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vcf-isec(1) [debian man page]

VCF-ISEC(1)							   User Commands						       VCF-ISEC(1)

NAME
vcf-isec - create intersections, unions, complements on bgzipped and tabix indexed VCF or tab-delimited files SYNOPSIS
vcf-isec [OPTIONS] file1.vcf file2.vcf ... DESCRIPTION
About: Create intersections, unions, complements on bgzipped and tabix indexed VCF or tab-delimited files. Note that lines from all files can be intermixed together on the output, which can yield unexpected results. OPTIONS
-C, --chromosomes <list|file> Process the given chromosomes (comma-separated list or one chromosome per line in a file). -c, --complement Output positions present in the first file but missing from the other files. -d, --debug Debugging information -f, --force Continue even if the script complains about differing columns. -o, --one-file-only Print only entries from the left-most file. Without -o, all unique positions will be printed. -n, --nfiles [+-=]<int> Output positions present in this many (=), this many or more (+), or this many or fewer (-) files. -p, --prefix <path> If present, multiple files will be created with all possible isec combinations. (Suitable for Venn Diagram analysis.) -t, --tab <chr:pos:file> Tab-delimited file with indexes of chromosome and position columns. (1-based indexes) -w, --win <int> In repetitive sequences, the same indel can be called at different positions. Consider records this far apart as matching (be it a SNP or an indel). -h, -?, --help This help message. EXAMPLES
bgzip file.vcf; tabix -p vcf file.vcf.gz bgzip file.tab; tabix -s 1 -b 2 -e 2 file.tab.gz vcf-isec 0.1.5 July 2011 VCF-ISEC(1)

Check Out this Related Man Page

VCF-COMPARE(1)							   User Commands						    VCF-COMPARE(1)

NAME
vcf-compare - compare bgzipped and tabix indexed VCF files SYNOPSIS
compare-vcf [OPTIONS] file1.vcf file2.vcf ... DESCRIPTION
About: Compare bgzipped and tabix indexed VCF files. (E.g. bgzip file.vcf; tabix -p vcf file.vcf.gz) OPTIONS
-c, --chromosomes <list|file> Same as -r, left for backward compatibility. Please do not use as it will be dropped in the future. -d, --debug Debugging information. Giving the option multiple times increases verbosity -H, --cmp-haplotypes Compare haplotypes, not only positions -m, --name-mapping <list|file> Use with -H when comparing files with differing column names. The argument to this options is a comma-separated list or one mapping per line in a file. The names are colon separated and must appear in the same order as the files on the command line. -R, --refseq <file> Compare the actual sequence, not just positions. Use with -w to compare indels. -r, --regions <list|file> Process the given regions (comma-separated list or one region per line in a file). -s, --samples <list> Process only the listed samples. Excluding unwanted samples may increase performance considerably. -w, --win <int> In repetitive sequences, the same indel can be called at different positions. Consider records this far apart as matching (be it a SNP or an indel). -h, -?, --help This help message. vcf-compare 0.1.5 July 2011 VCF-COMPARE(1)
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