Write vcf

R/gen_tibble.R

@@ -378,7 +378,7 @@ gt_write_bigsnp_from_dfs <- function(genotypes, indiv_meta, loci,
 
   map <- tibble(chromosome = loci$chromosome,
                 marker.ID = loci$name,
-                genetic.dist = loci$genetic_dist,
+                genetic.dist = as.double(loci$genetic_dist), ## make sure that genetic.dist is double
                 physical.pos = loci$position,
                 allele1 = loci$allele_alt,
                 allele2 = loci$allele_ref)

R/gt_as_vcf.R

@@ -35,11 +35,12 @@ gt_as_vcf <- function(x, file = NULL, chunk_size = NULL, overwrite = FALSE){
   }
 
   # set up chunks
-  chunks_vec <- c(
-    rep(chunk_size, floor(count_loci(x) / chunk_size)),
-    count_loci(x) %% chunk_size
-  )
-  chunks_vec_index <- c(1,cumsum(chunks_vec))
+  chunks_vec <- rep(chunk_size, floor(count_loci(x) / chunk_size))
+  if (count_loci(x) %% chunk_size != 0){
+    chunks_vec <- c(chunks_vec, count_loci(x) %% chunk_size)
+  }
+  chunks_vec_index <- c(0,cumsum(chunks_vec))
+
 
   # generate the header
   vcf_header <- c("##fileformat=VCFv4.3",
@@ -68,13 +69,13 @@ gt_as_vcf <- function(x, file = NULL, chunk_size = NULL, overwrite = FALSE){
   for (chunk_i in seq_along(chunks_vec)) {
     genotypes_matrix <- t(show_genotypes(x,
                                          loci_indices =
-                                           chunks_vec_index[chunk_i]:chunks_vec_index[chunk_i+1]))
+                                           (chunks_vec_index[chunk_i]+1):chunks_vec_index[chunk_i+1]))
     genotypes_matrix[genotypes_matrix==0] <- "0/0"
     genotypes_matrix[genotypes_matrix==1] <- "0/1"
     genotypes_matrix[genotypes_matrix==2] <- "1/1"
     genotypes_matrix[is.na(genotypes_matrix)] <- "./."
     # subset loci to this chunk
-    loci_sub <- show_loci(x)[chunks_vec_index[chunk_i]:chunks_vec_index[chunk_i+1],]
+    loci_sub <- show_loci(x)[(chunks_vec_index[chunk_i]+1):chunks_vec_index[chunk_i+1],]
     # add the other columns needed for the
     loci_cols <- c("chromosome", "position", "name", "allele_ref", "allele_alt")
     loci_sub <- loci_sub %>% select(any_of(loci_cols)) %>%

data-raw/ideas/allele_sharing.R

@@ -15,7 +15,7 @@ test_indiv_meta <- data.frame (id=c("a","b","c"),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=paste0("chr",c(1,1,1,1,2,2)),
                         position=as.integer(c(3,5,65,343,23,456)),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))
 

data-raw/ideas/fst_gt_compare_to_hier.R

@@ -10,7 +10,7 @@ test_indiv_meta <- data.frame (id=c("a","b","c","d","e","f","g"),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=paste0("chr",c(1,1,1,1,2,2)),
                         position=as.integer(c(3,5,65,343,23,456)),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))
 

data-raw/ideas/fst_hier.R

@@ -12,7 +12,7 @@ test_indiv_meta <- data.frame (id=c("a","b","c","d","e","f","g"),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=paste0("chr",c(1,1,1,1,2,2)),
                         position=as.integer(c(3,5,65,343,23,456)),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))
 

data-raw/ideas/fst_wc.R

@@ -10,7 +10,7 @@ test_indiv_meta <- data.frame (id=c("a","b","c","d","e","f","g"),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=paste0("chr",c(1,1,1,1,2,2)),
                         position=as.integer(c(3,5,65,343,23,456)),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))
 

data-raw/ideas/fst_wc2.R

@@ -10,7 +10,7 @@ test_indiv_meta <- data.frame (id=c("a","b","c","d","e","f","g"),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=paste0("chr",c(1,1,1,1,2,2)),
                         position=as.integer(c(3,5,65,343,23,456)),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))
 

data-raw/worked_comparisons/compare_fst.Rmd

@@ -25,7 +25,7 @@ test_indiv_meta <- data.frame (id=c("a","b","c","d","e","f","g"),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=paste0("chr",c(1,1,1,1,2,2)),
                         position=as.integer(c(3,5,65,343,23,456)),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))
 

tests/testthat/test_gen_tibble.R

@@ -7,7 +7,7 @@ test_genotypes <- rbind(c(1,1,0,1,1,0),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=paste0("chr",c(1,1,1,1,2,2)),
                         position=as.integer(c(3,5,65,343,23,456)),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))
 
