It generates a VCF file with simulated random variants based on the given probability model.
Usage: vcfy [OPTIONS] REFERENCE
Generate VCF file with simulated variants in specified range [low, high)
for the given region of the reference genome (in FASTA format). In case
that the region is not specified the first region is used. If no range is
provided, it is assumed that the variants are scattered throughout the
region.
For more information, consult with the README file.
Options:
-o, --output FILENAME Write to this file instead of standard output.
-m, --mutation-rate FLOAT Base mutation rate. [required]
-r, --region TEXT Region ID (default=first region in the reference)
-l, --low INTEGER Range lower bound (default=first locus in the
region)
-h, --high INTEGER Range upper bound (default=last locus in the
region)
--help Show this message and exit.
Usage: ksnper [OPTIONS] [VCF]
Report the number of SNPs in all k-mers. Specify the k and the VCF file,
it reports number of SNPS occurred in each k-mer.
Options:
-o, --output FILENAME Write to this file instead of standard
output.
-r, --reference FILENAME Reference genome FASTA file. It will be
inferred from VCF header, if not specified.
-k INTEGER The value of k. [required]
-c Set if the input VCF is compressed
-d, --dialect [unix|excel-tab|excel]
Use this CSV dialect. [default: unix]
--help Show this message and exit.