def calculate_significance(args, infmat, infmat_index, G, heat_permutations):
sizes = range(args.cc_start_size, args.cc_stop_size+1)
print "\t- Using no. of components >= k (k \\in",
print "[%s, %s]) as statistic" % (min(sizes), max(sizes))
#size2counts is dict(size -> (list of counts, 1 per permutation))
sizes2counts = stats.calculate_permuted_cc_counts(infmat, infmat_index, heat_permutations,
args.delta, sizes, args.parallel)
real_counts = stats.num_components_min_size(G, sizes)
size2real_counts = dict(zip(sizes, real_counts))
return stats.compute_statistics(size2real_counts, sizes2counts, args.num_permutations)
def calculate_significance(args, infmat, infmat_index, G, heat_permutations):
sizes = list(range(args.cc_start_size, args.cc_stop_size + 1))
print("\t- Using no. of components >= k (k \\in")
print("[%s, %s]) as statistic" % (min(sizes), max(sizes)))
#size2counts is dict(size -> (list of counts, 1 per permutation))
sizes2counts = stats.calculate_permuted_cc_counts(infmat, infmat_index,
heat_permutations,
args.delta, sizes,
args.parallel)
real_counts = stats.num_components_min_size(G, sizes)
size2real_counts = dict(list(zip(sizes, real_counts)))
return stats.compute_statistics(size2real_counts, sizes2counts,
args.num_permutations)
def run_helper(args, infmat, full_index2gene, G, nname, pnp, heat, hname, addtl_genes, get_deltas_fn, infmat_name="PPR", max_cc_sizes=[5, 10, 15, 20], verbose=0):
"""Helper shared by runHotNet2 and runClassicHotNet.
"""
# Perform delta selection (if necessary)
if args.deltas:
deltas = args.deltas
else:
deltas = get_deltas_fn(full_index2gene, heat, args.network_permutations, args.num_cores, infmat, addtl_genes, pnp, infmat_name, max_cc_sizes, verbose)
sim, index2gene = hn.similarity_matrix(infmat, full_index2gene, heat, True, verbose=verbose)
results = []
for delta in deltas:
# find connected components
G = hn.weighted_graph(sim, index2gene, delta, directed=True)
ccs = hn.connected_components(G, args.min_cc_size)
# calculate significance (using all genes with heat scores)
if verbose > 4:
print "* Performing permuted heat statistical significance..."
print "\t- Using no. of components >= k (k \\in",
print "[%s, %s]) as statistic" % (min(HN2_STATS_SIZES), max(HN2_STATS_SIZES))
heat_permutations = p.permute_heat(heat, full_index2gene.values(),
args.heat_permutations, addtl_genes,
args.num_cores)
sizes2counts = stats.calculate_permuted_cc_counts(infmat, full_index2gene,
heat_permutations, delta, HN2_STATS_SIZES, True,
args.num_cores)
real_counts = stats.num_components_min_size(G, HN2_STATS_SIZES)
size2real_counts = dict(zip(HN2_STATS_SIZES, real_counts))
sizes2stats = stats.compute_statistics(size2real_counts, sizes2counts,
args.heat_permutations)
# sort ccs list such that genes within components are sorted alphanumerically, and components
# are sorted first by length, then alphanumerically by name of the first gene in the component
ccs = [sorted(cc) for cc in ccs]
ccs.sort(key=lambda comp: comp[0])
ccs.sort(key=len, reverse=True)
# Record the results for this delta
results.append( (ccs, sizes2stats, delta) )
return results
def run_helper(args, infmat_name, get_deltas_fn, extra_delta_args):
"""Helper shared by simpleRun and simpleRunClassic.
