def process_upload(self, exp, *args, **kwargs):
"""
@param exp: Experiment
"""
self.clean_errors()
assay_df = pd.DataFrame.from_csv(self.es_matrix.get_file())
es = ExpressionSet(base_dir=exp.get_data_folder(),
base_filename="%s_annotation" % self.uuid)
pheno_df = pd.DataFrame.from_csv(self.pheno_matrix.get_file())
pheno_df.set_index(pheno_df.columns[0])
user_class_title = es.pheno_metadata["user_class_title"]
if user_class_title not in pheno_df.columns:
pheno_df[es.pheno_metadata["user_class_title"]] = ""
es.store_assay_data_frame(assay_df)
es.store_pheno_data_frame(pheno_df)
if self.working_unit:
es.working_unit = self.working_unit
self.set_out_var("expression_set", es)
exp.store_block(self)
self.do_action("success", exp)
def process_upload(self, exp, *args, **kwargs):
"""
@param exp: Experiment
"""
self.clean_errors()
assay_df = pd.DataFrame.from_csv(self.es_matrix.get_file())
es = ExpressionSet(base_dir=exp.get_data_folder(),
base_filename="%s_annotation" % self.uuid)
pheno_df = pd.DataFrame.from_csv(self.pheno_matrix.get_file())
pheno_df.set_index(pheno_df.columns[0])
user_class_title = es.pheno_metadata["user_class_title"]
if user_class_title not in pheno_df.columns:
pheno_df[es.pheno_metadata["user_class_title"]] = ""
# if matrix is bad oriented, then do transposition
if self.es_matrix_ori == "GxS":
assay_df = assay_df.T
es.store_assay_data_frame(assay_df)
es.store_pheno_data_frame(pheno_df)
if self.working_unit:
es.working_unit = self.working_unit
self.set_out_var("expression_set", es)
exp.store_block(self)
self.do_action("success", exp)
def process_upload(self, exp, *args, **kwargs):
"""
@param exp: Experiment
"""
# TODO: move to celery
self.clean_errors()
seq = []
sep = getattr(self, "csv_sep", " ")
try:
if len(self.pheno_matrices) != len(self.es_matrices):
raise RuntimeError(
"Different number of phenotypes and expression sets")
self.labels = es_matrix_names = sorted(self.es_matrices)
pheno_matrix_names = sorted(self.pheno_matrices)
self.pheno_by_es_names = {
es_name: pheno_name
for es_name, pheno_name in zip(es_matrix_names,
pheno_matrix_names)
}
for es_name, pheno_name in self.pheno_by_es_names.iteritems():
es_ufw = self.es_matrices[es_name]
es_df = es_ufw.get_as_data_frame(sep)
pheno_ufw = self.pheno_matrices[pheno_name]
pheno_df = pheno_ufw.get_as_data_frame(sep)
es_sample_names = sorted(es_df.columns.tolist())
pheno_sample_names = sorted(pheno_df.index.tolist())
if es_sample_names != pheno_sample_names:
raise RuntimeError("Couldn't match `%s` and `%s` due to "
"different sample name sets" %
(es_name, pheno_name))
es = ExpressionSet(base_dir=exp.get_data_folder(),
base_filename="%s_%s" %
(self.uuid, es_name))
es.store_assay_data_frame(es_df)
es.store_pheno_data_frame(pheno_df)
es.pheno_metadata["user_class_title"] = pheno_df.columns[0]
seq.append({"es": es, "__label__": es_name})
self.seq = seq
exp.store_block(self)
self.do_action("processing_done", exp, seq)
except Exception as e:
log.exception(e)
self.errors.append(e)
self.do_action("error_on_processing", exp, e)
def process_upload(self, exp, *args, **kwargs):
"""
@param exp: Experiment
"""
# TODO: move to celery
self.clean_errors()
seq = []
sep = getattr(self, "csv_sep", " ")
try:
if len(self.pheno_matrices) != len(self.es_matrices):
raise RuntimeError("Different number of phenotypes and expression sets")
self.labels = es_matrix_names = sorted(self.es_matrices)
pheno_matrix_names = sorted(self.pheno_matrices)
self.pheno_by_es_names = {
es_name: pheno_name for
es_name, pheno_name
in zip(es_matrix_names, pheno_matrix_names)
}
for es_name, pheno_name in self.pheno_by_es_names.iteritems():
