comparison cufflinks_wrapper.py @ 9:a1ea9af8d5f4 draft

planemo upload for repository https://github.com/galaxyproject/tools-devteam/tree/master/tool_collections/cufflinks/cufflinks commit a1517c9d22029095120643bbe2c8fa53754dd2b7

8:64698e16f4a6

#!/usr/bin/env python

import optparse, os, shutil, subprocess, sys, tempfile
from galaxy import eggs
from galaxy.datatypes.util.gff_util import parse_gff_attributes, gff_attributes_to_str

def stop_err( msg ):
    sys.stderr.write( "%s\n" % msg )
    sys.exit()
    
def __main__():
    #Parse Command Line
    parser = optparse.OptionParser()
    parser.add_option( '-1', '--input', dest='input', help=' file of RNA-Seq read alignments in the SAM format. SAM is a standard short read alignment, that allows aligners to attach custom tags to individual alignments, and Cufflinks requires that the alignments you supply have some of these tags. Please see Input formats for more details.' )
    parser.add_option( '-I', '--max-intron-length', dest='max_intron_len', help='The minimum intron length. Cufflinks will not report transcripts with introns longer than this, and will ignore SAM alignments with REF_SKIP CIGAR operations longer than this. The default is 300,000.' )

    parser.add_option( '-j', '--pre-mrna-fraction', dest='pre_mrna_fraction', help='Some RNA-Seq protocols produce a significant amount of reads that originate from incompletely spliced transcripts, and these reads can confound the assembly of fully spliced mRNAs. Cufflinks uses this parameter to filter out alignments that lie within the intronic intervals implied by the spliced alignments. The minimum depth of coverage in the intronic region covered by the alignment is divided by the number of spliced reads, and if the result is lower than this parameter value, the intronic alignments are ignored. The default is 5%.' )
    parser.add_option( '-p', '--num-threads', dest='num_threads', help='Use this many threads to align reads. The default is 1.' )
    parser.add_option( '-G', '--GTF', dest='GTF', help='Tells Cufflinks to use the supplied reference annotation to estimate isoform expression. It will not assemble novel transcripts, and the program will ignore alignments not structurally compatible with any reference transcript.' )
    parser.add_option("--compatible-hits-norm", dest='compatible_hits_norm', action="store_true", help='Count hits compatible with reference RNAs only')
    parser.add_option( '-g', '--GTF-guide', dest='GTFguide', help='use reference transcript annotation to guide assembly' )
    parser.add_option("--3-overhang-tolerance",dest='three_overhang_tolerance', help='The number of bp allowed to overhang the 3prime end of a reference transcript when determining if an assembled transcript should be merged with it (ie, the assembled transcript is not novel). The default is 600 bp.')
    parser.add_option("--intron-overhang-tolerance",dest='intron_overhang_tolerance',help='The number of bp allowed to enter the intron of a reference transcript when determining if an assembled transcript should be merged with it (ie, the assembled transcript is not novel). The default is 50 bp.')
    parser.add_option("--no-faux-reads", dest='no_faux_reads',help='This option disables tiling of the reference transcripts with faux reads. Use this if you only want to use sequencing reads in assembly but do not want to output assembled transcripts that lay within reference transcripts. All reference transcripts in the input annotation will also be included in the output.')
    parser.add_option( '-u', '--multi-read-correct', dest='multi_read_correct', action="store_true", help='Tells Cufflinks to do an initial estimation procedure to more accurately weight reads mapping to multiple locations in the genome')
    
    # Normalization options.
    parser.add_option( "--no-effective-length-correction", dest="no_effective_length_correction", action="store_true" ) 
    parser.add_option( "--no-length-correction", dest="no_length_correction", action="store_true" ) 

    # Wrapper / Galaxy options.
    parser.add_option( '-A', '--assembled-isoforms-output', dest='assembled_isoforms_output_file', help='Assembled isoforms output file; formate is GTF.' )

