/usr/bin/maq.pl is in maq 0.7.1-5.
This file is owned by root:root, with mode 0o755.
The actual contents of the file can be viewed below.
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# Author: lh3
use strict;
use warnings;
use Getopt::Std;
use File::Copy;
use File::Spec;
use Cwd qw/getcwd abs_path/;
my $version = '0.4.7';
&usage if (@ARGV < 1);
# global variables
my @nucl_type = (0, 1, 1, 2, 1, 2, 2, 3, 1, 2, 2, 3, 2, 3, 3, 4);
my @conv = split('', 'XACMGRSVTWYHKDBN');
my $command = shift(@ARGV);
my %func = (easyrun=>\&easyrun, chrpt2snp=>\&chrpt2snp, fastq2bfq=>\&fastq2bfq,
cat2pair=>\&cat2pair, SNPfilter=>\&SNPfilter, ucsc2snp=>\&ucsc2snp,
statmap=>\&statmap, sv=>\&sv, demo=>\&demo, splitread=>\&splitread,
indelpe=>\&indelpe);
die("Unknown command \"$command\".\n") if (!defined($func{$command}));
&{$func{$command}}();
exit(0);
#
# easyrun command
#
sub easyrun
{
my %opts = (d=>'easyrun', 1=>0, 2=>0, A=>'', n=>2000000, a=>250, e=>3, q=>40, m=>2,
D=>256, E=>20, N=>2, w=>5, b=>60, B=>2);
getopts('d:1:2:A:n:a:pe:q:E:D:m:N:b:B:S', \%opts);
die qq(
Usage: maq.pl easyrun [options] <ref.fa|bfa> <reads1.fq|bfq> [reads2.fastq]
Options: -d DIR output directory [$opts{d}]
-n INT number of reads in a split file [$opts{n}]
-1 INT length of read1 [$opts{1}]
-A FILE file that contains the 3'adapter [null]
-m INT number of mismatches in the seed [$opts{m}]
-N INT number of haplotypes [$opts{N}]
-b INT maximum sum of qualities of mismatches [$opts{b}]
-e INT minimum read depth to call a SNP [$opts{e}]
-D INT maximum read depth to call a SNP [$opts{D}]
-E INT minimum neighbour consensus quality to call a SNP [$opts{E}]
-q INT quality threshold for the final SNP calls [$opts{q}]
-w INT SNP within +/- INT distant to an indel to be filtered [$opts{w}]
-B INT maximum number of SNPs in a window [$opts{B}]
-S apply indel detection with the splitread (VERY SLOW)
-p mate-pair alignment (PE mode)
-2 INT length of read2 (PE only) [$opts{2}]
-a INT max insert size (PE only) [$opts{a}]
Notes: For pooled data, please specify the number of haplotypes in the
pool with `-N' and set `-E 0' at the same time. Do not try
`-N 1', which only causes segfault.
) if (@ARGV < 2);
if (defined($opts{p}) && @ARGV != 3) {
die("** for PE mode, two reads files should be specified.\n");
}
my $d = $opts{d};
my $cwd = getcwd;
my $mapopt = " -n $opts{m} -e ".($opts{b}+10);
map { $_ = File::Spec->rel2abs($_) } @ARGV; # change to absolute path
$mapopt .= $opts{1}? " -1 $opts{1}" : '';
$mapopt .= $opts{2}? " -2 $opts{2}" : '';
$mapopt .= $opts{A}? " -d " . File::Spec->rel2abs($opts{A}) : '';
my $filtopt = "-d $opts{e} -D $opts{D} -n $opts{E}";
my $exe = gwhich('maq') || die("** Cannot find 'maq' executable.");
my $pl = gwhich($0) || die("** Cannot find 'maq.pl' script. Should be a bug actually.");
mkdir($d) unless (-d $d);
# run fasta2bfa
my ($is_gzip, $first) = &test_file($ARGV[0]);
if (ord($first) == ord('>')) { # fasta format
if ($is_gzip) { # gzipped
&run_cmd("gzip -dc $ARGV[0] | $exe fasta2bfa - $d/ref.bfa 2> /dev/null");
} else { # plain
&run_cmd("$exe fasta2bfa $ARGV[0] $d/ref.bfa 2> /dev/null");
}
} else { # create a symbolic link
&run_cmd("ln -sf $ARGV[0] $d/ref.bfa");
}
# run fastq2bfq && match
shift(@ARGV);
my $i = 0;
my (@map_files, $map_file);
foreach my $file (@ARGV) {
++$i;
($is_gzip, $first) = &test_file($file);
if (ord($first) == ord('@')) { # fastq format
if ($is_gzip) { # gzipped
&run_cmd("gzip -dc $file | $exe fastq2bfq -n $opts{n} - $d/read$i");
} else { # plain fastq