es_ufw = self.es_matrices[es_name]
es_df = es_ufw.get_as_data_frame(sep)
pheno_ufw = self.pheno_matrices[pheno_name]
pheno_df = pheno_ufw.get_as_data_frame(sep)
es_sample_names = sorted(es_df.columns.tolist())
pheno_sample_names = sorted(pheno_df.index.tolist())
if es_sample_names != pheno_sample_names:
raise RuntimeError("Couldn't match `%s` and `%s` due to "
"different sample name sets" % (es_name, pheno_name))
es = ExpressionSet(
base_dir=exp.get_data_folder(),
base_filename="%s_%s" % (self.uuid, es_name)
)
es.store_assay_data_frame(es_df)
es.store_pheno_data_frame(pheno_df)
es.pheno_metadata["user_class_title"] = pheno_df.columns[0]
seq.append({"es": es, "__label__": es_name})
self.seq = seq
exp.store_block(self)
self.do_action("processing_done", exp, seq)
except Exception as e:
log.exception(e)
self.errors.append(e)
self.do_action("error_on_processing", exp, e)
def process_upload(self, exp, *args, **kwargs):
"""
@param exp: Experiment
"""
# TODO: move to celery
self.clean_errors()
sep = getattr(self, "csv_sep", " ")
try:
if not self.pheno_matrix:
self.warnings.append(Exception("Phenotype is undefined"))
pheno_df = None
else:
pheno_df = self.pheno_matrix.get_as_data_frame(sep)
pheno_df.set_index(pheno_df.columns[0])
# TODO: solve somehow better: Here we add empty column with user class assignment
pheno_df[ExpressionSet(None, None).pheno_metadata["user_class_title"]] = ""
if self.m_rna_matrix is not None:
m_rna_assay_df = self.m_rna_matrix.get_as_data_frame(sep)
m_rna_es = ExpressionSet(base_dir=exp.get_data_folder(),
base_filename="%s_m_rna_es" % self.uuid)
m_rna_es.store_assay_data_frame(m_rna_assay_df)
m_rna_es.store_pheno_data_frame(pheno_df)
m_rna_es.working_unit = self.m_rna_unit
self.set_out_var("m_rna_es", m_rna_es)
# TODO: fetch GPL annotation if GPL id was provided
if self.mi_rna_matrix is not None:
mi_rna_assay_df = self.mi_rna_matrix.get_as_data_frame(sep)
mi_rna_es = ExpressionSet(base_dir=exp.get_data_folder(),
base_filename="%s_mi_rna_es" % self.uuid)
mi_rna_es.store_assay_data_frame(mi_rna_assay_df)
mi_rna_es.store_pheno_data_frame(pheno_df)
self.set_out_var("mi_rna_es", mi_rna_es)
if self.methyl_matrix is not None:
methyl_assay_df = self.methyl_matrix.get_as_data_frame(sep)
methyl_es = ExpressionSet(base_dir=exp.get_data_folder(),
base_filename="%s_methyl_es" % self.uuid)
methyl_es.store_assay_data_frame(methyl_assay_df)
methyl_es.store_pheno_data_frame(pheno_df)
self.set_out_var("methyl_es", methyl_es)
self.do_action("success", exp)
except Exception as e:
ex_type, ex, tb = sys.exc_info()
traceback.print_tb(tb)
self.do_action("error", exp, e)
def preprocess_soft(exp, block, source_file):
#TODO: now we assume that we get GSE file
try:
soft = list(parse_geo(gzip.open(source_file.filepath)))
except:
raise RuntimeError("Bad source file, can't read")
assert soft[2].entity_type == "PLATFORM"
pl = soft[2].table_rows
id_idx = pl[0].index('ID')
entrez_idx = pl[0].index('ENTREZ_GENE_ID')
#TODO bug here
probe_to_genes_GS = GS()
for row in pl[1:]:
probe_to_genes_GS.description[row[id_idx]] = ""
probe_to_genes_GS.genes[row[id_idx]] = row[entrez_idx].split(" /// ")
platform_annotation = PlatformAnnotation(
"TODO:GET NAME FROM SOFT",
base_dir=exp.get_data_folder(),
base_filename="%s_annotation" % block.uuid
)
platform_annotation.gene_sets.metadata["gene_units"] = GeneUnits.ENTREZ_ID
platform_annotation.gene_sets.metadata["set_units"] = GeneUnits.PROBE_ID
platform_annotation.gene_sets.store_gs(probe_to_genes_GS)
id_ref_idx = soft[3].table_rows[0].index("ID_REF")
value_idx = soft[3].table_rows[0].index("VALUE")
assay_df = DataFrame(dict([
(
