/usr/include/htslib/vcfutils.h is in libhts-dev 1.2.1-2ubuntu1.
This file is owned by root:root, with mode 0o644.
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1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 | /* vcfutils.h -- allele-related utility functions.
Copyright (C) 2012, 2013 Genome Research Ltd.
Author: Petr Danecek <pd3@sanger.ac.uk>
Permission is hereby granted, free of charge, to any person obtaining a copy
of this software and associated documentation files (the "Software"), to deal
in the Software without restriction, including without limitation the rights
to use, copy, modify, merge, publish, distribute, sublicense, and/or sell
copies of the Software, and to permit persons to whom the Software is
furnished to do so, subject to the following conditions:
The above copyright notice and this permission notice shall be included in
all copies or substantial portions of the Software.
THE SOFTWARE IS PROVIDED "AS IS", WITHOUT WARRANTY OF ANY KIND, EXPRESS OR
IMPLIED, INCLUDING BUT NOT LIMITED TO THE WARRANTIES OF MERCHANTABILITY,
FITNESS FOR A PARTICULAR PURPOSE AND NONINFRINGEMENT. IN NO EVENT SHALL
THE AUTHORS OR COPYRIGHT HOLDERS BE LIABLE FOR ANY CLAIM, DAMAGES OR OTHER
LIABILITY, WHETHER IN AN ACTION OF CONTRACT, TORT OR OTHERWISE, ARISING
FROM, OUT OF OR IN CONNECTION WITH THE SOFTWARE OR THE USE OR OTHER
DEALINGS IN THE SOFTWARE. */
#ifndef HTSLIB_VCFUTILS_H
#define HTSLIB_VCFUTILS_H
#include "vcf.h"
/**
* bcf_trim_alleles() - remove ALT alleles unused in genotype fields
* @header: for access to BCF_DT_ID dictionary
* @line: VCF line obtain from vcf_parse1
*
* Returns the number of removed alleles on success or negative
* on error:
* -1 .. some allele index is out of bounds
*/
int bcf_trim_alleles(const bcf_hdr_t *header, bcf1_t *line);
/**
* bcf_remove_alleles() - remove ALT alleles according to bitmask @mask
* @header: for access to BCF_DT_ID dictionary
* @line: VCF line obtained from vcf_parse1
* @mask: alleles to remove
*/
void bcf_remove_alleles(const bcf_hdr_t *header, bcf1_t *line, int mask);
/**
* bcf_calc_ac() - calculate the number of REF and ALT alleles
* @header: for access to BCF_DT_ID dictionary
* @line: VCF line obtained from vcf_parse1
* @ac: array of length line->n_allele
* @which: determine if INFO/AN,AC and indv fields be used
*
* Returns 1 if the call succeeded, or 0 if the value could not
* be determined.
*
* The value of @which determines if existing INFO/AC,AN can be
* used (BCF_UN_INFO) and and if indv fields can be splitted
* (BCF_UN_FMT).
*/
int bcf_calc_ac(const bcf_hdr_t *header, bcf1_t *line, int *ac, int which);
/**
* bcf_gt_type() - determines type of the genotype
* @fmt_ptr: the GT format field as set for example by set_fmt_ptr
* @isample: sample index (starting from 0)
* @ial: index of the 1st non-reference allele (starting from 1)
* @jal: index of the 2nd non-reference allele (starting from 1)
*
* Returns the type of the genotype (one of GT_HOM_RR, GT_HET_RA,
* GT_HOM_AA, GT_HET_AA, GT_HAPL_R, GT_HAPL_A or GT_UNKN). If $ial
* is not NULL and the genotype has one or more non-reference
* alleles, $ial will be set. In case of GT_HET_AA, $ial is the
* position of the allele which appeared first in ALT. If $jal is
* not null and the genotype is GT_HET_AA, $jal will be set and is
* the position of the second allele in ALT.
*/
#define GT_HOM_RR 0 // note: the actual value of GT_* matters, used in dosage r2 calculation
#define GT_HOM_AA 1
#define GT_HET_RA 2
#define GT_HET_AA 3
#define GT_HAPL_R 4
#define GT_HAPL_A 5
#define GT_UNKN 6
int bcf_gt_type(bcf_fmt_t *fmt_ptr, int isample, int *ial, int *jal);
static inline int bcf_acgt2int(char c)
{
if ( (int)c>96 ) c -= 32;
if ( c=='A' ) return 0;
if ( c=='C' ) return 1;
if ( c=='G' ) return 2;
if ( c=='T' ) return 3;
return -1;
}
#define bcf_int2acgt(i) "ACGT"[i]
/**
* bcf_ij2G() - common task: allele indexes to Number=G index (diploid)
* @i,j: allele indexes, 0-based, i<=j
*
* Returns index to the Number=G diploid array
*/
#define bcf_ij2G(i, j) ((j)*((j)+1)/2+(i))
#endif
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