/usr/share/samtools/export2sam.pl is in samtools 0.1.19-1ubuntu1.
This file is owned by root:root, with mode 0o755.
The actual contents of the file can be viewed below.
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#
#
# export2sam.pl converts GERALD export files to SAM format.
#
#
#
########## License:
#
# The MIT License
#
# Original SAMtools work copyright (c) 2008-2009 Genome Research Ltd.
# Modified SAMtools work copyright (c) 2010 Illumina, Inc.
#
# 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.
#
#
#
#
########## ChangeLog:
#
# Version: 2.3.1 (18MAR2011)
#
# - Restore file '-' as stdin input.
#
# Version: 2.3.0 (24JAN2011)
#
# - Add support for export reserved chromosome name "CONTROL",
# which is translated to optional field "XC:Z:CONTROL".
# - Check for ".gz" file extension on export files and open
# these as gzip pipes when the extension is found.
#
# Version: 2.2.0 (16NOV2010)
#
# - Remove any leading zeros in export fields: RUNNO,LANE,TILE,X,Y
# - For export records with reserved chromosome name identifiers
# "QC" and "RM", add the optional field "XC:Z:QC" or "XC:Z:RM"
# to the SAM record, so that these cases can be distinguished
# from other unmatched reads.
#
# Version: 2.1.0 (21SEP2010)
#
# - Additional export record error checking.
# - Convert export records with chromomsome value of "RM" to unmapped
# SAM records.
#
# Version: 2.0.0 (15FEB2010)
#
# Script updated by Illumina in conjunction with CASAVA 1.7.0
# release.
#
# Major changes are as follows:
# - The CIGAR string has been updated to include all gaps from
# ELANDv2 alignments.
# - The ELAND single read alignment score is always stored in the
# optional "SM" field and the ELAND paired read alignment score
# is stored in the optional "AS" field when it exists.
# - The MAPQ value is set to the higher of the two alignment scores,
# but no greater than 254, i.e. min(254,max(SM,AS))
# - The SAM "proper pair" bit (0x0002) is now set for read pairs
# meeting ELAND's expected orientation and insert size criteria.
# - The default quality score translation is set for export files
# which contain Phread+64 quality values. An option,
# "--qlogodds", has been added to translate quality values from
# the Solexa+64 format used in export files prior to Pipeline
# 1.3
# - The export match descriptor is now reverse-complemented when
# necessary such that it always corresponds to the forward
# strand of the reference, to be consistent with other
# information in the SAM record. It is now written to the
# optional 'XD' field (rather than 'MD') to acknowledge its
# minor differences from the samtools match descriptor (see
# additional detail below).
# - An option, "--nofilter", has been added to include reads which
# have failed primary analysis quality filtration. Such reads
# will have the corresponding SAM flag bit (0x0200) set.
# - Labels in the export 'contig' field are preserved by setting
# RNAME to "$export_chromosome/$export_contig" when the contig
# label exists.
#
#
# Contact: lh3
# Version: 0.1.2 (03JAN2009)
#
#
#
########## Known Conversion Limitations:
#
# - Export records for reads that map to a position < 1 (allowed
# in export format), are converted to unmapped reads in the SAM
# record.
# - Export records contain the reserved chromosome names: "NM",
# "QC","RM" and "CONTROL". "NM" indicates that the aligner could
# not map the read to the reference sequence set. "QC" means that
# the aligner did not attempt to map the read due to some
# technical limitation. "RM" means that the read mapped to a set
# of 'contaminant' sequences specified in GERALD's RNA-seq
# workflow. "CONTROL" means that the read is a control. All of
# these alignment types are collapsed to the single unmapped
# alignment state in the SAM record, but the optional SAM "XC"
# field is used to record the original reserved chromosome name of
# the read for all but the "NM" case.
# - The export match descriptor is slightly different than the
# samtools match descriptor. For this reason it is stored in the
# optional SAM field 'XD' (and not 'MD'). Note that the export
# match descriptor differs from the samtools version in two
# respects: (1) indels are explicitly closed with the '$'
# character and (2) insertions must be enumerated in the match
# descriptor. For example a 35-base read with a two-base insertion
# is described as: 20^2$14
#
#
#
my $version = "2.3.1";
use strict;
use warnings;
use Getopt::Long;
use File::Spec;
use List::Util qw(min max);
use constant {
EXPORT_MACHINE => 0,
EXPORT_RUNNO => 1,
EXPORT_LANE => 2,
EXPORT_TILE => 3,
EXPORT_X => 4,
EXPORT_Y => 5,
EXPORT_INDEX => 6,
EXPORT_READNO => 7,
EXPORT_READ => 8,
EXPORT_QUAL => 9,
EXPORT_CHROM => 10,
EXPORT_CONTIG => 11,
EXPORT_POS => 12,
EXPORT_STRAND => 13,
EXPORT_MD => 14,
EXPORT_SEMAP => 15,
EXPORT_PEMAP => 16,
EXPORT_PASSFILT => 21,
EXPORT_SIZE => 22,
};
use constant {
SAM_QNAME => 0,
SAM_FLAG => 1,
SAM_RNAME => 2,
SAM_POS => 3,
SAM_MAPQ => 4,
SAM_CIGAR => 5,
SAM_MRNM => 6,
SAM_MPOS => 7,
SAM_ISIZE => 8,
SAM_SEQ => 9,
SAM_QUAL => 10,
};
# function prototypes for Richard's code
sub match_desc_to_cigar($);
sub match_desc_frag_length($);
sub reverse_compl_match_descriptor($);
sub write_header($;$;$);
&export2sam;
exit;
sub export2sam {
my $cmdline = $0 . " " . join(" ",@ARGV);
my $arg_count = scalar @ARGV;
my $progname = (File::Spec->splitpath($0))[2];
my $is_logodds_qvals = 0; # if true, assume files contain logodds (i.e. "solexa") quality values
my $is_nofilter = 0;
my $read1file;
my $read2file;
my $print_version = 0;
my $help = 0;
my $result = GetOptions( "qlogodds" => \$is_logodds_qvals,
"nofilter" => \$is_nofilter,
"read1=s" => \$read1file,
"read2=s" => \$read2file,
"version" => \$print_version,
"help" => \$help );
my $usage = <<END;
$progname converts GERALD export files to SAM format.
Usage: $progname --read1=FILENAME [ options ] | --version | --help
--read1=FILENAME read1 export file or '-' for stdin (mandatory)
(file may be gzipped with ".gz" extension)
