fprintf(stderr, "\n");
fprintf(stderr, "Usage: bcftools view [options] <in.bcf> [reg]\n\n");
fprintf(stderr, "Options: -c SNP calling\n");
+ fprintf(stderr, " -b output BCF instead of VCF\n");
fprintf(stderr, " -G suppress all individual genotype information\n");
fprintf(stderr, " -L discard the PL genotype field\n");
fprintf(stderr, " -v output potential variant sites only\n");