fine tune the wrapper scripts
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6
NEWS.md
6
NEWS.md
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@ -9,9 +9,9 @@ mapping, we start to provide a wrapper script and precompiled binaries since
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this release. Please check README-alt.md for details.
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Another major addition to BWA-MEM is HLA typing, which made possible with the
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new ALT mapping strategy. Necessary data and programs are also included in
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the binary release. The wrapper script also performs HLA typing when HLA genes
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are also included in the reference genome as additional ALT contigs.
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new ALT mapping strategy. Necessary data and programs are included in the
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binary release. The wrapper script also performs HLA typing when HLA genes are
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also included in the reference genome as additional ALT contigs.
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Other notable changes to BWA-MEM:
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7
bwa.1
7
bwa.1
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@ -1,4 +1,4 @@
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.TH bwa 1 "19 May 2014" "bwa-0.7.9-r783" "Bioinformatics tools"
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.TH bwa 1 "18 November 2014" "bwa-0.7.11-r999" "Bioinformatics tools"
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.SH NAME
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.PP
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bwa - Burrows-Wheeler Alignment Tool
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@ -233,8 +233,9 @@ more aggressive read pair. [17]
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.B INPUT/OUTPUT OPTIONS:
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.TP
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.B -p
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Assume the first input query file is interleaved paired-end FASTA/Q. See the
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command description for details.
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Smart pairing. If two adjacent reads have the same name, they are considered
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to form a read pair. This way, paired-end and single-end reads can be mixed
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in a single FASTA/Q stream.
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.TP
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.BI -R \ STR
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Complete read group header line. '\\t' can be used in
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@ -4,8 +4,8 @@ use strict;
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use warnings;
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use Getopt::Std;
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my %opts = (t=>1, n=>64);
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getopts("Sadsko:R:x:t:", \%opts);
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my %opts = (t=>1);
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getopts("SadskHo:R:x:t:", \%opts);
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die('
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Usage: run-bwamem [options] <idxbase> <file1> [file2]
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@ -22,6 +22,7 @@ Options: -o STR prefix for output files [inferred from
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-d mark duplicate (via samblaster)
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-S for SAM/BAM input, don\'t shuffle
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-s sort the output alignment (requring more RAM)
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-H skip HLA typing
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-k keep temporary files generated by typeHLA
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Examples:
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@ -31,15 +32,15 @@ Examples:
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run-bwamem -o prefix -t8 -R"@RG\tID:foo\tSM:bar" hs38d6.fa read1.fq.gz read2.fq.gz
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* Remap coordinate-sorted BAM, trim Illumina PE adapters and sort the output. The BAM
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may contain single-end or paired-end reads, or a mixture of the two types. The read
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groups are not transferred to the output BAM.
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may contain single-end or paired-end reads, or a mixture of the two types. Read groups
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are not transferred to the output BAM, though.
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run-bwamem -sao prefix hs38d6.fa old-srt.bam
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* Remap name-grouped BAM and mark duplicates. Note that in this case, all reads from
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a single library should be aligned at the same time. Paired-end only.
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run-bwamem -Sdo prefix hs38d6.fa old-unsrt.bam
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run-bwamem -Sdo prefix hs38d6.fa old-unsrt.bam
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Output files:
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@ -119,7 +120,7 @@ if ($is_sam || $is_bam) {
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my $bwa_opts = "-p " . ($opts{t} > 1? "-t$opts{t} " : "") . (defined($opts{x})? "-x $opts{x} " : "") . (defined($opts{R})? "-R'$opts{R}' " : "");
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$cmd .= " | $root/trimadap \\\n" if defined($opts{a});
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$cmd .= " | $root/trimadap 2> $prefix.log.trim \\\n" if defined($opts{a});
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$cmd .= " | $root/bwa mem $bwa_opts$ARGV[0] - 2> $prefix.log.bwamem \\\n";
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$cmd .= " | $root/samblaster 2> $prefix.log.dedup \\\n" if defined($opts{d});
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@ -138,8 +139,8 @@ if (-f "$ARGV[0].alt") {
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my $t_sort = $opts{t} < 4? $opts{t} : 4;
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$cmd .= defined($opts{s})? " | $root/samtools sort -@ $t_sort -m1G - $prefix.aln;\n" : " | $root/samtools view -1 - > $prefix.aln.bam;\n";
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if ($has_hla && (!defined($opts{x}) || $opts{x} eq 'intractg')) {
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$cmd .= "$root/run-HLA ". ($opts{x} eq 'intractg'? "-A " : "") . "$prefix.hla > $prefix.hla.top 2> $prefix.log.hla;\n";
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if ($has_hla && !defined($opts{H}) && (!defined($opts{x}) || $opts{x} eq 'intractg')) {
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$cmd .= "$root/run-HLA ". (defined($opts{x}) && $opts{x} eq 'intractg'? "-A " : "") . "$prefix.hla > $prefix.hla.top 2> $prefix.log.hla;\n";
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$cmd .= "cat $prefix.hla.HLA*.gt | grep ^GT | cut -f2- > $prefix.hla.all;\n";
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$cmd .= "rm -f $prefix.hla.HLA*;\n" unless defined($opts{k});
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}
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@ -20,7 +20,7 @@ if [ $is_ctg -eq 0 ]; then
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echo "** De novo assembling..." >&2
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len=`$root/seqtk comp $pre.fq | awk '{++x;y+=$2}END{printf("%.0f\n", y/x)}'`
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$root/fermi2.pl unitig -f $root/fermi2 -r $root/ropebwt2 -t2 -l$len -p $pre.tmp $pre.fq > $pre.tmp.mak
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make -f $pre.tmp.mak
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make -f $pre.tmp.mak >&2
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cp $pre.tmp.mag.gz $pre.mag.gz
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else
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rm -f $pre.tmp.mag.gz
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