&run_cmd("$exe fastq2bfq -n $opts{n} $file $d/read$i");
}
} elsif ($is_gzip) { # probably bfq
&run_cmd("ln -sf $file $d/read$i.bfq");
} else {
die("** Cannot guess the format of file '$file'.");
}
}
# run alignment
if (defined $opts{p}) { # paired reads
my @bfq_files = `(cd $d; find . -name "read1*.bfq")`;
foreach (@bfq_files) {
chomp;
/^\.\/read1(.*)\.bfq$/;
my $tag = $1;
my $bfqs = (-f "$d/read2$tag.bfq")? "read1$tag.bfq read2$tag.bfq" : "read1$tag.bfq";
&run_cmd("(cd $d; $exe map $mapopt aln$tag.map ref.bfa $bfqs 2> aln$tag.map.log)");
push(@map_files, "aln$tag.map");
}
} else { # unpaired reads
my @bfq_files = `(cd $d; find . -name "read*.bfq")`;
foreach (@bfq_files) {
chomp;
/^\.\/read(.*)\.bfq$/;
my $tag = $1;
&run_cmd("(cd $d; $exe map $mapopt -u unmap$tag.txt aln$tag.map ref.bfa read$tag.bfq 2> aln$tag.map.log)");
push(@map_files, "aln$tag.map");
}
}
if (@map_files > 1) { # we should merge them
&run_cmd("(cd $d; $exe mapmerge all.map @map_files)");
} else {
&run_cmd("(cd $d; mv $map_files[0] all.map)");
}
$map_file = "all.map";
&run_cmd("(cd $d; $exe mapcheck ref.bfa $map_file > mapcheck.txt)");
&run_cmd("(cd $d; $exe assemble -N $opts{N} -Q $opts{b} consensus.cns ref.bfa $map_file 2> assemble.log)");
&run_cmd("$exe cns2fq $d/consensus.cns > $d/cns.fq");
&run_cmd("$exe cns2snp $d/consensus.cns > $d/cns.snp");
&run_cmd("$exe cns2win $d/consensus.cns > $d/cns.win");
&run_cmd("$exe indelsoa $d/ref.bfa $d/$map_file > $d/cns.indelse");
if (defined $opts{p}) {
&run_cmd("$exe indelpe $d/ref.bfa $d/$map_file > $d/cns.indelpe");
&run_cmd("$pl SNPfilter -q $opts{q} -w $opts{w} -N $opts{B} -f $d/cns.indelse -F $d/cns.indelpe $filtopt -Q60 $d/cns.snp > $d/cns.final.snp");
} else {
&run_cmd("(cd $d; touch unmap.indel)");
if (!defined($opts{S})) {
&run_cmd("$pl SNPfilter -q $opts{q} -w $opts{w} -N $opts{B} -f $d/cns.indelse $filtopt $d/cns.snp > $d/cns.final.snp");
} else { # call splitread indels
&run_cmd("(cd $d; cat unmap*.txt | $pl splitread -p unmap - ref.bfa 2> unmap.log)");
&run_cmd("$pl SNPfilter -q $opts{q} -w $opts{w} -N $opts{B} -f $d/cns.indelse -S $d/unmap.indel $filtopt $d/cns.snp > $d/cns.final.snp");
}
}
&run_cmd("(cd $d; ln -s cns.final.snp cns.filter.snp)");
# my $maq_plot = gwhich("maq_plot.pl");
# my $gnuplot = gwhich("gnuplot");
# if ($maq_plot && $gnuplot) {
# &run_cmd("$maq_plot depth -x 0.2 $d/depth $d/cns.win");
# }
&run_cmd("$pl statmap $d/*.map.log");
}
sub statmap {
my ($is_paired, $n_reads1, $n_reads2, $n_moved_high, $n_moved_low, $n_mapped1, $n_mapped2, $n_paired, $n_added);
$is_paired = $n_reads1 = $n_reads2 = $n_moved_high = $n_moved_low = $n_mapped1 = $n_mapped2 = $n_paired = $n_added = 0;
while (<>) {
if (/^--\s*\(total,\s*isPE,.*\) .*=\s*\((\d+),\s*(\d+),\s*(\d+),\s*(\d+)\)/) {
$is_paired = $2;
if ($is_paired) { $n_reads2 += $1; $n_mapped2 += $3; }
else { $n_reads1 += $1; $n_mapped1 += $3; }
$n_paired += $4;
} elsif (/match_data2mapping.* (\d+) pairs are added/) {
$n_added += $1;
} elsif (/match_data2mapping.* first.*\((\d+), (\d+)\).*second.*\((\d+), (\d+)\)/) {
$n_moved_high += $1+$3;
$n_moved_low += $2+$4;
}
}
my $tot = $n_reads1 + $n_reads2;
my $map1_ratio = ($n_reads1 == 0)? 'NA' : int(10000 * $n_mapped1 / $n_reads1) / 100;
my $map2_ratio = ($n_reads2 == 0)? 'NA' : int(10000 * $n_mapped2 / $n_reads2) / 100;
my $pair_ratio = ($n_mapped2 == 0)? 'NA' : int(10000 * $n_paired / $n_mapped2) / 100;
my $add_ratio = ($n_paired == 0)? 'NA' : int(10000 * $n_added / $n_paired) / 100;
my $high_ratio = ($n_paired == 0)? 'NA' : int(10000 * $n_moved_high / $n_paired) / 100;
