#const
my $BURNIN = 200;
-my $CHAINLEN = 1000;
+my $NCV = 1000;
my $SAMPLEGAP = 1;
my $CONFIDENCE = 0.95;
my $NSPC = 50;
my $NMB = 1024; # default
-my $status;
+my $status = 0;
my $read_type = 1; # default, single end with qual
my $E = 99999999;
my $L = 25;
my $maxHits = 200;
+my $chunkMbs = 0; # 0 = use bowtie default
my $phred33 = 0;
my $phred64 = 0;
my $solexa = 0;
my $B = 20;
my $nThreads = 1;
-my $genBamF = 0;
+my $genBamF = 1; # default is generating transcript bam file
+my $genGenomeBamF = 0;
+my $sampling = 0;
my $calcCI = 0;
my $quiet = 0;
my $help = 0;
my $strand_specific = 0;
+my $mTime = 0;
+my ($time_start, $time_end, $time_alignment, $time_rsem, $time_ci) = (0, 0, 0, 0, 0);
+
GetOptions("keep-intermediate-files" => \$keep_intermediate_files,
"no-qualities" => \$no_qual,
"paired-end" => \$paired_end,
"bowtie-n=i" => \$C,
"bowtie-e=i" => \$E,
"bowtie-m=i" => \$maxHits,
+ "bowtie-chunkmbs=i" => \$chunkMbs,
"phred33-quals" => \$phred33,
"phred64-quals" => \$phred64, #solexa1.3-quals" => \$phred64,
"solexa-quals" => \$solexa,
"estimate-rspd" => \$estRSPD,
"num-rspd-bins=i" => \$B,
"p|num-threads=i" => \$nThreads,
- "out-bam" => \$genBamF,
+ "output-genome-bam" => \$genGenomeBamF,
+ "sampling-for-bam" => \$sampling,
"calc-ci" => \$calcCI,
"ci-memory=i" => \$NMB,
+ "time" => \$mTime,
"q|quiet" => \$quiet,
"h|help" => \$help) or pod2usage(-exitval => 2, -verbose => 2);
pod2usage(-msg => "Min fragment length should be smaller or equal to max fragment length!", -exitval => 2, -verbose => 2) if ($minL > $maxL);
pod2usage(-msg => "The memory allocated for calculating credibility intervals should be at least 1 MB!\n", -exitval => 2, -verbose => 2) if ($NMB < 1);
pod2usage(-msg => "Number of threads should be at least 1!\n", -exitval => 2, -verbose => 2) if ($nThreads < 1);
+pod2usage(-msg => "Seed length should be at least 5!\n", -exitval => 2, -verbose => 2) if ($L < 5);
+pod2usage(-msg => "--sampling-for-bam cannot be specified if --out-bam is not specified!\n", -exitval => 2, -verbose => 2) if ($sampling && !$genBamF);
+
+if ($L < 25) { print "Warning: the seed length set is less than 25! This is only allowed if the references are not added poly(A) tails.\n"; }
if ($strand_specific) { $probF = 1.0; }
my $mate2_list = "";
my $inpF = "";
-my ($refName, $taskName, $tmp_dir, $imdName) = ();
+my ($refName, $sampleName, $sampleToken, $temp_dir, $stat_dir, $imdName) = ();
my $gap = 32;
if ($paired_end) {
if ($is_sam || $is_bam) { $inpF = $ARGV[0]; }
else {$mate1_list = $ARGV[0]; }
$refName = $ARGV[1];
- $taskName = $ARGV[2];
+ $sampleName = $ARGV[2];
}
else {
$mate1_list = $ARGV[0];
$mate2_list = $ARGV[1];
$refName = $ARGV[2];
- $taskName = $ARGV[3];
+ $sampleName = $ARGV[3];
}
-$tmp_dir = $taskName.".temp";
-my $pos = rindex($taskName, '/');
-if ($pos < 0) {
- $imdName = "$tmp_dir/$taskName";
-}
-else {
- $imdName = $tmp_dir."/".substr($taskName, $pos + 1);
+if ($genGenomeBamF) {
+ open(INPUT, "$refName.ti");
+ my $line = <INPUT>; chomp($line);
+ close(INPUT);
+ my ($M, $type) = split(/ /, $line);
+ pod2usage(-msg => "No genome information provided, so genome bam file cannot be generated!\n", -exitval => 2, -verbose => 2) if ($type != 0);
}
+my $pos = rindex($sampleName, '/');
+if ($pos < 0) { $sampleToken = $sampleName; }
+else { $sampleToken = substr($sampleName, $pos + 1); }
+
+$temp_dir = "$sampleName.temp";
+$stat_dir = "$sampleName.stat";
+
+if (!(-d $temp_dir) && !mkdir($temp_dir)) { print "Fail to create folder $temp_dir.\n"; exit(-1); }
+if (!(-d $stat_dir) && !mkdir($stat_dir)) { print "Fail to create folder $stat_dir.\n"; exit(-1); }
+
+$imdName = "$temp_dir/$sampleToken";
+
