Mercurial > repos > devteam > cummerbund_to_tabular
comparison cummerbund_to_tabular.py @ 0:648c27c78eed draft
Initial commit with version 1.0.0 of the tool.
author | devteam |
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date | Tue, 23 Dec 2014 16:01:24 -0500 |
parents | |
children | 36f917aa4b60 |
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-1:000000000000 | 0:648c27c78eed |
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1 import os | |
2 import argparse | |
3 import sys | |
4 import string | |
5 | |
6 from galaxy.model.orm import * | |
7 import logging | |
8 from galaxy import eggs | |
9 eggs.require('SQLAlchemy') | |
10 import sqlalchemy | |
11 | |
12 | |
13 class CummerbundParser(object): | |
14 | |
15 def __init__(self, opts): | |
16 self.cummerbund_db = opts.filename | |
17 self.__connect_database() | |
18 | |
19 def generate_file( self, table ): | |
20 if hasattr( self, table ): | |
21 with open( '%s.tabular' % table, 'w' ) as self.fh: | |
22 getattr( self, table )() | |
23 else: | |
24 print 'Table %s is not supported or does not exist.' % table | |
25 | |
26 def __connect_database( self ): | |
27 database_connection = 'sqlite:///%s' % os.path.abspath( self.cummerbund_db ) | |
28 # Initialize the database connection. | |
29 engine = create_engine( database_connection ) | |
30 meta = MetaData( bind=engine ) | |
31 sa_sesssion = Session = scoped_session( sessionmaker( bind=engine, autoflush=False, autocommit=True ) ) | |
32 self.session = sa_sesssion | |
33 | |
34 def __write_line(self, line): | |
35 columns = [] | |
36 for col in line: | |
37 if isinstance( col, float ): | |
38 if str( col ) in [ '-inf', 'inf' ]: | |
39 columns.append( str( col ) ) | |
40 elif col == int(col): | |
41 columns.append( str( int( col ) ) ) | |
42 else: | |
43 columns.append( str( col ) ) | |
44 elif col is None: | |
45 columns.append( '-' ) | |
46 else: | |
47 columns.append( str( col ) ) | |
48 print >>self.fh, '\t'.join( columns ) | |
49 | |
50 def __get_diff_from_table( self, table, identifier ): | |
51 columns = [ '${table}.${identifier}', '${table}.gene_id', 'genes.gene_short_name', 'genes.locus', | |
52 '${table}.sample_1', '${table}.sample_2', '${table}.status', | |
53 '${table}.value_1', '${table}.value_2', '${table}.JS_dist', | |
54 '${table}.test_stat', '${table}.p_value', '${table}.q_value', | |
55 '${table}.significant' ] | |
56 query = string.Template( 'SELECT %s FROM ${table} JOIN genes on ${table}.gene_id = genes.gene_id' % ', '.join(columns) ) | |
57 result = self.session.execute( query.safe_substitute( table=table, identifier=identifier ) ) | |
58 self.__write_line( [ 'test_id', 'gene_id', 'gene', 'locus', 'sample_1', | |
59 'sample_2', 'status', 'value_1', 'value_2', 'sqrt(JS)', | |
60 'test_stat', 'p_value', 'q_value', 'significant' ] ) | |
61 for row in result: | |
62 self.__write_line( row ) | |
63 | |
64 def __get_read_group_data( self, table, identifier ): | |
65 header = [ 'tracking_id', 'condition', 'replicate', 'raw_frags', | |
66 'internal_scaled_frags', 'external_scaled_frags', 'FPKM', | |
67 'effective_length', 'status' ] | |
68 columns = [ identifier, 'sample_name', 'replicate', 'raw_frags', | |
69 'internal_scaled_frags', 'external_scaled_frags', 'fpkm', | |
70 'effective_length', 'status' ] | |
71 self.__write_line( header ) | |
72 for row in self.session.execute( 'SELECT %s FROM %s' % ( ', '.join( columns ), table ) ): | |
73 self.__write_line( row ) | |
74 | |
75 | |
76 def __get_exp_diff( self, table, data_table, data_table_as, column ): | |