--read2=FILENAME read2 export file or '-' for stdin
(file may be gzipped with ".gz" extension)
--nofilter include reads that failed the basecaller
purity filter
--qlogodds assume export file(s) use logodds quality values
as reported by OLB (Pipeline) prior to v1.3
(default: phred quality values)
END
my $version_msg = <<END;
$progname version: $version
END
if((not $result) or $help or ($arg_count==0)) {
die($usage);
}
if(@ARGV) {
print STDERR "\nERROR: Unrecognized arguments: " . join(" ",@ARGV) . "\n\n";
die($usage);
}
if($print_version) {
die($version_msg);
}
if(not defined($read1file)) {
print STDERR "\nERROR: read1 export file must be specified\n\n";
die($usage);
}
unless((-f $read1file) or ($read1file eq '-')) {
die("\nERROR: Can't find read1 export file: '$read1file'\n\n");
}
if (defined $read2file) {
unless((-f $read2file) or ($read2file eq '-')) {
die("\nERROR: Can't find read2 export file: '$read2file'\n\n");
}
if($read1file eq $read2file) {
die("\nERROR: read1 and read2 export filenames are the same: '$read1file'\n\n");
}
}
my ($fh1, $fh2, $is_paired);
my $read1cmd="$read1file";
$read1cmd = "gzip -dc $read1file |" if($read1file =~ /\.gz$/);
open($fh1, $read1cmd)
or die("\nERROR: Can't open read1 process: '$read1cmd'\n\n");
$is_paired = defined $read2file;
if ($is_paired) {
my $read2cmd="$read2file";
$read2cmd = "gzip -dc $read2file |" if($read2file =~ /\.gz$/);
open($fh2, $read2cmd)
or die("\nERROR: Can't open read2 process: '$read2cmd'\n\n");
}
# quality value conversion table
my @conv_table;
if($is_logodds_qvals){ # convert from solexa+64 quality values (pipeline pre-v1.3):
for (-64..64) {
$conv_table[$_+64] = int(33 + 10*log(1+10**($_/10.0))/log(10)+.499);
}
} else { # convert from phred+64 quality values (pipeline v1.3+):
for (-64..-1) {
$conv_table[$_+64] = undef;
}
for (0..64) {
$conv_table[$_+64] = int(33 + $_);
}
}
# write the header
print write_header( $progname, $version, $cmdline );
# core loop
my $export_line_count = 0;
while (<$fh1>) {
$export_line_count++;
my (@s1, @s2);
&export2sam_aux($_, $export_line_count, \@s1, \@conv_table, $is_paired, 1, $is_nofilter);
if ($is_paired) {
my $read2line = <$fh2>;
if(not $read2line){
die("\nERROR: read1 and read2 export files do not contain the same number of reads.\n Extra reads observed in read1 file at line no: $export_line_count.\n\n");
}
&export2sam_aux($read2line, $export_line_count, \@s2, \@conv_table, $is_paired, 2, $is_nofilter);
if (@s1 && @s2) { # then set mate coordinate
if($s1[SAM_QNAME] ne $s2[SAM_QNAME]){
die("\nERROR: Non-paired reads in export files on line: $export_line_count.\n Read1: $_ Read2: $read2line\n");
}
my $isize = 0;
if ($s1[SAM_RNAME] ne '*' && $s1[SAM_RNAME] eq $s2[SAM_RNAME]) { # then calculate $isize
my $x1 = ($s1[SAM_FLAG] & 0x10)? $s1[SAM_POS] + length($s1[SAM_SEQ]) : $s1[SAM_POS];
my $x2 = ($s2[SAM_FLAG] & 0x10)? $s2[SAM_POS] + length($s2[SAM_SEQ]) : $s2[SAM_POS];
$isize = $x2 - $x1;
}
