def read_genotype_file(self):
'''Read genotype from .geno file instead of database'''
#genotype_1 is Dataset Object without parents and f1
#genotype_2 is Dataset Object with parents and f1 (not for intercross)
genotype_1 = reaper.Dataset()
# reaper barfs on unicode filenames, so here we ensure it's a string
if self.genofile:
full_filename = str(locate(self.genofile, 'genotype'))
else:
full_filename = str(locate(self.name + '.geno', 'genotype'))
genotype_1.read(full_filename)
if genotype_1.type == "group" and self.parlist:
genotype_2 = genotype_1.add(Mat=self.parlist[0], Pat=self.parlist[1]) #, F1=_f1)
else:
genotype_2 = genotype_1
#determine default genotype object
if self.incparentsf1 and genotype_1.type != "intercross":
genotype = genotype_2
else:
self.incparentsf1 = 0
genotype = genotype_1
self.samplelist = list(genotype.prgy)
return genotype
def read_genotype_file(self, use_reaper=False):
'''Read genotype from .geno file instead of database'''
# genotype_1 is Dataset Object without parents and f1
# genotype_2 is Dataset Object with parents and f1 (not for intercross)
#genotype_1 = reaper.Dataset()
# reaper barfs on unicode filenames, so here we ensure it's a string
if self.genofile:
if "RData" in self.genofile: # ZS: This is a temporary fix; I need to change the way the JSON files that point to multiple genotype files are structured to point to other file types like RData
full_filename = str(
locate(self.genofile.split(".")[0] + ".geno", 'genotype'))
else:
full_filename = str(locate(self.genofile, 'genotype'))
else:
full_filename = str(locate(self.name + '.geno', 'genotype'))
genotype_1 = gen_geno_ob.genotype(full_filename)
if genotype_1.type == "group" and self.parlist:
genotype_2 = genotype_1.add(Mat=self.parlist[0],
Pat=self.parlist[1]) # , F1=_f1)
else:
genotype_2 = genotype_1
# determine default genotype object
if self.incparentsf1 and genotype_1.type != "intercross":
genotype = genotype_2
else:
self.incparentsf1 = 0
genotype = genotype_1
self.samplelist = list(genotype.prgy)
return genotype
def __init__(self, name):
json_data_fh = open(locate(name + ".json", 'genotype/json'))
try:
markers = []
with open(locate(name + "_snps.txt", 'r')) as bimbam_fh:
marker = {}
if len(bimbam_fh[0].split(", ")) > 2:
delimiter = ", "
elif len(bimbam_fh[0].split(",")) > 2:
delimiter = ","
elif len(bimbam_fh[0].split("\t")) > 2:
delimiter = "\t"
else:
delimiter = " "
for line in bimbam_fh:
marker['name'] = line.split(delimiter)[0]
marker['Mb']
marker['chr'] = line.split(delimiter)[2]
marker['cM']
markers.append(marker)
#try:
# markers = json.load(json_data_fh)
except:
markers = []
for marker in markers:
if (marker['chr'] != "X") and (marker['chr'] != "Y"):
marker['chr'] = int(marker['chr'])
marker['Mb'] = float(marker['Mb'])
self.markers = markers
def run_analysis(self, requestform):
print("Starting ePheWAS analysis on dataset")
genofilelocation = locate("BXD.geno", "genotype") # Get the location of the BXD genotypes
tissuealignerloc = locate("Tissue_color_aligner.csv", "auwerx") # Get the location of the Tissue_color_aligner
# Get user parameters, trait_id and dataset, and store/update them in self
self.trait_id = requestform["trait_id"]
self.datasetname = requestform["dataset"]
self.dataset = data_set.create_dataset(self.datasetname)
# Print some debug
print "self.trait_id:" + self.trait_id + "\n"
print "self.datasetname:" + self.datasetname + "\n"
print "self.dataset.type:" + self.dataset.type + "\n"
# Load in the genotypes file *sigh* to make the markermap
parser = genofile_parser.ConvertGenoFile(genofilelocation)
parser.process_csv()
snpinfo = []
for marker in parser.markers:
snpinfo.append(marker["name"]);
snpinfo.append(marker["chr"]);
snpinfo.append(marker["Mb"]);
rnames = r_seq(1, len(parser.markers))
# Create the snp aligner object out of the BXD genotypes
snpaligner = ro.r.matrix(snpinfo, nrow=len(parser.markers), dimnames = r_list(rnames, r_c("SNP", "Chr", "Pos")), ncol = 3, byrow=True)
# Create the phenotype aligner object using R
phenoaligner = self.r_create_Pheno_aligner()
print("Initialization of ePheWAS done !")