if (!$is_sam && !$is_bam && $phred33 + $phred64 + $solexa == 0) { $phred33 = 1; }
my ($mate_minL, $mate_maxL) = (1, $maxL);
-if (!(-d $tmp_dir) && !mkdir($tmp_dir)) { print "Fail to create the directory.\n"; exit(-1); }
-
if ($bowtie_path ne "") { $bowtie_path .= "/"; }
my ($fn, $dir, $suf) = fileparse($0);
else { print "Oh, no!!!"; exit(2); }
$command .= " -n $C -e $E -l $L";
-
if ($read_type == 2 || $read_type == 3) { $command .= " -I $minL -X $maxL"; }
+ if ($chunkMbs > 0) { $command .= " --chunkmbs $chunkMbs"; }
if ($strand_specific || $probF == 1.0) { $command .= " --norc"; }
elsif ($probF == 0.0) { $command .= " --nofw"; }
$command .= " -p $nThreads -a -m $maxHits -S";
- if ($quiet) { $command .= " --quiet"; }
-
+ if ($quiet) { $command .= " --quiet"; }
+
$command .= " $refName";
if ($read_type == 0 || $read_type == 1) {
$command .= " $mate1_list";
$command .= " -1 $mate1_list -2 $mate2_list";
}
- $command .= " | gzip > $imdName.sam.gz";
- print "$command\n";
- $status = system($command);
- if ($status != 0) {
- print "bowtie failed! Please check if you provide correct parameters/options for the pipeline!\n";
- exit(-1);
- }
- print "\n";
+ $command .= " | gzip > $sampleName.sam.gz";
- $inpF = "$imdName.sam.gz";
+ if ($mTime) { $time_start = time(); }
+
+ &runCommand($command);
+
+ if ($mTime) { $time_end = time(); $time_alignment = $time_end - $time_start; }
+
+ $inpF = "$sampleName.sam.gz";
$is_sam = 1; # output of bowtie is a sam file
}
-$command = $dir."rsem-parse-alignments $refName $imdName";
+if ($mTime) { $time_start = time(); }
+
+$command = $dir."rsem-parse-alignments $refName $sampleName $sampleToken";
my $samInpType;
if ($is_sam) { $samInpType = "s"; }
if ($tagName ne "") { $command .= " -tag $tagName"; }
if ($quiet) { $command .= " -q"; }
-print "$command\n";
-$status = system($command);
-if ($status != 0) {
- print "rsem-parse-alignments failed! Please check if you provide correct parameters/options for the pipeline!\n";
- exit(-1);
-}
-print "\n";
+&runCommand($command);
$command = $dir."rsem-build-read-index $gap";
switch($read_type) {
case 2 { $command .= " 0 $quiet $imdName\_alignable_1.fa $imdName\_alignable_2.fa"; }
case 3 { $command .= " 1 $quiet $imdName\_alignable_1.fq $imdName\_alignable_2.fq"; }
}
-print "$command\n";
-$status = system($command);
-if ($status != 0) {
- print "rsem-build-read-index failed! Please check if you provide correct parameters/options for the pipeline!\n";
- exit(-1);
-}
-print "\n";
+&runCommand($command);
-$status = open(OUTPUT, ">$imdName.mparams");
-if ($status == 0) { print "Cannot generate $imdName.mparams!\n"; exit(-1); }
+my $doesOpen = open(OUTPUT, ">$imdName.mparams");
+if ($doesOpen == 0) { print "Cannot generate $imdName.mparams!\n"; exit(-1); }
print OUTPUT "$minL $maxL\n";
print OUTPUT "$probF\n";
print OUTPUT "$estRSPD\n";
print OUTPUT "$L\n";
close(OUTPUT);
-$command = $dir."rsem-run-em $refName $read_type $imdName $taskName -p $nThreads";
+$command = $dir."rsem-run-em $refName $read_type $sampleName $sampleToken -p $nThreads";
if ($genBamF) {
$command .= " -b $samInpType $inpF";
if ($fn_list ne "") { $command .= " 1 $fn_list"; }
else { $command .= " 0"; }
+ if ($sampling) { $command .= " --sampling"; }
}
if ($calcCI) { $command .= " --gibbs-out"; }
if ($quiet) { $command .= " -q"; }
-print "$command\n";
-$status = system($command);
-if ($status != 0) {
- print "rsem-run-em failed! Please check if you provide correct parameters/options for the pipeline!\n";
- exit(-1);
-}
-print "\n";
+&runCommand($command);
if ($genBamF) {
- $command = $dir."sam/samtools sort $taskName.bam $taskName.sorted";
- print "$command\n";
