int main_flags(int argc, char *argv[])
{
if ( argc!=2 ) usage();
else
{
int mask = bam_str2flag(argv[1]);
if ( mask<0 ) { fprintf(pysamerr,"Error: Could not parse \"%s\"\n", argv[1]); usage(); return 1; }
printf("0x%x\t%d\t%s\n", mask, mask, bam_flag2str(mask));
}
return 0;
}
static void print_usage(FILE *fp, const mplp_conf_t *mplp)
{
char *tmp_require = bam_flag2str(mplp->rflag_require);
char *tmp_filter = bam_flag2str(mplp->rflag_filter);
// Display usage information, formatted for the standard 80 columns.
// (The unusual string formatting here aids the readability of this
// source code in 80 columns, to the extent that's possible.)
fprintf(fp,
"\n"
"Usage: bcftools mpileup [options] in1.bam [in2.bam [...]]\n"
"\n"
"Input options:\n"
" -6, --illumina1.3+ quality is in the Illumina-1.3+ encoding\n"
" -A, --count-orphans do not discard anomalous read pairs\n"
" -b, --bam-list FILE list of input BAM filenames, one per line\n"
" -B, --no-BAQ disable BAQ (per-Base Alignment Quality)\n"
" -C, --adjust-MQ INT adjust mapping quality; recommended:50, disable:0 [0]\n"
" -d, --max-depth INT max per-file depth; avoids excessive memory usage [%d]\n", mplp->max_depth);
fprintf(fp,
" -E, --redo-BAQ recalculate BAQ on the fly, ignore existing BQs\n"
" -f, --fasta-ref FILE faidx indexed reference sequence file\n"
" --no-reference do not require fasta reference file\n"
" -G, --read-groups FILE select or exclude read groups listed in the file\n"
" -q, --min-MQ INT skip alignments with mapQ smaller than INT [%d]\n", mplp->min_mq);
fprintf(fp,
" -Q, --min-BQ INT skip bases with baseQ/BAQ smaller than INT [%d]\n", mplp->min_baseQ);
fprintf(fp,
" -r, --regions REG[,...] comma separated list of regions in which pileup is generated\n"
" -R, --regions-file FILE restrict to regions listed in a file\n"
" --ignore-RG ignore RG tags (one BAM = one sample)\n"
" --rf, --incl-flags STR|INT required flags: skip reads with mask bits unset [%s]\n", tmp_require);
fprintf(fp,
" --ff, --excl-flags STR|INT filter flags: skip reads with mask bits set\n"
" [%s]\n", tmp_filter);
fprintf(fp,
" -s, --samples LIST comma separated list of samples to include\n"
" -S, --samples-file FILE file of samples to include\n"
" -t, --targets REG[,...] similar to -r but streams rather than index-jumps\n"
" -T, --targets-file FILE similar to -R but streams rather than index-jumps\n"
" -x, --ignore-overlaps disable read-pair overlap detection\n"
"\n"
"Output options:\n"
" -a, --annotate LIST optional tags to output; '?' to list []\n"
" -g, --gvcf INT[,...] group non-variant sites into gVCF blocks according\n"
" to minimum per-sample DP\n"
" --no-version do not append version and command line to the header\n"
" -o, --output FILE write output to FILE [standard output]\n"
" -O, --output-type TYPE 'b' compressed BCF; 'u' uncompressed BCF;\n"
" 'z' compressed VCF; 'v' uncompressed VCF [v]\n"
" --threads INT number of extra output compression threads [0]\n"
"\n"
"SNP/INDEL genotype likelihoods options:\n"
" -e, --ext-prob INT Phred-scaled gap extension seq error probability [%d]\n", mplp->extQ);
fprintf(fp,
" -F, --gap-frac FLOAT minimum fraction of gapped reads [%g]\n", mplp->min_frac);
fprintf(fp,
" -h, --tandem-qual INT coefficient for homopolymer errors [%d]\n", mplp->tandemQ);
fprintf(fp,
" -I, --skip-indels do not perform indel calling\n"
" -L, --max-idepth INT maximum per-file depth for INDEL calling [%d]\n", mplp->max_indel_depth);
fprintf(fp,
" -m, --min-ireads INT minimum number gapped reads for indel candidates [%d]\n", mplp->min_support);
fprintf(fp,
" -o, --open-prob INT Phred-scaled gap open seq error probability [%d]\n", mplp->openQ);
fprintf(fp,
" -p, --per-sample-mF apply -m and -F per-sample for increased sensitivity\n"
" -P, --platforms STR comma separated list of platforms for indels [all]\n"
"\n"
"Notes: Assuming diploid individuals.\n"
"\n");
free(tmp_require);
free(tmp_filter);
}
static void print_usage(FILE *fp, const mplp_conf_t *mplp)
{
char *tmp_require = bam_flag2str(mplp->rflag_require);
char *tmp_filter = bam_flag2str(mplp->rflag_filter);
// Display usage information, formatted for the standard 80 columns.
