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Update man page
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doc/bcftools.txt

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@@ -3827,14 +3827,14 @@ when piping!)
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non-missing genotype. Note that the missingness is determined from INFO/AN
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and AC tags when available to avoid parsing sample fields.
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*-v, --types* 'snps'|'indels'|'mnps'|'other'::
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*-v, --types* 'snps'|'indels'|'mnps'|'ref'|'bnd'|'other'|'overlap'::
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comma-separated list of variant types to select. Site is selected if
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any of the ALT alleles is of the type requested. Types are determined
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by comparing the REF and ALT alleles in the VCF record not INFO tags
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like INFO/INDEL or INFO/VT. Use *--include* to select based on INFO
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tags.
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*-V, --exclude-types* 'snps'|'indels'|'mnps'|'ref'|'bnd'|'other'::
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*-V, --exclude-types* 'snps'|'indels'|'mnps'|'ref'|'bnd'|'other'|'overlap'::
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comma-separated list of variant types to exclude. Site is excluded if
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any of the ALT alleles is of the type requested. Types are determined
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by comparing the REF and ALT alleles in the VCF record not INFO tags

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