    # Advanced Options:	
    parser.add_option( "--library-type",dest="library_type",help=' library prep used for input reads, default fr-unstranded')
    parser.add_option( '-M','--mask-file', dest='mask_file', help='Tells Cufflinks to ignore all reads that could have come from transcripts in this GTF file. \
                                                                   We recommend including any annotated rRNA, mitochondrial transcripts other abundant transcripts \
                                                                   you wish to ignore in your analysis in this file. Due to variable efficiency of mRNA enrichment \
                                                                   methods and rRNA depletion kits, masking these transcripts often improves the overall robustness \
                                                                   of transcript abundance estimates.')
    parser.add_option( '-m', '--inner-mean-dist', dest='inner_mean_dist', help='This is the expected (mean) inner distance between mate pairs. \
                                                                                For, example, for paired end runs with fragments selected at 300bp, \
                                                                                where each end is 50bp, you should set -r to be 200. The default is 45bp.') # cufflinks: --frag-len-mean

    parser.add_option( '-s', '--inner-dist-std-dev', dest='inner_dist_std_dev', help='The standard deviation for the distribution on inner distances between mate pairs. The default is 20bp.' )  # cufflinks: --frag-len-std-dev
    parser.add_option( '--max-mle-iterations', dest='max_mle_iterations', help='Sets the number of iterations allowed during maximum likelihood estimation of abundances. Default: 5000' )
    parser.add_option( '--junc-alpha', dest='junc_alpha', help='Alpha value for the binomial test used during false positive spliced alignment filtration. Default: 0.001' )
    parser.add_option( '--small-anchor-fraction', dest='small_anchor_fraction', help='Spliced reads with less than this percent of their length on each side of\

    parser.add_option( '--max-bundle-frags', dest='max_bundle_frags', help='Sets the maximum number of fragments a locus may have before being skipped. Skipped loci are listed in skipped.gtf. Default: 1,000,000' )
    parser.add_option( '--min-intron-length', dest='min_intron_length', help='Minimal allowed intron size. Default: 50' )
    parser.add_option( '--trim-3-avgcov-thresh', dest='trim_three_avgcov_thresh', help='Minimum average coverage required to attempt 3prime trimming. Default: 10' )
    parser.add_option( '--trim-3-dropoff-frac', dest='trim_three_dropoff_frac', help='The fraction of average coverage below which to trim the 3prime end of an assembled transcript. Default: 0.1' )


    # Bias correction options.
    parser.add_option( '-b', dest='do_bias_correction', action="store_true", help='Providing Cufflinks with a multifasta file via this option instructs it to run our new bias detection and correction algorithm which can significantly improve accuracy of transcript abundance estimates.')
    parser.add_option( '', '--index', dest='index', help='The path of the reference genome' )
    parser.add_option( '', '--ref_file', dest='ref_file', help='The reference dataset from the history' )
    
    # Global model (for trackster).
    parser.add_option( '', '--global_model', dest='global_model_file', help='Global model used for computing on local data' )
    
    (options, args) = parser.parse_args()
    
    # output version # of tool
    try:
        tmp = tempfile.NamedTemporaryFile().name
        tmp_stdout = open( tmp, 'wb' )
        proc = subprocess.Popen( args='cufflinks --no-update-check 2>&1', shell=True, stdout=tmp_stdout )

            sys.stdout.write( '%s\n' % stdout )
        else:
            raise Exception
    except:
        sys.stdout.write( 'Could not determine Cufflinks version\n' )
    
    # If doing bias correction, set/link to sequence file.
    if options.do_bias_correction:
        if options.ref_file:
            # Sequence data from history.
            # Create symbolic link to ref_file so that index will be created in working directory.

            if not os.path.exists( options.index ):
                stop_err( 'Reference genome %s not present, request it by reporting this error.' % options.index )
            seq_path = options.index

    # Build command.
    
    # Base; always use quiet mode to avoid problems with storing log output.
    cmd = "cufflinks -q --no-update-check"
    
    # Add options.
    if options.max_intron_len:
        cmd += ( " -I %i" % int ( options.max_intron_len ) )
    if options.min_isoform_fraction:
        cmd += ( " -F %f" % float ( options.min_isoform_fraction ) )
    if options.pre_mrna_fraction:
        cmd += ( " -j %f" % float ( options.pre_mrna_fraction ) )    
    if options.num_threads:
        cmd += ( " -p %i" % int ( options.num_threads ) )
    if options.GTF:
        cmd += ( " -G %s" % options.GTF )
    if options.compatible_hits_norm:
        cmd += ( " --compatible-hits-norm" )
    if options.GTFguide:
        cmd += ( " -g %s" % options.GTFguide )
        cmd += ( " --3-overhang-tolerance %i" % int ( options.three_overhang_tolerance ) )
        cmd += ( " --intron-overhang-tolerance %i" % int ( options.intron_overhang_tolerance ) )
    if options.no_faux_reads:
        cmd += ( " --no-faux-reads" )
    if options.multi_read_correct:
        cmd += ( " -u" )

