X-Git-Url: https://git.donarmstrong.com/?a=blobdiff_plain;f=misc%2Fsam2vcf.pl;h=afaf91e1dcf60894f195bed3580b6712dc0457df;hb=0b3418cf166ce4a58cedf0d9a2df5ec3dd4cc5fa;hp=c2644f53d1210669c04bbbdb02559b0b966259cc;hpb=8443a8179d04a83464fe514e8b9b40e7f456b0fe;p=samtools.git diff --git a/misc/sam2vcf.pl b/misc/sam2vcf.pl index c2644f5..afaf91e 100755 --- a/misc/sam2vcf.pl +++ b/misc/sam2vcf.pl @@ -3,7 +3,7 @@ # VCF specs: http://www.1000genomes.org/wiki/doku.php?id=1000_genomes:analysis:vcf3.3 # # Contact: pd3@sanger -# Version: 2009-12-08 +# Version: 2010-04-23 use strict; use warnings; @@ -23,10 +23,12 @@ sub error die "Usage: sam2vcf.pl [OPTIONS] < in.pileup > out.vcf\n", "Options:\n", - " -r, --refseq The reference sequence, required when indels are present.\n", - " -s, --snps-only Ignore indels.\n", - " -t, --column-title The column title.\n", - " -h, -?, --help This help message.\n", + " -h, -?, --help This help message.\n", + " -i, --indels-only Ignore SNPs.\n", + " -r, --refseq The reference sequence, required when indels are present.\n", + " -R, --keep-ref Print reference alleles as well.\n", + " -s, --snps-only Ignore indels.\n", + " -t, --column-title The column title.\n", "\n"; } @@ -40,9 +42,11 @@ sub parse_params while (my $arg=shift(@ARGV)) { + if ( $arg eq '-R' || $arg eq '--keep-ref' ) { $opts{keep_ref}=1; next; } if ( $arg eq '-r' || $arg eq '--refseq' ) { $opts{refseq}=shift(@ARGV); next; } if ( $arg eq '-t' || $arg eq '--column-title' ) { $opts{title}=shift(@ARGV); next; } if ( $arg eq '-s' || $arg eq '--snps-only' ) { $opts{snps_only}=1; next; } + if ( $arg eq '-i' || $arg eq '--indels-only' ) { $opts{indels_only}=1; next; } if ( $arg eq '-?' || $arg eq '-h' || $arg eq '--help' ) { error(); } error("Unknown parameter \"$arg\". Run -h for help.\n"); @@ -103,6 +107,8 @@ sub do_pileup_to_vcf my ($prev_chr,$prev_pos,$prev_ref); my $refseq; my $ignore_indels = $$opts{snps_only} ? 1 : 0; + my $ignore_snps = $$opts{indels_only} ? 1 : 0; + my $keep_ref = $$opts{keep_ref} ? 1 : 0; my $title = exists($$opts{title}) ? $$opts{title} : 'data'; print $fh_out @@ -117,28 +123,43 @@ sub do_pileup_to_vcf while (my $line=<$fh_in>) { chomp($line); - my ($chr,$pos,$ref,$cons,$cons_qual,$snp_qual,$rms_qual,$depth,@items) = split(/\t/,$line); + my (@items) = split(/\t/,$line); + if ( scalar @items<8 ) + { + error("\nToo few columns, does not look like output of 'samtools pileup -c': $line\n"); + } + my ($chr,$pos,$ref,$cons,$cons_qual,$snp_qual,$rms_qual,$depth,$a1,$a2) = @items; + $ref = uc($ref); + $cons = uc($cons); my ($alt,$gt); if ( $ref eq '*' ) { # An indel is involved. - if ( $ignore_indels ) { next; } + if ( $ignore_indels ) + { + $prev_ref = $ref; + $prev_pos = $pos; + $prev_chr = $chr; + next; + } - if ($chr ne $prev_chr || $pos ne $prev_pos) + if (!defined $prev_chr || $chr ne $prev_chr || $pos ne $prev_pos) { if ( !$$opts{refseq} ) { error("Cannot do indels without the reference.\n"); } if ( !$refseq ) { $refseq = Fasta->new(file=>$$opts{refseq}); } $ref = $refseq->get_base($chr,$pos); + $ref = uc($ref); } else { $ref = $prev_ref; } - # One of the alleles can be a reference and it can come in arbitrary order + # One of the alleles can be a reference and it can come in arbitrary order. In some + # cases */* can be encountered. In such a case, look in the additional columns. my ($al1,$al2) = split(m{/},$cons); + if ( $al1 eq $al2 && $al1 eq '*' ) { $al1=$a1; $al2=$a2; } my $alt1 = parse_indel($al1); my $alt2 = parse_indel($al2); if ( !$alt1 && !$alt2 ) { error("FIXME: could not parse indel:\n", $line); } - if ( $alt1 && $alt2 && $alt1 eq $alt2 ) { $alt2=''; } if ( !$alt1 ) { $alt=$alt2; @@ -149,7 +170,12 @@ sub do_pileup_to_vcf $alt=$alt1; $gt='0/1'; } - else + elsif ( $alt1 eq $alt2 ) + { + $alt="$alt1"; + $gt='1/1'; + } + else { $alt="$alt1,$alt2"; $gt='1/2'; @@ -157,6 +183,14 @@ sub do_pileup_to_vcf } else { + if ( $ignore_snps || (!$keep_ref && $ref eq $cons) ) + { + $prev_ref = $ref; + $prev_pos = $pos; + $prev_chr = $chr; + next; + } + # SNP ($alt,$gt) = iupac_to_gtype($ref,$cons); }