Mercurial > repos > devteam > cummerbund_to_tabular
comparison cummerbund_to_tabular.py @ 0:21d03c46f286 draft default tip
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author | devteam |
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date | Thu, 02 Apr 2015 16:13:37 -0400 |
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-1:000000000000 | 0:21d03c46f286 |
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1 import os | |
2 import argparse | |
3 import sys | |
4 import string | |
5 import sqlite3 | |
6 | |
7 import logging | |
8 | |
9 | |
10 class CummerbundParser(object): | |
11 | |
12 def __init__(self, opts): | |
13 self.cummerbund_db = opts.filename | |
14 self.session = sqlite3.connect( os.path.abspath( self.cummerbund_db ) ) | |
15 | |
16 def generate_file( self, table ): | |
17 if hasattr( self, table ): | |
18 with open( '%s.tabular' % table, 'w' ) as self.fh: | |
19 getattr( self, table )() | |
20 else: | |
21 print 'Table %s is not supported or does not exist.' % table | |
22 | |
23 def __write_line(self, line): | |
24 columns = [] | |
25 for col in line: | |
26 if isinstance( col, float ): | |
27 if str( col ) in [ '-inf', 'inf' ]: | |
28 columns.append( str( col ) ) | |
29 elif col == int(col): | |
30 columns.append( str( int( col ) ) ) | |
31 else: | |
32 columns.append( str( col ) ) | |
33 elif col is None: | |
34 columns.append( '-' ) | |
35 else: | |
36 columns.append( str( col ) ) | |
37 print >>self.fh, '\t'.join( columns ) | |
38 | |
39 def __get_diff_from_table( self, table, identifier ): | |
40 columns = [ '${table}.${identifier}', '${table}.gene_id', 'genes.gene_short_name', 'genes.locus', | |
41 '${table}.sample_1', '${table}.sample_2', '${table}.status', | |
42 '${table}.value_1', '${table}.value_2', '${table}.JS_dist', | |
43 '${table}.test_stat', '${table}.p_value', '${table}.q_value', | |
44 '${table}.significant' ] | |
45 query = string.Template( 'SELECT %s FROM ${table} JOIN genes on ${table}.gene_id = genes.gene_id' % ', '.join(columns) ) | |
46 result = self.session.execute( query.safe_substitute( table=table, identifier=identifier ) ) | |
47 self.__write_line( [ 'test_id', 'gene_id', 'gene', 'locus', 'sample_1', | |
48 'sample_2', 'status', 'value_1', 'value_2', 'sqrt(JS)', | |
49 'test_stat', 'p_value', 'q_value', 'significant' ] ) | |
50 for row in result: | |
51 self.__write_line( row ) | |
52 | |
53 def __get_read_group_data( self, table, identifier ): | |
54 header = [ 'tracking_id', 'condition', 'replicate', 'raw_frags', | |
55 'internal_scaled_frags', 'external_scaled_frags', 'FPKM', | |
56 'effective_length', 'status' ] | |
57 columns = [ identifier, 'sample_name', 'replicate', 'raw_frags', | |
58 'internal_scaled_frags', 'external_scaled_frags', 'fpkm', | |
59 'effective_length', 'status' ] | |
60 self.__write_line( header ) | |
61 for row in self.session.execute( 'SELECT %s FROM %s' % ( ', '.join( columns ), table ) ): | |
62 self.__write_line( row ) | |
63 | |
64 | |
65 def __get_exp_diff( self, table, data_table, data_table_as, column ): | |
66 header = [ 'test_id', 'gene_id', 'gene', 'locus', 'sample_1', 'sample_2', | |
67 'status', 'value_1', 'value_2', 'log2(fold_change)', 'test_stat', | |
68 'p_value', 'q_value', 'significant' ] | |
69 columns = [ '${dtas}.${column}', '${table}.gene_id', '${table}.gene_short_name', '${table}.locus', | |