- $status = system($command);
- if ($status != 0) {
- print "sam/samtools sort failed! Please check if you provide correct parameters/options for the pipeline!\n";
- exit(-1);
+ $command = $dir."sam/samtools sort $sampleName.transcript.bam $sampleName.transcript.sorted";
+ &runCommand($command);
+ $command = $dir."sam/samtools index $sampleName.transcript.sorted.bam";
+ &runCommand($command);
+
+ if ($genGenomeBamF) {
+ $command = $dir."rsem-tbam2gbam $refName $sampleName.transcript.bam $sampleName.genome.bam";
+ &runCommand($command);
+ $command = $dir."sam/samtools sort $sampleName.genome.bam $sampleName.genome.sorted";
+ &runCommand($command);
+ $command = $dir."sam/samtools index $sampleName.genome.sorted.bam";
+ &runCommand($command);
}
- print "\n";
- $command = $dir."sam/samtools index $taskName.sorted.bam";
- print "$command\n";
- $status = system($command);
- if ($status != 0) {
- print "sam/samtools index failed! Please check if you provide correct parameters/options for the pipeline!\n";
- exit(-1);
- }
- print "\n";
}
-&collectResults("$imdName.iso_res", "$taskName.isoforms.results"); # isoform level
-&collectResults("$imdName.gene_res", "$taskName.genes.results"); # gene level
+&collectResults("$imdName.iso_res", "$sampleName.isoforms.results"); # isoform level
+&collectResults("$imdName.gene_res", "$sampleName.genes.results"); # gene level
+
+if ($mTime) { $time_end = time(); $time_rsem = $time_end - $time_start; }
+
+if ($mTime) { $time_start = time(); }
if ($calcCI) {
- $command = $dir."rsem-run-gibbs $refName $taskName $imdName $BURNIN $CHAINLEN $SAMPLEGAP";
+ $command = $dir."rsem-run-gibbs $refName $sampleName $sampleToken $BURNIN $NCV $SAMPLEGAP";
+ $command .= " -p $nThreads";
if ($quiet) { $command .= " -q"; }
- print "$command\n";
- $status = system($command);
- if ($status != 0) {
- print "rsem-run-gibbs failed! Please check if you provide correct parameters/options for the pipeline!\n";
- exit(-1);
- }
- print "\n";
+ &runCommand($command);
- system("mv $taskName.isoforms.results $imdName.isoforms.results.bak1");
- system("mv $taskName.genes.results $imdName.genes.results.bak1");
- &collectResults("$imdName.iso_res", "$taskName.isoforms.results"); # isoform level
- &collectResults("$imdName.gene_res", "$taskName.genes.results"); # gene level
+ system("mv $sampleName.isoforms.results $imdName.isoforms.results.bak1");
+ system("mv $sampleName.genes.results $imdName.genes.results.bak1");
+ &collectResults("$imdName.iso_res", "$sampleName.isoforms.results"); # isoform level
+ &collectResults("$imdName.gene_res", "$sampleName.genes.results"); # gene level
- $command = $dir."rsem-calculate-credibility-intervals $refName $taskName $imdName $CONFIDENCE $NSPC $NMB";
+ $command = $dir."rsem-calculate-credibility-intervals $refName $sampleName $sampleToken $CONFIDENCE $NCV $NSPC $NMB";
+ $command .= " -p $nThreads";
if ($quiet) { $command .= " -q"; }
- print "$command\n";
- $status = system($command);
- if ($status != 0) {
- print "rsem-calculate-credibility-intervals failed! Please check if you provide correct parameters/options for the pipeline!\n";
- exit(-1);
- }
- print "\n";
+ &runCommand($command);
- system("mv $taskName.isoforms.results $imdName.isoforms.results.bak2");
- system("mv $taskName.genes.results $imdName.genes.results.bak2");
- &collectResults("$imdName.iso_res", "$taskName.isoforms.results"); # isoform level
- &collectResults("$imdName.gene_res", "$taskName.genes.results"); # gene level
+ system("mv $sampleName.isoforms.results $imdName.isoforms.results.bak2");
+ system("mv $sampleName.genes.results $imdName.genes.results.bak2");