def read_genotype_file(self):
'''Read genotype from .geno file instead of database'''
#genotype_1 is Dataset Object without parents and f1
#genotype_2 is Dataset Object with parents and f1 (not for intercross)
genotype_1 = reaper.Dataset()
# reaper barfs on unicode filenames, so here we ensure it's a string
if self.genofile:
full_filename = str(locate(self.genofile, 'genotype'))
else:
full_filename = str(locate(self.name + '.geno', 'genotype'))
genotype_1.read(full_filename)
if genotype_1.type == "group" and self.parlist:
genotype_2 = genotype_1.add(Mat=self.parlist[0], Pat=self.parlist[1]) #, F1=_f1)
else:
genotype_2 = genotype_1
#determine default genotype object
if self.incparentsf1 and genotype_1.type != "intercross":
genotype = genotype_2
else:
self.incparentsf1 = 0
genotype = genotype_1
self.samplelist = list(genotype.prgy)
return genotype
def __init__(self, name):
json_data_fh = open(locate(name + ".json",'genotype/json'))
try:
markers = []
with open(locate(name + "_snps.txt", 'r')) as bimbam_fh:
marker = {}
if len(bimbam_fh[0].split(", ")) > 2:
delimiter = ", "
elif len(bimbam_fh[0].split(",")) > 2:
delimiter = ","
elif len(bimbam_fh[0].split("\t")) > 2:
delimiter = "\t"
else:
delimiter = " "
for line in bimbam_fh:
marker['name'] = line.split(delimiter)[0]
marker['Mb']
marker['chr'] = line.split(delimiter)[2]
marker['cM']
markers.append(marker)
#try:
# markers = json.load(json_data_fh)
except:
markers = []
for marker in markers:
if (marker['chr'] != "X") and (marker['chr'] != "Y"):
marker['chr'] = int(marker['chr'])
marker['Mb'] = float(marker['Mb'])
self.markers = markers
def __init__(self, name):
json_data_fh = open(locate(name + ".json", 'genotype/json'))
markers = []
with open("%s/%s_snps.txt" % (flat_files('genotype/bimbam'), name),
'r') as bimbam_fh:
if len(bimbam_fh.readline().split(", ")) > 2:
delimiter = ", "
elif len(bimbam_fh.readline().split(",")) > 2:
delimiter = ","
elif len(bimbam_fh.readline().split("\t")) > 2:
delimiter = "\t"
else:
delimiter = " "
for line in bimbam_fh:
marker = {}
marker['name'] = line.split(delimiter)[0].rstrip()
marker['Mb'] = float(
line.split(delimiter)[1].rstrip()) / 1000000
marker['chr'] = line.split(delimiter)[2].rstrip()
markers.append(marker)
for marker in markers:
if (marker['chr'] != "X") and (marker['chr'] !=
"Y") and (marker['chr'] != "M"):
marker['chr'] = int(marker['chr'])
marker['Mb'] = float(marker['Mb'])
self.markers = markers
def gen_human_results(self, pheno_vector, key, temp_uuid):
file_base = locate(self.dataset.group.name, "mapping")
plink_input = input.plink(file_base, type='b')
input_file_name = os.path.join(webqtlConfig.SNP_PATH,
self.dataset.group.name + ".snps.gz")
pheno_vector = pheno_vector.reshape((len(pheno_vector), 1))
covariate_matrix = np.ones((pheno_vector.shape[0], 1))
kinship_matrix = np.fromfile(open(file_base + '.kin', 'r'), sep=" ")
kinship_matrix.resize(
(len(plink_input.indivs), len(plink_input.indivs)))
logger.debug("Before creating params")
params = dict(
pheno_vector=pheno_vector.tolist(),
covariate_matrix=covariate_matrix.tolist(),
input_file_name=input_file_name,
kinship_matrix=kinship_matrix.tolist(),
refit=False,
temp_uuid=temp_uuid,
# meta data
timestamp=datetime.datetime.now().isoformat(),
)
logger.debug("After creating params")
json_params = json.dumps(params)
Redis.set(key, json_params)
Redis.expire(key, 60 * 60)
logger.debug("Before creating the command")
command = PYLMM_COMMAND + ' --key {} --species {}'.format(key, "human")
logger.debug("command is:", command)
os.system(command)
json_results = Redis.blpop("pylmm:results:" + temp_uuid, 45 * 60)
results = json.loads(json_results[1])
t_stats = results['t_stats']
p_values = results['p_values']
#p_values, t_stats = lmm.run_human(key)
#p_values, t_stats = lmm.run_human(
# pheno_vector,
# covariate_matrix,
# input_file_name,
# kinship_matrix,
# loading_progress=tempdata
# )
return p_values, t_stats
def generate_cross_from_rdata(dataset):
rdata_location = locate(dataset.group.name + ".RData", "genotype/rdata")
ro.r("""
generate_cross_from_rdata <- function(filename = '%s') {
load(file=filename)
cross = cunique
return(cross)
}
""" % (rdata_location))
def gen_human_results(self, pheno_vector, key, temp_uuid):
file_base = locate(self.dataset.group.name,"mapping")
plink_input = input.plink(file_base, type='b')
input_file_name = os.path.join(webqtlConfig.SNP_PATH, self.dataset.group.name + ".snps.gz")
pheno_vector = pheno_vector.reshape((len(pheno_vector), 1))
covariate_matrix = np.ones((pheno_vector.shape[0],1))
kinship_matrix = np.fromfile(open(file_base + '.kin','r'),sep=" ")
kinship_matrix.resize((len(plink_input.indivs),len(plink_input.indivs)))
logger.debug("Before creating params")
params = dict(pheno_vector = pheno_vector.tolist(),
covariate_matrix = covariate_matrix.tolist(),
input_file_name = input_file_name,
kinship_matrix = kinship_matrix.tolist(),
refit = False,
temp_uuid = temp_uuid,
# meta data
timestamp = datetime.datetime.now().isoformat(),
)
logger.debug("After creating params")
