Description Usage Arguments Value
This funtion reads a set of VCF files and creates a table of SNPs with SNP IDs as rows and sample names (one per file) as columns
1 |
subsetByChromosome |
Chromosome number to use for comparison, left NULL if using SNP list |
snps |
List of SNP IDs to use for comparison |
input |
Input Directory Containing annotated VCF files |
Matrix containing SNP calls for all samples
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