"""
# create output directory if doesn't exist; warn if it exists and is not empty
if not os.path.exists(args.output_directory):
os.makedirs(args.output_directory)
if len(os.listdir(args.output_directory)) > 0:
print("WARNING: Output directory is not empty. Any conflicting files will be overwritten. "
"(Ctrl-c to cancel).")
infmat = hnio.load_infmat(args.infmat_file, infmat_name)
full_index2gene = hnio.load_index(args.infmat_index_file)
using_json_heat = os.path.splitext(args.heat_file.lower())[1] == '.json'
if using_json_heat:
heat = json.load(open(args.heat_file))['heat']
else:
heat = hnio.load_heat_tsv(args.heat_file)
print "* Loaded heat scores for %s genes" % len(heat)
# filter out genes not in the network
heat = hnheat.filter_heat_to_network_genes(heat, set(full_index2gene.values()))
# genes with score 0 cannot be in output components, but are eligible for heat in permutations
heat, addtl_genes = hnheat.filter_heat(heat, None, False, 'There are ## genes with heat score 0')
deltas = get_deltas_fn(full_index2gene, heat, args.delta_permutations, args.num_cores, infmat, addtl_genes, *extra_delta_args)
sim, index2gene = hn.similarity_matrix(infmat, full_index2gene, heat, True)
results_files = []
for delta in deltas:
# create output directory
delta_out_dir = args.output_directory + "/delta_" + str(delta)
if not os.path.isdir(delta_out_dir):
os.mkdir(delta_out_dir)
# find connected components
G = hn.weighted_graph(sim, index2gene, delta, directed=True)
ccs = hn.connected_components(G, args.min_cc_size)
# calculate significance (using all genes with heat scores)
print "* Performing permuted heat statistical significance..."
heat_permutations = p.permute_heat(heat, full_index2gene.values(),
args.significance_permutations, addtl_genes,
args.num_cores)
sizes = range(2, 11)
print "\t- Using no. of components >= k (k \\in",
print "[%s, %s]) as statistic" % (min(sizes), max(sizes))
sizes2counts = stats.calculate_permuted_cc_counts(infmat, full_index2gene,
heat_permutations, delta, sizes, True,
args.num_cores)
real_counts = stats.num_components_min_size(G, sizes)
size2real_counts = dict(zip(sizes, real_counts))
sizes2stats = stats.compute_statistics(size2real_counts, sizes2counts,
args.significance_permutations)
# sort ccs list such that genes within components are sorted alphanumerically, and components
# are sorted first by length, then alphanumerically by name of the first gene in the component
ccs = [sorted(cc) for cc in ccs]
ccs.sort(key=lambda comp: comp[0])
ccs.sort(key=len, reverse=True)
# write output
if not using_json_heat:
heat_dict = {"heat": heat, "parameters": {"heat_file": args.heat_file}}
heat_out = open(os.path.abspath(delta_out_dir) + "/" + HEAT_JSON, 'w')
json.dump(heat_dict, heat_out, indent=4)
heat_out.close()
args.heat_file = os.path.abspath(delta_out_dir) + "/" + HEAT_JSON
args.delta = delta # include delta in parameters section of output JSON
output_dict = {"parameters": vars(args), "sizes": hn.component_sizes(ccs),
"components": ccs, "statistics": sizes2stats}
hnio.write_significance_as_tsv(os.path.abspath(delta_out_dir) + "/" + SIGNIFICANCE_TSV,
sizes2stats)
json_out = open(os.path.abspath(delta_out_dir) + "/" + JSON_OUTPUT, 'w')
json.dump(output_dict, json_out, indent=4)
json_out.close()
results_files.append( os.path.abspath(delta_out_dir) + "/" + JSON_OUTPUT )
hnio.write_components_as_tsv(os.path.abspath(delta_out_dir) + "/" + COMPONENTS_TSV, ccs)
# create the hierarchy if necessary
if args.output_hierarchy:
from bin import createDendrogram as CD
hierarchy_out_dir = '{}/hierarchy/'.format(args.output_directory)
if not os.path.isdir(hierarchy_out_dir): os.mkdir(hierarchy_out_dir)
params = vars(args)
CD.createDendrogram( sim, index2gene.values(), hierarchy_out_dir, params, verbose=False)
hierarchyFile = '{}/viz_files/{}'.format(str(hn.__file__).rsplit('/', 1)[0], HIERARCHY_WEB_FILE)
shutil.copy(hierarchyFile, '{}/index.html'.format(hierarchy_out_dir))
# write visualization output if edge file given
if args.edge_file:
from bin import makeResultsWebsite as MRW
viz_args = [ "-r" ] + results_files
viz_args += ["-ef", args.edge_file, "-o", args.output_directory + "/viz" ]
if args.network_name: viz_args += [ "-nn", args.network_name ]
if args.display_score_file: viz_args += [ "-dsf", args.display_score_file ]
if args.display_name_file: viz_args += [ "-dnf", args.display_name_file ]
MRW.run( MRW.get_parser().parse_args(viz_args) )
def run_helper(args, infmat_name, get_deltas_fn, extra_delta_args):
"""Helper shared by simpleRun and simpleRunClassic.