// (The unusual string formatting here aids the readability of this
// source code in 80 columns, to the extent that's possible.)
fprintf(fp,
"\n"
"Usage: samtools mpileup [options] in1.bam [in2.bam [...]]\n"
"\n"
"Input options:\n"
" -6, --illumina1.3+ quality is in the Illumina-1.3+ encoding\n"
" -A, --count-orphans do not discard anomalous read pairs\n"
" -b, --bam-list FILE list of input BAM filenames, one per line\n"
" -B, --no-BAQ disable BAQ (per-Base Alignment Quality)\n"
" -C, --adjust-MQ INT adjust mapping quality; recommended:50, disable:0 [0]\n"
" -d, --max-depth INT max per-BAM depth; avoids excessive memory usage [%d]\n", mplp->max_depth);
fprintf(fp,
" -E, --redo-BAQ recalculate BAQ on the fly, ignore existing BQs\n"
" -f, --fasta-ref FILE faidx indexed reference sequence file\n"
" -G, --exclude-RG FILE exclude read groups listed in FILE\n"
" -l, --positions FILE skip unlisted positions (chr pos) or regions (BED)\n"
" -q, --min-MQ INT skip alignments with mapQ smaller than INT [%d]\n", mplp->min_mq);
fprintf(fp,
" -Q, --min-BQ INT skip bases with baseQ/BAQ smaller than INT [%d]\n", mplp->min_baseQ);
fprintf(fp,
" -r, --region REG region in which pileup is generated\n"
" -R, --ignore-RG ignore RG tags (one BAM = one sample)\n"
" --rf, --incl-flags STR|INT required flags: skip reads with mask bits unset [%s]\n", tmp_require);
fprintf(fp,
" --ff, --excl-flags STR|INT filter flags: skip reads with mask bits set\n"
" [%s]\n", tmp_filter);
fprintf(fp,
" -x, --ignore-overlaps disable read-pair overlap detection\n"
"\n"
"Output options:\n"
" -o, --output FILE write output to FILE [standard output]\n"
" -g, --BCF generate genotype likelihoods in BCF format\n"
" -v, --VCF generate genotype likelihoods in VCF format\n"
"\n"
"Output options for mpileup format (without -g/-v):\n"
" -O, --output-BP output base positions on reads\n"
" -s, --output-MQ output mapping quality\n"
"\n"
"Output options for genotype likelihoods (when -g/-v is used):\n"
" -t, --output-tags LIST optional tags to output: DP,DPR,DV,DP4,INFO/DPR,SP []\n"
" -u, --uncompressed generate uncompressed VCF/BCF output\n"
"\n"
"SNP/INDEL genotype likelihoods options (effective with -g/-v):\n"
" -e, --ext-prob INT Phred-scaled gap extension seq error probability [%d]\n", mplp->extQ);
fprintf(fp,
" -F, --gap-frac FLOAT minimum fraction of gapped reads [%g]\n", mplp->min_frac);
fprintf(fp,
" -h, --tandem-qual INT coefficient for homopolymer errors [%d]\n", mplp->tandemQ);
fprintf(fp,
" -I, --skip-indels do not perform indel calling\n"
" -L, --max-idepth INT maximum per-sample depth for INDEL calling [%d]\n", mplp->max_indel_depth);
fprintf(fp,
" -m, --min-ireads INT minimum number gapped reads for indel candidates [%d]\n", mplp->min_support);
fprintf(fp,
" -o, --open-prob INT Phred-scaled gap open seq error probability [%d]\n", mplp->openQ);
fprintf(fp,
" -p, --per-sample-mF apply -m and -F per-sample for increased sensitivity\n"
" -P, --platforms STR comma separated list of platforms for indels [all]\n"
"\n"
"Notes: Assuming diploid individuals.\n");
free(tmp_require);
free(tmp_filter);
}
