20e6eff593096b1ec381de4ee5058c5edafd2bba
mmaddren
  Tue Aug 30 15:47:54 2011 -0700
added protocol checking functionality, partial support for deprecated, and revised the error messages to be more consistent
diff --git python/programs/mkGeoPkg/mkGeoPkg python/programs/mkGeoPkg/mkGeoPkg
index 5dd0ec7..a83a9bb 100755
--- python/programs/mkGeoPkg/mkGeoPkg
+++ python/programs/mkGeoPkg/mkGeoPkg
@@ -1,575 +1,579 @@
 #!/hive/groups/encode/dcc/bin/python
 import sys, os, shutil, stat, argparse, datetime
 from ucscgenomics.compositetrack.CompositeTrack import *
 from ucscgenomics.rafile.RaFile import *
 from ucscgenomics.softfile.SoftFile import *
 from ucscgenomics.cvfile.CvFile import *
 
 class DataType(object):
 
 	def __init__(self, molecule, strategy, source, selection, soft):
 		self.molecule = molecule
 		self.strategy = strategy
 		self.source = source
 		self.selection = selection
 		self.soft = soft
 
 datatypes = {
 	'Cage': DataType('OVERRIDE RNA', 'OTHER', 'transcriptomic', 'CAGE', HighThroughputSoftFile),
 	'ChipSeq': DataType('genomic DNA', 'ChIP-Seq', 'genomic', 'ChIP', HighThroughputSoftFile),
 	'DnaPet': DataType('genomic DNA', 'OTHER', 'genomic', 'size fractionation', HighThroughputSoftFile),
 	'DnaseDgf': DataType('genomic DNA', 'DNase-Hypersensitivity', 'genomic', 'DNase', HighThroughputSoftFile),
 	'DnaseSeq': DataType('genomic DNA', 'DNase-Hypersensitivity', 'genomic', 'DNase', HighThroughputSoftFile),
 	'FaireSeq': DataType('genomic DNA', 'OTHER', 'genomic', 'other', HighThroughputSoftFile),
 	'MethylSeq': DataType('genomic DNA', 'MRE-Seq', 'genomic', 'Restriction Digest', HighThroughputSoftFile),
 	'MethylRrbs': DataType('genomic DNA', 'Bisulfite-Seq', 'genomic', 'Reduced Representation', HighThroughputSoftFile),
 	'Orchid': DataType('genomic DNA', 'OTHER', 'genomic', 'other', HighThroughputSoftFile),
 	'Proteogenomics': DataType('protein', 'mass spectrometry-based proteogenomic mapping', 'protein', 'chromatographically fractionated peptides', HighThroughputSoftFile),
 	'RnaPet': DataType('OVERRIDE RNA', 'OTHER', 'transcriptomic', 'other', HighThroughputSoftFile),
 	'RnaSeq': DataType('OVERRIDE RNA', 'RNA-Seq', 'transcriptomic', 'cDNA', HighThroughputSoftFile),
 	
 	#these need to be curated
 	'5C': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'AffyExonArray': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', MicroArraySoftFile),
 	'Bip': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'Cluster': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'Cnv': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'Combined': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'Genotype': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'Gencode': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'ChiaPet': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'Mapability': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'MethylArray': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'NRE': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'Nucleosome': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'RnaChip': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'RipGeneSt': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'RipTiling': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'RipChip': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'RipSeq': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'Switchgear': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None),
 	'TfbsValid': DataType('REPLACE', 'REPLACE', 'REPLACE', 'REPLACE', None)
 }
 
 #compare this to the source in datatype, give GP ids depending on the type
 gpIds = {
-	'genomic': '63443',
-	'transcriptomic': '30709',
-	'protein': '63447'
+	'human genomic': '63443',
+	'human transcriptomic': '30709',
+	'human protein': '63447',
+	
+	'mouse genomic': '63471',
+	'mouse transcriptomic': '66167',
+	'mouse protein': '63475'
 }
 
 cvDetails = {
 	'cell':	[ 'organism', 'description', 'karyotype', 'lineage', 'sex' ],
 	'antibody': [ 'antibodyDescription', 'targetDescription', 'vendorName', 'vendorId' ]
 }
 
 #if the term appears in the mdb and must overriding the value in the cv
 cvOverride = [ 'sex' ]
 