json_params = json.dumps(params)
Redis.set(key, json_params)
Redis.expire(key, 60*60)
logger.debug("Before creating the command")
command = PYLMM_COMMAND+' --key {} --species {}'.format(key,
"human")
logger.debug("command is:", command)
os.system(command)
json_results = Redis.blpop("pylmm:results:" + temp_uuid, 45*60)
results = json.loads(json_results[1])
t_stats = results['t_stats']
p_values = results['p_values']
#p_values, t_stats = lmm.run_human(key)
#p_values, t_stats = lmm.run_human(
# pheno_vector,
# covariate_matrix,
# input_file_name,
# kinship_matrix,
# loading_progress=tempdata
# )
return p_values, t_stats
def run_analysis(self, requestform):
print("Starting ePheWAS analysis on dataset")
genofilelocation = locate(
"BXD.geno", "genotype") # Get the location of the BXD genotypes
tissuealignerloc = locate(
"Tissue_color_aligner.csv",
"auwerx") # Get the location of the Tissue_color_aligner
# Get user parameters, trait_id and dataset, and store/update them in self
self.trait_id = requestform["trait_id"]
self.datasetname = requestform["dataset"]
self.dataset = data_set.create_dataset(self.datasetname)
# Print some debug
print "self.trait_id:" + self.trait_id + "\n"
print "self.datasetname:" + self.datasetname + "\n"
print "self.dataset.type:" + self.dataset.type + "\n"
# Load in the genotypes file *sigh* to make the markermap
parser = genofile_parser.ConvertGenoFile(genofilelocation)
parser.process_csv()
snpinfo = []
for marker in parser.markers:
snpinfo.append(marker["name"])
snpinfo.append(marker["chr"])
snpinfo.append(marker["Mb"])
rnames = r_seq(1, len(parser.markers))
# Create the snp aligner object out of the BXD genotypes
snpaligner = ro.r.matrix(snpinfo,
nrow=len(parser.markers),
dimnames=r_list(rnames,
r_c("SNP", "Chr", "Pos")),
ncol=3,
byrow=True)
# Create the phenotype aligner object using R
phenoaligner = self.r_create_Pheno_aligner()
print("Initialization of ePheWAS done !")
def run_rqtl(trait_name, vals, samples, dataset, mapping_scale, model, method,
num_perm, perm_strata_list, do_control, control_marker,
manhattan_plot, cofactors):
"""Run R/qtl by making a request to the GN3 endpoint and reading in the output file(s)"""
pheno_file = write_phenotype_file(trait_name, samples, vals, dataset,
cofactors, perm_strata_list)
if dataset.group.genofile:
geno_file = locate(dataset.group.genofile, "genotype")
else:
geno_file = locate(dataset.group.name + ".geno", "genotype")
post_data = {
"pheno_file": pheno_file,
"geno_file": geno_file,
"model": model,
"method": method,
"nperm": num_perm,
"scale": mapping_scale
}
if do_control == "true" and control_marker:
post_data["control"] = control_marker
if not manhattan_plot:
post_data["interval"] = True
if cofactors:
post_data["addcovar"] = True
if perm_strata_list:
post_data["pstrata"] = True
rqtl_output = requests.post(GN3_LOCAL_URL + "api/rqtl/compute",
data=post_data).json()
if num_perm > 0:
return rqtl_output['perm_results'], rqtl_output[
'suggestive'], rqtl_output['significant'], rqtl_output['results']
else:
return rqtl_output['results']
def __init__(self, name):
json_data_fh = open(locate(name + '.json','genotype/json'))
try:
markers = json.load(json_data_fh)
except:
markers = []
for marker in markers:
if (marker['chr'] != "X") and (marker['chr'] != "Y"):
marker['chr'] = int(marker['chr'])
marker['Mb'] = float(marker['Mb'])
self.markers = markers
def __init__(self, name):
json_data_fh = open(locate(name + ".json",'genotype/json'))
try:
markers = json.load(json_data_fh)
except:
markers = []
for marker in markers:
if (marker['chr'] != "X") and (marker['chr'] != "Y"):
marker['chr'] = int(marker['chr'])
marker['Mb'] = float(marker['Mb'])
self.markers = markers
def __init__(self, name, specified_markers = []):
marker_data_fh = open(locate('genotype') + '/' + name + '.bim')
self.markers = []
for line in marker_data_fh:
splat = line.strip().split()
#logger.debug("splat:", splat)
if len(specified_markers) > 0:
if splat[1] in specified_markers:
marker = {}
marker['chr'] = int(splat[0])
marker['name'] = splat[1]
marker['Mb'] = float(splat[3]) / 1000000
else:
continue
else:
marker = {}
marker['chr'] = int(splat[0])
marker['name'] = splat[1]
marker['Mb'] = float(splat[3]) / 1000000
self.markers.append(marker)
def __init__(self, name, specified_markers = []):
marker_data_fh = open(locate('genotype') + '/' + name + '.bim')
self.markers = []
for line in marker_data_fh:
splat = line.strip().split()
#logger.debug("splat:", splat)
if len(specified_markers) > 0:
if splat[1] in specified_markers:
marker = {}
marker['chr'] = int(splat[0])
marker['name'] = splat[1]
marker['Mb'] = float(splat[3]) / 1000000
else:
continue
else:
marker = {}
marker['chr'] = int(splat[0])
marker['name'] = splat[1]
marker['Mb'] = float(splat[3]) / 1000000
self.markers.append(marker)
def run_analysis(self, requestform):
print("Starting CTL analysis on dataset")
self.trait_db_list = [trait.strip() for trait in requestform['trait_list'].split(',')]
self.trait_db_list = [x for x in self.trait_db_list if x]