"""
# create output directory if doesn't exist; warn if it exists and is not empty
if not os.path.exists(args.output_directory):
os.makedirs(args.output_directory)
if len(os.listdir(args.output_directory)) > 0:
print("WARNING: Output directory is not empty. Any conflicting files will be overwritten. "
"(Ctrl-c to cancel).")
infmat = scipy.io.loadmat(args.infmat_file)[infmat_name]
full_index2gene = hnio.load_index(args.infmat_index_file)
using_json_heat = os.path.splitext(args.heat_file.lower())[1] == '.json'
if using_json_heat:
heat = json.load(open(args.heat_file))['heat']
else:
heat = hnio.load_heat_tsv(args.heat_file)
print "* Loaded heat scores for %s genes" % len(heat)
# filter out genes not in the network
heat = hnheat.filter_heat_to_network_genes(heat, set(full_index2gene.values()))
# genes with score 0 cannot be in output components, but are eligible for heat in permutations
heat, addtl_genes = hnheat.filter_heat(heat, None, False, 'There are ## genes with heat score 0')
deltas = get_deltas_fn(full_index2gene, heat, args.delta_permutations, args.num_cores, infmat, addtl_genes, *extra_delta_args)
sim, index2gene = hn.similarity_matrix(infmat, full_index2gene, heat, True)
results_files = []
for delta in deltas:
# create output directory
delta_out_dir = args.output_directory + "/delta_" + str(delta)
if not os.path.isdir(delta_out_dir):
os.mkdir(delta_out_dir)
# find connected components
G = hn.weighted_graph(sim, index2gene, delta, directed=True)
ccs = hn.connected_components(G, args.min_cc_size)
# calculate significance (using all genes with heat scores)
print "* Performing permuted heat statistical significance..."
heat_permutations = p.permute_heat(heat, full_index2gene.values(),
args.significance_permutations, addtl_genes,
args.num_cores)
sizes = range(2, 11)
print "\t- Using no. of components >= k (k \\in",
print "[%s, %s]) as statistic" % (min(sizes), max(sizes))
sizes2counts = stats.calculate_permuted_cc_counts(infmat, full_index2gene,
heat_permutations, delta, sizes, True,
args.num_cores)
real_counts = stats.num_components_min_size(G, sizes)
size2real_counts = dict(zip(sizes, real_counts))
sizes2stats = stats.compute_statistics(size2real_counts, sizes2counts,
args.significance_permutations)
# sort ccs list such that genes within components are sorted alphanumerically, and components
# are sorted first by length, then alphanumerically by name of the first gene in the component
ccs = [sorted(cc) for cc in ccs]
ccs.sort(key=lambda comp: comp[0])
ccs.sort(key=len, reverse=True)
# write output
if not using_json_heat:
heat_dict = {"heat": heat, "parameters": {"heat_file": args.heat_file}}
heat_out = open(os.path.abspath(delta_out_dir) + "/" + HEAT_JSON, 'w')
json.dump(heat_dict, heat_out, indent=4)
heat_out.close()
args.heat_file = os.path.abspath(delta_out_dir) + "/" + HEAT_JSON
args.delta = delta # include delta in parameters section of output JSON
output_dict = {"parameters": vars(args), "sizes": hn.component_sizes(ccs),
"components": ccs, "statistics": sizes2stats}
hnio.write_significance_as_tsv(os.path.abspath(delta_out_dir) + "/" + SIGNIFICANCE_TSV,
sizes2stats)
json_out = open(os.path.abspath(delta_out_dir) + "/" + JSON_OUTPUT, 'w')
json.dump(output_dict, json_out, indent=4)
json_out.close()
results_files.append( os.path.abspath(delta_out_dir) + "/" + JSON_OUTPUT )
hnio.write_components_as_tsv(os.path.abspath(delta_out_dir) + "/" + COMPONENTS_TSV, ccs)
# write visualization output if edge file given
if args.edge_file:
from bin import makeResultsWebsite as MRW
viz_args = [ "-r" ] + results_files
viz_args += ["-ef", args.edge_file, "-o", args.output_directory + "/viz" ]
if args.network_name: viz_args += [ "-nn", args.network_name ]
if args.display_score_file: viz_args += [ "-dsf", args.display_score_file ]
MRW.run( MRW.get_parser().parse_args(viz_args) )
def run_helper(args,
infmat,
full_index2gene,
G,
nname,
pnp,
heat,
hname,
addtl_genes,
get_deltas_fn,
infmat_name="PPR",
max_cc_sizes=[5, 10, 15, 20],
verbose=0):
"""Helper shared by runHotNet2 and runClassicHotNet."""