 #talk to Venkat lol
 cvPretend = { 'antibody Input': 'control' }
 
 #if its not in cvDetails, which things should we check by default
 cvDefaults = [ 'description' ]
 
 mdbWhitelist = [
 	'age',
 	'bioRep',
 	'control',
 	'controlId',
 	'fragSize',
 	'labExpId',
 	'labVersion',
 	'mapAlgorithm',
 	'obtainedBy',
 	'phase',
 	'readType',
 	'region',
 	'replicate',
 	'restrictionEnzyme',
 	'run',
 	'softwareVersion',
 	'spikeInPool',
 	'strain'
 ]
 
 # if the molecule is RNA, we need to map our data into !Sample_molecule, which only takes certain fields
 # first we check rnaExtractMapping. If its not there, we use the localization. This is because (at current)
 # polyA is the most important trait, otherwise its going to be nonPolyA which GEO doesn't accept that. 
 rnaExtractMapping = {
 	'shortPolyA': 'polyA RNA', 
 	'longPolyA': 'polyA RNA', 
 	'polyA': 'polyA RNA'
 }
 
 localizationMapping = {
 	'cytosol': 'cytoplasmic RNA', 
 	'polysome': 'cytoplasmic RNA',
 	'membraneFraction': 'cytoplasmic RNA',
 	'mitochondria': 'cytoplasmic RNA',
 	'nucleus': 'nuclear RNA', 
 	'nucleolus': 'nuclear RNA', 
 	'nucleoplasm': 'nuclear RNA', 
 	'nuclearMatrix': 'nuclear RNA', 
 	'chromatin': 'nuclear RNA',
 	'cell': 'total RNA'
 }
 
 # map our instrument names to GEO's names
 instrumentModels = {
 	'Illumina_GA2x': 'Illumina Genome Analyzer II',
 	'Illumina_GA2': 'Illumina Genome Analyzer II',
 	'Illumina_HiSeq_2000': 'Illumina HiSeq 2000'
 }
 
 	
 def isRawFile(file):
 	return (file.extension == 'fastq' or file.extension == 'fasta')
 	
 def isSupplimentaryFile(file):
 	return not isRawFile(file)
 
-def sampleTitle(stanza, expVars):
+def sampleTitle(stanza, expVars, warn=False):
 	concat = stanza[expVars[0]].replace('-m', '')
 	for expVar in expVars[1:len(expVars)]:
-		if expVar in stanza:
+		if expVar in stanza and stanza[expVar] != 'None':
 			concat += '_' + stanza[expVar]
-		else:
-			print 'warning: %s not in %s' % (expVar, stanza.name)
+		elif warn:
+			print 'warning: %s is None or not in %s' % (expVar, stanza.name)
 	return concat
 	
 def createMappings(mdb):
 	expIds = dict()
 	geoMapping = dict()
 	expVars = None
 	series = None
 	datatype = None
 	
 	for stanza in mdb.itervalues():
 		
 		if 'objType' in stanza and stanza['objType'] == 'composite':
 			series = stanza
 			expVars = stanza['expVars'].split(',')
 			continue
 
 		if 'expId' not in stanza:
 			print stanza.name + ': no expId'
 			continue
 
 		if 'geoSampleAccession' not in stanza:
 			# if this hasn't been submitted to GEO yet, we'll add it to the submission list
 			if stanza['expId'] not in expIds:
 				expIds[stanza['expId']] = list()
 				
 			expIds[stanza['expId']].append(stanza)
 		
 		else:
 			# otherwise we keep track of the geo number for partially submitted samples
 			if stanza['expId'] not in geoMapping:
 				geoMapping[stanza['expId']] = stanza['geoSampleAccession']
 			elif geoMapping[stanza['expId']] != 'Inconsistent' and geoMapping[stanza['expId']] != stanza['geoSampleAccession']:
 				geoMapping[stanza['expId']] = 'Inconsistent'
 				print stanza.name + ': inconsistent geo mapping'
 		
 		if datatype == None and 'dataType' in stanza:
 			datatype = stanza['dataType']
 		elif datatype != None and 'dataType' in stanza and datatype != stanza['dataType']:
 			raise KeyError(stanza.name + ': inconsistent data type') 
 
 	datatype = datatypes[datatype]
 	
 	return expIds, expVars, geoMapping, series, datatype
 	
 	
 def createSeries(softfile, compositeTrack, expIds, expVars, geoMapping, series, datatype, replace):
 	
 	if 'geoSeriesAccession' in series:
 		print 'Existing series ' + series['composite'] + ' using geoSeriesAccession ' + series['geoSeriesAccession']
 		return
 		