    if options.library_type and options.library_type != 'auto':
        cmd += ( " --library-type %s" % options.library_type)
    if options.mask_file:
        cmd += ( " --mask-file %s" % options.mask_file )
    if options.inner_mean_dist:
        cmd += ( " -m %i" % int ( options.inner_mean_dist ) )
    if options.inner_dist_std_dev:
        cmd += ( " -s %i" % int ( options.inner_dist_std_dev ) )
    if options.max_mle_iterations:
        cmd += ( " --max-mle-iterations %i" % int ( options.max_mle_iterations ) )
    if options.junc_alpha:
        cmd += ( " --junc-alpha %f" % float ( options.junc_alpha) ) 
    if options.small_anchor_fraction:
        cmd += ( " --small-anchor-fraction %f" % float (options.small_anchor_fraction ) )
    if options.overhang_tolerance:
        cmd += ( " --overhang-tolerance %i" % int ( options.overhang_tolerance ) )
    if options.max_bundle_length:
        cmd += ( " --max-bundle-length %i" % int ( options.max_bundle_length ) ) 
    if options.max_bundle_frags:
        cmd += ( " --max-bundle-frags %i" % int ( options.max_bundle_frags ) )
    if options.min_intron_length:
        cmd += ( " --min-intron-length %i" % int ( options.min_intron_length ) )
    if options.trim_three_avgcov_thresh:
        cmd += ( " --trim-3-avgcov-thresh %i" % int ( options.trim_three_avgcov_thresh ) ) 
    if options.trim_three_dropoff_frac:
        cmd += ( " --trim-3-dropoff-frac %f" % float ( options.trim_three_dropoff_frac ) ) 

    if options.do_bias_correction:
        cmd += ( " -b %s" % seq_path )
    if options.no_effective_length_correction:
        cmd += ( " --no-effective-length-correction" )
    if options.no_length_correction:
        cmd += ( " --no-length-correction" )
        
    # Add input files.
    cmd += " " + options.input
   
    # Debugging.
    print cmd
 
    #
    # Run command and handle output.
    #
    try:
        #

        tmp_name = tempfile.NamedTemporaryFile( dir="." ).name
        tmp_stderr = open( tmp_name, 'wb' )
        proc = subprocess.Popen( args=cmd, shell=True, stderr=tmp_stderr.fileno() )
        returncode = proc.wait()
        tmp_stderr.close()
        
        # Error checking.
        if returncode != 0:
            raise Exception, "return code = %i" % returncode
        
        #
        # Handle output.
        # 
        
        # Read standard error to get total map/upper quartile mass.
        total_map_mass = -1
        tmp_stderr = open( tmp_name, 'r' )
        for line in tmp_stderr:
            if line.lower().find( "map mass" ) >= 0 or line.lower().find( "upper quartile" ) >= 0:
                total_map_mass = float( line.split(":")[1].strip() )
                break
        tmp_stderr.close()
        
        #
        # If there's a global model provided, use model's total map mass
        # to adjust FPKM + confidence intervals.
        #
        if options.global_model_file:        
            # Global model is simply total map mass from original run.
            global_model_file = open( options.global_model_file, 'r' )
            global_model_total_map_mass = float( global_model_file.readline() )
            global_model_file.close()
        
            # Ratio of global model's total map mass to original run's map mass is
            # factor used to adjust FPKM.
            fpkm_map_mass_ratio = total_map_mass / global_model_total_map_mass
        
            # Update FPKM values in transcripts.gtf file.
            transcripts_file = open( "transcripts.gtf", 'r' )
            tmp_transcripts = tempfile.NamedTemporaryFile( dir="." ).name
            new_transcripts_file = open( tmp_transcripts, 'w' )
            for line in transcripts_file:

                fields[8] = gff_attributes_to_str( attrs, "GTF" )
                new_transcripts_file.write( "%s\n" % '\t'.join( fields ) )
            transcripts_file.close()
            new_transcripts_file.close()
            shutil.copyfile( tmp_transcripts, "transcripts.gtf" )
            
        # TODO: update expression files as well.
                    
        # Set outputs. Transcript and gene expression handled by wrapper directives.
        shutil.copyfile( "transcripts.gtf" , options.assembled_isoforms_output_file )
        if total_map_mass > -1:
            f = open( "global_model.txt", 'w' )
            f.write( "%f\n" % total_map_mass )
            f.close()
    except Exception, e:

                if not stderr or len( stderr ) % buffsize != 0:
                    break
        except OverflowError:
            pass
        tmp_stderr.close()
        
        stop_err( 'Error running cufflinks.\n%s\n%s' % ( str( e ), stderr ) )

if __name__=="__main__": __main__()