soft[i].entity_attributes['Sample_geo_accession'],
Series(dict([(row[id_ref_idx], row[value_idx]) for row in soft[i].table_rows[1:]]))
)
for i in range(3, len(soft))
]))
expression_set = ExpressionSet(exp.get_data_folder(), "%s_es" % block.uuid)
expression_set.store_assay_data_frame(assay_df)
raw_factors = [soft[i].entity_attributes
for i in range(3, len(soft))]
pheno_index = []
# Here we trying to guess sub columns
one_factor_row = raw_factors[0]
pheno_complex_columns_def = {}
for col_name, col in one_factor_row.iteritems():
if type(col) in [str, unicode]:
continue
else:
if all([":" in sub_col for sub_col in col]):
mb_sub_col_names_sets = [
tuple(map(lambda x: x.split(":")[0], row[col_name]))
for row in raw_factors
]
if len(set(mb_sub_col_names_sets)) == 1:
pheno_complex_columns_def[col_name] = "dict"
else:
pheno_complex_columns_def[col_name] = "list"
else:
pheno_complex_columns_def[col_name] = "list"
factors = []
for idx, factor in enumerate(raw_factors):
pheno_index.append(factor.pop('Sample_geo_accession', idx))
factor.pop('sample_table_begin', None)
factor.pop('sample_table_end', None)
fixed_factor = {}
for col_name, col in factor.iteritems():
# Special treat for sub columns
if col_name in pheno_complex_columns_def:
if pheno_complex_columns_def[col_name] == "list":
for sub_idx, sub_col in enumerate(col):
fixed_factor["%s_%s" % (col_name, sub_idx + 1)] = sub_col
elif pheno_complex_columns_def[col_name] == "dict":
for sub_col in col:
sub_name, sub_value = sub_col.split(":", 1)
fixed_factor["%s_%s" % (col_name, sub_name)] = sub_value
else:
fixed_factor[col_name] = col
factors.append(fixed_factor)
# TODO: add ordering to phenotype features
pheno_df = DataFrame([Series(factor) for factor in factors], index=pheno_index)
if expression_set.pheno_metadata["user_class_title"] not in pheno_df.columns:
pheno_df[expression_set.pheno_metadata["user_class_title"]] = ""
pheno_df.index.name = 'Sample_geo_accession'
expression_set.store_pheno_data_frame(pheno_df)
return [expression_set, platform_annotation], {}
def preprocess_soft(exp, block, source_file):
#TODO: now we assume that we get GSE file
try:
soft = list(parse_geo(gzip.open(source_file.filepath)))
except:
raise RuntimeError("Bad source file, can't read")
assert soft[2].entity_type == "PLATFORM"
pl = soft[2].table_rows
id_idx = pl[0].index('ID')
# entrez_idx = pl[0].index('ENTREZ_GENE_ID')
refseq_idx = [i for i, item in enumerate(pl[0]) if re.search('.*refseq.*', item, re.IGNORECASE)]
if refseq_idx == []:
refseq_idx = [i for i, item in enumerate(pl[0]) if re.search('.*mirna.*', item, re.IGNORECASE)][0]
else:
refseq_idx = refseq_idx[0]
probe_to_genes_GS = GS()
for row in pl[1:]:
probe_to_genes_GS.description[row[id_idx]] = ""
probe_to_genes_GS.genes[row[id_idx]] = [row[refseq_idx].split(" /// ")[0]]
# platform_annotation = PlatformAnnotation(
# "TODO:GET NAME FROM SOFT",
# base_dir=exp.get_data_folder(),
# base_filename="%s_annotation" % block.uuid
# )
#
# platform_annotation.gene_sets.metadata["gene_units"] = GeneUnits.ENTREZ_ID
# platform_annotation.gene_sets.metadata["set_units"] = GeneUnits.PROBE_ID
# platform_annotation.gene_sets.store_gs(probe_to_genes_GS)
if settings.CELERY_DEBUG:
import sys
sys.path.append('/Migration/skola/phd/projects/miXGENE/mixgene_project/wrappers/pycharm-debug.egg')
import pydevd
pydevd.settrace('localhost', port=6901, stdoutToServer=True, stderrToServer=True)
id_ref_idx = soft[3].table_rows[0].index("ID_REF")
value_idx = soft[3].table_rows[0].index("VALUE")
assay_df = DataFrame(dict([
(
soft[i].entity_attributes['Sample_geo_accession'],
Series(dict(
