Last updated: 2023-08-08

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Rmd 0c24851 mcmero 2023-08-08 Added human mixture variant analysis

Human samples are duplicate of 1% spike-in of 8393 (son of Chinese ancestry HG-005) in 8391 (son of Eastern European Ashkenazi Jewish ancestry HG-0020). Reference.

library(ggplot2)
library(data.table)
library(dplyr)
library(here)
library(tibble)
library(stringr)
library(Rsamtools)
library(GenomicRanges)
library(seqinr)
library(parallel)
library(readxl)
library(patchwork)
library(RColorBrewer)
library(UpSetR)
library(vcfR)
library(R.utils)
library(knitr)
source(here('code/load_data.R'))
source(here('code/plot.R'))
source(here('code/efficiency_nanoseq_functions.R'))
variant_dir <- here('data/human_mixture_vars')
region_bed <- here('data/human_mixture_capture_region.bed')
hg002_var_file <- here('data/human_mixture_refs/HG002_GRCh38_1_22_v4.2.1_benchmark.vcf.gz')
hg005_var_file <- here('data/human_mixture_refs/HG005_GRCh38_1_22_v4.2.1_benchmark.vcf.gz')
sample_names <- c('Human1pR1', 'Human1pR2')

# load variant data
var_df <- load_variants(variant_dir, sample_names)
hg002_vars <- read.vcfR(hg002_var_file, verbose = FALSE)
hg005_vars <- read.vcfR(hg005_var_file, verbose = FALSE)

hg002v <- data.frame(hg002_vars@fix)
hg005v <- data.frame(hg005_vars@fix)

# get capture regions
regions <- read.delim(region_bed, sep = '\t', header = FALSE)

Variant Upset plot

Here we remove any “N” variant calls and INDELs and compare the overlaps for on- and off-target variant calls.

# remove any N calls and INDELs
var_df <- filter(var_df, ALT != "N") %>%
            filter(., (ALT %>% str_split("") %>% lapply(., length) %>% unlist) == 1) %>%
            filter(., (REF %>% str_split("") %>% lapply(., length) %>% unlist) == 1) %>%
            calculate_vafs_nvc(.)

# get capture region range
grx <- GRanges(seqnames = paste0("chr", regions$V1),
               ranges = IRanges(start = regions$V2, end = regions$V3))
vrx <- GRanges(seqnames = var_df$CHROM,
               ranges = IRanges(start = as.numeric(var_df$POS),
                                end = as.numeric(var_df$POS) + 1))
var_df$on_target <- overlapsAny(vrx, grx)

# make upsetplot
ulist <- NULL
for(sample in sample_names) {
    ont_ids <- var_df[var_df$sample %in% sample & var_df$on_target,]$id
    oft_ids <- var_df[var_df$sample %in% sample & !var_df$on_target,]$id
    ulist[[paste(sample, "ontarget")]] <- ont_ids
    ulist[[paste(sample, "offtarget")]] <- oft_ids
    
}

upset(fromList(ulist), order.by='freq', nsets=4)

Variant allele frequencies

Here we plot the allelic frequencies per-replicate in three plots:

  • all filtered variant calls: no frequency or target filtering
  • on-target variant calls: only on-target variant calls (in capture region)
  • VAF-filtered on-target variant calls: all on-target variants under <0.3% VAF
ggplot(var_df, aes(VAF)) +
    geom_histogram(binwidth = 0.05) +
    facet_grid(~sample) +
    theme_minimal() +
    ggtitle("All filtered variant calls")

ggplot(var_df[var_df$on_target,], aes(VAF)) +
    geom_histogram(binwidth = 0.05) +
    facet_grid(~sample) +
    theme_minimal() +
    ggtitle("On-target variant calls")

ggplot(var_df[var_df$on_target & var_df$VAF < 0.3,], aes(VAF)) +
    geom_histogram(binwidth = 0.01) +
    facet_grid(~sample) +
    theme_minimal() +
    ggtitle("On-target variant calls < 0.3 VAF")

Variant comparison

Given the referene information, we check how many SNPs are present in the capture area. We also filter out any variants that are common between the two samples (if the same variant appears in both samples, we can’t differentiate the calls without some kind of phasing).

# filter out any INDELs
hg005v <- filter(hg005v, (ALT %>% str_split("") %>% lapply(., length) %>% unlist) == 1) %>%
          filter(., (REF %>% str_split("") %>% lapply(., length) %>% unlist) == 1)

# construct Granges for hg005 SNPs and keep only SNPs in capture area
hg5x <- GRanges(seqnames = hg005v$CHROM,
                ranges = IRanges(start = as.numeric(hg005v$POS),
                                 end = as.numeric(hg005v$POS) + 1),
                variant = hg005v$ALT)
hg5x <- hg5x[overlapsAny(hg5x, grx) %>% suppressWarnings()]

# construct Granges for hg002
hg2x <- GRanges(seqnames = hg002v$CHROM,
                ranges = IRanges(start = as.numeric(hg002v$POS),
                                 end = as.numeric(hg002v$POS) + 1),
                variant = hg002v$ALT)