9:a1ea9af8d5f4

#!/usr/bin/env python

import optparse
import os
import shutil
import subprocess
import sys
import tempfile
from galaxy.datatypes.util.gff_util import parse_gff_attributes, gff_attributes_to_str


def stop_err( msg ):
    sys.exit( "%s\n" % msg )


def __main__():
    #Parse Command Line
    parser = optparse.OptionParser()
    parser.add_option( '-1', '--input', dest='input', help=' file of RNA-Seq read alignments in the SAM format. SAM is a standard short read alignment, that allows aligners to attach custom tags to individual alignments, and Cufflinks requires that the alignments you supply have some of these tags. Please see Input formats for more details.' )
    parser.add_option( '-I', '--max-intron-length', dest='max_intron_len', help='The minimum intron length. Cufflinks will not report transcripts with introns longer than this, and will ignore SAM alignments with REF_SKIP CIGAR operations longer than this. The default is 300,000.' )

    parser.add_option( '-j', '--pre-mrna-fraction', dest='pre_mrna_fraction', help='Some RNA-Seq protocols produce a significant amount of reads that originate from incompletely spliced transcripts, and these reads can confound the assembly of fully spliced mRNAs. Cufflinks uses this parameter to filter out alignments that lie within the intronic intervals implied by the spliced alignments. The minimum depth of coverage in the intronic region covered by the alignment is divided by the number of spliced reads, and if the result is lower than this parameter value, the intronic alignments are ignored. The default is 5%.' )
    parser.add_option( '-p', '--num-threads', dest='num_threads', help='Use this many threads to align reads. The default is 1.' )
    parser.add_option( '-G', '--GTF', dest='GTF', help='Tells Cufflinks to use the supplied reference annotation to estimate isoform expression. It will not assemble novel transcripts, and the program will ignore alignments not structurally compatible with any reference transcript.' )
    parser.add_option("--compatible-hits-norm", dest='compatible_hits_norm', action="store_true", help='Count hits compatible with reference RNAs only')
    parser.add_option( '-g', '--GTF-guide', dest='GTFguide', help='use reference transcript annotation to guide assembly' )
    parser.add_option("--3-overhang-tolerance", dest='three_overhang_tolerance', help='The number of bp allowed to overhang the 3prime end of a reference transcript when determining if an assembled transcript should be merged with it (ie, the assembled transcript is not novel). The default is 600 bp.')
    parser.add_option("--intron-overhang-tolerance", dest='intron_overhang_tolerance', help='The number of bp allowed to enter the intron of a reference transcript when determining if an assembled transcript should be merged with it (ie, the assembled transcript is not novel). The default is 50 bp.')
    parser.add_option("--no-faux-reads", dest='no_faux_reads', help='This option disables tiling of the reference transcripts with faux reads. Use this if you only want to use sequencing reads in assembly but do not want to output assembled transcripts that lay within reference transcripts. All reference transcripts in the input annotation will also be included in the output.')
    parser.add_option( '-u', '--multi-read-correct', dest='multi_read_correct', action="store_true", help='Tells Cufflinks to do an initial estimation procedure to more accurately weight reads mapping to multiple locations in the genome')

    # Normalization options.
    parser.add_option( "--no-effective-length-correction", dest="no_effective_length_correction", action="store_true" )
    parser.add_option( "--no-length-correction", dest="no_length_correction", action="store_true" )

    # Wrapper / Galaxy options.
    parser.add_option( '-A', '--assembled-isoforms-output', dest='assembled_isoforms_output_file', help='Assembled isoforms output file; formate is GTF.' )

