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 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 131 132 133 134 135 136 137 138 139 140 141 142 143 144 145 146 147 148 149 150 151 152 153 154 155 156 157 158 159 160 161 162 163 164 165 166 167 168 169 170 171 172 173 174 175 176 177 178 179 180 181 182 183 184 185 186 187 188 189 190 191 192 193 194 195 196 197 198 199 200 201 202 203 204 205 206 207 208 209 210 211 212 213 214 215 216 217 218 219 220 221 222 223 224 225 226 227 228 229
|
#include "bcftools.pysam.h"
/* gvcf.c -- support for gVCF files.
Copyright (C) 2014-2015 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. */
#include "gvcf.h"
#include "bcftools.h"
struct _gvcf_t
{
int *dp_range, ndp_range; // per-sample DP ranges
int prev_range; // 0 if not in a block
int32_t *dp, mdp, *pl, mpl, npl;
int32_t *tmp, mtmp, *gts, ngts,mgts, nqsum,mqsum;
float *qsum;
int32_t rid, start, end, min_dp;
kstring_t als;
bcf1_t *line;
};
void gvcf_update_header(gvcf_t *gvcf, bcf_hdr_t *hdr)
{
bcf_hdr_append(hdr,"##INFO=<ID=END,Number=1,Type=Integer,Description=\"End position of the variant described in this record\">");
bcf_hdr_append(hdr,"##INFO=<ID=MinDP,Number=1,Type=Integer,Description=\"Minimum per-sample depth in this gVCF block\">");
}
gvcf_t *gvcf_init(const char *dp_ranges)
{
gvcf_t *gvcf = (gvcf_t*) calloc(1,sizeof(gvcf_t));
gvcf->line = bcf_init();
int n = 1;
const char *ss = dp_ranges;
while ( *ss )
{
if ( *ss==',' ) n++;
ss++;
}
gvcf->ndp_range = n;
gvcf->dp_range = (int*) malloc(sizeof(int)*gvcf->ndp_range);
n = 0;
ss = dp_ranges;
while ( *ss )
{
char *se = (char*) ss;
gvcf->dp_range[n++] = strtol(ss,&se,10);
if ( se==ss ) return NULL;
if ( *se==',' && se[1] ) { ss = se+1; continue; }
else if ( !*se ) break;
return NULL;
}
return gvcf;
}
void gvcf_destroy(gvcf_t *gvcf)
{
free(gvcf->dp_range);
free(gvcf->dp);
free(gvcf->pl);
free(gvcf->tmp);
free(gvcf->qsum);
free(gvcf->gts);
free(gvcf->als.s);
if ( gvcf->line ) bcf_destroy(gvcf->line);
free(gvcf);
}
bcf1_t *gvcf_write(gvcf_t *gvcf, htsFile *fh, bcf_hdr_t *hdr, bcf1_t *rec, int is_ref)
{
int i, ret, nsmpl = bcf_hdr_nsamples(hdr);
int can_collapse = is_ref ? 1 : 0;
int32_t dp_range = 0, min_dp = 0;
// No record and nothing to flush?
if ( !rec && !gvcf->prev_range ) return NULL;
// Flush gVCF block if there are no more records, chr changed, a gap
// encountered, or other conditions not met (block broken by a non-ref or DP too low).
int needs_flush = can_collapse ? 0 : 1;
// Can the record be included in a gVCF block? That is, is this a ref-only site?
if ( rec && can_collapse )
{
bcf_unpack(rec, BCF_UN_ALL);
// per-sample depth
ret = bcf_get_format_int32(hdr, rec, "DP", &gvcf->tmp, &gvcf->mtmp);
if ( ret==nsmpl )
{
min_dp = gvcf->tmp[0];
for (i=1; i<nsmpl; i++)
if ( min_dp > gvcf->tmp[i] ) min_dp = gvcf->tmp[i];
for (i=0; i<gvcf->ndp_range; i++)
if ( min_dp < gvcf->dp_range[i] ) break;
dp_range = i;
if ( !dp_range )
{
// leave the record unchanged, DP is too small. Alternatively, return NULL here
// to skip these sites
needs_flush = 1;
can_collapse = 0;
}
}
else
needs_flush = 1; // DP field not present
}
if ( gvcf->prev_range && gvcf->prev_range!=dp_range ) needs_flush = 1;
if ( !rec || gvcf->rid!=rec->rid || rec->pos > gvcf->end+1 ) needs_flush = 1;
// If prev_range is set, something can be flushed
if ( gvcf->prev_range && needs_flush )
{
// mpileup can output two records with the same position, SNP and
// indel. Make sure the end position does not include the non-variant
// SNP position just before the indel.
