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
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.