print("strategy:", requestform.get("strategy"))
strategy = requestform.get("strategy")
print("nperm:", requestform.get("nperm"))
nperm = int(requestform.get("nperm"))
print("parametric:", requestform.get("parametric"))
parametric = bool(requestform.get("parametric"))
print("significance:", requestform.get("significance"))
significance = float(requestform.get("significance"))
# Get the name of the .geno file belonging to the first phenotype
datasetname = self.trait_db_list[0].split(":")[1]
dataset = data_set.create_dataset(datasetname)
genofilelocation = locate(dataset.group.name + ".geno", "genotype")
parser = genofile_parser.ConvertGenoFile(genofilelocation)
parser.process_csv()
# Create a genotype matrix
individuals = parser.individuals
markers = []
markernames = []
for marker in parser.markers:
markernames.append(marker["name"])
markers.append(marker["genotypes"])
genotypes = list(itertools.chain(*markers))
print(len(genotypes) / len(individuals), "==", len(parser.markers))
rGeno = r_t(ro.r.matrix(r_unlist(genotypes), nrow=len(markernames), ncol=len(individuals), dimnames = r_list(markernames, individuals), byrow=True))
# Create a phenotype matrix
traits = []
for trait in self.trait_db_list:
print("retrieving data for", trait)
if trait != "":
ts = trait.split(':')
gt = TRAIT.GeneralTrait(name = ts[0], dataset_name = ts[1])
gt.retrieve_sample_data(individuals)
for ind in individuals:
if ind in gt.data.keys():
traits.append(gt.data[ind].value)
else:
traits.append("-999")
rPheno = r_t(ro.r.matrix(r_as_numeric(r_unlist(traits)), nrow=len(self.trait_db_list), ncol=len(individuals), dimnames = r_list(self.trait_db_list, individuals), byrow=True))
# Use a data frame to store the objects
rPheno = r_data_frame(rPheno)
rGeno = r_data_frame(rGeno)
# Debug: Print the genotype and phenotype files to disk
#r_write_table(rGeno, "~/outputGN/geno.csv")
#r_write_table(rPheno, "~/outputGN/pheno.csv")
# Perform the CTL scan
res = self.r_CTLscan(rGeno, rPheno, strategy = strategy, nperm = nperm, parametric = parametric, ncores = 6)
# Get significant interactions
significant = self.r_CTLsignificant(res, significance = significance)
# Create an image for output
self.results = {}
self.results['imgurl1'] = webqtlUtil.genRandStr("CTLline_") + ".png"
self.results['imgloc1'] = GENERATED_IMAGE_DIR + self.results['imgurl1']
self.results['ctlresult'] = significant
self.results['requestform'] = requestform # Store the user specified parameters for the output page
# Create the lineplot
r_png(self.results['imgloc1'], width=1000, height=600)
self.r_lineplot(res, significance = significance)
r_dev_off()
n = 2
for trait in self.trait_db_list:
# Create the QTL like CTL plots
self.results['imgurl' + str(n)] = webqtlUtil.genRandStr("CTL_") + ".png"
self.results['imgloc' + str(n)] = GENERATED_IMAGE_DIR + self.results['imgurl' + str(n)]
r_png(self.results['imgloc' + str(n)], width=1000, height=600)
self.r_plotCTLobject(res, (n-1), significance = significance, main='Phenotype ' + trait)
r_dev_off()
n = n + 1
# Flush any output from R
sys.stdout.flush()
def run_rqtl_geno(self):
print("Calling R/qtl")
self.geno_to_rqtl_function()
## Get pointers to some common R functions
r_library = ro.r["library"] # Map the library function
r_c = ro.r["c"] # Map the c function
r_sum = ro.r["sum"] # Map the sum function
plot = ro.r["plot"] # Map the plot function
postscript = ro.r["postscript"] # Map the postscript function
png = ro.r["png"] # Map the png function
dev_off = ro.r["dev.off"] # Map the device off function
print(r_library("qtl")) # Load R/qtl
## Get pointers to some R/qtl functions
scanone = ro.r["scanone"] # Map the scanone function
scantwo = ro.r["scantwo"] # Map the scantwo function
calc_genoprob = ro.r["calc.genoprob"] # Map the calc.genoprob function
read_cross = ro.r["read.cross"] # Map the read.cross function
write_cross = ro.r["write.cross"] # Map the write.cross function
GENOtoCSVR = ro.r["GENOtoCSVR"] # Map the local GENOtoCSVR function
crossname = self.dataset.group.name
genofilelocation = locate(crossname + ".geno", "genotype")
crossfilelocation = TMPDIR + crossname + ".cross"
print("Conversion of geno to cross at location:", genofilelocation, " to ", crossfilelocation)
cross_object = GENOtoCSVR(genofilelocation, crossfilelocation) # TODO: Add the SEX if that is available
if self.manhattan_plot:
cross_object = calc_genoprob(cross_object)
else:
cross_object = calc_genoprob(cross_object, step=1, stepwidth="max")
cross_object = self.add_phenotype(cross_object, self.sanitize_rqtl_phenotype()) # Add the phenotype
# for debug: write_cross(cross_object, "csvr", "test.csvr")
# Scan for QTLs
covar = self.create_covariates(cross_object) # Create the additive covariate matrix
if self.pair_scan:
if self.do_control == "true": # If sum(covar) > 0 we have a covariate matrix
print("Using covariate"); result_data_frame = scantwo(cross_object, pheno = "the_pheno", addcovar = covar, model=self.model, method=self.method, n_cluster = 16)
else:
print("No covariates"); result_data_frame = scantwo(cross_object, pheno = "the_pheno", model=self.model, method=self.method, n_cluster = 16)
print("Pair scan results:", result_data_frame)
self.pair_scan_filename = webqtlUtil.genRandStr("scantwo_") + ".png"
png(file=TMPDIR+self.pair_scan_filename)
plot(result_data_frame)
dev_off()
return self.process_pair_scan_results(result_data_frame)
else:
if self.do_control == "true":
print("Using covariate"); result_data_frame = scanone(cross_object, pheno = "the_pheno", addcovar = covar, model=self.model, method=self.method)
else:
print("No covariates"); result_data_frame = scanone(cross_object, pheno = "the_pheno", model=self.model, method=self.method)
if int(self.num_perm) > 0: # Do permutation (if requested by user)
if self.do_control == "true":
perm_data_frame = scanone(cross_object, pheno_col = "the_pheno", addcovar = covar, n_perm = int(self.num_perm), model=self.model, method=self.method)
else:
perm_data_frame = scanone(cross_object, pheno_col = "the_pheno", n_perm = int(self.num_perm), model=self.model, method=self.method)
self.process_rqtl_perm_results(perm_data_frame) # Functions that sets the thresholds for the webinterface
return self.process_rqtl_results(result_data_frame)
def run_analysis(self, requestform):
logger.info("Starting PheWAS analysis on dataset")
genofilelocation = locate(
"BXD.geno", "genotype") # Get the location of the BXD genotypes
precompfile = locate_phewas(
"PheWAS_pval_EMMA_norm.RData",
"auwerx") # Get the location of the pre-computed EMMA results
# Get user parameters, trait_id and dataset, and store/update them in self
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"])
# Logger.Info some debug
logger.info("self.trait_id:" + self.trait_id + "\n")
logger.info("self.datasetname:" + self.datasetname + "\n")
logger.info("self.dataset.type:" + self.dataset.type + "\n")
# GN Magic ?
self.this_trait = GeneralTrait(dataset=self.dataset,
name=self.trait_id,
get_qtl_info=False,
get_sample_info=False)
logger.info(vars(self.this_trait))
# Set the values we need
self.chr = str(self.this_trait.chr)
self.mb = int(self.this_trait.mb)
# logger.info some debug
logger.info("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)
parser.process_csv()
snpinfo = []
for marker in parser.markers:
snpinfo.append(marker["name"])
snpinfo.append(marker["chr"])
snpinfo.append(marker["Mb"])
rnames = r_seq(1, len(parser.markers))
# Create the snp aligner object out of the BXD genotypes
snpaligner = ro.r.matrix(snpinfo,
nrow=len(parser.markers),
dimnames=r_list(rnames,
r_c("SNP", "Chr", "Pos")),
ncol=3,
byrow=True)
# Create the phenotype aligner object using R
phenoaligner = self.r_create_Pheno_aligner()
self.results = {}
self.results['imgurl1'] = webqtlUtil.genRandStr("phewas_") + ".png"
self.results['imgloc1'] = GENERATED_IMAGE_DIR + self.results['imgurl1']
self.results['mtadjust'] = self.mtadjust
logger.info("IMAGE AT:", self.results['imgurl1'])
logger.info("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
assert (precompfile)
assert (phenoaligner)
assert (snpaligner)
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]
self.results['R_debuglog'] = phewasres[3]
#self.r_PheWASManhattan(allpvalues)
#self.r_Stop()
logger.info("Initialization of PheWAS done !")
def run_rqtl_geno(vals, dataset, method, model, permCheck, num_perm,
do_control, control_marker, manhattan_plot, pair_scan):
geno_to_rqtl_function(dataset)
## Get pointers to some common R functions
r_library = ro.r["library"] # Map the library function
r_c = ro.r["c"] # Map the c function
r_sum = ro.r["sum"] # Map the sum function
plot = ro.r["plot"] # Map the plot function
postscript = ro.r["postscript"] # Map the postscript function
png = ro.r["png"] # Map the png function
dev_off = ro.r["dev.off"] # Map the device off function
print(r_library("qtl")) # Load R/qtl
## Get pointers to some R/qtl functions
scanone = ro.r["scanone"] # Map the scanone function
scantwo = ro.r["scantwo"] # Map the scantwo function
calc_genoprob = ro.r["calc.genoprob"] # Map the calc.genoprob function
read_cross = ro.r["read.cross"] # Map the read.cross function
write_cross = ro.r["write.cross"] # Map the write.cross function
GENOtoCSVR = ro.r["GENOtoCSVR"] # Map the local GENOtoCSVR function
crossname = dataset.group.name
genofilelocation = locate(crossname + ".geno", "genotype")
crossfilelocation = TMPDIR + crossname + ".cross"
#print("Conversion of geno to cross at location:", genofilelocation, " to ", crossfilelocation)
cross_object = GENOtoCSVR(
genofilelocation,
crossfilelocation) # TODO: Add the SEX if that is available
if manhattan_plot:
cross_object = calc_genoprob(cross_object)
else:
cross_object = calc_genoprob(cross_object, step=1, stepwidth="max")
cross_object = add_phenotype(
cross_object, sanitize_rqtl_phenotype(vals)) # Add the phenotype
# for debug: write_cross(cross_object, "csvr", "test.csvr")
# Scan for QTLs
covar = create_covariates(
control_marker, cross_object) # Create the additive covariate matrix
if pair_scan:
if do_control == "true": # If sum(covar) > 0 we have a covariate matrix
print("Using covariate")
result_data_frame = scantwo(cross_object,
pheno="the_pheno",
addcovar=covar,
model=model,
method=method,
n_cluster=16)
else:
print("No covariates")
result_data_frame = scantwo(cross_object,
pheno="the_pheno",
model=model,
method=method,
n_cluster=16)
#print("Pair scan results:", result_data_frame)
pair_scan_filename = webqtlUtil.genRandStr("scantwo_") + ".png"
png(file=TEMPDIR + pair_scan_filename)
plot(result_data_frame)
dev_off()
return process_pair_scan_results(result_data_frame)
else:
if do_control == "true":
print("Using covariate")
result_data_frame = scanone(cross_object,
pheno="the_pheno",
addcovar=covar,
model=model,
method=method)
else:
print("No covariates")
result_data_frame = scanone(cross_object,
pheno="the_pheno",
model=model,
method=method)
if num_perm > 0 and permCheck == "ON": # Do permutation (if requested by user)
if do_control == "true":
perm_data_frame = scanone(cross_object,
pheno_col="the_pheno",
addcovar=covar,
n_perm=num_perm,
model=model,
method=method)
else:
perm_data_frame = scanone(cross_object,
pheno_col="the_pheno",
n_perm=num_perm,
model=model,
method=method)
perm_output, suggestive, significant = process_rqtl_perm_results(
num_perm, perm_data_frame
) # Functions that sets the thresholds for the webinterface
return perm_output, suggestive, significant, process_rqtl_results(
result_data_frame)
else:
return process_rqtl_results(result_data_frame)
def run_analysis(self, requestform):
logger.info("Starting PheWAS analysis on dataset")
genofilelocation = locate("BXD.geno", "genotype") # Get the location of the BXD genotypes
precompfile = locate_phewas("PheWAS_pval_EMMA_norm.RData", "auwerx") # Get the location of the pre-computed EMMA results
# Get user parameters, trait_id and dataset, and store/update them in self
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"])
# Logger.Info some debug
logger.info("self.trait_id:" + self.trait_id + "\n")
logger.info("self.datasetname:" + self.datasetname + "\n")
logger.info("self.dataset.type:" + self.dataset.type + "\n")
# GN Magic ?
self.this_trait = GeneralTrait(dataset=self.dataset, name = self.trait_id, get_qtl_info = False, get_sample_info=False)
logger.info(vars(self.this_trait))
# Set the values we need
self.chr = str(self.this_trait.chr);
self.mb = int(self.this_trait.mb);
# logger.info some debug
logger.info("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)
parser.process_csv()
snpinfo = []
for marker in parser.markers:
snpinfo.append(marker["name"]);
snpinfo.append(marker["chr"]);
snpinfo.append(marker["Mb"]);
rnames = r_seq(1, len(parser.markers))
# Create the snp aligner object out of the BXD genotypes
snpaligner = ro.r.matrix(snpinfo, nrow=len(parser.markers), dimnames = r_list(rnames, r_c("SNP", "Chr", "Pos")), ncol = 3, byrow=True)
# Create the phenotype aligner object using R
phenoaligner = self.r_create_Pheno_aligner()
self.results = {}
self.results['imgurl1'] = webqtlUtil.genRandStr("phewas_") + ".png"
self.results['imgloc1'] = GENERATED_IMAGE_DIR + self.results['imgurl1']
self.results['mtadjust'] = self.mtadjust
logger.info("IMAGE AT:", self.results['imgurl1'] )
logger.info("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
assert(precompfile)
assert(phenoaligner)
assert(snpaligner)
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]
self.results['R_debuglog'] = phewasres[3]
#self.r_PheWASManhattan(allpvalues)
#self.r_Stop()
logger.info("Initialization of PheWAS done !")
def run_rqtl_geno(vals, samples, dataset, method, model, permCheck, num_perm, perm_strata_list, do_control, control_marker, manhattan_plot, pair_scan, cofactors):
## Get pointers to some common R functions
r_library = ro.r["library"] # Map the library function
r_c = ro.r["c"] # Map the c function
plot = ro.r["plot"] # Map the plot function
png = ro.r["png"] # Map the png function
dev_off = ro.r["dev.off"] # Map the device off function
print(r_library("qtl")) # Load R/qtl
## Get pointers to some R/qtl functions
scanone = ro.r["scanone"] # Map the scanone function
scantwo = ro.r["scantwo"] # Map the scantwo function
calc_genoprob = ro.r["calc.genoprob"] # Map the calc.genoprob function
crossname = dataset.group.name
#try:
# generate_cross_from_rdata(dataset)
# read_cross_from_rdata = ro.r["generate_cross_from_rdata"] # Map the local read_cross_from_rdata function
# genofilelocation = locate(crossname + ".RData", "genotype/rdata")
# cross_object = read_cross_from_rdata(genofilelocation) # Map the local GENOtoCSVR function
#except:
generate_cross_from_geno(dataset)
GENOtoCSVR = ro.r["GENOtoCSVR"] # Map the local GENOtoCSVR function
crossfilelocation = TMPDIR + crossname + ".cross"
if dataset.group.genofile:
genofilelocation = locate(dataset.group.genofile, "genotype")
else:
genofilelocation = locate(dataset.group.name + ".geno", "genotype")
cross_object = GENOtoCSVR(genofilelocation, crossfilelocation) # TODO: Add the SEX if that is available
if manhattan_plot:
cross_object = calc_genoprob(cross_object)
else:
cross_object = calc_genoprob(cross_object, step=1, stepwidth="max")
pheno_string = sanitize_rqtl_phenotype(vals)
cross_object = add_phenotype(cross_object, pheno_string, "the_pheno") # Add the phenotype
# Scan for QTLs
marker_covars = create_marker_covariates(control_marker, cross_object) # Create the additive covariate markers
if cofactors != "":
cross_object, trait_covars = add_cofactors(cross_object, dataset, cofactors, samples) # Create the covariates from selected traits
ro.r('all_covars <- cbind(marker_covars, trait_covars)')
else:
ro.r('all_covars <- marker_covars')
covars = ro.r['all_covars']
if pair_scan:
if do_control == "true":
logger.info("Using covariate"); result_data_frame = scantwo(cross_object, pheno = "the_pheno", addcovar = covars, model=model, method=method, n_cluster = 16)
else:
logger.info("No covariates"); result_data_frame = scantwo(cross_object, pheno = "the_pheno", model=model, method=method, n_cluster = 16)
pair_scan_filename = webqtlUtil.genRandStr("scantwo_") + ".png"
png(file=TEMPDIR+pair_scan_filename)
plot(result_data_frame)
dev_off()
return process_pair_scan_results(result_data_frame)
else:
if do_control == "true" or cofactors != "":
logger.info("Using covariate"); result_data_frame = scanone(cross_object, pheno = "the_pheno", addcovar = covars, model=model, method=method)
else:
logger.info("No covariates"); result_data_frame = scanone(cross_object, pheno = "the_pheno", model=model, method=method)
if num_perm > 0 and permCheck == "ON": # Do permutation (if requested by user)
if len(perm_strata_list) > 0: #ZS: The strata list would only be populated if "Stratified" was checked on before mapping
cross_object, strata_ob = add_perm_strata(cross_object, perm_strata_list)
if do_control == "true" or cofactors != "":
perm_data_frame = scanone(cross_object, pheno_col = "the_pheno", addcovar = covars, n_perm = int(num_perm), perm_strata = strata_ob, model=model, method=method)
else:
perm_data_frame = scanone(cross_object, pheno_col = "the_pheno", n_perm = num_perm, perm_strata = strata_ob, model=model, method=method)
else:
if do_control == "true" or cofactors != "":
perm_data_frame = scanone(cross_object, pheno_col = "the_pheno", addcovar = covars, n_perm = int(num_perm), model=model, method=method)
else:
perm_data_frame = scanone(cross_object, pheno_col = "the_pheno", n_perm = num_perm, model=model, method=method)
perm_output, suggestive, significant = process_rqtl_perm_results(num_perm, perm_data_frame) # Functions that sets the thresholds for the webinterface
the_scale = check_mapping_scale(genofilelocation)
return perm_output, suggestive, significant, process_rqtl_results(result_data_frame, dataset.group.species), the_scale
else:
the_scale = check_mapping_scale(genofilelocation)
return process_rqtl_results(result_data_frame, dataset.group.species), the_scale
def run_analysis(self, requestform):
print("Starting CTL analysis on dataset")
self.trait_db_list = [trait.strip() for trait in requestform['trait_list'].split(',')]
self.trait_db_list = [x for x in self.trait_db_list if x]
print("strategy:", requestform.get("strategy"))
strategy = requestform.get("strategy")
print("nperm:", requestform.get("nperm"))
nperm = int(requestform.get("nperm"))
print("parametric:", requestform.get("parametric"))
parametric = bool(requestform.get("parametric"))
print("significance:", requestform.get("significance"))
significance = float(requestform.get("significance"))
# Get the name of the .geno file belonging to the first phenotype
datasetname = self.trait_db_list[0].split(":")[1]
dataset = data_set.create_dataset(datasetname)
genofilelocation = locate(dataset.group.name + ".geno", "genotype")
parser = genofile_parser.ConvertGenoFile(genofilelocation)
parser.process_csv()
print(dataset.group)
# Create a genotype matrix
individuals = parser.individuals
markers = []
markernames = []
for marker in parser.markers:
markernames.append(marker["name"])
markers.append(marker["genotypes"])
genotypes = list(itertools.chain(*markers))
print(len(genotypes) / len(individuals), "==", len(parser.markers))
rGeno = r_t(ro.r.matrix(r_unlist(genotypes), nrow=len(markernames), ncol=len(individuals), dimnames = r_list(markernames, individuals), byrow=True))
# Create a phenotype matrix
traits = []
for trait in self.trait_db_list:
print("retrieving data for", trait)
if trait != "":
ts = trait.split(':')
gt = TRAIT.GeneralTrait(name = ts[0], dataset_name = ts[1])
gt = TRAIT.retrieve_sample_data(gt, dataset, individuals)
for ind in individuals:
if ind in gt.data.keys():
traits.append(gt.data[ind].value)
else:
traits.append("-999")
rPheno = r_t(ro.r.matrix(r_as_numeric(r_unlist(traits)), nrow=len(self.trait_db_list), ncol=len(individuals), dimnames = r_list(self.trait_db_list, individuals), byrow=True))
print(rPheno)
# Use a data frame to store the objects
rPheno = r_data_frame(rPheno, check_names = False)
rGeno = r_data_frame(rGeno, check_names = False)
# Debug: Print the genotype and phenotype files to disk
#r_write_table(rGeno, "~/outputGN/geno.csv")