@@ -112,7 +112,7 @@ test_that("gen_tibble loci is dataframe or tbl",{
   test_loci <- data.frame(name=paste0("rs",1:6),
                           chromosome=paste0("chr",c(1,1,1,1,2,2)),
                           position=as.integer(c(3,5,65,343,23,456)),
-                          genetic_dist = as.integer(rep(0,6)),
+                          genetic_dist = as.double(rep(0,6)),
                           allele_ref = c("A","T","C","G","C","T"),
                           allele_alt = c("T","C", NA,"C","G","A"))
   wrong_loci_matrix <- as.matrix(test_loci)
@@ -150,7 +150,7 @@ test_that("gen_tibble identifies wrong loci table columns",{
   wrong_loci <- data.frame(a=paste0("rs",1:6),
                           b=paste0("chr",c(1,1,1,1,2,2)),
                           c=as.integer(c(3,5,65,343,23,456)),
-                          d = as.integer(rep(0,6)),
+                          d = as.double(rep(0,6)),
                           e = c("A","T","C","G","C","T"),
                           f = c("T","C", NA,"C","G","A"))
   expect_error(test_dfs_gt <- gen_tibble(test_genotypes, indiv_meta = test_indiv_meta,
@@ -437,7 +437,7 @@ test_genotypes <- rbind(c(1,1,0,1,1,0),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=paste0("chr",c(1,1,1,1,2,2)),
                         position=as.integer(c(3,5,65,343,23,456)),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))
 
@@ -492,7 +492,7 @@ test_that("chr_int is always an integer",{
   test_loci_fac <- data.frame(name=paste0("rs",1:6),
                           chromosome=as.factor(paste0("chr",c(1,1,1,1,2,2))),
                           position=as.integer(c(3,5,65,343,23,456)),
-                          genetic_dist = as.integer(rep(0,6)),
+                          genetic_dist = as.double(rep(0,6)),
                           allele_ref = c("A","T","C","G","C","T"),
                           allele_alt = c("T","C", NA,"C","G","A"))
   test_gt <- gen_tibble(x = test_genotypes, loci = test_loci_fac, indiv_meta = test_indiv_meta, quiet = TRUE)
@@ -531,7 +531,7 @@ test_genotypes <- rbind(c(1,1,0,1,1,0),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=paste0("chr",c(1,1,1,1,2,2)),
                         position=as.integer(c(3,5,65,343,23,456)),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))
 
@@ -590,7 +590,7 @@ test_that("additional vcf tests with larger file",{
 #   test_loci <- data.frame(name=paste0("rs",1:6),
 #                           chromosome=paste0("chr",c(1,1,1,1,2,2)),
 #                           position=as.integer(c(3,5,65,343,23,456)),
-#                           genetic_dist = as.integer(rep(0,6)),
+#                           genetic_dist = as.double(rep(0,6)),
 #                           allele_ref = c("A","T","C","G","C","T"),
 #                           allele_alt = c("T","C", NA,"C","G","A"))
 #   test_loci_wrong <- test_loci

tests/testthat/test_gen_tibble_save_load.R

@@ -7,7 +7,7 @@ test_genotypes <- rbind(c(1,1,0,1,1,0),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=paste0("chr",c(1,1,1,1,2,2)),
                         position=as.integer(c(3,5,65,343,23,456)),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))
 

tests/testthat/test_group_by.R

@@ -7,7 +7,7 @@ test_genotypes <- rbind(c(1,1,0,1,1,0),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=paste0("chr",c(1,1,1,1,2,2)),
                         position=as.integer(c(3,5,65,343,23,456)),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))
 

tests/testthat/test_gt_as_.R

@@ -11,7 +11,7 @@ test_that("show_loci gets and sets information",{
   test_loci <- data.frame(name=paste0("rs",1:6),
                           chromosome=paste0("chr",c(1,1,1,1,2,2)),
                           position=as.integer(c(3,5,65,343,23,456)),
-                          genetic_dist = as.integer(rep(0,6)),
+                          genetic_dist = as.double(rep(0,6)),
                           allele_ref = c("A","T","C","G","C","T"),
                           allele_alt = c("T","C", NA,"C","G","A"))
 

tests/testthat/test_gt_as_plink.R

@@ -7,7 +7,7 @@ test_genotypes <- rbind(c(1,1,0,1,1,0),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=paste0("chr",c(1,1,1,1,2,2)),
                         position=as.integer(c(3,5,65,343,23,456)),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))
 

tests/testthat/test_gt_as_vcf.R

@@ -8,7 +8,7 @@ test_genotypes <- rbind(c(1,1,0,1,1,0),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=paste0("chr",c(1,1,1,1,2,2)),
                         position=as.integer(c(3,5,65,343,23,456)),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))
 