+ &collectResults("$imdName.iso_res", "$sampleName.isoforms.results"); # isoform level
+ &collectResults("$imdName.gene_res", "$sampleName.genes.results"); # gene level
}
+if ($mTime) { $time_end = time(); $time_ci = $time_end - $time_start; }
+
+if ($mTime) { $time_start = time(); }
+
if (!$keep_intermediate_files) {
- $status = system ("rm -rf $tmp_dir");
- if ($status != 0) {
- print "Fail to delete the temporary folder!\n";
+ &runCommand("rm -rf $temp_dir", "Fail to delete the temporary folder!");
+}
+
+if ($mTime) { $time_end = time(); }
+
+if ($mTime) {
+ open(OUTPUT, ">$sampleName.time");
+ print OUTPUT "Aligning reads: $time_alignment s.\n";
+ print OUTPUT "Estimating expression levels: $time_rsem s.\n";
+ print OUTPUT "Calculating credibility intervals: $time_ci s.\n";
+ my $time_del = $time_end - $time_start;
+# print OUTPUT "Delete: $time_del s.\n";
+ close(OUTPUT);
+}
+
+# command, {err_msg}
+sub runCommand {
+ print $_[0]."\n";
+ my $status = system($_[0]);
+ if ($status != 0) {
+ my $errmsg;
+ if (scalar(@_) > 1) { $errmsg = $_[1]; }
+ else { $errmsg = "\"$command\" failed! Plase check if you provide correct parameters/options for the pipeline!"; }
+ print $errmsg."\n";
exit(-1);
}
+ print "\n";
}
# inpF, outF
sub collectResults {
my $local_status;
my ($inpF, $outF);
- my (@results, @comment) = ();
+ my (@results, @ids) = ();
my $line;
my $cnt;
++$cnt;
chomp($line);
my @local_arr = split(/\t/, $line);
- if ($cnt == 4) { @comment = @local_arr; }
+ if ($cnt == 4) { @ids = @local_arr; }
else { push(@results, \@local_arr); }
}
- push(@results, \@comment);
+ push(@results, \@ids);
close(INPUT);
$local_status = open(OUTPUT, ">$outF");
Number of threads to use. Both Bowtie and expression estimation will use this many threads. (Default: 1)
-=item B<--out-bam>
+=item B<--output-genome-bam>
+
+Generate a BAM file, 'sample_name.genome.bam', with alignments mapped to genomic coordinates and annotated with their posterior probabilities. In addition, RSEM will call samtools (included in RSEM package) to sort and index the bam file. 'sample_name.genome.sorted.bam' and 'sample_name.genome.sorted.bam.bai' will be generated. (Default: off)
+
+=item B<--sampling-for-bam>
-Generate a BAM file, 'sample_name.bam', with alignments mapped to genomic coordinates and annotated with their posterior probabilities. In addition, RSEM will call samtools (included in RSEM package) to sort and index the bam file. 'sample_name.sorted.bam' and 'sample_name.sorted.bam.bai' will be generated. (Default: off)
+When RSEM generates a BAM file, instead of outputing all alignments a read has with their posterior probabilities, one alignment is sampled and outputed according to the posterior probabilities. If the sampling result is that the read comes from the "noise" transcript, nothing is outputed. (Default: off)
=item B<--calc-ci>
=item B<--seed-length> <int>
-Seed length used by the read aligner. Providing the correct value for this parameter is important for RSEM's accuracy if the data are single-end reads. If RSEM runs Bowtie, it uses this value for Bowtie's seed length parameter. (Default: 25)
+Seed length used by the read aligner. Providing the correct value is important for RSEM. If RSEM runs Bowtie, it uses this value for Bowtie's seed length parameter. Any read with its or at least one of its mates' (for paired-end reads) length less than this value will be ignored. If the references are not added poly(A) tails, the minimum allowed value is 5, otherwise, the minimum allowed value is 25. Note that this script will only check if the value >= 5 and give a warning message if the value < 25 but >= 5. (Default: 25)
=item B<--tag> <string>