map_probes_to_refseqs(probe_to_genes_GS.genes, [(row[id_ref_idx], row[value_idx]) for row in soft[i].table_rows[1:]])
))
)
for i in range(3, len(soft))
]))
expression_set = ExpressionSet(exp.get_data_folder(), "%s_es" % block.uuid)
expression_set.store_assay_data_frame(assay_df.T)
raw_factors = [soft[i].entity_attributes
for i in range(3, len(soft))]
pheno_index = []
# Here we trying to guess sub columns
one_factor_row = raw_factors[0]
pheno_complex_columns_def = {}
for col_name, col in one_factor_row.iteritems():
if type(col) in [str, unicode]:
continue
else:
if all([":" in sub_col for sub_col in col]):
mb_sub_col_names_sets = [
tuple(map(lambda x: x.split(":")[0], row[col_name]))
for row in raw_factors
]
if len(set(mb_sub_col_names_sets)) == 1:
pheno_complex_columns_def[col_name] = "dict"
else:
pheno_complex_columns_def[col_name] = "list"
else:
pheno_complex_columns_def[col_name] = "list"
factors = []
for idx, factor in enumerate(raw_factors):
pheno_index.append(factor.pop('Sample_geo_accession', idx))
factor.pop('sample_table_begin', None)
factor.pop('sample_table_end', None)
fixed_factor = {}
for col_name, col in factor.iteritems():
# Special treat for sub columns
if col_name in pheno_complex_columns_def:
if pheno_complex_columns_def[col_name] == "list":
for sub_idx, sub_col in enumerate(col):
fixed_factor["%s_%s" % (col_name, sub_idx + 1)] = sub_col
elif pheno_complex_columns_def[col_name] == "dict":
for sub_col in col:
sub_name, sub_value = sub_col.split(":", 1)
fixed_factor["%s_%s" % (col_name, sub_name)] = sub_value
else:
fixed_factor[col_name] = col
factors.append(fixed_factor)
# TODO: add ordering to phenotype features
pheno_df = DataFrame([Series(factor) for factor in factors], index=pheno_index)
if expression_set.pheno_metadata["user_class_title"] not in pheno_df.columns:
pheno_df[expression_set.pheno_metadata["user_class_title"]] = ""
pheno_df.index.name = 'Sample_geo_accession'
expression_set.store_pheno_data_frame(pheno_df)
return [expression_set], {}
def preprocess_soft(exp, block, source_file):
#TODO: now we assume that we get GSE file
try:
soft = list(parse_geo(gzip.open(source_file.filepath)))
except:
raise RuntimeError("Bad source file, can't read")
assert soft[2].entity_type == "PLATFORM"
pl = soft[2].table_rows
id_idx = pl[0].index('ID')
# entrez_idx = pl[0].index('ENTREZ_GENE_ID')
refseq_idx = [
i for i, item in enumerate(pl[0])
if re.search('.*refseq.*', item, re.IGNORECASE)
]
if refseq_idx == []:
refseq_idx = [
i for i, item in enumerate(pl[0])
if re.search('.*mirna.*', item, re.IGNORECASE)
][0]
else:
refseq_idx = refseq_idx[0]
probe_to_genes_GS = GS()
for row in pl[1:]:
probe_to_genes_GS.description[row[id_idx]] = ""
probe_to_genes_GS.genes[row[id_idx]] = [
row[refseq_idx].split(" /// ")[0]
]
# platform_annotation = PlatformAnnotation(
# "TODO:GET NAME FROM SOFT",
# base_dir=exp.get_data_folder(),
# base_filename="%s_annotation" % block.uuid
# )
#
# platform_annotation.gene_sets.metadata["gene_units"] = GeneUnits.ENTREZ_ID
# platform_annotation.gene_sets.metadata["set_units"] = GeneUnits.PROBE_ID
# platform_annotation.gene_sets.store_gs(probe_to_genes_GS)
if settings.CELERY_DEBUG:
import sys
sys.path.append(
'/Migration/skola/phd/projects/miXGENE/mixgene_project/wrappers/pycharm-debug.egg'
)
import pydevd
pydevd.settrace('localhost',
port=6901,
stdoutToServer=True,
stderrToServer=True)
id_ref_idx = soft[3].table_rows[0].index("ID_REF")
value_idx = soft[3].table_rows[0].index("VALUE")
assay_df = DataFrame(
dict([(soft[i].entity_attributes['Sample_geo_accession'],
Series(
dict(
map_probes_to_refseqs(
probe_to_genes_GS.genes,
[(row[id_ref_idx], row[value_idx])
for row in soft[i].table_rows[1:]]))))