70 '${dtas}.sample_1', '${dtas}.sample_2', '${dtas}.status', | |
71 '${dtas}.value_1', '${dtas}.value_2', '${dtas}.log2_fold_change', | |
72 '${dtas}.test_stat', '${dtas}.p_value', '${dtas}.q_value', | |
73 '${dtas}.significant' ] | |
74 query = string.Template( 'SELECT %s FROM ${dtab} as ${dtas} JOIN ${table} on ${dtas}.${column} = ${table}.${column}' % ', '.join( columns ) ) | |
75 self.__write_line( header ) | |
76 for row in self.session.execute( query.safe_substitute( dtas=data_table_as, dtab=data_table, table=table, column=column ) ): | |
77 self.__write_line( row ) | |
78 | |
79 def __get_per_sample_fpkm( self, identifiers, table, column ): | |
80 columns = [] | |
81 for identifier in identifiers: | |
82 samples = self.session.execute( "SELECT sample_name FROM %s WHERE %s = '%s' ORDER BY sample_name ASC" % ( table, column, identifier[0] ) ) | |
83 for sample in samples: | |
84 sample_name = sample[0] | |
85 columns.extend( [ '%s_FPKM' % sample_name, | |
86 '%s_conf_lo' % sample_name, | |
87 '%s_conf_hi' % sample_name, | |
88 '%s_status' % sample_name ] ) | |
89 return columns | |
90 | |
91 def __get_fpkms( self, table, data_table, column ): | |
92 tss_columns = [ column, 'class_code', 'nearest_ref_id', 'gene_id', | |
93 'gene_short_name', column, 'locus', 'length', 'coverage' ] | |
94 output_cols = [ 'tracking_id', 'class_code', 'nearest_ref_id', 'gene_id', 'gene_short_name', | |
95 'tss_id', 'locus', 'length', 'coverage' ] | |
96 tss_groups = self.session.execute( 'SELECT %s FROM %s LIMIT 1' % ( ', '.join( tss_columns ), table ) ) | |
97 output_cols.extend( self.__get_per_sample_fpkm( identifiers=tss_groups, column=column, table=data_table ) ) | |
98 self.__write_line( output_cols ) | |
99 tss_groups = self.session.execute( 'SELECT %s FROM %s' % ( ', '.join( tss_columns ), table ) ) | |
100 for tss_group in tss_groups: | |
101 out_data = list( tss_group ) | |
102 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] ) ) | |
103 for sample in samples: | |
104 out_data.extend( list( sample ) ) | |
105 self.__write_line( out_data ) | |
106 | |
107 def __get_count_data( self, table, column ): | |
108 output_cols = [ 'tracking_id' ] | |
109 tss_groups = self.session.execute( 'SELECT %s FROM %s LIMIT 1' % ( column, table ) ) | |
110 output_cols.extend( self.__get_per_sample_count_cols( identifiers=tss_groups, table=table, column=column ) ) | |
111 self.__write_line( output_cols ) | |
112 self.__get_per_sample_count_data( table=table, column=column ) | |
113 | |
114 def __get_per_sample_count_data( self, table, column ): | |
115 result = self.session.execute( 'SELECT DISTINCT(%s) FROM %s' % ( column, table ) ) | |
116 for row in result: | |
117 isoform_id = row[0] | |
118 output_data = [ isoform_id ] | |
119 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 ) ) | |
120 for samplerow in per_sample: | |
121 output_data.extend( list( samplerow ) ) | |
122 self.__write_line( output_data ) | |
123 | |
124 def __get_per_sample_count_cols( self, identifiers, table, column ): | |
125 columns = [] | |
126 for identifier in identifiers: | |
127 samples = self.session.execute( "SELECT sample_name FROM %s WHERE %s = '%s' ORDER BY sample_name ASC" % ( table, column, identifier[0] ) ) | |
128 for sample in samples: | |
