X-Git-Url: https://git.donarmstrong.com/?a=blobdiff_plain;f=bcftools%2Fvcfout.c;h=dfcb25a4c0a40cadda0cadf1c702545e0aa1a01b;hb=94027d8bf194b5e62b98d8a2b240a3ab1c439b46;hp=989e831aff90dffc3f53eb984e90bfadca949740;hpb=ed5305b1d40c8d34c26221a6a897c8ebb9f4d5c6;p=samtools.git

diff --git a/bcftools/vcfout.c b/bcftools/vcfout.c
index 989e831..dfcb25a 100644
--- a/bcftools/vcfout.c
+++ b/bcftools/vcfout.c
@@ -175,6 +175,7 @@ int bcfview(int argc, char *argv[])
 		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");