forked from samtools/bcftools
-
Notifications
You must be signed in to change notification settings - Fork 0
/
gvcf.c
226 lines (196 loc) · 7.93 KB
/
gvcf.c
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
/* gvcf.c -- support for gVCF files.
Copyright (C) 2014-2015 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. */
#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=MIN_DP,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, "MIN_DP", &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);
if ( bcf_write1(fh, hdr, gvcf->line)!=0 ) error("[%s] Error: failed to write the record\n", __func__);
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, "MIN_DP", &min_dp, 1);
return rec;
}