@@ -43,3 +43,46 @@ test_that("test reading and writing is equivalent",{
   expect_true(identical(show_genotypes(pop_a_vcf), show_genotypes(pop_a_vcf_rewrite)))
   expect_true(identical(show_loci(pop_a_vcf), show_loci(pop_a_vcf_rewrite)))
 })
+
+
+test_that("test reading and writing with chunking is equivalent cpp",{
+  # write out to vcf with chunk size - smaller chunk size = more duplicates
+  vcf_path_chunked <- gt_as_vcf(test_gt, file = paste0(tempfile(),".vcf"), chunk_size = 2)
+  # read vcf back in with cpp
+  test_gt_chunked <- gen_tibble(vcf_path_chunked, quiet=TRUE, parser = "cpp", backingfile = tempfile("anolis_chunk_"))
+  # check they are the same
+  expect_true(identical(show_genotypes(test_gt), show_genotypes(test_gt_chunked)))
+  expect_true(identical(show_loci(test_gt), show_loci(test_gt_chunked)))
+  expect_equal(count_loci(test_gt_chunked), count_loci(test_gt))
+
+  # now do the same with chunk size that is not an exact divisor of the number of loci
+  vcf_path_chunked <- gt_as_vcf(test_gt, file = paste0(tempfile(),".vcf"), chunk_size = 4)
+  # read vcf back in with cpp
+  test_gt_chunked <- gen_tibble(vcf_path_chunked, quiet=TRUE, parser = "cpp", backingfile = tempfile("anolis_chunk_"))
+  # check they are the same
+  expect_true(identical(show_genotypes(test_gt), show_genotypes(test_gt_chunked)))
+  expect_true(identical(show_loci(test_gt), show_loci(test_gt_chunked)))
+  expect_equal(count_loci(test_gt_chunked), count_loci(test_gt))
+
+
+})
+
+
+test_that("test reading and writing with chunking is equivalent rvcf",{
+  # write out to vcf with chunk size
+  vcf_path_chunked <- gt_as_vcf(test_gt, file = paste0(tempfile(),".vcf"), chunk_size = 2)
+  # read vcf back in with vcfR
+  test_gt_chunked <- gen_tibble(vcf_path_chunked, quiet=TRUE, parser = "vcfR", backingfile = tempfile("anolis_chunk_"))
+  # check they are the same
+  expect_true(identical(show_genotypes(test_gt), show_genotypes(test_gt_chunked)))
+  expect_true(identical(show_loci(test_gt), show_loci(test_gt_chunked)))
+  expect_equal(count_loci(test_gt_chunked), count_loci(test_gt))
+})
+
+
+
+
+
+
+
+

tests/testthat/test_gt_extract_f2.R

@@ -10,7 +10,7 @@ test_indiv_meta <- data.frame (id=c("a","b","c","d","e","f","g"),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=paste0("chr",c(1,1,1,1,2,2)),
                         position=as.integer(c(3,5,65,343,23,456)),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))
 

tests/testthat/test_indiv_het_obs.R

@@ -7,7 +7,7 @@ test_that("indiv_het_obs computes correctly",{
   test_loci <- data.frame(name=paste0("rs",1:6),
                           chromosome=c(1,1,1,1,2,2),
                           position=c(3,5,65,343,23,456),
-                          genetic_dist = as.integer(rep(0,6)),
+                          genetic_dist = as.double(rep(0,6)),
                           allele_ref = c("A","T","C","G","C","T"),
                           allele_alt = c("T","C", NA,"C","G","A"))
 
@@ -33,7 +33,7 @@ test_that("indiv_het_obs returns 0's when all genotypes are homozygous", {
   test_loci <- data.frame(name=paste0("rs",1:6),
                           chromosome=c(1,1,1,1,2,2),
                           position=c(3,5,65,343,23,456),
-                          genetic_dist = as.integer(rep(0,6)),
+                          genetic_dist = as.double(rep(0,6)),
                           allele_ref = c("A","T","C","G","C","T"),
                           allele_alt = c("T","C", NA,"C","G","A"))
 

tests/testthat/test_indiv_missingness.R

@@ -6,7 +6,7 @@ test_genotypes <- rbind(c(1,1,0,1,1,2),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=c(1,1,1,1,2,2),
                         position=c(3,5,65,343,23,456),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))
 