 	print 'Writing series ' + series['composite']
 	
 	seriesStanza = SeriesStanza()
 	seriesStanza['^SERIES'] = series['composite']
 	seriesStanza['!Series_title'] = compositeTrack.trackDb[compositeTrack.name]['longLabel'] #STILL INCORRECT
 	
 	if '!Series_summary' in replace:
 		seriesStanza['!Series_summary'] = replace['!Series_summary']
 	else:
-		raise Error('no series summary found. Please include in replace file.')
+		print 'warning: no series summary found. Please include in replace file.'
 		seriesStanza['!Series_summary'] = '[REPLACE]'
 		
 	if '!Series_overall_design' in replace:
 		seriesStanza['!Series_overall_design'] = replace['!Series_overall_design']
 	else:
-		raise Error('no series overall design found. Please include in replace file.')
+		print 'no series overall design found. Please include in replace file.'
 		seriesStanza['!Series_overall_design'] = '[REPLACE]'
 		
 	seriesStanza['!Series_web_link'] = [ compositeTrack.url, 'http://www.ncbi.nlm.nih.gov/geo/info/ENCODE.html' ]
 	
 	if '!Series_contributor' in replace:
 		seriesStanza['!Series_contributor'] = replace['!Series_contributor']
 	else:
 		seriesStanza['!Series_contributor'] = '[REPLACE]'
 		
-	seriesStanza['!Series_gp_id'] = gpIds[datatype.source]
+	seriesStanza['!Series_gp_id'] = gpIds[compositeTrack.organism + ' ' + datatype.source]
 	
 	# could use !Series_variable_* and !Series_repeats_*
 	
 	seriesStanza['!Series_sample_id'] = list()
 	
 	for idNum in expIds.iterkeys():
 		if idNum in geoMapping and geoMapping[idNum] != 'Inconsistent':
 			seriesStanza['!Series_sample_id'].append(geoMapping[idNum])
 		else:
 			seriesStanza['!Series_sample_id'].append(sampleTitle(expIds[idNum][0], expVars))
 	
 	softfile[series['composite']] = seriesStanza
 	
 def createHighThroughputSoftFile(compositeTrack, cv, expIds, expVars, geoMapping, series, datatype, instrument, replace):
 	
 	print 'Creating HighThroughput soft file'
 
 	softfile = HighThroughputSoftFile()
 	fileList = list()
 	
 	createSeries(softfile, compositeTrack, expIds, expVars, geoMapping, series, datatype, replace)
 		
 	for idNum in expIds.iterkeys():
 		
 		expId = expIds[idNum]
 		firstStanza = expId[0]
 		print 'Writing sample ' + firstStanza['metaObject'] + ' (' + idNum + ')'
 		sample = HighThroughputSampleStanza()
 
-		sample['^SAMPLE'] = sampleTitle(firstStanza, expVars)
+		sample['^SAMPLE'] = sampleTitle(firstStanza, expVars, 1)
 		sample['!Sample_type'] = 'SRA'
 		sample['!Sample_title'] = sample['^SAMPLE']
 		
 		if 'geoSeriesAccession' in series:
 			sample['!Sample_series_id'] = series['geoSeriesAccession']
 			
 		count = 1
 		
 		for stanza in expId:
 		
 			file = compositeTrack.files[stanza['fileName']]
 			
 			if isRawFile(file):
 				sample['!Sample_raw_file_' + str(count)] = file.name
 				sample['!Sample_raw_file_type_' + str(count)] = file.extension
 				
 				if file.md5sum != None:
 					sample['!Sample_raw_file_checksum_' + str(count)] = file.md5sum
 
 				fileList.append(file)	
 				count = count + 1
 			
 		count = 1
 			
 		for stanza in expId:
 		
 			file = compositeTrack.files[stanza['fileName']]
 		
 			if isSupplimentaryFile(file):
 				sample['!Sample_supplementary_file_' + str(count)] = file.name
 				
 				if file.md5sum != None:
 					sample['!Sample_supplementary_file_checksum_' + str(count)] = file.md5sum
 				
 				sample['!Sample_supplementary_file_build_' + str(count)] = compositeTrack.database
 				
 				fileList.append(file)
 				count = count + 1
 			
 		sample['!Sample_source_name'] = firstStanza['cell']
 		sample['!Sample_organism'] = compositeTrack.organism
 		