129 sample_name = sample[0] | |
130 columns.extend( [ '%s_count' % sample_name, | |
131 '%s_count_variance' % sample_name, | |
132 '%s_count_uncertainty_var' % sample_name, | |
133 '%s_count_dispersion_var' % sample_name, | |
134 '%s_status' % sample_name ] ) | |
135 return columns | |
136 | |
137 def splicing_diff( self ): | |
138 self.__get_diff_from_table( 'splicingDiffData', 'TSS_group_id' ) | |
139 | |
140 def promoters_diff( self ): | |
141 self.__get_diff_from_table( 'promoterDiffData', 'gene_id' ) | |
142 | |
143 def cds_diff( self ): | |
144 self.__get_diff_from_table( 'CDSDiffData', 'gene_id' ) | |
145 | |
146 def tss_fpkm( self ): | |
147 data_table = 'TSSData' | |
148 table = 'TSS' | |
149 column = 'TSS_group_id' | |
150 self.__get_fpkms( data_table=data_table, table=table, column=column ) | |
151 | |
152 def isoform_fpkm( self ): | |
153 data_table = 'isoformData' | |
154 table = 'isoforms' | |
155 column = 'isoform_id' | |
156 self.__get_fpkms( data_table=data_table, table=table, column=column ) | |
157 | |
158 def genes_fpkm( self ): | |
159 output_cols = [ 'tracking_id', 'class_code', 'nearest_ref_id', 'gene_id', 'gene_short_name', | |
160 'tss_id', 'locus', 'length', 'coverage' ] | |
161 iso_groups = self.session.execute( 'SELECT gene_id FROM genes LIMIT 1' ) | |
162 output_cols.extend( self.__get_per_sample_fpkm( identifiers=iso_groups, column='gene_id', table='geneData' ) ) | |
163 self.__write_line( output_cols ) | |
164 data_columns = [ 'genes.gene_id', 'genes.class_code', 'genes.nearest_ref_id', 'genes.gene_id', 'genes.gene_short_name', | |
165 'GROUP_CONCAT(TSS.TSS_group_id)', 'genes.locus', 'genes.length', 'genes.coverage' ] | |
166 query = 'SELECT %s FROM genes JOIN TSS on TSS.gene_id = genes.gene_id GROUP BY genes.gene_id' % ', '.join( data_columns ) | |
167 result = self.session.execute( query ) | |
168 for row in result: | |
169 gene_id = row[0] | |
170 output_data = list( row ) | |
171 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 ) | |
172 for samplerow in per_sample: | |
173 output_data.extend( list( samplerow ) ) | |
174 self.__write_line( output_data ) | |
175 | |
176 def cds_fpkm( self ): | |
177 output_cols = [ 'tracking_id', 'class_code', 'nearest_ref_id', 'gene_id', 'gene_short_name', | |
178 'tss_id', 'locus', 'length', 'coverage' ] | |
179 iso_groups = self.session.execute( 'SELECT CDS_id FROM CDS LIMIT 1' ) | |
180 output_cols.extend( self.__get_per_sample_fpkm( identifiers=iso_groups, column='CDS_id', table='CDSData' ) ) | |
181 self.__write_line( output_cols ) | |
182 data_columns = [ 'CDS_id', 'class_code', 'nearest_ref_id', 'gene_id', 'gene_short_name', | |
183 'GROUP_CONCAT(TSS_group_id)', 'locus', 'length', 'coverage' ] | |
184 query = 'SELECT %s FROM CDS GROUP BY CDS_id' % ', '.join( data_columns ) | |
185 result = self.session.execute( query ) | |
186 for row in result: | |
187 CDS_id = row[0] | |
188 output_data = list( row ) | |
189 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 ) | |
190 for samplerow in per_sample: | |
191 output_data.extend( list( samplerow ) ) | |
192 self.__write_line( output_data ) | |
193 | |
194 def tss_count_tracking( self ): | |
195 self.__get_count_data( table='TSSCount', column='TSS_group_id' ) | |
196 | |
197 def isoform_count( self ): | |