foreach ([\@s1,\@s2,$isize],[\@s2,\@s1,-$isize]){
my ($sa,$sb,$is) = @{$_};
if ($sb->[SAM_RNAME] ne '*') {
$sa->[SAM_MRNM] = ($sb->[SAM_RNAME] eq $sa->[SAM_RNAME]) ? "=" : $sb->[SAM_RNAME];
$sa->[SAM_MPOS] = $sb->[SAM_POS];
$sa->[SAM_ISIZE] = $is;
$sa->[SAM_FLAG] |= 0x20 if ($sb->[SAM_FLAG] & 0x10);
} else {
$sa->[SAM_FLAG] |= 0x8;
}
}
}
}
print join("\t", @s1), "\n" if (@s1);
print join("\t", @s2), "\n" if (@s2 && $is_paired);
}
close($fh1);
if($is_paired) {
while(my $read2line = <$fh2>){
$export_line_count++;
die("\nERROR: read1 and read2 export files do not contain the same number of reads.\n Extra reads observed in read2 file at line no: $export_line_count.\n\n");
}
close($fh2);
}
}
sub export2sam_aux {
my ($line, $line_no, $s, $ct, $is_paired, $read_no, $is_nofilter) = @_;
chomp($line);
my @t = split("\t", $line);
if(scalar(@t) < EXPORT_SIZE) {
my $msg="\nERROR: Unexpected number of fields in export record on line $line_no of read$read_no export file. Found " . scalar(@t) . " fields but expected " . EXPORT_SIZE . ".\n";
$msg.="\t...erroneous export record:\n" . $line . "\n\n";
die($msg);
}
@$s = ();
my $isPassFilt = ($t[EXPORT_PASSFILT] eq 'Y');
return if(not ($isPassFilt or $is_nofilter));
# read name
my $samQnamePrefix = $t[EXPORT_MACHINE] . (($t[EXPORT_RUNNO] ne "") ? "_" . int($t[EXPORT_RUNNO]) : "");
$s->[SAM_QNAME] = join(':', $samQnamePrefix, int($t[EXPORT_LANE]), int($t[EXPORT_TILE]),
int($t[EXPORT_X]), int($t[EXPORT_Y]));
# initial flag (will be updated later)
$s->[SAM_FLAG] = 0;
if($is_paired) {
if($t[EXPORT_READNO] != $read_no){
die("\nERROR: read$read_no export file contains record with read number: " .$t[EXPORT_READNO] . " on line: $line_no\n\n");
}
$s->[SAM_FLAG] |= 1 | 1<<(5 + $read_no);
}
$s->[SAM_FLAG] |= 0x200 if (not $isPassFilt);
# read & quality
my $is_export_rev = ($t[EXPORT_STRAND] eq 'R');
if ($is_export_rev) { # then reverse the sequence and quality
$s->[SAM_SEQ] = reverse($t[EXPORT_READ]);
$s->[SAM_SEQ] =~ tr/ACGTacgt/TGCAtgca/;
$s->[SAM_QUAL] = reverse($t[EXPORT_QUAL]);
} else {
$s->[SAM_SEQ] = $t[EXPORT_READ];
$s->[SAM_QUAL] = $t[EXPORT_QUAL];
}
my @convqual = ();
foreach (unpack('C*', $s->[SAM_QUAL])){
my $val=$ct->[$_];
if(not defined $val){
my $msg="\nERROR: can't interpret export quality value: " . $_ . " in read$read_no export file, line: $line_no\n";
if( $_ < 64 ) { $msg .= " Use --qlogodds flag to translate logodds (solexa) quality values.\n"; }
die($msg . "\n");
}
push @convqual,$val;
}
$s->[SAM_QUAL] = pack('C*',@convqual); # change coding
# coor
my $has_coor = 0;
$s->[SAM_RNAME] = "*";
if (($t[EXPORT_CHROM] eq 'NM') or
($t[EXPORT_CHROM] eq 'QC') or
($t[EXPORT_CHROM] eq 'RM') or
($t[EXPORT_CHROM] eq 'CONTROL')) {
$s->[SAM_FLAG] |= 0x4; # unmapped
push(@$s,"XC:Z:".$t[EXPORT_CHROM]) if($t[EXPORT_CHROM] ne 'NM');
} elsif ($t[EXPORT_CHROM] =~ /(\d+):(\d+):(\d+)/) {
$s->[SAM_FLAG] |= 0x4; # TODO: should I set BAM_FUNMAP in this case?