(Bowtie parameter) suppress all alignments for a read if > <int> valid alignments exist. (Default: 200)
+=item B<--bowtie-chunkmbs> <int>
+
+(Bowtie parameter) memory allocated for best first alignment calculation (Default: 0 - use bowtie's default)
+
=item B<--phred33-quals>
Input quality scores are encoded as Phred+33. (Default: on)
=item B<--phred64-quals>
-
+
Input quality scores are encoded as Phred+64 (default for GA Pipeline ver. >= 1.3). (Default: off)
=item B<--solexa-quals>
-
+
Input quality scores are solexa encoded (from GA Pipeline ver. < 1.3). (Default: off)
=item B<--forward-prob> <double>
=item B<--ci-memory> <int>
-Amount of memory (in MB) RSEM is allowed to use for computing credibility intervals. (Default: 1024)
+Maximum size (in memory, MB) of the auxiliary buffer used for computing credibility intervals (CI). Set it larger for a faster CI calculation. However, leaving 2 GB memory free for other usage is recommended. (Default: 1024)
=item B<--keep-intermediate-files>
Keep temporary files generated by RSEM. RSEM creates a temporary directory, 'sample_name.temp', into which it puts all intermediate output files. If this directory already exists, RSEM overwrites all files generated by previous RSEM runs inside of it. By default, after RSEM finishes, the temporary directory is deleted. Set this option to prevent the deletion of this directory and the intermediate files inside of it. (Default: off)
+=item B<--time>
+
+Output time consumed by each step of RSEM to 'sample_name.time'. (Default: off)
+
=item B<-q/--quiet>
Suppress the output of logging information. (Default: off)
=head1 DESCRIPTION
-In its default mode, this program aligns input reads against a reference transcriptome with Bowtie and calculates expression values using the alignments. RSEM assumes the data are single-end reads with quality scores, unless the '--paired-end' or '--no-qualities' options are specified. Users may use an alternative aligner by specifying one of the --sam and --bam options, and providing an alignment file in the specified format. However, users should make sure the alignment file satisfies the requirements mentioned in ARGUMENTS section.
+In its default mode, this program aligns input reads against a reference transcriptome with Bowtie and calculates expression values using the alignments. RSEM assumes the data are single-end reads with quality scores, unless the '--paired-end' or '--no-qualities' options are specified. Users may use an alternative aligner by specifying one of the --sam and --bam options, and providing an alignment file in the specified format. However, users should make sure that they align against the indices generated by 'rsem-prepare-reference' and the alignment file satisfies the requirements mentioned in ARGUMENTS section.
-One simple way to make the alignment file (e.g. input.sam) satisfying RSEM's requirements (assuming the aligner used put mates in a paired-end read adjacent) is to use the following command:
+One simple way to make the alignment file satisfying RSEM's requirements (assuming the aligner used put mates in a paired-end read adjacent) is to use 'convert-sam-for-rsem' script. This script only accept SAM format files as input. If a BAM format file is obtained, please use samtools to convert it to a SAM file first. For example, if '/ref/mouse_125' is the 'reference_name' and the SAM file is named 'input.sam', you can run the following command:
- sort -k 1,1 -s input.sam > input.sorted.sam
+ convert-sam-for-rsem /ref/mouse_125 input.sam -o input_for_rsem.sam
-The SAM/BAM format RSEM uses is v1.3. However, it is compatible with old SAM/BAM format.
