Simplify multi-nucleotide variants (MNPs) into more basic/primitive alleles.
java -jar GenomeAnalysisTK.jar -T VariantsToAllelicPrimitives -R reference.fasta -V input.vcf -o output.vcf
Argument name(s) | Default value | Summary | |
---|---|---|---|
Required Inputs | |||
--variant  -V | NA | Input VCF file | |
Optional Outputs | |||
--out  -o | stdout | File to which variants should be written |