push(@$s, "H0:i:$1", "H1:i:$2", "H2:i:$3")
} elsif ($t[EXPORT_POS] < 1) {
$s->[SAM_FLAG] |= 0x4; # unmapped
} else {
$s->[SAM_RNAME] = $t[EXPORT_CHROM];
$s->[SAM_RNAME] .= "/" . $t[EXPORT_CONTIG] if($t[EXPORT_CONTIG] ne '');
$has_coor = 1;
}
$s->[SAM_POS] = $has_coor? $t[EXPORT_POS] : 0;
# print STDERR "t[14] = " . $t[14] . "\n";
my $matchDesc = '';
$s->[SAM_CIGAR] = "*";
if($has_coor){
$matchDesc = ($is_export_rev) ? reverse_compl_match_descriptor($t[EXPORT_MD]) : $t[EXPORT_MD];
if($matchDesc =~ /\^/){
# construct CIGAR string using Richard's function
$s->[SAM_CIGAR] = match_desc_to_cigar($matchDesc); # indel processing
} else {
$s->[SAM_CIGAR] = length($s->[SAM_SEQ]) . "M";
}
}
# print STDERR "cigar_string = $cigar_string\n";
$s->[SAM_FLAG] |= 0x10 if ($has_coor && $is_export_rev);
if($has_coor){
my $semap = ($t[EXPORT_SEMAP] ne '') ? $t[EXPORT_SEMAP] : 0;
my $pemap = 0;
if($is_paired) {
$pemap = ($t[EXPORT_PEMAP] ne '') ? $t[EXPORT_PEMAP] : 0;
# set `proper pair' bit if non-blank, non-zero PE alignment score:
$s->[SAM_FLAG] |= 0x02 if ($pemap > 0);
}
$s->[SAM_MAPQ] = min(254,max($semap,$pemap));
} else {
$s->[SAM_MAPQ] = 0;
}
# mate coordinate
$s->[SAM_MRNM] = '*';
$s->[SAM_MPOS] = 0;
$s->[SAM_ISIZE] = 0;
# aux
push(@$s, "BC:Z:$t[EXPORT_INDEX]") if ($t[EXPORT_INDEX]);
if($has_coor){
# The export match descriptor differs slightly from the samtools match descriptor.
# In order for the converted SAM files to be as compliant as possible,
# we put the export match descriptor in optional field 'XD' rather than 'MD':
push(@$s, "XD:Z:$matchDesc");
push(@$s, "SM:i:$t[EXPORT_SEMAP]") if ($t[EXPORT_SEMAP] ne '');
push(@$s, "AS:i:$t[EXPORT_PEMAP]") if ($is_paired and ($t[EXPORT_PEMAP] ne ''));
}
}
#
# the following code is taken from Richard Shaw's sorted2sam.pl file
#
sub reverse_compl_match_descriptor($)
{
# print "\nREVERSING THE MATCH DESCRIPTOR!\n";
my ($match_desc) = @_;
my $rev_compl_match_desc = reverse($match_desc);
$rev_compl_match_desc =~ tr/ACGT\^\$/TGCA\$\^/;
# Unreverse the digits of numbers.
$rev_compl_match_desc = join('',
map {($_ =~ /\d+/)
? join('', reverse(split('', $_)))
: $_} split(/(\d+)/,
$rev_compl_match_desc));
return $rev_compl_match_desc;
}
sub match_desc_to_cigar($)
{
my ($match_desc) = @_;
my @match_desc_parts = split(/(\^.*?\$)/, $match_desc);
my $cigar_str = '';
my $cigar_del_ch = 'D';
my $cigar_ins_ch = 'I';
my $cigar_match_ch = 'M';
foreach my $match_desc_part (@match_desc_parts) {
next if (!$match_desc_part);
if ($match_desc_part =~ /^\^([ACGTN]+)\$$/) {
# Deletion
$cigar_str .= (length($1) . $cigar_del_ch);
} elsif ($match_desc_part =~ /^\^(\d+)\$$/) {
# Insertion
$cigar_str .= ($1 . $cigar_ins_ch);
} else {
$cigar_str .= (match_desc_frag_length($match_desc_part)
. $cigar_match_ch);
}
}
return $cigar_str;
}
#------------------------------------------------------------------------------
sub match_desc_frag_length($)
{
my ($match_desc_str) = @_;
my $len = 0;
my @match_desc_fields = split(/([ACGTN]+)/, $match_desc_str);
foreach my $match_desc_field (@match_desc_fields) {
next if ($match_desc_field eq '');
$len += (($match_desc_field =~ /(\d+)/)
? $1 : length($match_desc_field));
}
return $len;
}
# argument holds the command line
sub write_header($;$;$)
{
my ($progname,$version,$cl) = @_;
my $complete_header = "";
$complete_header .= "\@PG\tID:$progname\tVN:$version\tCL:$cl\n";
return $complete_header;
}
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