my $low_ratio = ($n_paired == 0)? 'NA' : int(10000 * $n_moved_low / $n_paired) / 100;
print qq(
-- == statmap report ==\n
-- # single end (SE) reads: $n_reads1
-- # mapped SE reads: $n_mapped1 (/ $n_reads1 = $map1_ratio%)
-- # paired end (PE) reads: $n_reads2
-- # mapped PE reads: $n_mapped2 (/ $n_reads2 = $map2_ratio%)
-- # reads that are mapped in pairs: $n_paired (/ $n_mapped2 = $pair_ratio%)
-- # Q>=30 reads that are moved to meet mate-pair requirement: $n_moved_high (/ $n_paired = $high_ratio%)
-- # Q<30 reads that are moved to meet mate-pair requirement: $n_moved_low ($low_ratio%)
\n);
}
#
# SNPfilter command
#
sub SNPfilter {
my %opts = (f=>'', S=>'', s=>3, m=>1, Q=>40, d=>3, F=>'', w=>5, D=>256, N=>2, W=>10, n=>20, c=>-1.0, q=>20);
getopts('af:s:m:Q:d:D:w:F:W:N:c:n:S:q:', \%opts);
die(qq{
Usage: maq.pl SNPfilter [options] <cns2snp.snp>
Options: -d INT minimum depth to call a SNP [$opts{d}]
-D INT maximum depth (<=254), otherwise ignored [$opts{D}]
-n INT minimum neighbouring quality [$opts{n}]
-Q INT required max mapping quality of the reads covering the SNP [$opts{Q}]
-q INT minimum consensus quality [$opts{q}]
-w INT size of the window in which SNPs should be filtered out [$opts{w}]
-S FILE splitread output [null]
-F FILE indelpe output [null]
-f FILE indelsoa output [null]
-s INT indelsoa score (= left_clip + right_clip - across) [$opts{s}]
-m INT indelsoa: max number of reads mapped across the indel [$opts{m}]
-W INT window size for filtering dense SNPs [$opts{W}]
-N INT maximum number of SNPs in a window [$opts{N}]
-a alternative filter for single end reads
\n}) unless (@ARGV);
my (%hash, $fh);
my $skip = $opts{w};
if ($opts{f}) { # for indelsoa
my $n = 0;
open($fh, $opts{f}) || die;
while (<$fh>) {
my @t = split;
next unless ($t[4]+$t[5]-$t[3] >= $opts{s} && $t[3] <= $opts{m}); # a simple filter
++$n;
if ($t[2] < 0) { # potential deletion
for (my $x = $t[1] + $t[2] - $skip; $x <= $t[1] + $skip; ++$x) {
$hash{$t[0],$x} = 1;
}
} else { # potential insertion
for (my $x = $t[1] - $skip; $x <= $t[1] + $t[2] + $skip; ++$x) {
$hash{$t[0],$x} = 1;
}
}
}
close($fh);
warn("-- $n potential soa-indels pass the filter.\n");
}
if ($opts{F}) { # for indelpe
my $n = 0;
open($fh, $opts{F}) || die;
while (<$fh>) {
my @t = split;
next unless ($t[2] eq '*' || $t[2] eq '+');
++$n;
for (my $x = $t[1] - 1; $x < $t[1] + 2*$skip; ++$x) {
$hash{$t[0],$x} = 1;
}
}
close($fh);
warn("-- $n potential pe-indels pass the filter.\n");
}
if ($opts{S}) { # for splitread
my $n = 0;
open($fh, $opts{S}) || die;
while (<$fh>) {
next unless (/^VR/);
my @t = split;
next if ($t[5] < 2 || ($t[5] < 4 && $t[4] == 0));
++$n;
$hash{$t[1],$_} = 1 for ($t[2] .. $t[3]);
}
close($fh);
warn("-- $n potential splitread-indels pass the filter.\n");
}
my $is_alter = defined($opts{a});
my (@last, $last_chr);
$last_chr = '';
while (<>) {
my @t = split;
next if ($hash{$t[0],$t[1]});
my $is_good;
if (!$is_alter) { # the default filter
$is_good = ($t[5] >= $opts{d} && $t[5] <= $opts{D} && $t[6] > $opts{c} && $t[7] >= $opts{Q} && $t[8] >= $opts{n})? 1 : 0;
} else { # the alternative filter for SE reads
$is_good = ($t[5] >= $opts{d} && $t[5] <= $opts{D} && $t[6] > $opts{c} && $t[6] <= 4.0 && $t[8] >= $opts{n})? 1 : 0;
}
$is_good = 0 unless ($t[4] >= $opts{q} || ($t[2] ne $t[9] && $t[4]+$t[10] >= $opts{q})); # consensus quality filter
next unless ($is_good); # drop
if ($t[0] ne $last_chr) { # a different chr, print
map { print $_->{L} if ($_->{F}) } @last;
@last = ();
$last_chr = $t[0];
