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bcf_sr_sort.h
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bcf_sr_sort.h
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/*
Copyright (C) 2017-2019,2024 Genome Research Ltd.
Author: Petr Danecek <[email protected]>
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.
*/
/*
Reorder duplicate lines so that compatible variant types are
returned together by bcf_sr_next_line()
- readers grouped by variants. Even with many readers there will be
typically only several groups
*/
#ifndef BCF_SR_SORT_H
#define BCF_SR_SORT_H
#include "htslib/synced_bcf_reader.h"
#include "htslib/kbitset.h"
typedef struct
{
int nrec, mrec;
bcf1_t **rec;
}
vcf_buf_t;
typedef struct
{
char *str; // "A>C" for biallelic records or "A>C,A>CC" for multiallelic records
int type; // VCF_SNP, VCF_REF, etc.
int nalt; // number of alternate alleles in this record
int nvcf, mvcf, *vcf; // the list of readers with the same variants
bcf1_t **rec; // list of VCF records in the readers
kbitset_t *mask; // which groups contain the variant
}
var_t;
// Group is a set of variants in duplicate records within one VCF. They are identified with a key (used only
// for debugging), such as C>A,C>G;C>T. Commas separate alleles in a multiallelic record, semicolons separate
// VCF lines.
typedef struct
{
char *key; // only for debugging
int nvar, mvar, *var; // the variants and their type
int nvcf; // number of readers with the same variants
}
grp_t;
typedef struct
{
int nvar, mvar, *var; // list of compatible variants that can be output together
int cnt; // number of readers in this group
kbitset_t *mask; // which groups are populated in this set
}
varset_t;
typedef struct
{
uint8_t score[256];
int nvar, mvar;
var_t *var; // list of all variants from all readers
int nvset, mvset;
int mpmat, *pmat; // pairing matrix, i-th vset and j-th group accessible as i*ngrp+j
int ngrp, mgrp;
int mcnt, *cnt; // number of VCF covered by a varset
grp_t *grp; // list of VCF representatives, each with a unique combination of duplicate lines
varset_t *vset; // list of variant sets - combinations of compatible variants across multiple groups ready for output
vcf_buf_t *vcf_buf; // records sorted in output order, for each VCF
bcf_srs_t *sr;
void *grp_str2int;
void *var_str2int;
kstring_t str;
int moff, noff, *off, mcharp;
char **charp;
const char *chr;
hts_pos_t pos;
int nsr, msr;
int pair;
int nactive, mactive, *active; // list of readers with lines at the current pos
}
sr_sort_t;
sr_sort_t *bcf_sr_sort_init(sr_sort_t *srt);
void bcf_sr_sort_reset(sr_sort_t *srt);
int bcf_sr_sort_next(bcf_srs_t *readers, sr_sort_t *srt, const char *chr, hts_pos_t pos);
// initialize a new position using the i-th reader
int bcf_sr_sort_set_active(sr_sort_t *srt, int i);
// add i-th reader with the same position, assumed bcf_sr_sort_set_active() was called with another reader
int bcf_sr_sort_add_active(sr_sort_t *srt, int i);
void bcf_sr_sort_destroy(sr_sort_t *srt);
void bcf_sr_sort_remove_reader(bcf_srs_t *readers, sr_sort_t *srt, int i);
#endif