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RhAMPseq: Analysis of rhAmpSeq data logo

R build status

Installation

You can install the development version from GitHub with:

# install.packages(c("hexSticker", "remotes")
remotes::install_github("villegar/RhAMPseq")

Data description

Author: J.L.

Files

  • hap_genotype: haplotype genotyping data for all samples. This is in a number code. The number code corresponds to a specific sequenced haplotype at each locus.
  • HaplotypeAllele.fasta: each marker is a conserved region of the genome, so the haplotype allele may differ only by a single SNP, or it could be many SNPS or indels.
  • readCountMatrixFile: number of read for each amplicon and each sample. This data is also provided in the hap_genotype file.

Example

Locus Haplotypes blank__vDNAfen551A01_A01 160_271_303__vDNAfen551A01_A02 160_271_311__vDNAfen551A01_A03
rh_chr1_10143990 2(0.37);4(0.16);9(0.10);5(0.09);1(0.07);3(0.07);8(0.05);13(0.04);6(0.03);7(0.03); ./.:0 4/2:34,24 2/2:71

where:

  • Locus is the marker.

  • Haplotypes lists the frequency of haplotypes at this Locus in the ENTIRE dataset, not just our samples. You can mostly ignore this.

  • Next column starts with blank, this is a blank control well in the plate. Here at this Locus it sequenced as ./., which means NULL. and :0 which is the read depth.

  • Next column is sample 303 from our mapping family, its on the fen551 plate. Here you see we detect 4/2 and 34, 24 for haplotype 4 with 34 reads, and 2 with 24 reads. This locus is heterozygous.

  • Next column is sample 311 from our mapping family. Here you see we only detect haplotype 2 at 71 reads. This is homozygous.

So, if we wanted to know the DNA sequence of this marker, we would look up haplotypes 4 and 2 from the HaplotypeAllele.fasta file.

One other thing to note that is very important. the marker name, rh_ch1_10143990 stands for rhampseq, chromosome 1, position 10143990. This position information does not indicate the position of the polymorphism detected at this marker, it is the position of the primer sequence. So when we map these markers, they will be very near, but not exactly at, these positions.

Initial analysis

Raw data

Load raw data from the 3 files previously described.

raw <- load_data(fasta = "data/HaplotypeAllele.fasta", 
                 hap_geno = "data/hap_genotype",
                 count_mat = "data/readCountMatrixFile")

Haplotypes

# Load haplotypes for mapping family
mapping_family <- read_excel_col("data/Rhampseq_populations.xlsx", "A")
mapping_family_short <- unlist(lapply(mapping_family, 
                                      function(x) gsub("__.*", "", x)))
mapping_family_short <- unique(mapping_family_short)

## Extract genotypes from the hap_genotype file
hap_geno_names <- names(raw$hap_geno)
hap_geno_names_blank <- hap_geno_names[grepl("*blank*", hap_geno_names)]
## Drop "blank" genotypes
# hap_geno_names <- hap_geno_names[!grepl("*blank*", hap_geno_names)]
## Trim 'X' from genotypes [added when importing the data]
hap_geno_names <- gsub("X*", "", hap_geno_names)
## Further trimming of genotypes: 160_271_001__vDNAlon499A03_A01 -> 160_271_001
hap_geno_names <- unlist(lapply(hap_geno_names, 
                                function(x) gsub("__.*", "", x)))

## Lookup for mapping_family genotypes
hap_geno_names_idx <- hap_geno_names %in% mapping_family_short
## Extract matching genotypes
hap_geno_names_sub <- hap_geno_names[hap_geno_names_idx]
hap_geno_sub <- raw$hap_geno[hap_geno_names_idx]

## Extract locus data
locus <- raw$hap_geno$Locus

# Start parallel backend
tictoc::tic("Parallel") # ~12.719 sec (2 CPUs); ~7.923 sec (4 CPUs)
cores <- parallel::detectCores() - 1
cpus <- ifelse(cores > 2, 2, 1)
cl <- parallel::makeCluster(cpus, setup_strategy = "sequential")
doParallel::registerDoParallel(cl)

# Load binary operator for backend
`%dopar%` <- foreach::`%dopar%`
map <- foreach::foreach(i = 1:length(hap_geno_sub), 
                        .combine = cbind) %dopar% {
                          unlist(lapply(hap_geno_sub[, i], get_geno))
                        }
parallel::stopCluster(cl) # Stop cluster
tictoc::toc()
colnames(map) <- names(hap_geno_sub)
rownames(map) <- locus
# map <- cbind(Locus = locus, map)
map_t <- t(map)
colnames(map_t) <- col(map)
rownames(map_t) <- gsub("X*", "", rownames(map_t))
write.csv(map_t, "data/pseudomap.csv")
# map_t[1:5,1:5]

Pseudo-genetic map sample (map_t)

X rhMAS_5GT_cons95 rhMAS_SDI_p2_AG11_chr18_30Mb rhMAS_SDI_p3_AGL11 rhMAS_SDI_p4_AGL11 rhMAS_5GT_700
160_271_303__vDNAfen551A01_A02 NP NP NP NP NN
160_271_311__vDNAfen551A01_A03 NN NN NP NP NN
160_271_319__vDNAfen551A01_A04 NP NP NN NN NN
160_271_327__vDNAfen551A01_A05 NP NP NP NP NN
160_271_335__vDNAfen551A01_A06 NP NP NP NP NN

Other stuff

  • Extract marker names and drop their “repeat ID”, #X. e.g. rhMAS_5GT_cons95#1 -> rhMAS_5GT_cons95
marker_names <- names(raw$fasta)
marker_names_no_repeats <- lapply(marker_names, function(x) gsub("#.*", "", x))

length(marker_names_no_repeats) # 984030
length(unique(marker_names_no_repeats)) # 2055
  • Something that might not make sense …
sum_stats <- list() #data.frame(marker = NA, non_zero = NA)
for (loc in raw$hap_geno$Locus) {
  # repeats_idx <- which(marker_names_no_repeats == loc)
  # repeats <- raw$fasta[repeats_idx]
  # repeats_seq <- lapply(repeats, get_seq)
  
  count_mat_idx <- which(loc == names(raw$count_mat))
  count_mat_sub <- raw$count_mat[count_mat_idx]
  sum_stats[[loc]] <- list(idx = which(count_mat_sub > 0), count = length(unlist(count_mat_sub)))
  #sum_stats <- rbind(sum_stats, c(loc, length(which(count_mat_sub > 0))))
}
# sum_stats[1, ] <- NULL