--allele_frequency_bins --af_bins | | Allele frequency bins, a list of bin values (0.1,0.5,1).
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--allele_frequency_bins_file --af_bins_file | | Same as allele_frequency_bins, but in a file.
Format of file is one value per line.
e.g.
0.1
0.5
1
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--allele_frequency_tag --af_tag | | Allele frequency tag to use, by default estimated from AN,AC or GT.
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--first_allele_only --first_only | | Include only 1st allele at multiallelic sites.
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| | Treat as identical records with <snps|indels|both|all|some|none>.
See https://samtools.github.io/bcftools/bcftools.html#common_options for details.
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| | Depth distribution: min,max,bin size.
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| | Exclude sites for which the expression is true.
See https://samtools.github.io/bcftools/bcftools.html#expressions for details.
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| | tab-delimited file with exons for indel frameshifts statistics.
The columns of the file are CHR, FROM, TO, with 1-based, inclusive, positions.
The file is BGZF-compressed and indexed with tabix (e.g. tabix -s1 -b2 -e3 file.gz).
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| | Require at least one of the listed FILTER strings (e.g. "PASS,.").
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| | Faidx indexed reference sequence file to determine INDEL context.
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| | Select sites for which the expression is true.
See https://samtools.github.io/bcftools/bcftools.html#expressions for details.
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| | Collect stats for sites with ID separately (known vs novel).
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| | Restrict to comma-separated list of regions.
Following formats are supported: chr|chr:pos|chr:beg-end|chr:beg-[,…​].
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| | Restrict to regions listed in a file.
Regions can be specified either on a VCF, BED, or tab-delimited file (the default).
For more information check manual.
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| | This option controls how overlapping records are determined:
set to 'pos' or '0' if the VCF record has to have POS inside a region (this corresponds to the default behavior of -t/-T);
set to 'record' or '1' if also overlapping records with POS outside a region should be included (this is the default behavior of -r/-R,
and includes indels with POS at the end of a region, which are technically outside the region);
or set to 'variant' or '2' to include only true overlapping variation (compare the full VCF representation "TA>T-" vs the true sequence variation "A>-").
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| | List of samples for sample stats, "-" to include all samples.
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| | File of samples to include.
e.g.
sample1 1
sample2 2
sample3 2
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| | Similar as -r, --regions, but the next position is accessed by streaming the whole VCF/BCF
rather than using the tbi/csi index. Both -r and -t options can be applied simultaneously: -r uses the
index to jump to a region and -t discards positions which are not in the targets. Unlike -r, targets
can be prefixed with "^" to request logical complement. For example, "^X,Y,MT" indicates that
sequences X, Y and MT should be skipped. Yet another difference between the -t/-T and -r/-R is
that -r/-R checks for proper overlaps and considers both POS and the end position of an indel,
while -t/-T considers the POS coordinate only (by default; see also --regions-overlap and --targets-overlap).
Note that -t cannot be used in combination with -T.
Following formats are supported: chr|chr:pos|chr:beg-end|chr:beg-[,…​].
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| | Similar to --regions_file option but streams rather than index-jumps.
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| | Include if POS in the region (0), record overlaps (1), variant overlaps (2).
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| | Collect Ts/Tv stats for any tag using the given binning [0:1:100].
Format is <TAG[:min:max:n]>.
A subfield can be selected as e.g. 'PV4[0]', here the first value of the PV4 tag.
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| | Produce verbose per-site and per-sample output.
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