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tpoorten · Jul 3, 2014 · b8d247a · b8d247a
1 parent b61f334
commit b8d247a
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diff --git a/vcf_to_genotypeTab.R b/vcf_to_genotypeTab.R
@@ -11,6 +11,7 @@
 #         0 represents homozygous reference allele
 #         1 represents heterozygous
 #         2 represents homozygous alternative allele
+#  	      NA represents missing data
 
 ## set working directory to the path where vcf file is located
 setwd("~/Dropbox/bioinfo/snps/")

diff --git a/vcf_to_genotypeTab.Rscript b/vcf_to_genotypeTab.Rscript
@@ -11,6 +11,7 @@
 #         0 represents homozygous reference allele
 #         1 represents heterozygous
 #         2 represents homozygous alternative allele
+#		  NA represents missing data
 
 ## set working directory to the path where vcf file is located
 # setwd("~/Dropbox/bioinfo/snps/")

diff --git a/vcf_to_genotypeTab_meta.R b/vcf_to_genotypeTab_meta.R
@@ -11,6 +11,7 @@
 #         0 represents homozygous reference allele
 #         1 represents heterozygous
 #         2 represents homozygous alternative allele
+#  	      NA represents missing data
 
 ## set working directory to the path where vcf file is located
 setwd("~/Dropbox/bioinfo/snps/SNP_data_analysis/")

diff --git a/vcf_to_genotypeTab_meta.Rscript b/vcf_to_genotypeTab_meta.Rscript
@@ -15,6 +15,7 @@
 #         0 represents homozygous reference allele
 #         1 represents heterozygous
 #         2 represents homozygous alternative allele
+#		  NA represents missing data
 
 ## set working directory to the path where vcf file is located
 #setwd("~/Dropbox/bioinfo/snps/SNP_data_analysis/")