Esempio n. 1
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    def __linkToFile(self, source, target, relative=True, dry_run=False):
        """Create symbolic link to a file
        
        Internal function to make symbolic links to primary data. Checks that the
        target links don't already exist, or if they do that the current source
        file is the same as that specified in the method call.

        Arguments:
          source: the file to be linked to
          target: the name of the link pointing to source
          relative: if True then make a relative link (if possible); otherwise
            link to the target as given (default)
          dry_run: if True then only report the actions that would be performed
            (default is False, perform the actions)
        """
        # Check if target file already exists
        if os.path.exists(target):
            logging.warning("Target file %s already exists" % target)
            # Test if the sources match
            if os.readlink(target) != source:
                logging.error("Different sources for %s" % target)
            return
        if not dry_run:
            # Make symbolic links
            bcf_utils.mklink(source, target, relative=relative)
        else:
            # Report what would have been done
            print "ln -s %s %s" % (source, target)
Esempio n. 2
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    def __linkToFile(self,source,target,relative=True,dry_run=False):
        """Create symbolic link to a file
        
        Internal function to make symbolic links to primary data. Checks that the
        target links don't already exist, or if they do that the current source
        file is the same as that specified in the method call.

        Arguments:
          source: the file to be linked to
          target: the name of the link pointing to source
          relative: if True then make a relative link (if possible); otherwise
            link to the target as given (default)
          dry_run: if True then only report the actions that would be performed
            (default is False, perform the actions)
        """
        # Check if target file already exists
        if os.path.exists(target):
            logging.warning("Target file %s already exists" % target)
            # Test if the sources match
            if os.readlink(target) != source:
                logging.error("Different sources for %s" % target)
            return
        if not dry_run:
            # Make symbolic links
            bcf_utils.mklink(source,target,relative=relative)
        else:
            # Report what would have been done
            print "ln -s %s %s" % (source,target)
Esempio n. 3
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def create_analysis_dir(project,
                        top_dir=None,
                        merge_replicates=False,
                        keep_names=False,
                        dry_run=False):
    """Create and populate analysis directory for an IlluminaProject

    Creates a new directory and populates either with links to FASTQ
    files, or with 'merged' FASTQ files created by concatenating
    multiple FASTQs for each sample (which can happen for multiplexed
    runs where samples are split across multiple lanes).

    Project directory names are made up of the project name and then
    the experiment type, or just the project name if experiment type
    is not set.

    Arguments:
      project   : populated IlluminaProject object
      top_dir   : parent directory to create analysis subdirectory
                  under. Defaults to cwd if not explicitly specified
      merge_replicates: if True then creates a single FASTQ file for
                  each sample by merging multiple FASTQs together
      keep_names: if True then links to FASTQ files will have the same
                  names as the original files; by default links use the
                  shortest unique name
      dry_run   : if True then report what would be done but don't
                  actually perform any action

    Returns:
      Name of the project directory.
    
    """
    project_dir = os.path.join(top_dir,project.full_name)
    print "Creating analysis directory for project '%s'..." % project.full_name
    # Check for & create directory
    if os.path.exists(project_dir):
        print "-> %s already exists" % project_dir
    else:
        print "Making analysis directory for %s" % project.name
        if not dry_run:
            bcf_utils.mkdir(project_dir,mode=0775)
    # Make an empty ScriptCode directory
    scriptcode_dir = os.path.join(project_dir,"ScriptCode")
    if os.path.exists(scriptcode_dir):
        print "'ScriptCode' directory %s already exists" % scriptcode_dir
    else:
        print "Making 'ScriptCode' directory for %s" % project.name
        if not dry_run:
            bcf_utils.mkdir(scriptcode_dir,mode=0775)
    # Check for & create links to fastq files
    if not merge_replicates:
        for sample in project.samples:
            fastq_names = IlluminaData.get_unique_fastq_names(sample.fastq)
            for fastq in sample.fastq:
                fastq_file = os.path.join(sample.dirn,fastq)
                if keep_names:
                    fastq_ln = os.path.join(project_dir,fastq)
                else:
                    fastq_ln = os.path.join(project_dir,fastq_names[fastq])
                if os.path.exists(fastq_ln):
                    logging.error("Failed to link to %s: %s already exists" %
                                  (fastq_file,os.path.basename(fastq_ln)))
                else:
                    print "Linking to %s" % fastq
                    if not dry_run:
                        bcf_utils.mklink(fastq_file,fastq_ln,relative=True)
    else:
        # Merge files for replicates within each sample
        for sample in project.samples:
            replicates = {}
            # Gather replicates to be merged
            for fastq in sample.fastq:
                fastq_data = IlluminaData.IlluminaFastq(fastq)
                name = "%s_%s_R%d" % (fastq_data.sample_name,
                                      fastq_data.barcode_sequence,
                                      fastq_data.read_number)
                if name not in replicates:
                    replicates[name] = []
                replicates[name].append(os.path.join(sample.dirn,fastq))
                # Sort into order
                replicates[name].sort()
            # Report detected replicates
            print "Sample %s" % sample.name
            for name in replicates:
                print "\tReplicate '%s'" % name
                for fastq in replicates[name]:
                    print "\t\t%s" % fastq
            # Do the merge
            for name in replicates:
                merged_fastq = os.path.join(project_dir,name+'.fastq')
                bcf_utils.concatenate_fastq_files(merged_fastq,replicates[name])
    # Return directory name
    return project_dir
 if not options.merge_replicates:
     for sample in project.samples:
         fastq_names = get_unique_fastqs(sample)
         for fastq in sample.fastq:
             fastq_file = os.path.join(sample.dirn,fastq)
             if options.keep_names:
                 fastq_ln = os.path.join(project_dir,fastq)
             else:
                 fastq_ln = os.path.join(project_dir,fastq_names[fastq])
             if os.path.exists(fastq_ln):
                 logging.error("Failed to link to %s: %s already exists" %
                               (fastq_file,os.path.basename(fastq_ln)))
             else:
                 print "Linking to %s" % fastq
                 if not options.dry_run:
                     bcf_utils.mklink(fastq_file,fastq_ln,relative=True)
 else:
     # Merge files for replicates within each sample
     for sample in project.samples:
         replicates = {}
         # Gather replicates to be merged
         for fastq in sample.fastq:
             fastq_data = IlluminaData.IlluminaFastq(fastq)
             name = "%s_%s_R%d" % (fastq_data.sample_name,
                                   fastq_data.barcode_sequence,
                                   fastq_data.read_number)
             if name not in replicates:
                 replicates[name] = []
             replicates[name].append(os.path.join(sample.dirn,fastq))
             # Sort into order
             replicates[name].sort()