+For details, please refer to 'convert-sam-for-rsem's documentation page.
+
+The SAM/BAM format RSEM uses is v1.4. However, it is compatible with old SAM/BAM format. However, RSEM cannot recognize 0x100 in the FLAG field. In addition, RSEM requires SEQ and QUAL are not '*'.
The user must run 'rsem-prepare-reference' with the appropriate reference before using this program.
The temporary directory and all intermediate files will be removed when RSEM finishes unless '--keep-intermediate-files' is specified.
-With the "--calc-ci" option, 95% credibility intervals and posterior mean estimates will be calculated in addition to maximum likelihood estimates.
+With the '--calc-ci' option, 95% credibility intervals and posterior mean estimates will be calculated in addition to maximum likelihood estimates.
=head1 OUTPUT
means the lower bound of the credibility intervals, ci_upper_bound(u)
means the upper bound of the credibility intervals. So the credibility
interval is [l, u]. 'transcript_id_list' is a space-separated list of
-transcript_ids belonging to the gene.
+transcript_ids belonging to the gene. If no gene information is
+provided, this file has the same content as
+'sample_name.isoforms.results'.
=item B<sample_name.isoforms.results>
File containing isoform level expression values. The format of each
line in this file is:
-transcript_id expected_counts tau_value [pmc_value tau_pme_value tau_ci_lower_bound tau_ci_upper_bound] other_attributes
+transcript_id expected_counts tau_value [pmc_value tau_pme_value tau_ci_lower_bound tau_ci_upper_bound] gene_id
+
+Fields are separated by the tab character. 'gene_id' is the gene_id of
+the gene which this transcript belongs to. If no gene information is
+provided, 'gene_id' and 'transcript_id' are the same.
-Fields are separated by the tab character. 'other_attributes' are all
-other attributes after attribute 'transcript_id' field in the GTF
-file. If no other attributes are given or no GTF file is provided in
-'rsem-prepare-reference', there will be no tab after the
-tau_value field.
+=item B<sample_name.transcript.bam, sample_name.transcript.sorted.bam and sample_name.transcript.sorted.bam.bai>
-=item B<sample_name.model> and B<sample_name.theta>
+'sample_name.transcript.bam' is a BAM-formatted file of read
+alignments in transcript coordinates. The MAPQ field of each alignment
+is set to min(100, floor(-10 * log10(1.0 - w) + 0.5)), where w is the
+posterior probability of that alignment being the true mapping of a
+read. In addition, RSEM pads a new tag ZW:f:value, where value is a
+single precision floating number representing the posterior
+probability.
-Output files used by RSEM internally for tasks like simulation,
-compute credibility intervals etc.
+'sample_name.transcript.sorted.bam' and
+'sample_name.transcript.sorted.bam.bai' are the sorted BAM file and
+indices generated by samtools (included in RSEM package).
-=item B<sample_name.bam, sample_name.sorted.bam and sample_name.sorted.bam.bai>
+=item B<sample_name.genome.bam, sample_name.genome.sorted.bam and sample_name.genome.sorted.bam.bai>
-Only generated when --out-bam is specified.
+Only generated when --output-genome-bam is specified.
-'sample_name.bam' is a BAM-formatted file of read alignments in
+'sample_name.genome.bam' is a BAM-formatted file of read alignments in
genomic coordinates. Alignments of reads that have identical genomic
coordinates (i.e., alignments to different isoforms that share the
same genomic region) are collapsed into one alignment. The MAPQ field
-of each alignment is set to max(100, floor(-10 * log10(1.0 - w) +
+of each alignment is set to min(100, floor(-10 * log10(1.0 - w) +
0.5)), where w is the posterior probability of that alignment being
the true mapping of a read. In addition, RSEM pads a new tag
ZW:f:value, where value is a single precision floating number
-representing the posterior probability.
+representing the posterior probability. If an alignment is spliced, a
+XS:A:value tag is also added, where value is either '+' or '-'
+indicating the strand of the transcript it aligns to.
