/usr/bin/maq.pl is in maq 0.7.1-6.
This file is owned by root:root, with mode 0o755.
The actual contents of the file can be viewed below.
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 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 121 122 123 124 125 126 127 128 129 130 131 132 133 134 135 136 137 138 139 140 141 142 143 144 145 146 147 148 149 150 151 152 153 154 155 156 157 158 159 160 161 162 163 164 165 166 167 168 169 170 171 172 173 174 175 176 177 178 179 180 181 182 183 184 185 186 187 188 189 190 191 192 193 194 195 196 197 198 199 200 201 202 203 204 205 206 207 208 209 210 211 212 213 214 215 216 217 218 219 220 221 222 223 224 225 226 227 228 229 230 231 232 233 234 235 236 237 238 239 240 241 242 243 244 245 246 247 248 249 250 251 252 253 254 255 256 257 258 259 260 261 262 263 264 265 266 267 268 269 270 271 272 273 274 275 276 277 278 279 280 281 282 283 284 285 286 287 288 289 290 291 292 293 294 295 296 297 298 299 300 301 302 303 304 305 306 307 308 309 310 311 312 313 314 315 316 317 318 319 320 321 322 323 324 325 326 327 328 329 330 331 332 333 334 335 336 337 338 339 340 341 342 343 344 345 346 347 348 349 350 351 352 353 354 355 356 357 358 359 360 361 362 363 364 365 366 367 368 369 370 371 372 373 374 375 376 377 378 379 380 381 382 383 384 385 386 387 388 389 390 391 392 393 394 395 396 397 398 399 400 401 402 403 404 405 406 407 408 409 410 411 412 413 414 415 416 417 418 419 420 421 422 423 424 425 426 427 428 429 430 431 432 433 434 435 436 437 438 439 440 441 442 443 444 445 446 447 448 449 450 451 452 453 454 455 456 457 458 459 460 461 462 463 464 465 466 467 468 469 470 471 472 473 474 475 476 477 478 479 480 481 482 483 484 485 486 487 488 489 490 491 492 493 494 495 496 497 498 499 500 501 502 503 504 505 506 507 508 509 510 511 512 513 514 515 516 517 518 519 520 521 522 523 524 525 526 527 528 529 530 531 532 533 534 535 536 537 538 539 540 541 542 543 544 545 546 547 548 549 550 551 552 553 554 555 556 557 558 559 560 561 562 563 564 565 566 567 568 569 570 571 572 573 574 575 576 577 578 579 580 581 582 583 584 585 586 587 588 589 590 591 592 593 594 595 596 597 598 599 600 601 602 603 604 605 606 607 608 609 610 611 612 613 614 615 616 617 618 619 620 621 622 623 624 625 626 627 628 629 630 631 632 633 634 635 636 637 638 639 640 641 642 643 644 645 646 647 648 649 650 651 652 653 654 655 656 657 658 659 660 661 662 663 664 665 666 667 668 669 670 671 672 673 674 675 676 677 678 679 680 681 682 683 684 685 686 687 688 689 690 691 692 693 694 695 696 697 698 699 700 701 702 703 704 705 706 707 708 709 710 711 712 713 714 715 716 717 718 719 720 721 722 723 724 725 726 727 728 729 730 731 732 733 734 735 736 737 738 739 740 741 742 743 744 745 746 747 748 749 750 751 752 753 754 755 756 757 758 759 760 761 762 763 764 765 766 767 768 769 770 771 772 773 774 775 776 777 778 779 780 781 782 783 784 785 786 787 788 789 790 791 792 793 794 795 796 797 798 799 800 801 802 803 804 805 806 807 808 809 810 811 812 813 814 815 816 817 818 819 820 821 822 823 824 825 826 827 828 829 830 831 832 833 834 835 836 837 838 839 840 841 842 843 844 845 846 847 848 849 850 851 852 853 854 855 856 857 858 859 860 861 862 863 864 865 866 867 868 869 870 871 872 873 874 875 876 877 878 879 880 881 882 883 884 885 886 | #!/usr/bin/perl -w
# 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;
}
}
|