for i in range(3, len(soft))]))
expression_set = ExpressionSet(exp.get_data_folder(), "%s_es" % block.uuid)
expression_set.store_assay_data_frame(assay_df.T)
raw_factors = [soft[i].entity_attributes for i in range(3, len(soft))]
pheno_index = []
# Here we trying to guess sub columns
one_factor_row = raw_factors[0]
pheno_complex_columns_def = {}
for col_name, col in one_factor_row.iteritems():
if type(col) in [str, unicode]:
continue
else:
if all([":" in sub_col for sub_col in col]):
mb_sub_col_names_sets = [
tuple(map(lambda x: x.split(":")[0], row[col_name]))
for row in raw_factors
]
if len(set(mb_sub_col_names_sets)) == 1:
pheno_complex_columns_def[col_name] = "dict"
else:
pheno_complex_columns_def[col_name] = "list"
else:
pheno_complex_columns_def[col_name] = "list"
factors = []
for idx, factor in enumerate(raw_factors):
pheno_index.append(factor.pop('Sample_geo_accession', idx))
factor.pop('sample_table_begin', None)
factor.pop('sample_table_end', None)
fixed_factor = {}
for col_name, col in factor.iteritems():
# Special treat for sub columns
if col_name in pheno_complex_columns_def:
if pheno_complex_columns_def[col_name] == "list":
for sub_idx, sub_col in enumerate(col):
fixed_factor["%s_%s" %
(col_name, sub_idx + 1)] = sub_col
elif pheno_complex_columns_def[col_name] == "dict":
for sub_col in col:
sub_name, sub_value = sub_col.split(":", 1)
fixed_factor["%s_%s" %
(col_name, sub_name)] = sub_value
else:
fixed_factor[col_name] = col
factors.append(fixed_factor)
# TODO: add ordering to phenotype features
pheno_df = DataFrame([Series(factor) for factor in factors],
index=pheno_index)
if expression_set.pheno_metadata[
"user_class_title"] not in pheno_df.columns:
pheno_df[expression_set.pheno_metadata["user_class_title"]] = ""
pheno_df.index.name = 'Sample_geo_accession'
expression_set.store_pheno_data_frame(pheno_df)
return [expression_set], {}
def process_upload(self, exp, *args, **kwargs):
"""
@param exp: Experiment
"""
# TODO: move to celery
self.clean_errors()
sep = getattr(self, "csv_sep", " ")
try:
if not self.pheno_matrix:
self.warnings.append(Exception("Phenotype is undefined"))
pheno_df = None
else:
pheno_df = self.pheno_matrix.get_as_data_frame(sep)
pheno_df.set_index(pheno_df.columns[0])
# TODO: solve somehow better: Here we add empty column with user class assignment
pheno_df[ExpressionSet(
None, None).pheno_metadata["user_class_title"]] = ""
if self.m_rna_matrix is not None:
m_rna_assay_df = self.m_rna_matrix.get_as_data_frame(sep)
m_rna_es = ExpressionSet(base_dir=exp.get_data_folder(),
base_filename="%s_m_rna_es" %
self.uuid)
m_rna_es.store_assay_data_frame(m_rna_assay_df)
m_rna_es.store_pheno_data_frame(pheno_df)
m_rna_es.working_unit = self.m_rna_unit
self.set_out_var("m_rna_es", m_rna_es)
# TODO: fetch GPL annotation if GPL id was provided
if self.mi_rna_matrix is not None:
mi_rna_assay_df = self.mi_rna_matrix.get_as_data_frame(sep)
mi_rna_es = ExpressionSet(base_dir=exp.get_data_folder(),
base_filename="%s_mi_rna_es" %
self.uuid)
mi_rna_es.store_assay_data_frame(mi_rna_assay_df)
mi_rna_es.store_pheno_data_frame(pheno_df)
self.set_out_var("mi_rna_es", mi_rna_es)
if self.methyl_matrix is not None:
methyl_assay_df = self.methyl_matrix.get_as_data_frame(sep)
methyl_es = ExpressionSet(base_dir=exp.get_data_folder(),
base_filename="%s_methyl_es" %
self.uuid)
methyl_es.store_assay_data_frame(methyl_assay_df)
methyl_es.store_pheno_data_frame(pheno_df)
self.set_out_var("methyl_es", methyl_es)
self.do_action("success", exp)
except Exception as e:
ex_type, ex, tb = sys.exc_info()
traceback.print_tb(tb)
self.do_action("error", exp, e)