77 header = [ 'test_id', 'gene_id', 'gene', 'locus', 'sample_1', 'sample_2', | |
78 'status', 'value_1', 'value_2', 'log2(fold_change)', 'test_stat', | |
79 'p_value', 'q_value', 'significant' ] | |
80 columns = [ '${dtas}.${column}', '${table}.gene_id', '${table}.gene_short_name', '${table}.locus', | |
81 '${dtas}.sample_1', '${dtas}.sample_2', '${dtas}.status', | |
82 '${dtas}.value_1', '${dtas}.value_2', '${dtas}.log2_fold_change', | |
83 '${dtas}.test_stat', '${dtas}.p_value', '${dtas}.q_value', | |
84 '${dtas}.significant' ] | |
85 query = string.Template( 'SELECT %s FROM ${dtab} as ${dtas} JOIN ${table} on ${dtas}.${column} = ${table}.${column}' % ', '.join( columns ) ) | |
86 self.__write_line( header ) | |
87 for row in self.session.execute( query.safe_substitute( dtas=data_table_as, dtab=data_table, table=table, column=column ) ): | |
88 self.__write_line( row ) | |
89 | |
90 def __get_per_sample_fpkm( self, identifiers, table, column ): | |
91 columns = [] | |
92 for identifier in identifiers: | |
93 samples = self.session.execute( "SELECT sample_name FROM %s WHERE %s = '%s' ORDER BY sample_name ASC" % ( table, column, identifier[0] ) ) | |
94 for sample in samples: | |
95 sample_name = sample[0] | |
96 columns.extend( [ '%s_FPKM' % sample_name, | |
97 '%s_conf_lo' % sample_name, | |
98 '%s_conf_hi' % sample_name, | |
99 '%s_status' % sample_name ] ) | |
100 return columns | |
101 | |
102 def __get_fpkms( self, table, data_table, column ): | |
103 tss_columns = [ column, 'class_code', 'nearest_ref_id', 'gene_id', | |
104 'gene_short_name', column, 'locus', 'length', 'coverage' ] | |
105 output_cols = [ 'tracking_id', 'class_code', 'nearest_ref_id', 'gene_id', 'gene_short_name', | |
106 'tss_id', 'locus', 'length', 'coverage' ] | |
107 tss_groups = self.session.execute( 'SELECT %s FROM %s LIMIT 1' % ( ', '.join( tss_columns ), table ) ) | |
108 output_cols.extend( self.__get_per_sample_fpkm( identifiers=tss_groups, column=column, table=data_table ) ) | |
109 self.__write_line( output_cols ) | |
110 tss_groups = self.session.execute( 'SELECT %s FROM %s' % ( ', '.join( tss_columns ), table ) ) | |
111 for tss_group in tss_groups: | |
112 out_data = list( tss_group ) | |
113 samples = self.session.execute( "SELECT fpkm, conf_hi, conf_lo, quant_status FROM %s WHERE %s = '%s' ORDER BY sample_name ASC" % ( data_table, column, tss_group[0] ) ) | |
114 for sample in samples: | |
115 out_data.extend( list( sample ) ) | |
116 self.__write_line( out_data ) | |
117 | |
118 def __get_count_data( self, table, column ): | |
119 output_cols = [ 'tracking_id' ] | |
120 tss_groups = self.session.execute( 'SELECT %s FROM %s LIMIT 1' % ( column, table ) ) | |
121 output_cols.extend( self.__get_per_sample_count_cols( identifiers=tss_groups, table=table, column=column ) ) | |
122 self.__write_line( output_cols ) | |
123 self.__get_per_sample_count_data( table=table, column=column ) | |
124 | |
125 def __get_per_sample_count_data( self, table, column ): | |
126 result = self.session.execute( 'SELECT DISTINCT(%s) FROM %s' % ( column, table ) ) | |
127 for row in result: | |
128 isoform_id = row[0] | |
129 output_data = [ isoform_id ] | |
130 per_sample = self.session.execute( "SELECT count, variance, uncertainty, dispersion, status FROM %s WHERE %s = '%s' ORDER BY sample_name ASC" % ( table, column, isoform_id ) ) | |
131 for samplerow in per_sample: | |
132 output_data.extend( list( samplerow ) ) | |
133 self.__write_line( output_data ) | |
134 | |