-'sample_name.sorted.bam' and 'sample_name.sorted.bam.bai' are the
+'sample_name.genome.sorted.bam' and 'sample_name.genome.sorted.bam.bai' are the
sorted BAM file and indices generated by samtools (included in RSEM package).
+=item B<sample_name.sam.gz>
+
+Only generated when the input files are raw reads instead of SAM/BAM format files
+
+It is the gzipped SAM output produced by bowtie aligner.
+
+=item B<sample_name.time>
+
+Only generated when --time is specified.
+
+It contains time (in seconds) consumed by aligning reads, estimating expression levels and calculating credibility intervals.
+
+=item B<sample_name.stat>
+
+This is a folder instead of a file. All model related statistics are stored in this folder. Use 'rsem-plot-model' can generate plots using this folder.
=back
=head1 EXAMPLES
-Assume the path to the bowtie executables is in the user's PATH environment variable. Reference files are under '/ref' with name 'mm9'.
+Assume the path to the bowtie executables is in the user's PATH environment variable. Reference files are under '/ref' with name 'mouse_125'.
-1) '/data/mmliver.fq', single-end reads with quality scores. Quality scores are encoded as for 'GA pipeline version >= 1.3'. We want to use 8 threads and generate a BAM file:
+1) '/data/mmliver.fq', single-end reads with quality scores. Quality scores are encoded as for 'GA pipeline version >= 1.3'. We want to use 8 threads and generate a genome BAM file:
rsem-calculate-expression --phred64-quals \
-p 8 \
- --out-bam \
+ --output-genome-bam \
/data/mmliver.fq \
- /ref/mm9 \
+ /ref/mouse_125 \
mmliver_single_quals
-2) '/data/mmliver_1.fq' and '/data/mmliver_2.fq', paired-end reads with quality scores. Quality scores are in SANGER format. We want to use 8 threads and do not generate a BAM file:
+2) '/data/mmliver_1.fq' and '/data/mmliver_2.fq', paired-end reads with quality scores. Quality scores are in SANGER format. We want to use 8 threads and do not generate a genome BAM file:
rsem-calculate-expression -p 8 \
--paired-end \
/data/mmliver_1.fq \
/data/mmliver_2.fq \
- /ref/mm9 \
+ /ref/mouse_125 \
mmliver_paired_end_quals
-3) '/data/mmliver.fa', single-end reads without quality scores. We want to use 8 threads and generate a BAM file:
+3) '/data/mmliver.fa', single-end reads without quality scores. We want to use 8 threads:
rsem-calculate-expression -p 8 \
--no-qualities \
/data/mmliver.fa \
- /ref/mm9 \
+ /ref/mouse_125 \
mmliver_single_without_quals
-4) Data are the same as 1). We want to take a fragment length distribution into consideration. We set the fragment length mean to 150 and the standard deviation to 35. In addition to a BAM file, we also want to generate credibility intervals. We allow RSEM to use 1GB of memory for CI calculation.
+4) Data are the same as 1). We want to take a fragment length distribution into consideration. We set the fragment length mean to 150 and the standard deviation to 35. In addition to a BAM file, we also want to generate credibility intervals. We allow RSEM to use 1GB of memory for CI calculation:
rsem-calculate-expression --bowtie-path /sw/bowtie \
--phred64-quals \
--fragment-length-mean 150.0 \
--fragment-length-sd 35.0 \
-p 8 \
- --out-bam \
+ --output-genome-bam \
--calc-ci \
--ci-memory 1024 \
/data/mmliver.fq \
- /ref/mm9 \
+ /ref/mouse_125 \
mmliver_single_quals
-5) '/data/mmliver_paired_end_quals.bam', paired-end reads with quality scores. We want to use 8 threads and do not generate a BAM file:
+5) '/data/mmliver_paired_end_quals.bam', paired-end reads with quality scores. We want to use 8 threads:
rsem-calculate-expression --paired-end \
--bam \
-p 8 \
/data/mmliver_paired_end_quals.bam \
- /ref/mm9 \
+ /ref/mouse_125 \
mmliver_paired_end_quals
=cut
projects / rsem.git / blobdiff