, map, chr = chrom, lodcolumn=i, col="slateblue", ylim=c(0, ymx+0.5))
##legend("topright", lwd=2, colnames(out)[i], bg="gray90")
#title(main = paste0(colnames(out)[i], " - chr", chrom, " [positions in cM]\n(using same scale as eoi vs. ici for easier comparison)"))
#add_threshold(map, summary(operm,alpha=0.1), col = 'purple')
#add_threshold(map, summary(operm, alpha=0.05), col = 'red')
#add_threshold(map, summary(operm, alpha=0.01), col = 'blue')
}
}
for(i in unique(peaks$chr)){
#for (i in 1:nrow(peaks)){
#plot_lod_chr(out,gm$gmap, peaks$chr[i])
plot_lod_chr(out,gm$gmap, i)
}
} else {
print(paste0("There are no peaks that have a LOD that reaches suggestive (p<0.05) level of ",summary(operm,alpha=0.05)$A, " [autosomes]/",summary(operm,alpha=0.05)$X, " [x-chromosome]"))
}
[1] “There are no peaks that have a LOD that reaches suggestive (p<0.05) level of 0 [autosomes]/0 [x-chromosome]”
print("peaks in MB positions")
[1] “peaks in MB positions”
peaks_mba <- find_peaks(out, gm$pmap, threshold=summary(operm,alpha=0.05)$A, thresholdX = summary(operm,alpha=0.05)$X, peakdrop=3, drop=1.5)
if(nrow(peaks) >0){
peaks_mba$marker <- find_marker(gm$pmap, chr=peaks_mba$chr,pos=peaks_mba$pos)
names(peaks_mba)[2] <- c("phenotype")
peaks_mba <- peaks_mba[-1]
rownames(peaks_mba) <- NULL
print(kable(peaks_mba, escape = F, align = c("cccccccc"), "html")
%>% kable_styling("striped", full_width = T)%>%
column_spec(1, bold=TRUE)
)
plot_lod_chr_mb<-function(out,map,chrom){
for (i in 1:dim(out)[2]){
#png(filename=paste0("/Users/chenm/Documents/qtl/Jai/",colnames(out)[i], "_lod.png"))
#par(mar=c(5.1, 6.1, 1.1, 1.1))
ymx <- maxlod(out) # overall maximum LOD score
plot(out, map, chr = chrom, lodcolumn=i, col="slateblue", ylim=c(0, ymx+0.5))
#legend("topright", lwd=2, colnames(out)[i], bg="gray90")
title(main = paste0(colnames(out)[i], " - chr", chrom, " [positions in MB]"))
add_threshold(map, summary(operm,alpha=0.1), col = 'purple')
add_threshold(map, summary(operm, alpha=0.05), col = 'red')
add_threshold(map, summary(operm, alpha=0.01), col = 'blue')
#for (j in 1: dim(summary_table)[1]){
# abline(h=summary_table[j, i],col="red")
# text(x=400, y =summary_table[j, i]+0.12, labels = paste("p=", row.names(summary_table)[j]))
#}
#dev.off()
#ymx <- 11
#plot(out, map, chr = chrom, lodcolumn=i, col="slateblue", ylim=c(0, ymx+0.5))
##legend("topright", lwd=2, colnames(out)[i], bg="gray90")
#title(main = paste0(colnames(out)[i], " - chr", chrom, " [positions in MB]\n(using same scale as eoi vs. ici for easier comparison)"))
#add_threshold(map, summary(operm,alpha=0.1), col = 'purple')
#add_threshold(map, summary(operm, alpha=0.05), col = 'red')
#add_threshold(map, summary(operm, alpha=0.01), col = 'blue')
}
}
for(i in unique(peaks_mba$chr)){
#for (i in 1:nrow(peaks_mba)){
#plot_lod_chr_mb(out,gm$pmap, peaks_mba$chr[i])
plot_lod_chr_mb(out,gm$pmap,i)
}
} else {
print(paste0("There are no peaks that have a LOD that reaches suggestive (p<0.05) level of ",summary(operm,alpha=0.05)$A, " [autosomes]/",summary(operm,alpha=0.05)$X, " [x-chromosome]"))
}
[1] “There are no peaks that have a LOD that reaches suggestive (p<0.05) level of 0 [autosomes]/0 [x-chromosome]”
For each peak LOD location we give a list of gene
query_variants <- create_variant_query_func("code/cc_variants.sqlite")
query_genes <- create_gene_query_func("code/mouse_genes_mgi.sqlite")
if(nrow(peaks) >0){
for (i in 1:nrow(peaks)){
g <- maxmarg(pr.qc, gm$gmap, chr=peaks$chr[i], pos=peaks$pos[i], return_char=TRUE)
#png(filename=paste0("/Users/chenm/Documents/qtl/Jai/","qtl_effect_", i, ".png"))
#par(mar=c(4.1, 4.1, 1.5, 0.6))
plot_pxg(g, covars[,peaks$phenotype[i]], ylab=peaks$phenotype[i], sort=FALSE)
title(main = paste0("chr: ", chr=peaks$chr[i],"; pos: ", peaks$pos[i], "cM /",peaks_mba$pos[i],"MB\n(",peaks$phenotype[i]," )"), line=0.2)