 		sample['!Sample_characteristics'] = list()
 		allVars = expVars + mdbWhitelist
 		
 		for var in allVars:
 			if var in firstStanza:
 				foobar = var
 				sample['!Sample_characteristics'].append(var + ': ' + firstStanza[var])
 				for pretend in cvPretend.iterkeys():
 					if var + ' ' + firstStanza[var] == pretend:
 						foobar = cvPretend[pretend]
 				if foobar in cvDetails:
 					for cvVar in cvDetails[foobar]:
 						if cvVar in cvOverride and cvVar in firstStanza:
 							sample['!Sample_characteristics'].append(var + ' ' + cvVar + ': ' + firstStanza[cvVar])
 						elif cvVar in cv[firstStanza[var]]:
 							sample['!Sample_characteristics'].append(var + ' ' + cvVar + ': ' + cv[firstStanza[var]][cvVar])
 				else:
 					for cvVar in cvDefaults:
 						if firstStanza[var] in cv and cvVar in cv[firstStanza[var]]:
 							sample['!Sample_characteristics'].append(var + ' ' +  cvVar + ': ' + cv[firstStanza[var]][cvVar])
 				
 		sample['!Sample_biomaterial_provider'] = cv[firstStanza['cell']]['vendorName']
 		
 		if 'treatment' in firstStanza:
 			sample['!Sample_treatment_protocol'] = firstStanza['treatment']
 		
 		if 'protocol' in cv[firstStanza['cell']]:
 			for protocol in cv[firstStanza['cell']]['protocol'].split(' '):
 					key, val = protocol.split(':')
 					if key == 'ENCODE' or key == cv[firstStanza['lab']]['labPi']:
 						sample['!Sample_growth_protocol'] = val
 		
 		if datatype.molecule == 'OVERRIDE RNA':
 			if firstStanza['rnaExtract'] in rnaExtractMapping:
 				sample['!Sample_molecule'] = rnaExtractMapping[firstStanza['rnaExtract']]
 			elif firstStanza['localization'] in localizationMapping:
 				sample['!Sample_molecule'] = localizationMapping[firstStanza['localization']]
 				
 		else:
 			sample['!Sample_molecule'] = datatype.molecule
 			
 		sample['!Sample_extract_protocol'] = compositeTrack.url
 		sample['!Sample_library_strategy'] = datatype.strategy
 		sample['!Sample_library_source'] = datatype.source
 		sample['!Sample_library_selection'] = datatype.selection
 		
 		# set to replace for if nothing has a seqPlatform and no instrument model is specified.
 		sample['!Sample_instrument_model'] = '[REPLACE]'
 		for stanza in expId:	
 			if 'seqPlatform' in stanza:
 				sample['!Sample_instrument_model'] = instrumentModels[stanza['seqPlatform']]
 				break
 			elif instrument != None:
 				sample['!Sample_instrument_model'] = instrumentModels[instrument]
 				break
 		if sample['!Sample_instrument_model'] == '[REPLACE]':
 			if '!Sample_instrument_model' in replace:
 				sample['!Sample_instrument_model'] = replace['!Sample_instrument_model']
 				
 		sample['!Sample_data_processing'] = compositeTrack.url
 
 		if idNum in geoMapping and geoMapping[idNum] != 'Inconsistent':
 			sample['!Sample_geo_accession'] = geoMapping[idNum]
 		
 		softfile[firstStanza['metaObject']] = sample
 		
 	return softfile, fileList
 		
 		
 def createMicroArraySoftFile(database, composite, organism, compositeUrl, mdb, cv, track, md5sums, expIds, expVars, geoMapping, series, datatype):
 	
 	raise KeyError('microarray')
 	
 	print 'Creating MicroArray soft file'
 
 	softfile = SoftFile()
 	fileList = list()
 	
 	createSeries(softfile, composite, compositeUrl, track, expIds, geoMapping, series)
 	
 	for idNum in expIds.iterkeys():
 		
 		expId = expIds[idNum]
 		firstStanza = expId[0]
 		print 'Writing sample ' + firstStanza['metaObject'] + ' (' + idNum + ')'
 		sample = MicroArraySampleStanza()
 			
 		sample['^SAMPLE'] = sampleTitle(firstStanza, expVars)
 		
 		if 'geoSeriesAccession' in series:
 			sample['!Sample_series_id'] = series['geoSeriesAccession']	
 			
 		sample['!Sample_title'] = concat
 		
 		count = 1
 			
 		for stanza in expId:
 		
 			if isSupplimentaryFile(stanza['fileName']):
 				sample['!Sample_supplementary_file_' + str(count)] = stanza['fileName']
 				