}
# The following block provided by Nathans Weeks. Thanks, Nathans.
push(@last, {L => $_, X => $t[1], F => 1}); # Enqueue current SNP
if ($#last == $opts{N}) { # number of SNPs in queue is N+1
if ($last[$#last]{X} - $last[0]{X} < $opts{W}) { # if all within window W
map {$_->{F} = 0} @last; # all SNPs in the window of size W are "bad"
}
print STDOUT $last[0]{L} if ($last[0]{F}); # print first SNP if good
shift @last # dequeue first SNP
}
}
# print the last few lines if applicable
map { print $_->{L} if ($_->{F}) } @last;
}
#
# splitread
#
sub splitread {
my %opts = (1=>12, 2=>12, p=>'splitread', a=>20);
getopts('1:2:p:a:', \%opts);
die(qq/
Usage: maq.pl splitread [options] <input.unmap> <in.bfa>
Options: -1 INT length of read1 [$opts{1}]
-2 INT length of read2 [$opts{2}]
-a INT maximum indel size [$opts{a}]
-p STR prefix [$opts{p}]
/) if (@ARGV < 2);
my $maq = gwhich('maq') || die("[splitread] fail to locate 'maq'. Abort!\n");
my ($l1, $l2) = ($opts{1}, $opts{2});
my ($n, $fh, $fh1, $fh2);
# generate fastq
warn("-- generate paired end reads\n");
open($fh, ($ARGV[0]=~/\.gz$/)? "gzip -dc $ARGV[0]" : $ARGV[0]) || die;
open($fh1, ">$opts{p}1.fq") || die;
open($fh2, ">$opts{p}2.fq") || die;
while (<$fh>) {
my @t = split;
next if ($t[1] != 99);
my $l = length($t[2]);
die("[splitread] reads are too short!\n") if ($l < $l1 + $l2);
# sequence
my ($s1, $s2) = (substr($t[2], 0, $l1), substr($t[2], -$l2));
# discard poor reads
next if ($s1 =~ /N/i || $s2 =~ /N/i);
$n = ($s1 =~ tr/A/A/);
next if ($n == $l1);
$n = ($s2 =~ tr/A/A/);
next if ($n == $l2);
# reverse $s2
$s2 = reverse($s2);
$s2 =~ tr/ACGTN/TGCAN/;
# quality
my ($q1, $q2) = (substr($t[3], 0, $l1), substr($t[3], -$l2));
$q2 = reverse($q2);
# output
print $fh1 "\@$t[0]_$l/1\n$s1\n+\n$q1\n";
print $fh2 "\@$t[0]_$l/2\n$s2\n+\n$q2\n";
}
close($fh); close($fh1); close($fh2);
# paired end alignment
my $ins_size = $l1 + $l2 + $opts{a};
&run_cmd("$maq fastq2bfq $opts{p}1.fq $opts{p}1.bfq");
&run_cmd("$maq fastq2bfq $opts{p}2.fq $opts{p}2.bfq");
&run_cmd("$maq map -Pn1 -a $ins_size $opts{p}.map $ARGV[1] $opts{p}1.bfq $opts{p}2.bfq");
# get indel sites
my @last = ('', 0, 0, 0, 0); # name, begin, end,
open($fh, "$maq mapview $opts{p}.map |") || die;
open($fh1, ">$opts{p}.indel") || die;
print $fh1 qq{CC\tCC comments
CC\tRD read_id chr begin end ins_size
CC\tVR chr begin end ins_size n_reads
CC
CC\tIn VR lines, zero ins_size indicates that there are indels of different
CC\tlengths. In addition, indels supported by one read is not reliable.