##dev.off()
chr = peaks$chr[i]
# Plot 2
pr_sub <- pull_genoprobint(pr.qc, gm$gmap, chr, c(peaks$ci_lo[i], peaks$ci_hi[i]))
blup <- scan1blup(pr.qc[,chr], covars[peaks$phenotype[i]],addcovar = addcovar)
blup_sub <- scan1blup(pr_sub[,chr], covars[peaks$phenotype[i]], addcovar = addcovar)
write.csv(as.data.frame(blup_sub), paste0("data/myo-yes.vs.myo-no_blup_sub_chr-",chr,"_peak.marker-",peaks$marker[i],"_lod.drop-1.5_snpsqc_7.batches_myo.csv"), quote=F)
plot_coef(blup,
gm$gmap, columns=1:2,
bgcolor="gray95", legend="bottomleft",
main = paste0("chr: ", chr=peaks$chr[i],"; pos: ", peaks$pos[i], "cM /",peaks_mba$pos[i],"MB\n(",peaks$phenotype[i]," [scan1blup; positions in cM])")
)
plot_coef(blup_sub,
gm$gmap, columns=1:2,
bgcolor="gray95", legend="bottomleft",
main = paste0("chr: ", chr=peaks$chr[i],"; pos: ", peaks$pos[i], "cM /",peaks_mba$pos[i],"MB\n(",peaks$phenotype[i],"; 1.5 LOD drop interval [scan1blup; positions in cM])")
)
#Table 1
chr = peaks_mba$chr[i]
start=as.numeric(peaks_mba$ci_lo[i])
end=as.numeric(peaks_mba$ci_hi[i])
genesgss = query_genes(chr, start, end)
write.csv(genesgss, file=paste0("data/myo-yes.vs.myo-no_genes_chr-",chr,"_peak.marker-",peaks$marker[i],"_lod.drop-1.5_snpsqc_7.batches_myo.csv"), quote=F)
rownames(genesgss) <- NULL
genesgss$strand_old = genesgss$strand
genesgss$strand[genesgss$strand=="+"] <- "positive"
genesgss$strand[genesgss$strand=="-"] <- "negative"
print(kable(genesgss[,c("chr","type","start","stop","strand","ID","Name","Dbxref","gene_id","mgi_type","description")], "html") %>% kable_styling("striped", full_width = T))
}
} else {
print(paste0("There are no peaks that have a LOD that reaches suggestive (p<0.05) level of ",summary(operm,alpha=0.05)$A, " [autosomes]/",summary(operm,alpha=0.05)$X, " [x-chromosome]"))
}
[1] “There are no peaks that have a LOD that reaches suggestive (p<0.05) level of 0 [autosomes]/0 [x-chromosome]”
R version 4.0.3 (2020-10-10)
Platform: x86_64-pc-linux-gnu (64-bit)
Running under: Ubuntu 20.04.5 LTS
Matrix products: default
BLAS: /usr/lib/x86_64-linux-gnu/openblas-pthread/libblas.so.3
LAPACK: /usr/lib/x86_64-linux-gnu/openblas-pthread/liblapack.so.3
locale:
[1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
[3] LC_TIME=en_US.UTF-8 LC_COLLATE=en_US.UTF-8
[5] LC_MONETARY=en_US.UTF-8 LC_MESSAGES=en_US.UTF-8
[7] LC_PAPER=en_US.UTF-8 LC_NAME=C
[9] LC_ADDRESS=C LC_TELEPHONE=C
[11] LC_MEASUREMENT=en_US.UTF-8 LC_IDENTIFICATION=C
attached base packages:
[1] stats graphics grDevices utils datasets methods base
other attached packages:
[1] abind_1.4-5 qtl2_0.24 reshape2_1.4.4 ggplot2_3.3.3
[5] tibble_3.0.6 psych_2.0.12 readxl_1.3.1 cluster_2.1.0
[9] dplyr_1.0.4 optparse_1.6.6 rhdf5_2.34.0 mclust_5.4.7
[13] tidyr_1.1.2 data.table_1.13.6 knitr_1.31 kableExtra_1.3.1
[17] workflowr_1.6.2
loaded via a namespace (and not attached):
[1] Rcpp_1.0.10 lattice_0.20-41 assertthat_0.2.1 rprojroot_2.0.2
[5] digest_0.6.27 R6_2.5.0 cellranger_1.1.0 plyr_1.8.6
[9] RSQLite_2.2.3 evaluate_0.14 httr_1.4.2 highr_0.8
[13] pillar_1.4.7 rlang_0.4.10 rstudioapi_0.13 blob_1.2.1
[17] rmarkdown_2.6 webshot_0.5.2 stringr_1.4.0 bit_4.0.4
[21] munsell_0.5.0 compiler_4.0.3 httpuv_1.5.5 xfun_0.21
[25] pkgconfig_2.0.3 mnormt_2.0.2 tmvnsim_1.0-2 htmltools_0.5.1.1
[29] tidyselect_1.1.0 viridisLite_0.3.0 crayon_1.4.1 withr_2.4.1
[33] later_1.1.0.1 rhdf5filters_1.2.1 grid_4.0.3 nlme_3.1-152
[37] gtable_0.3.0 lifecycle_0.2.0 DBI_1.1.1 git2r_0.28.0
[41] magrittr_2.0.1 scales_1.1.1 cachem_1.0.3 stringi_1.5.3
[45] fs_1.5.0 promises_1.1.1 getopt_1.20.3 xml2_1.3.2
[49] ellipsis_0.3.1 generics_0.1.0 vctrs_0.3.6 Rhdf5lib_1.12.1
[53] tools_4.0.3 bit64_4.0.5 glue_1.4.2 purrr_0.3.4
[57] fastmap_1.1.0 parallel_4.0.3 yaml_2.2.1 colorspace_2.0-0
[61] rvest_0.3.6 memoise_2.0.0