 				if 'checksum' in stanza:
 					sample['!Sample_supplementary_file_checksum_' + str(count)] = stanza['checksum']
 				elif md5sums != None and stanza['fileName'] in md5sums:
 					sample['!Sample_supplementary_file_checksum_' + str(count)] = md5sums[stanza['fileName']]
 				
 				fileList.append(stanza['fileName'])
 				count = count + 1
 
 		# sample['!Sample_table'] = KeyOptional # CEL file
 		sample['!Sample_source_name_ch_1'] = '[REPLACE]' #KeyOnePlusNumbered
 		sample['!Sample_organism_ch_1'] = '[REPLACE]' #KeyOnePlusNumbered
 		sample['!Sample_characteristics_ch_1'] = '[REPLACE]' #KeyOnePlusNumbered
 		# sample['!Sample_biomaterial_provider_ch'] = KeyZeroPlusNumbered
 		# sample['!Sample_treatment_protocol_ch'] = KeyZeroPlusNumbered
 		# sample['!Sample_growth_protocol_ch'] = KeyZeroPlusNumbered
 		sample['!Sample_molecule_ch_1'] = '[REPLACE]' #KeyOnePlusNumbered
 		sample['!Sample_extract_protocol_ch_1'] = '[REPLACE]' #KeyOnePlusNumbered
 		sample['!Sample_label_ch_1'] = '[REPLACE]' #KeyOnePlusNumbered
 		sample['!Sample_label_protocol_ch_1'] = '[REPLACE]' #KeyOnePlusNumbered
 		sample['!Sample_hyb_protocol'] = '[REPLACE]' #KeyOnePlus
 		sample['!Sample_scan_protocol'] = '[REPLACE]' #KeyOnePlus
 		sample['!Sample_data_processing'] = '[REPLACE]' #KeyOnePlus
 		sample['!Sample_description'] = '[REPLACE]' #KeyZeroPlus
 		sample['!Sample_platform_id'] = '[REPLACE]'
 		# sample['!Sample_geo_accession'] = KeyOptional
 		# sample['!Sample_anchor'] = KeyRequired SAGE ONLY
 		# sample['!Sample_type'] = KeyRequired SAGE ONLY
 		# sample['!Sample_tag_count'] = KeyRequired SAGE ONLY
 		# sample['!Sample_tag_length'] = KeyRequired SAGE ONLY
 		sample['!Sample_table_begin'] = ''
 		sample['!Sample_table_end'] = ''
 	
 		softfile[firstStanza['accession']] = sample
 		
 	return softfile, fileList
 	
 	
 def createSpecialSoftFile(database, composite, organism, compositeUrl, mdb, cv, track, md5sums, expIds, expVars, geoMapping, series, datatype):
 	softfile = SoftFile()
 	fileList = list()
 	
 	createSeries(softfile, composite, compositeUrl, track, expIds, geoMapping, series)
 	
 	for idNum in expIds.iterkeys():
 		
 		expId = expIds[idNum]
 		firstStanza = expId[0]
 		print 'Writing sample ' + firstStanza['metaObject'] + ' (' + idNum + ')'
 		sample = HighThroughputSampleStanza()
 		
 		hasbigwig = 0
 		for stanza in expId:
 		
 			if getFileType(stanza['fileName']) == 'bigWig':
 				hasbigwig = 1
 				
 		if hasbigwig == 0:
 			continue
 		
 		sample['^SAMPLE'] = firstStanza['geoSampleAccession']
 		
 		if 'geoSeriesAccession' in series:
 			sample['!Sample_series_id'] = series['geoSeriesAccession']
 			
 		sample['!Sample_geo_accession'] = firstStanza['geoSampleAccession']
 		
 		count = 1
 			
 		for stanza in expId:
 		
 			if getFileType(stanza['fileName']) == 'bigWig':
 				sample['!Sample_supplementary_file_' + str(count)] = stanza['fileName']
 				
 				if 'checksum' in stanza:
 					sample['!Sample_supplementary_file_checksum_' + str(count)] = stanza['checksum']
 				elif md5sums != None and stanza['fileName'] in md5sums:
 					sample['!Sample_supplementary_file_checksum_' + str(count)] = md5sums[stanza['fileName']]
 				