# check variants that overlap, we will keep these if they call a different base
unique_vars <- hg5x[overlapsAny(hg5x, hg2x)]$variant != hg2x[overlapsAny(hg2x, hg5x)]$variant
hg5x <- c(hg5x[!overlapsAny(hg5x, hg2x)], hg5x[overlapsAny(hg5x, hg2x)][unique_vars])

kable(hg5x)
seqnames start end width strand variant
chr1 114714012 114714013 2 * G
chr3 128486108 128486109 2 * T
chr5 177516672 177516673 2 * T
chr9 5069837 5069838 2 * A
chr10 87970403 87970404 2 * T
chr11 32396399 32396400 2 * C
chr11 64805130 64805131 2 * A
chr11 64810148 64810149 2 * C
chr17 7676301 7676302 2 * T
kable(var_df[var_df$POS %in% start(hg5x) & var_df$CHROM %in% seqnames(hg5x),])
CHROM POS ID REF ALT QUAL FILTER INFO FORMAT Sample1 sample id VAF on_target
127 chr5 177516672 NA C T NA NA AC=2;AF=0.0104712041885 GT:AC:AF:NC 0:2:0.0104712041885:C=189,T=2, Human1pR1 chr5_177516672 0.0104712 TRUE
231 chr10 87970403 NA C T NA NA AC=2;AF=0.00393700787402 GT:AC:AF:NC 0:2:0.00393700787402:C=506,T=2, Human1pR1 chr10_87970403 0.0039370 TRUE
260 chr11 32396399 NA T C NA NA AC=4;AF=0.0121951219512 GT:AC:AF:NC 0:4:0.0121951219512:C=4,T=324, Human1pR1 chr11_32396399 0.0121951 TRUE
517 chr3 128486108 NA C T NA NA AC=3;AF=0.0260869565217 GT:AC:AF:NC 0:3:0.0260869565217:C=112,T=3, Human1pR2 chr3_128486108 0.0260870 TRUE
732 chr11 32396399 NA T C NA NA AC=3;AF=0.0125 GT:AC:AF:NC 0:3:0.0125:C=3,T=237, Human1pR2 chr11_32396399 0.0125000 TRUE

sessionInfo()
R version 4.3.0 (2023-04-21)
Platform: x86_64-pc-linux-gnu (64-bit)
Running under: CentOS Linux 7 (Core)

Matrix products: default
BLAS:   /stornext/System/data/apps/R/R-4.3.0/lib64/R/lib/libRblas.so 
LAPACK: /stornext/System/data/apps/R/R-4.3.0/lib64/R/lib/libRlapack.so;  LAPACK version 3.11.0

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       

time zone: Australia/Melbourne
tzcode source: system (glibc)

attached base packages:
[1] parallel  stats4    stats     graphics  grDevices utils     datasets 
[8] methods   base     

other attached packages:
 [1] knitr_1.43           R.utils_2.12.2       R.oo_1.25.0         
 [4] R.methodsS3_1.8.2    vcfR_1.14.0          UpSetR_1.4.0        
 [7] RColorBrewer_1.1-3   patchwork_1.1.2      readxl_1.4.3        
[10] seqinr_4.2-30        Rsamtools_2.16.0     Biostrings_2.68.1   
[13] XVector_0.40.0       GenomicRanges_1.52.0 GenomeInfoDb_1.36.1 
[16] IRanges_2.34.1       S4Vectors_0.38.1     BiocGenerics_0.46.0 
[19] stringr_1.5.0        tibble_3.2.1         here_1.0.1          
[22] dplyr_1.1.2          data.table_1.14.8    ggplot2_3.4.2       
[25] workflowr_1.7.0     

loaded via a namespace (and not attached):
 [1] ade4_1.7-22             tidyselect_1.2.0        viridisLite_0.4.2      
 [4] farver_2.1.1            bitops_1.0-7            fastmap_1.1.1          
 [7] RCurl_1.98-1.12         promises_1.2.0.1        digest_0.6.33          
[10] lifecycle_1.0.3         cluster_2.1.4           processx_3.8.2         
[13] magrittr_2.0.3          compiler_4.3.0          rlang_1.1.1            
[16] sass_0.4.7              tools_4.3.0             utf8_1.2.3             
[19] yaml_2.3.7              labeling_0.4.2          plyr_1.8.8             
[22] BiocParallel_1.34.2     memuse_4.2-3            withr_2.5.0            
[25] grid_4.3.0              fansi_1.0.4             git2r_0.32.0           
[28] colorspace_2.1-0        scales_1.2.1            MASS_7.3-58.4          
[31] cli_3.6.1               rmarkdown_2.23          vegan_2.6-4            
[34] crayon_1.5.2            generics_0.1.3          rstudioapi_0.15.0      
[37] httr_1.4.6              ape_5.7-1               cachem_1.0.8           
[40] zlibbioc_1.46.0         splines_4.3.0           cellranger_1.1.0       
[43] vctrs_0.6.3             Matrix_1.5-4            jsonlite_1.8.7         
[46] callr_3.7.3             jquerylib_0.1.4         glue_1.6.2             
[49] codetools_0.2-19        ps_1.7.5                stringi_1.7.12         
[52] gtable_0.3.3            later_1.3.1             munsell_0.5.0          
[55] pillar_1.9.0            htmltools_0.5.5         GenomeInfoDbData_1.2.10
[58] R6_2.5.1                pinfsc50_1.2.0          rprojroot_2.0.3        
[61] evaluate_0.21           lattice_0.21-8          highr_0.10             
[64] httpuv_1.6.11           bslib_0.5.0             Rcpp_1.0.11            
[67] gridExtra_2.3           nlme_3.1-162            permute_0.9-7          
[70] mgcv_1.8-42             whisker_0.4.1           xfun_0.39              
[73] fs_1.6.3                getPass_0.2-2           pkgconfig_2.0.3