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Consensus/variant calling options:

       -c        SNP calling (force -e)
       -d FLOAT  skip loci where less than FLOAT fraction of samples covered [0]
       -e        likelihood based analyses
       -g        call genotypes at variant sites (force -c)
       -i FLOAT  indel-to-substitution ratio [-1]
       -I        skip indels
       -m FLOAT  alternative model for multiallelic and rare-variant calling, include if P(chi^2)>=FLOAT
       -p FLOAT  variant if P(ref|D)<FLOAT [0.5]
       -P STR    type of prior: full, cond2, flat [full]
       -t FLOAT  scaled substitution mutation rate [0.001]
       -T STR    constrained calling; STR can be: pair, trioauto, trioxd and trioxs (see manual) [null]
       -v        output potential variant sites only (force -c)