135 def __get_per_sample_count_cols( self, identifiers, table, column ): | |
136 columns = [] | |
137 for identifier in identifiers: | |
138 samples = self.session.execute( "SELECT sample_name FROM %s WHERE %s = '%s' ORDER BY sample_name ASC" % ( table, column, identifier[0] ) ) | |
139 for sample in samples: | |
140 sample_name = sample[0] | |
141 columns.extend( [ '%s_count' % sample_name, | |
142 '%s_count_variance' % sample_name, | |
143 '%s_count_uncertainty_var' % sample_name, | |
144 '%s_count_dispersion_var' % sample_name, | |
145 '%s_status' % sample_name ] ) | |
146 return columns | |
147 | |
148 def splicing_diff( self ): | |
149 self.__get_diff_from_table( 'splicingDiffData', 'TSS_group_id' ) | |
150 | |
151 def promoters_diff( self ): | |
152 self.__get_diff_from_table( 'promoterDiffData', 'gene_id' ) | |
153 | |
154 def cds_diff( self ): | |
155 self.__get_diff_from_table( 'CDSDiffData', 'gene_id' ) | |
156 | |
157 def tss_fpkm( self ): | |
158 data_table = 'TSSData' | |
159 table = 'TSS' | |
160 column = 'TSS_group_id' | |
161 self.__get_fpkms( data_table=data_table, table=table, column=column ) | |
162 | |
163 def isoform_fpkm( self ): | |
164 data_table = 'isoformData' | |
165 table = 'isoforms' | |
166 column = 'isoform_id' | |
167 self.__get_fpkms( data_table=data_table, table=table, column=column ) | |
168 | |
169 def genes_fpkm( self ): | |
170 output_cols = [ 'tracking_id', 'class_code', 'nearest_ref_id', 'gene_id', 'gene_short_name', | |
171 'tss_id', 'locus', 'length', 'coverage' ] | |
172 iso_groups = self.session.execute( 'SELECT gene_id FROM genes LIMIT 1' ) | |
173 output_cols.extend( self.__get_per_sample_fpkm( identifiers=iso_groups, column='gene_id', table='geneData' ) ) | |
174 self.__write_line( output_cols ) | |
175 data_columns = [ 'genes.gene_id', 'genes.class_code', 'genes.nearest_ref_id', 'genes.gene_id', 'genes.gene_short_name', | |
176 'GROUP_CONCAT(TSS.TSS_group_id)', 'genes.locus', 'genes.length', 'genes.coverage' ] | |
177 query = 'SELECT %s FROM genes JOIN TSS on TSS.gene_id = genes.gene_id GROUP BY genes.gene_id' % ', '.join( data_columns ) | |
178 result = self.session.execute( query ) | |
179 for row in result: | |
180 gene_id = row[0] | |
181 output_data = list( row ) | |
182 per_sample = self.session.execute( "SELECT fpkm, conf_lo, conf_hi, quant_status FROM geneData WHERE gene_id = '%s' ORDER BY sample_name ASC" % gene_id ) | |
183 for samplerow in per_sample: | |
184 output_data.extend( list( samplerow ) ) | |
185 self.__write_line( output_data ) | |
186 | |
187 def cds_fpkm( self ): | |
188 output_cols = [ 'tracking_id', 'class_code', 'nearest_ref_id', 'gene_id', 'gene_short_name', | |
189 'tss_id', 'locus', 'length', 'coverage' ] | |
190 iso_groups = self.session.execute( 'SELECT CDS_id FROM CDS LIMIT 1' ) | |
191 output_cols.extend( self.__get_per_sample_fpkm( identifiers=iso_groups, column='CDS_id', table='CDSData' ) ) | |
192 self.__write_line( output_cols ) | |
193 data_columns = [ 'CDS_id', 'class_code', 'nearest_ref_id', 'gene_id', 'gene_short_name', | |
194 'GROUP_CONCAT(TSS_group_id)', 'locus', 'length', 'coverage' ] | |
195 query = 'SELECT %s FROM CDS GROUP BY CDS_id' % ', '.join( data_columns ) | |
196 result = self.session.execute( query ) | |
197 for row in result: | |
198 CDS_id = row[0] | |
199 output_data = list( row ) | |
200 per_sample = self.session.execute( "SELECT fpkm, conf_lo, conf_hi, quant_status FROM CDSData WHERE CDS_id = '%s' ORDER BY sample_name ASC" % CDS_id ) | |
201 for samplerow in per_sample: | |
202 output_data.extend( list( samplerow ) ) | |