CC
};
while (<$fh>) {
my @t = split;
next if ($t[5] != 18 || $t[8] == 0 || $t[4] < 0);
$t[0] =~ /^(\S+)_(\d+)\/[12]$/;
my ($name, $l) = ($1, $2);
next if ($t[4] == $l); # no indel
if ($last[0] ne $t[1]) {
if ($last[0]) {
print $fh1 join("\t", "VR", @last), "\n";
}
@last = ($t[1], 0, 0, 0, 0);
}
my ($b, $e, $s) = ($t[2], $t[2]+$t[4]-1, $l - $t[4]);
if ($last[1] == 0) { # the first
@last = ($t[1], $b, $e, $s, 1);
} elsif ($b <= $last[2]) { # overlap
if ($s != $last[3]) { # conflict
$last[3] = 0;
}
++$last[4];
$last[1] = $b;
} else { # non-overlap
print $fh1 join("\t", "VR", @last), "\n";
@last = ($t[1], $b, $e, $s, 1);
}
print $fh1 join("\t", 'RD', $name, $t[1], $b, $e, $s), "\n";
}
close($fh); close($fh1);
}
#
# for Sanger's PE read format only
#
sub cat2pair
{
my %opts = (1=>0, 2=>0);
getopts('1:2:', \%opts);
die qq(Usage: maq.pl cat2pair [-1 $opts{1}] [-2 $opts{2}] <read1_len> <input.fastq> [output.fastq]\n) if (@ARGV < 2);
my ($tl1, $tl2) = ($opts{1}, $opts{2});
my $size1 = $ARGV[0];
my $fn = $ARGV[1];
my $fn_out = (@ARGV >= 3)? $ARGV[2] : $ARGV[1];
$fn_out =~ s/^.*\/([^\/\s]+)$/$1/ if ($fn_out =~ /\//);
$fn_out =~ s/\.gz$// if ($fn_out =~ /\.gz$/);
mkdir("read1"); mkdir("read2");
my ($fh1, $fh2, $fhin);
$fn = "gzip -dc $fn |" if ($fn =~ /\.gz$/);
open($fhin, $fn) || die;
open($fh1, ">read1/$fn_out") || die;
open($fh2, ">read2/$fn_out") || die;
while (<$fhin>) {
if (/^@/) {
chomp; print $fh1 "$_/1\n"; print $fh2 "$_/2\n";
$_ = <$fhin>; chomp; # sequence
print $fh1 substr($_, $tl1, $size1-$tl1), "\n+\n";
print $fh2 substr($_, $size1+$tl2), "\n+\n";
<$fhin>; $_ = <$fhin>; chomp; # qualities
print $fh1 substr($_, $tl1, $size1-$tl1), "\n";
print $fh2 substr($_, $size1+$tl2), "\n";
}
}
close($fhin); close($fh1); close($fh2);
}
#
# for Sanger's farm only
#
sub fastq2bfq {
my %opts = (s=>1000000, e=>'fastq', d=>'', r=>'', a=>250);
getopts('s:e:Ed:r:a:', \%opts);
die qq(
Usage: maq.pl fastq2bfq [-s nreads] [-e ext] <src_dir> <dst_dir>\n
Options: -s INT number of reads per file [1000000]
-e STR extension of the read files [fastq]
-d FILE adapter sequence file [null]
-r FILE reference genome [hg18_male.bfa]
-a INT maximum insert size [$opts{a}]
-E the input in is Solexa's "export" format
\n) if (@ARGV < 2);
my ($size, $ext) = ($opts{s}, $opts{e});
my $is_export = (defined $opts{E})? 1 : 0;
my ($src_dir, $dst_dir) = ($ARGV[0], $ARGV[1]);
$dst_dir =~ s/\/$//;
my ($fh_lst, $fh_pl);
open($fh_lst, ">$dst_dir.lst") || die;
open($fh_pl, ">$dst_dir.pl") || die;
my $tmp_dir = "$dst_dir/tmp";
my $cwd = getcwd;
die("FATAL ERROR: source directory '$src_dir' does not exist!\n") unless (-d $src_dir);
mkdir($dst_dir) unless (-d $dst_dir);
mkdir($tmp_dir) unless (-d $tmp_dir);
chdir($src_dir);
my @list = `(find . -name "*.$ext" -follow; find . -name "*.$ext.gz" -follow)`; # get the list of files
chdir($cwd);
$size = $size >> 1 << 1;
# run 'maq fastq2bfq'
my $maq = gwhich("maq") || die("ERROR: Cannot find maq\n");
my $fq_all2std = gwhich("fq_all2std.pl") || die("ERROR: Cannot find fq_all2std.pl\n");
foreach (@list) {
chomp; s/^\.\///;
my $ori = $_;
my $prog = (/\.gz$/i? 'zcat' : 'cat') . " $src_dir/$ori";
if ($is_export) {
next if ($ori !~ /export/i);
$prog = "$prog | $fq_all2std export2sol | $maq sol2sanger - -";
}
s/\//-/g; s/\.gz$//i; s/\.$ext$//;
my ($cur_size, $name);