 				# sample['!Sample_supplementary_file_build_' + str(count)] = database
 				
 				fileList.append(stanza['fileName'])
 				count = count + 1
 				
 		softfile[firstStanza['geoSampleAccession']] = sample
 		
 	return softfile, fileList
 		
 def main():
 
 	parser = argparse.ArgumentParser(description = 'Prepares a submission to GEO. Creates a soft file and shell script with the correct call to aspera.')
 	parser.add_argument('-t', '--trackPath', help='Overrides the default track path ~/kent/src/hg/makeDb/trackDb/')
 	parser.add_argument('-i', '--instrument', help='If specified, expIds without instruments listed will default to this value. Use the no-spacing name eg Illumina_GA2')
 	parser.add_argument('-r', '--replace', help='Give the name of a file that has contents to be used to replace unspecified tags in metadata (description, contributers, etc)')
 	parser.add_argument('database', help='The database, typically hg19 or mm9')
 	parser.add_argument('composite', help='The composite name, wgEncodeCshlLongRnaSeq for instance')
 	parser.add_argument('expIds', nargs='*', help='Any number of expIds separated by spaces, you can also specify a range by using a hyphen, "140 150 160-170" for instance, or leave blank to specify the entire file')
 	
 	if len(sys.argv) == 1:
 		parser.print_usage()
 		return
 	
 	args = parser.parse_args(sys.argv[1:])
 		
 	compositeTrack = CompositeTrack(args.database, args.composite, args.trackPath)
 
 	cvPath = compositeTrack.trackPath + 'cv/alpha/cv.ra'
 	cv = CvFile(cvPath)
 	
 	replace = dict()
 	if args.replace != None:
 		for line in open(args.replace):
 			if line == '':
 				continue
 			key, val = map(str.strip, line.split('=', 1))
 			if key not in replace:
 				replace[key] = list()
 			replace[key].append(val)
 		
 	
 	ids = list()
 	
 	for id in args.expIds:
 		if '-' in id:
 			start, end = id.split('-', 1)
 			ids.extend(range(int(start), int(end) + 1))
 		else:
 			ids.append(int(id))
 	
 	expIds, expVars, geoMapping, series, datatype = createMappings(compositeTrack.alphaMetaDb)
 	
 	submission = dict()
 	if len(ids) == 0:
 		submission = expIds
 	else:
 		for expId in ids:
-			submission[expId] = expIds[expId]
+			submission[str(expId)] = expIds[str(expId)]
 	
 	expIdStr = ' '
 	for id in args.expIds:
 		expIdStr = expIdStr + id + ',' 
 	expIdStr = expIdStr[:len(expIdStr) - 1]
 	print 'Generating soft using expIds ' + expIdStr
 	
 	if datatype.soft == HighThroughputSoftFile:
 		softfile, fileList = createHighThroughputSoftFile(compositeTrack, cv, submission, expVars, geoMapping, series, datatype, args.instrument, replace)
 	elif datatype.soft == MicroArraySoftFile:
 		softfile, fileList = createMicroArraySoftFile(compositeTrack, cv, submission, expVars, geoMapping, series, datatype)
 	else:
 		raise KeyError('unsupported type')
 	
 	print 'Creating directory'
 	
 	d = datetime.datetime.today()
 	datestring = '%4d-%02d-%02d' % (d.year, d.month, d.day)
 	
 	dirname = '%s_%s/' % (compositeTrack.name, datestring)
 	os.mkdir(dirname)
 	
 	print 'Writing file'
 	
 	outfileName = '%s%s.soft' % (dirname, compositeTrack.name)
 	outfile = open(outfileName, 'w')
 	outfile.write(str(softfile))
 	fileslistname = '%sfiles.txt' % dirname
 	fileslist = open(fileslistname, 'w')
 	scriptname = '%supload.sh' % dirname
 	outscript = open(scriptname, 'w')
 	outscript.write('#!/bin/sh\n\n')
 	outscript.write('/opt/aspera/connect/bin/ascp -i ~/encode_geo_key/encode_geo_key.ppk -QTr -l300m \\\n')
 	
 	for file in fileList:
 		if not os.path.exists(file.path):
 			print IOError(file.path + ' does not exist')
 		else:
 			outscript.write(file.path + ' \\\n')
 			fileslist.write(file.name + '\n')
 	
 	outscript.write('asp-geo@upload.ncbi.nlm.nih.gov:ENCODE\n')
 	outscript.close()
 	fileslist.close()
 
 	os.system('chmod +x ' + scriptname)
 		
 	print 'Finished!'
 	
 if __name__ == '__main__':
 	main()
\ No newline at end of file