203 self.__write_line( output_data ) | |
204 | |
205 def tss_count_tracking( self ): | |
206 self.__get_count_data( table='TSSCount', column='TSS_group_id' ) | |
207 | |
208 def isoform_count( self ): | |
209 self.__get_count_data( table='isoformCount', column='isoform_id' ) | |
210 | |
211 def genes_count( self ): | |
212 self.__get_count_data( table='geneCount', column='gene_id' ) | |
213 | |
214 def cds_count( self ): | |
215 self.__get_count_data( table='CDSCount', column='CDS_id' ) | |
216 | |
217 def tss_group_exp( self ): | |
218 columns = [ 'TEDD.TSS_group_id', 'TSS.gene_id', 'TSS.gene_short_name', 'TSS.locus', | |
219 'TEDD.sample_1', 'TEDD.sample_2', 'TEDD.status', | |
220 'TEDD.value_1', 'TEDD.value_2', 'TEDD.log2_fold_change', | |
221 'TEDD.test_stat', 'TEDD.p_value', 'TEDD.q_value', 'TEDD.significant' ] | |
222 query = [ 'SELECT %s FROM TSSExpDiffData AS TEDD' % ', '.join(columns), | |
223 'JOIN TSS on TEDD.TSS_group_id = TSS.TSS_group_id' ] | |
224 self.__write_line( [ 'test_id', 'gene_id', 'gene', 'locus', | |
225 'sample_1', 'sample_2', 'status', 'value_1', | |
226 'value_2', 'log2(fold_change)', 'test_stat', | |
227 'p_value', 'q_value', 'significant' ] ) | |
228 for row in self.session.execute( ' '.join( query ) ): | |
229 self.__write_line( row ) | |
230 | |
231 def run_info( self ): | |
232 self.__write_line( [ 'param', 'value' ] ) | |
233 for row in self.session.execute( 'SELECT param, value FROM runInfo' ): | |
234 self.__write_line( row ) | |
235 | |
236 def read_groups( self ): | |
237 self.__write_line( [ 'file', 'condition', 'replicate_num', 'total_mass', 'norm_mass', 'internal_scale', 'external_scale' ] ) | |
238 for row in self.session.execute( 'SELECT file, sample_name, replicate, total_mass, norm_mass, internal_scale, external_scale FROM replicates' ): | |
239 self.__write_line( row ) | |
240 | |
241 def isoform_exp_diff( self ): | |
242 self.__get_exp_diff( table='isoforms', data_table='isoformExpDiffData', data_table_as='iED', column='isoform_id' ) | |
243 | |
244 def gene_exp_diff( self ): | |
245 self.__get_exp_diff( table='genes', data_table='geneExpDiffData', data_table_as='gEDD', column='gene_id' ) | |
246 | |
247 def cds_exp_diff( self ): | |
248 self.__get_exp_diff( table='CDS', data_table='CDSExpDiffData', data_table_as='CED', column='CDS_id' ) | |
249 | |
250 def tss_rg( self ): | |
251 self.__get_read_group_data( table='TSSReplicateData', identifier='TSS_group_id' ) | |
252 | |
253 def isoform_rg( self ): | |
254 self.__get_read_group_data( table='isoformReplicateData', identifier='isoform_id' ) | |
255 | |
256 def gene_rg( self ): | |
257 self.__get_read_group_data( table='geneReplicateData', identifier='gene_id' ) | |
258 | |
259 def cds_rg( self ): | |
260 self.__get_read_group_data( table='CDSReplicateData', identifier='CDS_id' ) | |
261 | |
262 def var_model( self ): | |
263 header = [ 'condition', 'locus', 'compatible_count_mean', 'compatible_count_var', 'total_count_mean', 'total_count_var', 'fitted_var' ] | |
264 self.__write_line( header ) | |
265 for row in self.session.execute( 'SELECT %s FROM varModel' % ', '.join( header ) ): | |
266 self.__write_line( row ) | |
267 | |
268 if __name__ == '__main__': | |
269 parser = argparse.ArgumentParser() | |
270 parser.add_argument( '--file', dest='filename' ) | |
271 parser.add_argument( '--tables', dest='tables', action='append' ) | |
272 opts = parser.parse_args() | |
273 cb = CummerbundParser( opts ) | |
274 for table in opts.tables: | |
275 cb.generate_file( table ) |