#r_write_table(rPheno, "~/outputGN/pheno.csv")
# Perform the CTL scan
res = self.r_CTLscan(rGeno, rPheno, strategy = strategy, nperm = nperm, parametric = parametric, ncores = 6)
# Get significant interactions
significant = self.r_CTLsignificant(res, significance = significance)
# Create an image for output
self.results = {}
self.results['imgurl1'] = webqtlUtil.genRandStr("CTLline_") + ".png"
self.results['imgloc1'] = GENERATED_IMAGE_DIR + self.results['imgurl1']
self.results['ctlresult'] = significant
self.results['requestform'] = requestform # Store the user specified parameters for the output page
# Create the lineplot
r_png(self.results['imgloc1'], width=1000, height=600, type='cairo-png')
self.r_lineplot(res, significance = significance)
r_dev_off()
n = 2 # We start from 2, since R starts from 1 :)
for trait in self.trait_db_list:
# Create the QTL like CTL plots
self.results['imgurl' + str(n)] = webqtlUtil.genRandStr("CTL_") + ".png"
self.results['imgloc' + str(n)] = GENERATED_IMAGE_DIR + self.results['imgurl' + str(n)]
r_png(self.results['imgloc' + str(n)], width=1000, height=600, type='cairo-png')
self.r_plotCTLobject(res, (n-1), significance = significance, main='Phenotype ' + trait)
r_dev_off()
n = n + 1
# Flush any output from R
sys.stdout.flush()
# Create the interactive graph for cytoscape visualization (Nodes and Edges)
print(type(significant))
if not type(significant) == ri.RNULLType:
for x in range(len(significant[0])):
print(significant[0][x], significant[1][x], significant[2][x]) # Debug to console
tsS = significant[0][x].split(':') # Source
tsT = significant[2][x].split(':') # Target
gtS = TRAIT.GeneralTrait(name = tsS[0], dataset_name = tsS[1]) # Retrieve Source info from the DB
gtT = TRAIT.GeneralTrait(name = tsT[0], dataset_name = tsT[1]) # Retrieve Target info from the DB
self.addNode(gtS)
self.addNode(gtT)
self.addEdge(gtS, gtT, significant, x)
significant[0][x] = gtS.symbol + " (" + gtS.name + ")" # Update the trait name for the displayed table
significant[2][x] = gtT.symbol + " (" + gtT.name + ")" # Update the trait name for the displayed table
self.elements = json.dumps(self.nodes_list + self.edges_list)
def run_rqtl_geno(vals, dataset, method, model, permCheck, num_perm, do_control, control_marker, manhattan_plot, pair_scan):
geno_to_rqtl_function(dataset)
## Get pointers to some common R functions
r_library = ro.r["library"] # Map the library function
r_c = ro.r["c"] # Map the c function
plot = ro.r["plot"] # Map the plot function
png = ro.r["png"] # Map the png function
dev_off = ro.r["dev.off"] # Map the device off function
print(r_library("qtl")) # Load R/qtl
## Get pointers to some R/qtl functions
scanone = ro.r["scanone"] # Map the scanone function
scantwo = ro.r["scantwo"] # Map the scantwo function
calc_genoprob = ro.r["calc.genoprob"] # Map the calc.genoprob function
GENOtoCSVR = ro.r["GENOtoCSVR"] # Map the local GENOtoCSVR function
crossname = dataset.group.name
genofilelocation = locate(crossname + ".geno", "genotype")
crossfilelocation = TMPDIR + crossname + ".cross"
cross_object = GENOtoCSVR(genofilelocation, crossfilelocation) # TODO: Add the SEX if that is available
if manhattan_plot:
cross_object = calc_genoprob(cross_object)
else:
cross_object = calc_genoprob(cross_object, step=1, stepwidth="max")
cross_object = add_phenotype(cross_object, sanitize_rqtl_phenotype(vals)) # Add the phenotype
# Scan for QTLs
covar = create_covariates(control_marker, cross_object) # Create the additive covariate matrix
if pair_scan:
if do_control == "true":
logger.info("Using covariate"); result_data_frame = scantwo(cross_object, pheno = "the_pheno", addcovar = covar, model=model, method=method, n_cluster = 16)
else:
logger.info("No covariates"); result_data_frame = scantwo(cross_object, pheno = "the_pheno", model=model, method=method, n_cluster = 16)
pair_scan_filename = webqtlUtil.genRandStr("scantwo_") + ".png"
png(file=TEMPDIR+pair_scan_filename)
plot(result_data_frame)
dev_off()
return process_pair_scan_results(result_data_frame)
else:
if do_control == "true":
logger.info("Using covariate"); result_data_frame = scanone(cross_object, pheno = "the_pheno", addcovar = covar, model=model, method=method)
else:
logger.info("No covariates"); result_data_frame = scanone(cross_object, pheno = "the_pheno", model=model, method=method)
if num_perm > 0 and permCheck == "ON": # Do permutation (if requested by user)
if do_control == "true":
perm_data_frame = scanone(cross_object, pheno_col = "the_pheno", addcovar = covar, n_perm = num_perm, model=model, method=method)
else:
perm_data_frame = scanone(cross_object, pheno_col = "the_pheno", n_perm = num_perm, model=model, method=method)
perm_output, suggestive, significant = process_rqtl_perm_results(num_perm, perm_data_frame) # Functions that sets the thresholds for the webinterface
return perm_output, suggestive, significant, process_rqtl_results(result_data_frame)
else:
return process_rqtl_results(result_data_frame)