if ($is_export) {
# IMPORTANT: I do not know what single end reads look like.
# possibly this part does not work well for SE reads.
if (/s_\d+_([12])_/) { # paired
$cur_size = int($size/2);
$name = "reads$1";
s/(s_\d+_)[12]_/$1/;
}
} else {
if (/read(s?)[12]/) { # paired
$cur_size = int($size/2);
$name = (/read(s?)1/i)? "reads1" : "reads2";
s/read(s?)[12]//i;
} else {
$cur_size = $size;
$name = "reads.bfq";
}
}
s/--/-/g; s/^-//;
$name = (($name =~ /[12]/)? "$_-PE" : "$_-SE") . ":$name";
&run_cmd("$prog | $maq fastq2bfq -n $cur_size - $tmp_dir/$name");
}
# move files to separate directories
my $n_jobs = 0;
@list = `(cd $tmp_dir; ls)`;
foreach (@list) {
chomp;
if (/(.*):(reads[12]?)\@(\d+)\.bfq$/) {
my $d = "$dst_dir/$1\@$3";
my $t = "$d/$2.bfq";
unless (/reads2\@\d+\.bfq/) {
++$n_jobs;
print $fh_lst "$d\n";
mkdir($d);
}
move("$tmp_dir/$_", $t);
}
}
system("rm -fr $tmp_dir");
close($fh_lst);
# generate configuration file for farm-run.pl
$opts{d} = "-d ".abs_path($opts{d}) if ($opts{d});
if ($opts{r}) {
$opts{r} = abs_path($opts{r});
} else {
$opts{r} = '../../human_male.bfa';
}
print $fh_pl qq(\%fr_config =
(
# The list of directories that should be processed. Do NOT change this.
run_list=>'$dst_dir.lst',
# number of LSF jobs at a time
n_jobs=>$n_jobs,
LSF_queue=>'long',
LSF_resource=>'select[mem>800 && type==X86_64] rusage[mem=800]',
# dir of the executables
binary_path=>"$ENV{HOME}/lsf-prog",
# dir of the scripts, if it is different from binary_path
script_path=>"$ENV{HOME}/lsf-prog/scripts",
# in each working directory, this function will be called.
action=>\\&func
);
sub func
{
my \$dir = shift; # the working directory
# The current working dir is the one where *.bfq are staying.
# usually the reference sequence is put two-level higher than
# the current working dir.
my \$maq_comm = "maq map -a $opts{a} $opts{d} $dst_dir.map $opts{r}";
if (-f "reads.bfq") { # single end
system("\$maq_comm reads.bfq");
} elsif (-f "reads1.bfq" && ! -f "reads2.bfq") { # single end
system("\$maq_comm reads1.bfq");
} elsif (-f "reads1.bfq" && -f "reads2.bfq") { # paired end
system("\$maq_comm reads1.bfq reads2.bfq");
}
}
);
close($fh_pl);
}
sub sv {
my %opts = (i=>150, l=>35, q=>35, s=>7);
getopts('s:i:l:q:', \%opts);
die("
Usage: maq.pl sv <in.mapview>\n
Options: -i INT maximum insert size [$opts{i}]
-l INT average read length [$opts{l}]
-q INT minimum alternative mapping quality [$opts{q}]
-s INT minimum length of a region [$opts{s}]\n
") unless (@ARGV);
my $d = $opts{i} - $opts{l};
my ($begins, $beginc, $lasts, $lastc) = ('', -1, '', -1);
my (@regs, %read, @reg_name);
my @reg_seq;
warn("-- read the mapview output\n");
while (<>) {
my @t = split;
next if ($t[8] <= $opts{q});
next if ($t[5] == 18 || $t[5] == 64 || $t[5] == 130);
my $do_break = ($t[1] ne $lasts || $t[2] - $lastc > $d)? 1 : 0;
if ($do_break) {
if ($lastc - $beginc > $opts{s}) { # skip short/unreliable regions
my $k = @regs;
my $flag = ($lastc - $beginc < $opts{i})? '*' : '.';
push(@reg_name, "$begins\t$beginc\t$lastc\t$flag");
my $p = \@{$regs[$k]};
foreach (@reg_seq) {
push(@$p, $_);
my @s = split;
push(@{$read{$s[0]}}, $k);
}
}
($begins, $beginc) = @t[1..2];
@reg_seq = ();
}
$t[0] =~ s/\/[12]$//;
push(@reg_seq, join(" ", @t[0..3,5,8,13]));
($lasts, $lastc) = @t[1..2];
}
# build connections
warn("-- link regions\n");
my %link;
foreach my $x (keys %read) {
my $p = $read{$x};
next if (@$p != 2);
my $key = sprintf("%.10d %.10d", $p->[0], $p->[1]); # $p->[0] < $p->[1] always stands
if (defined $link{$key}) {
++$link{$key};
