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-rw-r--r--wqflask/wqflask/auwerx/phewas_analysis.py7
1 files changed, 5 insertions, 2 deletions
diff --git a/wqflask/wqflask/auwerx/phewas_analysis.py b/wqflask/wqflask/auwerx/phewas_analysis.py
index ed2df01f..b9789404 100644
--- a/wqflask/wqflask/auwerx/phewas_analysis.py
+++ b/wqflask/wqflask/auwerx/phewas_analysis.py
@@ -55,6 +55,8 @@ class PheWAS(object):
self.trait_id = requestform["trait_id"]
self.datasetname = requestform["dataset"]
self.dataset = data_set.create_dataset(self.datasetname)
+ self.region = int(requestform["num_region"])
+ self.mtadjust = str(requestform["sel_mtadjust"])
# Print some debug
print "self.trait_id:" + self.trait_id + "\n"
@@ -70,7 +72,7 @@ class PheWAS(object):
self.mb = int(self.this_trait.mb);
# print some debug
- print "location:" + self.chr + ":" + str(self.mb) + "\n"
+ print "location:" + self.chr + ":" + str(self.mb) + "+/-" + str(self.region) + "\n"
# Load in the genotypes file *sigh* to make the markermap
parser = genofile_parser.ConvertGenoFile(genofilelocation)
@@ -92,11 +94,12 @@ class PheWAS(object):
self.results = {}
self.results['imgurl1'] = webqtlUtil.genRandStr("phewas_") + ".png"
self.results['imgloc1'] = GENERATED_IMAGE_DIR + self.results['imgurl1']
+ self.results['mtadjust'] = self.mtadjust
print("IMAGE AT:", self.results['imgurl1'] )
print("IMAGE AT:", self.results['imgloc1'] )
# Create the PheWAS plot (The gene/probe name, chromosome and gene/probe positions should come from the user input)
# TODO: generate the PDF in the temp folder, with a unique name
- phewasres = self.r_PheWASManhattan("Test", precompfile, phenoaligner, snpaligner, "None", self.chr, self.mb, self.mb, self.results['imgloc1'] )
+ phewasres = self.r_PheWASManhattan("Test", precompfile, phenoaligner, snpaligner, "None", self.chr, self.mb, self.region, self.results['imgloc1'] , self.mtadjust)
self.results['phewas1'] = phewasres[0]
self.results['phewas2'] = phewasres[1]
self.results['tabulardata'] = phewasres[2]