if ( rec && rec->rid==gvcf->rid && rec->pos==gvcf->end ) gvcf->end--;
gvcf->end++; // from 0-based to 1-based coordinate
bcf_clear1(gvcf->line);
gvcf->line->rid = gvcf->rid;
gvcf->line->pos = gvcf->start;
gvcf->line->rlen = gvcf->end - gvcf->start;
bcf_update_alleles_str(hdr, gvcf->line, gvcf->als.s);
if ( gvcf->start+1 < gvcf->end ) // create gVCF record only if it spans at least two sites
bcf_update_info_int32(hdr, gvcf->line, "END", &gvcf->end, 1);
bcf_update_info_int32(hdr, gvcf->line, "MinDP", &gvcf->min_dp, 1);
if ( gvcf->nqsum>0 )
bcf_update_info_float(hdr, gvcf->line, "QS", gvcf->qsum, gvcf->nqsum);
if ( gvcf->ngts )
bcf_update_genotypes(hdr,gvcf->line,gvcf->gts,gvcf->ngts);
if ( gvcf->npl>0 )
bcf_update_format_int32(hdr, gvcf->line, "PL", gvcf->pl, gvcf->npl);
bcf_update_format_int32(hdr, gvcf->line, "DP", gvcf->dp, nsmpl);
bcf_write1(fh, hdr, gvcf->line);
gvcf->prev_range = 0;
gvcf->rid = -1;
gvcf->npl = 0;
gvcf->nqsum = 0;
gvcf->ngts = 0;
if ( !rec ) return NULL; // just flushing the buffer, this was last record
}
if ( can_collapse )
{
if ( !gvcf->prev_range )
{
hts_expand(int32_t,nsmpl,gvcf->mdp,gvcf->dp);
memcpy(gvcf->dp,gvcf->tmp,nsmpl*sizeof(int32_t)); // tmp still contains DP from rec
gvcf->npl = bcf_get_format_int32(hdr, rec, "PL", &gvcf->pl, &gvcf->mpl);
gvcf->nqsum = bcf_get_info_float(hdr,rec,"QS",&gvcf->qsum,&gvcf->mqsum);
gvcf->ngts = bcf_get_genotypes(hdr,rec,&gvcf->gts,&gvcf->mgts);
gvcf->rid = rec->rid;
gvcf->start = rec->pos;
gvcf->als.l = 0;
kputs(rec->d.allele[0],&gvcf->als);
for (i=1; i<rec->n_allele; i++)
{
kputc(',',&gvcf->als);
kputs(rec->d.allele[i],&gvcf->als);
}
gvcf->min_dp = min_dp;
}
else
{
if ( gvcf->min_dp > min_dp ) gvcf->min_dp = min_dp;
for (i=0; i<nsmpl; i++)
if ( gvcf->dp[i] > gvcf->tmp[i] ) gvcf->dp[i] = gvcf->tmp[i];
ret = bcf_get_format_int32(hdr, rec, "PL", &gvcf->tmp, &gvcf->mtmp);
if ( ret>=0 )
{
if ( ret!=nsmpl*3 ) error("Unexpected number of PL fields\n");
for (i=0; i<nsmpl; i++)
{
if ( gvcf->pl[3*i+1] > gvcf->tmp[3*i+1] )
{
gvcf->pl[3*i+1] = gvcf->tmp[3*i+1];
gvcf->pl[3*i+2] = gvcf->tmp[3*i+2];
}
else if ( gvcf->pl[3*i+1]==gvcf->tmp[3*i+1] && gvcf->pl[3*i+2] > gvcf->tmp[3*i+2] )
gvcf->pl[3*i+2] = gvcf->tmp[3*i+2];
}
}
else
gvcf->npl = 0;
}
gvcf->prev_range = dp_range;
if ( bcf_get_info_int32(hdr,rec,"END",&gvcf->tmp,&gvcf->mtmp)==1 )
gvcf->end = gvcf->tmp[0] - 1; // from 1-based to 0-based
else
gvcf->end = rec->pos;
return NULL;
}
if ( is_ref && min_dp )
bcf_update_info_int32(hdr, rec, "MinDP", &min_dp, 1);
return rec;
}
|