198 self.__get_count_data( table='isoformCount', column='isoform_id' ) | |
199 | |
200 def genes_count( self ): | |
201 self.__get_count_data( table='geneCount', column='gene_id' ) | |
202 | |
203 def cds_count( self ): | |
204 self.__get_count_data( table='CDSCount', column='CDS_id' ) | |
205 | |
206 def tss_group_exp( self ): | |
207 columns = [ 'TEDD.TSS_group_id', 'TSS.gene_id', 'TSS.gene_short_name', 'TSS.locus', | |
208 'TEDD.sample_1', 'TEDD.sample_2', 'TEDD.status', | |
209 'TEDD.value_1', 'TEDD.value_2', 'TEDD.log2_fold_change', | |
210 'TEDD.test_stat', 'TEDD.p_value', 'TEDD.q_value', 'TEDD.significant' ] | |
211 query = [ 'SELECT %s FROM TSSExpDiffData AS TEDD' % ', '.join(columns), | |
212 'JOIN TSS on TEDD.TSS_group_id = TSS.TSS_group_id' ] | |
213 self.__write_line( [ 'test_id', 'gene_id', 'gene', 'locus', | |
214 'sample_1', 'sample_2', 'status', 'value_1', | |
215 'value_2', 'log2(fold_change)', 'test_stat', | |
216 'p_value', 'q_value', 'significant' ] ) | |
217 for row in self.session.execute( ' '.join( query ) ): | |
218 self.__write_line( row ) | |
219 | |
220 def run_info( self ): | |
221 self.__write_line( [ 'param', 'value' ] ) | |
222 for row in self.session.execute( 'SELECT param, value FROM runInfo' ): | |
223 self.__write_line( row ) | |
224 | |
225 def read_groups( self ): | |
226 self.__write_line( [ 'file', 'condition', 'replicate_num', 'total_mass', 'norm_mass', 'internal_scale', 'external_scale' ] ) | |
227 for row in self.session.execute( 'SELECT file, sample_name, replicate, total_mass, norm_mass, internal_scale, external_scale FROM replicates' ): | |
228 self.__write_line( row ) | |
229 | |
230 def isoform_exp_diff( self ): | |
231 self.__get_exp_diff( table='isoforms', data_table='isoformExpDiffData', data_table_as='iED', column='isoform_id' ) | |
232 | |
233 def gene_exp_diff( self ): | |
234 self.__get_exp_diff( table='genes', data_table='geneExpDiffData', data_table_as='gEDD', column='gene_id' ) | |
235 | |
236 def cds_exp_diff( self ): | |
237 self.__get_exp_diff( table='CDS', data_table='CDSExpDiffData', data_table_as='CED', column='CDS_id' ) | |
238 | |
239 def tss_rg( self ): | |
240 self.__get_read_group_data( table='TSSReplicateData', identifier='TSS_group_id' ) | |
241 | |
242 def isoform_rg( self ): | |
243 self.__get_read_group_data( table='isoformReplicateData', identifier='isoform_id' ) | |
244 | |
245 def gene_rg( self ): | |
246 self.__get_read_group_data( table='geneReplicateData', identifier='gene_id' ) | |
247 | |
248 def cds_rg( self ): | |
249 self.__get_read_group_data( table='CDSReplicateData', identifier='CDS_id' ) | |
250 | |
251 def var_model( self ): | |
252 header = [ 'condition', 'locus', 'compatible_count_mean', 'compatible_count_var', 'total_count_mean', 'total_count_var', 'fitted_var' ] | |
253 self.__write_line( header ) | |
254 for row in self.session.execute( 'SELECT %s FROM varModel' % ', '.join( header ) ): | |
255 self.__write_line( row ) | |
256 | |
257 if __name__ == '__main__': | |
258 parser = argparse.ArgumentParser() | |
259 parser.add_argument( '--file', dest='filename' ) | |
260 parser.add_argument( '--tables', dest='tables', action='append' ) | |
261 opts = parser.parse_args() | |
262 cb = CummerbundParser( opts ) | |
263 for table in opts.tables: | |
264 cb.generate_file( table ) |