} else {
$link{$key} = 1;
}
}
# print connected regions
warn("-- print result\n");
foreach (reverse sort{$link{$a}<=>$link{$b}} keys %link) {
my @s = split;
my $x = $_;
my @count;
$count[$_] = 0 for (0..3);
foreach my $y (@{$regs[$s[0]]}) {
my @t = split(" ", $y);
++$count[($t[3] eq '+')? 0 : 1];
}
foreach my $y (@{$regs[$s[1]]}) {
my @t = split(" ", $y);
++$count[($t[3] eq '+')? 2 : 3];
}
# infer flag
my $flag = ($s[0] == $s[1])? 'LOP' : '';
if (!$flag) {
my @t1 = split(/\s+/, $reg_name[$s[0]]);
my @t2 = split(/\s+/, $reg_name[$s[1]]);
if ($t1[0] ne $t2[0]) {
$flag = 'DIF';
} elsif (($count[1] == 0 && 2*$count[2] < $count[3])
|| ($count[2] == 0 && 2*$count[1] < $count[0])) {
$flag = 'DEL';
} else {
$flag = 'AMB';
}
}
print "$flag\t$link{$x}\t$reg_name[$s[0]]\t$count[0]\t$count[1]\t$reg_name[$s[1]]\t$count[2]\t$count[3]\n";
}
}
#
# chrpt2snp command
#
sub chrpt2snp
{
# calculate @mm
my @mm;
die("Usage: maq.pl chrpt2snp <chr_rpt.dbSNP>\n") unless (@ARGV);
for (my $i = 0; $i != 0x10000; ++$i) {
my ($x, $k) = (1, 0);
for (my $l = 0; $l != 16; ++$l, $x <<= 1) {
++$k if ($i & $x);
}
$mm[$i] = $k;
}
my $fh;
open($fh, "| sort -k1,1 -k2,2n");
while (<>) {
next unless (/^\d+/ && /reference$/);
my @t = split("\t", $_);
next unless ($t[11] =~ /^\d+/); # no position
my $vs = $mm[$t[16]&0xffff] + $mm[$t[16]>>16&0xffff];
printf $fh ("chr$t[6]\t$t[11]\tN\tN\t%d\t%.3f\n", $vs*10, ($t[13] ne ' ')? $t[13] : 0.0);
}
close($fh);
}
#
# ucsc2snp command
#
sub ucsc2snp {
warn("-- only one-basepair substitutions and indels will be retained.\n");
my %conv = (AC=>'M', CA=>'M', AG=>'R', GA=>'R',
AT=>'W', TA=>'W', CG=>'S', GC=>'S',
CT=>'Y', TC=>'Y', GT=>'K', TG=>'K');
my ($n_not2, $n_not1) = (0, 0);
while (<>) {
my @t = split;
if ($t[9] !~ /-/) {
if (length($t[9]) != 3 || length($t[7]) != 1) {
++$n_not1;
next;
}
}
my ($a1, $a2) = split("/", $t[9]);
my $SNP;
if ($t[11] eq 'single') {
$SNP = $conv{"$a1$a2"};
} else {
if ($t[7] eq '-') {
$SNP = ($a1 ne '-')? $a1 : $a2;
} else {
$SNP = '-';
}
}
my $qual = 0;
if ($t[12] ne 'unknown') {
my @s = split(",", $t[12]);
$qual = @s * 10;
}
my $ref = (length($t[7]) == 1)? $t[7] : 'N';
print "$t[1]\t$t[3]\t$ref\t$SNP\t$qual\t$t[13]\t$t[15]\n";
}
warn("-- discarded: ($n_not1, $n_not2)\n");
}
sub demo {
my %opts = (N=>1000000, d=>'maqdemo');
getopts('N:d:hs', \%opts);
die("
Usage: maq.pl demo [-N npairs] [-d outdir] [-h] <in.fa> <in.simudat>\n
Options: -N INT number of read pairs [$opts{N}]
-d DIR output directory [$opts{d}]
-s single-end mode in alignment
-h haploid mode in simulation\n
") if (@ARGV < 2);
my $peopt = (defined $opts{s})? '' : '-p';
my $simuopt = "-N $opts{N}";
$simuopt .= " -h" if (defined $opts{h});
my $maq = gwhich("maq");
my $maq_pl = gwhich("maq.pl");
my $eval_pl = gwhich("maq_eval.pl");
die("** 'maq', 'maq.pl' and 'maq_eval.pl' MUST be on the \$PATH\n") unless ($maq && $maq_pl && $eval_pl);
&run_cmd("mkdir -p $opts{d}");
&run_cmd("$maq simulate $simuopt $opts{d}/r1.fq $opts{d}/r2.fq $ARGV[0] $ARGV[1] > $opts{d}/true.snp");
&run_cmd("$maq fasta2bfa $ARGV[0] $opts{d}/ref.bfa");
&run_cmd("(cd $opts{d}; $maq_pl easyrun $peopt -d easyrun ref.bfa r1.fq r2.fq)");
&run_cmd("(cd $opts{d}; $maq simustat easyrun/all.map > eval.simustat)");
&run_cmd("(cd $opts{d}; $eval_pl sub -p eval.sub true.snp true.snp easyrun/cns.filter.snp)");
&run_cmd("(cd $opts{d}; $eval_pl indelpe true.snp easyrun/cns.indelpe > eval.indelpe)") if ($peopt);
&run_cmd("(cd $opts{d}; $eval_pl indelsoa true.snp easyrun/cns.indelse > eval.indelse)");