    # Advanced Options:
    parser.add_option( "--library-type", dest="library_type", help=' library prep used for input reads, default fr-unstranded')
    parser.add_option( '-M', '--mask-file', dest='mask_file', help='Tells Cufflinks to ignore all reads that could have come from transcripts in this GTF file. \
                                                                   We recommend including any annotated rRNA, mitochondrial transcripts other abundant transcripts \
                                                                   you wish to ignore in your analysis in this file. Due to variable efficiency of mRNA enrichment \
                                                                   methods and rRNA depletion kits, masking these transcripts often improves the overall robustness \
                                                                   of transcript abundance estimates.')
    parser.add_option( '-m', '--inner-mean-dist', dest='inner_mean_dist', help='This is the expected (mean) inner distance between mate pairs. \
                                                                                For, example, for paired end runs with fragments selected at 300bp, \
                                                                                where each end is 50bp, you should set -r to be 200. The default is 45bp.')  # cufflinks: --frag-len-mean

    parser.add_option( '-s', '--inner-dist-std-dev', dest='inner_dist_std_dev', help='The standard deviation for the distribution on inner distances between mate pairs. The default is 20bp.' )  # cufflinks: --frag-len-std-dev
    parser.add_option( '--max-mle-iterations', dest='max_mle_iterations', help='Sets the number of iterations allowed during maximum likelihood estimation of abundances. Default: 5000' )
    parser.add_option( '--junc-alpha', dest='junc_alpha', help='Alpha value for the binomial test used during false positive spliced alignment filtration. Default: 0.001' )
    parser.add_option( '--small-anchor-fraction', dest='small_anchor_fraction', help='Spliced reads with less than this percent of their length on each side of\

    parser.add_option( '--max-bundle-frags', dest='max_bundle_frags', help='Sets the maximum number of fragments a locus may have before being skipped. Skipped loci are listed in skipped.gtf. Default: 1,000,000' )
    parser.add_option( '--min-intron-length', dest='min_intron_length', help='Minimal allowed intron size. Default: 50' )
    parser.add_option( '--trim-3-avgcov-thresh', dest='trim_three_avgcov_thresh', help='Minimum average coverage required to attempt 3prime trimming. Default: 10' )
    parser.add_option( '--trim-3-dropoff-frac', dest='trim_three_dropoff_frac', help='The fraction of average coverage below which to trim the 3prime end of an assembled transcript. Default: 0.1' )

    # Bias correction options.
    parser.add_option( '-b', dest='do_bias_correction', action="store_true", help='Providing Cufflinks with a multifasta file via this option instructs it to run our new bias detection and correction algorithm which can significantly improve accuracy of transcript abundance estimates.')
    parser.add_option( '', '--index', dest='index', help='The path of the reference genome' )
    parser.add_option( '', '--ref_file', dest='ref_file', help='The reference dataset from the history' )

    # Global model (for trackster).
    parser.add_option( '', '--global_model', dest='global_model_file', help='Global model used for computing on local data' )

    (options, args) = parser.parse_args()

    # output version # of tool
    try:
        tmp = tempfile.NamedTemporaryFile().name
        tmp_stdout = open( tmp, 'wb' )
        proc = subprocess.Popen( args='cufflinks --no-update-check 2>&1', shell=True, stdout=tmp_stdout )

            sys.stdout.write( '%s\n' % stdout )
        else:
            raise Exception
    except:
        sys.stdout.write( 'Could not determine Cufflinks version\n' )

    # If doing bias correction, set/link to sequence file.
    if options.do_bias_correction:
        if options.ref_file:
            # Sequence data from history.
            # Create symbolic link to ref_file so that index will be created in working directory.

            if not os.path.exists( options.index ):
                stop_err( 'Reference genome %s not present, request it by reporting this error.' % options.index )
            seq_path = options.index

    # Build command.

    # Base; always use quiet mode to avoid problems with storing log output.
    cmd = "cufflinks -q --no-update-check"

    # Add options.
    if options.max_intron_len:
        cmd += ( " -I %i" % int( options.max_intron_len ) )
    if options.min_isoform_fraction:
        cmd += ( " -F %f" % float( options.min_isoform_fraction ) )
    if options.pre_mrna_fraction:
        cmd += ( " -j %f" % float( options.pre_mrna_fraction ) )
    if options.num_threads:
        cmd += ( " -p %i" % int( options.num_threads ) )
    if options.GTF:
        cmd += ( " -G %s" % options.GTF )
    if options.compatible_hits_norm:
        cmd += ( " --compatible-hits-norm" )
    if options.GTFguide:
        cmd += ( " -g %s" % options.GTFguide )
        cmd += ( " --3-overhang-tolerance %i" % int( options.three_overhang_tolerance ) )
        cmd += ( " --intron-overhang-tolerance %i" % int( options.intron_overhang_tolerance ) )
    if options.no_faux_reads:
        cmd += ( " --no-faux-reads" )
    if options.multi_read_correct:
        cmd += ( " -u" )