tests/testthat/test_loci_freq.R

@@ -7,7 +7,7 @@ test_that("loci_alt_freq and loci_maf computes correctly",{
   test_loci <- data.frame(name=paste0("rs",1:6),
                           chromosome=c(1,1,1,1,2,2),
                           position=c(3,5,65,343,23,456),
-                          genetic_dist = as.integer(rep(0,6)),
+                          genetic_dist = as.double(rep(0,6)),
                           allele_ref = c("A","T","C","G","C","T"),
                           allele_alt = c("T","C", NA,"C","G","A"))
   test_gt <- gen_tibble(x = test_genotypes, loci = test_loci, indiv_meta = test_indiv_meta, quiet = TRUE)
@@ -77,7 +77,7 @@ test_that("loci_alt_freq and loci_maf on grouped tibbles",{
   test_loci <- data.frame(name=paste0("rs",1:6),
                           chromosome=paste0("chr",c(1,1,1,1,2,2)),
                           position=as.integer(c(3,5,65,343,23,456)),
-                          genetic_dist = as.integer(rep(0,6)),
+                          genetic_dist = as.double(rep(0,6)),
                           allele_ref = c("A","T","C","G","C","T"),
                           allele_alt = c("T","C", NA,"C","G","A"))
 

tests/testthat/test_loci_ld_clump.R

@@ -6,7 +6,7 @@ test_genotypes <- rbind(c(2,2,0,1,1,2),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=c(1,1,1,1,2,2),
                         position=c(3,5,65,343,23,456),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))
 
@@ -99,7 +99,7 @@ test_that("loci order",{
   test_loci <- data.frame(name=paste0("rs",1:6),
                           chromosome=c("chr2","chr1","chr1","chr1","chr2","chr1"),
                           position=c(3,5,65,343,23,456),
-                          genetic_dist = as.integer(rep(0,6)),
+                          genetic_dist = as.double(rep(0,6)),
                           allele_ref = c("A","T","C","G","C","T"),
                           allele_alt = c("T","C", NA,"C","G","A"))
 

tests/testthat/test_loci_missingness.R

@@ -7,7 +7,7 @@ test_that("loci_missingness",{
   test_loci <- data.frame(name=paste0("rs",1:6),
                           chromosome=c(1,1,1,1,2,2),
                           position=c(3,5,65,343,23,456),
-                          genetic_dist = as.integer(rep(0,6)),
+                          genetic_dist = as.double(rep(0,6)),
                           allele_ref = c("A","T","C","G","C","T"),
                           allele_alt = c("T","C", NA,"C","G","A"))
 
@@ -48,7 +48,7 @@ test_that("loci_missingness on grouped tibble",{
   test_loci <- data.frame(name=paste0("rs",1:6),
                           chromosome=paste0("chr",c(1,1,1,1,2,2)),
                           position=as.integer(c(3,5,65,343,23,456)),
-                          genetic_dist = as.integer(rep(0,6)),
+                          genetic_dist = as.double(rep(0,6)),
                           allele_ref = c("A","T","C","G","C","T"),
                           allele_alt = c("T","C", NA,"C","G","A"))
 

tests/testthat/test_loci_transversions_transitions.R

@@ -7,7 +7,7 @@ test_that("find transitions and transversions",{
   test_loci <- data.frame(name=paste0("rs",1:6),
                           chromosome=c(1,1,1,1,2,2),
                           position=c(3,5,65,343,23,456),
-                          genetic_dist = as.integer(rep(0,6)),
+                          genetic_dist = as.double(rep(0,6)),
                           allele_ref = c("A","T","C","G","C","T"),
                           allele_alt = c("T","C", NA,"C","G","A"))
 
@@ -26,7 +26,7 @@ test_that("check warning message for different alleles",{
   test_loci <- data.frame(name=paste0("rs",1:6),
                           chromosome=c(1,1,1,1,2,2),
                           position=c(3,5,65,343,23,456),
-                          genetic_dist = as.integer(rep(0,6)),
+                          genetic_dist = as.double(rep(0,6)),
                           allele_ref = c("a","t","c","g","c","t"),
                           allele_alt = c("t","c", NA,"c","g","a"))
 

tests/testthat/test_pairwise_allele_sharing.R

@@ -6,7 +6,7 @@ test_indiv_meta <- data.frame (id=c("a","b","c"),
 test_loci <- data.frame(name=paste0("rs",1:6),
                         chromosome=paste0("chr",c(1,1,1,1,2,2)),
                         position=as.integer(c(3,5,65,343,23,456)),
-                        genetic_dist = as.integer(rep(0,6)),
+                        genetic_dist = as.double(rep(0,6)),
                         allele_ref = c("A","T","C","G","C","T"),
                         allele_alt = c("T","C", NA,"C","G","A"))