warn("++ $opts{d}/easyrun/cns.filter.snp gives the SNPs that passes most of filters.\n");
warn("++ $opts{d}/easyrun/cns.final.snp is the high-quality subset of the previous SNPs.\n");
warn("++ $opts{d}/easyrun/mapcheck.txt gives some statistics about qualities.\n");
warn("++ $opts{d}/true.snp contains all variants used in simulation.\n");
warn("++ $opts{d}/eval.* give various benchmarks. Their formats will be documented later.\n");
}
#
#
#
sub indelpe {
my %opts = (m=>6, n=>4);
getopts('m:n:', \%opts);
die("Usage: maq.pl indelpe [-m $opts{m}] [-n $opts{n}] <in.indelpe>\n") if (@ARGV == 0 && -t STDIN);
my ($om, $on) = ($opts{m}, $opts{n});
while (<>) {
my @t = split;
# calculate length of homopolymer tract
$_ = $t[8];
my $c = substr($_, 0, 1);
/^($c+)/;
my $n_hpt = length($1);
$n_hpt = length($1) if (/^(${c}{3,}[^$c\s]{1,2}${c}{3,})/);
$n_hpt = length($1) if (/^(${c}{4,}[^$c\s]{1,4}${c}{4,})/);
# get rid of reads afftected by homopolymer tract
my (@b, @e, @mm, @nb, @ne, @nmm);
$_ = $t[10]; s/^@//; @b = split(',', $_);
$_ = $t[11]; s/^@//; @e = split(',', $_);
$_ = $t[12]; s/^@//; @mm = split(',', $_);
for my $i (0 .. $#b) {
if ($b[$i] > $om && $e[$i] > $om && $e[$i] > $n_hpt + $on && $mm[$i] <= 2) {
push(@nb, $b[$i]);
push(@ne, $e[$i]);
push(@nmm, $mm[$i]);
}
}
$t[3] = $t[5] + $t[6] + @nb;
$t[9] = @nb;
$t[10] = "@".join(",", @nb).",";
$t[11] = "@".join(",", @ne).",";
$t[12] = "@".join(",", @nmm).",";
print join("\t", @t), "\n";
}
}
#
# Usage
#
sub usage
{
die qq(
Program: maq.pl (helper script for maq)
Version: $version
Contact: Heng Li <lh3\@sanger.ac.uk>
Usage: maq.pl <command> [options] <input> [...]
Command: easyrun simple pipeline for small dataset
demo demonstration of maq functionalities (for SE only)
SNPfilter filter SNPs
statmap extract statistics from the error output of 'maq map'
chrpt2snp convert dbSNP's chr_rpt file to .snp file
ucsc2snp convert UCSC's SNP dump to .snp file
fastq2bfq convert fastq in batch
cat2pair convert paired end reads format
sv call structural variations
indelpe post-processing indelpe output
\n);
}
#
# Other utilities
#
sub test_file
{
my ($file) = @_;
my $gzip = gwhich('gzip') || die;
my ($is_gzip, $fh, $first);
if (system("$gzip -l $file >/dev/null 2>&1")) {
$is_gzip = 0;
open($fh, $file);
} else {
$is_gzip = 1;
open($fh, "$gzip -dc $file |");
}
read($fh, $first, 1);
close($fh);
return ($is_gzip, $first);
}
sub run_cmd
{
my ($cmd) = @_;
warn("-- CMD: $cmd\n");
system("$cmd") && die("** fail to run command '$cmd'");
}
# the following codes are copied from treefam::generic
sub dirname
{
my $prog = shift;
my $cwd = getcwd;
return $cwd if ($prog !~ /\//);
$prog =~ s/\/[^\s\/]+$//g;
return $prog;
}
sub which
{
my $file = shift;
my $path = (@_)? shift : $ENV{PATH};
return if (!defined($path));
foreach my $x (split(":", $path)) {
$x =~ s/\/$//;
return "$x/$file" if (-x "$x/$file" && -f "$x/$file");
}
return;
}
sub gwhich
{
my $progname = shift;
my $addtional_path = shift if (@_);
my $dirname = &dirname($0);
my $tmp;
chomp($dirname);
if (-x $progname && -f $progname) {
return abs_path($progname);
} elsif (defined($addtional_path) && ($tmp = &which($progname, $addtional_path))) {
return $tmp; # lh3: Does it work? I will come back to this later
} elsif (defined($dirname) && (-x "$dirname/$progname" && -f "$dirname/$progname")) {
return abs_path("$dirname/$progname");
} elsif (($tmp = &which($progname))) { # on the $PATH
return $tmp;
} else {
warn("[gwhich] fail to find executable $progname anywhere.");
return;
}
}
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