    if options.library_type and options.library_type != 'auto':
        cmd += ( " --library-type %s" % options.library_type)
    if options.mask_file:
        cmd += ( " --mask-file %s" % options.mask_file )
    if options.inner_mean_dist:
        cmd += ( " -m %i" % int( options.inner_mean_dist ) )
    if options.inner_dist_std_dev:
        cmd += ( " -s %i" % int( options.inner_dist_std_dev ) )
    if options.max_mle_iterations:
        cmd += ( " --max-mle-iterations %i" % int( options.max_mle_iterations ) )
    if options.junc_alpha:
        cmd += ( " --junc-alpha %f" % float( options.junc_alpha) )
    if options.small_anchor_fraction:
        cmd += ( " --small-anchor-fraction %f" % float(options.small_anchor_fraction ) )
    if options.overhang_tolerance:
        cmd += ( " --overhang-tolerance %i" % int( options.overhang_tolerance ) )
    if options.max_bundle_length:
        cmd += ( " --max-bundle-length %i" % int( options.max_bundle_length ) )
    if options.max_bundle_frags:
        cmd += ( " --max-bundle-frags %i" % int( options.max_bundle_frags ) )
    if options.min_intron_length:
        cmd += ( " --min-intron-length %i" % int( options.min_intron_length ) )
    if options.trim_three_avgcov_thresh:
        cmd += ( " --trim-3-avgcov-thresh %i" % int( options.trim_three_avgcov_thresh ) )
    if options.trim_three_dropoff_frac:
        cmd += ( " --trim-3-dropoff-frac %f" % float( options.trim_three_dropoff_frac ) )

    if options.do_bias_correction:
        cmd += ( " -b %s" % seq_path )
    if options.no_effective_length_correction:
        cmd += ( " --no-effective-length-correction" )
    if options.no_length_correction:
        cmd += ( " --no-length-correction" )

    # Add input files.
    cmd += " " + options.input

    # Debugging.
    print cmd

    #
    # Run command and handle output.
    #
    try:
        #

        tmp_name = tempfile.NamedTemporaryFile( dir="." ).name
        tmp_stderr = open( tmp_name, 'wb' )
        proc = subprocess.Popen( args=cmd, shell=True, stderr=tmp_stderr.fileno() )
        returncode = proc.wait()
        tmp_stderr.close()

        # Error checking.
        if returncode != 0:
            raise Exception("return code = %i" % returncode)

        #
        # Handle output.
        #

        # Read standard error to get total map/upper quartile mass.
        total_map_mass = -1
        tmp_stderr = open( tmp_name, 'r' )
        for line in tmp_stderr:
            if line.lower().find( "map mass" ) >= 0 or line.lower().find( "upper quartile" ) >= 0:
                total_map_mass = float( line.split(":")[1].strip() )
                break
        tmp_stderr.close()

        #
        # If there's a global model provided, use model's total map mass
        # to adjust FPKM + confidence intervals.
        #
        if options.global_model_file:
            # Global model is simply total map mass from original run.
            global_model_file = open( options.global_model_file, 'r' )
            global_model_total_map_mass = float( global_model_file.readline() )
            global_model_file.close()

            # Ratio of global model's total map mass to original run's map mass is
            # factor used to adjust FPKM.
            fpkm_map_mass_ratio = total_map_mass / global_model_total_map_mass

            # Update FPKM values in transcripts.gtf file.
            transcripts_file = open( "transcripts.gtf", 'r' )
            tmp_transcripts = tempfile.NamedTemporaryFile( dir="." ).name
            new_transcripts_file = open( tmp_transcripts, 'w' )
            for line in transcripts_file:

                fields[8] = gff_attributes_to_str( attrs, "GTF" )
                new_transcripts_file.write( "%s\n" % '\t'.join( fields ) )
            transcripts_file.close()
            new_transcripts_file.close()
            shutil.copyfile( tmp_transcripts, "transcripts.gtf" )

        # TODO: update expression files as well.

        # Set outputs. Transcript and gene expression handled by wrapper directives.
        shutil.copyfile( "transcripts.gtf", options.assembled_isoforms_output_file )
        if total_map_mass > -1:
            f = open( "global_model.txt", 'w' )
            f.write( "%f\n" % total_map_mass )
            f.close()
    except Exception, e:

                if not stderr or len( stderr ) % buffsize != 0:
                    break
        except OverflowError:
            pass
        tmp_stderr.close()
        stop_err( 'Error running cufflinks.\n%s\n%s' % ( str( e ), stderr ) )

if __name__ == "__main__":
    __main__()