# Perform delta selection (if necessary)
if args.deltas:
deltas = args.deltas
else:
deltas = get_deltas_fn(full_index2gene, heat,
args.network_permutations, args.num_cores,
infmat, addtl_genes, pnp, infmat_name,
max_cc_sizes, verbose)
sim, index2gene = hn.similarity_matrix(infmat,
full_index2gene,
heat,
True,
verbose=verbose)
results = []
"""Change from here """
#permuted_sub_score_delta = []
#subnet_geneScore_delta = []
#Alpha_sig_delta = []
#Subnetscore_sig_delta = []
#Conponet_sig_delta = []
#sig_Conp_delta = []
#sig_Count_delta = []
#degree_delta = []
#permuted_degree_delta = []
#degree_weighted_score_delta = []
#cent_weighted_score_delta = []
My_results = []
"""end here"""
for delta in deltas:
"""Change from here"""
simG = hn.weighted_graph(sim, index2gene, delta, directed=True)
ccs = hn.connected_components(simG, args.min_cc_size)
"""end here"""
# calculate significance (using all genes with heat scores)
if verbose > 4:
print "* Performing permuted heat statistical significance..."
print "\t- Using no. of components >= k (k \\in",
print "[%s, %s]) as statistic" % (min(HN2_STATS_SIZES),
max(HN2_STATS_SIZES))
heat_permutations = p.permute_heat(heat, full_index2gene.values(),
args.heat_permutations, addtl_genes,
args.num_cores)
#print heat_permutations
#print heat_permutations[0]
"""change from here"""
permuted_sub_score, permuted_gene_degree, permuted_degree_weighted_score, permuted_centality_weighted_score = my.calculate_permuted_subnetScore(
infmat, full_index2gene, heat_permutations, delta, verbose,
args.min_cc_size, G, args.num_cores)
#permuted_sub_score_delta.append((permuted_sub_score, delta))
#permuted_degree_delta.append((permuted_gene_degree,delta))
#print permuted_sub_score_delta
####print permuted_degree_weighted_score
#print permuted_degree_delta
####calcaule the degree of gene in each permuted subnetwork
""" End here """
sizes2counts = stats.calculate_permuted_cc_counts(
infmat, full_index2gene, heat_permutations, delta, HN2_STATS_SIZES,
True, args.num_cores)
real_counts = stats.num_components_min_size(simG, HN2_STATS_SIZES)
size2real_counts = dict(zip(HN2_STATS_SIZES, real_counts))
sizes2stats = stats.compute_statistics(size2real_counts, sizes2counts,
args.heat_permutations)
#print ccs
# sort ccs list such that genes within components are sorted alphanumerically, and components
# are sorted first by length, then alphanumerically by name of the first gene in the component
ccs = [sorted(cc) for cc in ccs]
ccs.sort(key=lambda comp: comp[0])
ccs.sort(key=len, reverse=True)
#print ccs
"""changing here"""
#####calculate all the gene score for gene list
genelist, scoreVec = my.score_vec(infmat, full_index2gene, heat)
#gene_socre = np.column_stack((genelist, scoreVec))
subnet_geneScore = my.Matchscore_Permuted_fun(genelist, scoreVec, ccs)
#print subnet_geneScore
####output the subnetwork with score only
#print ccs
#subnet_geneScore_delta.append((subnet_geneScore,delta))
####calculate the gene degree within each subnetwork
gene_degree = my.Gene_Degree_func(G, ccs)
#degree_delta.append((gene_degree,delta))
#####find score weighted by degree
degree_weighted_score = my.Product_func(subnet_geneScore, gene_degree)
#degree_weighted_score_delta.append((degree_weighted_score,delta))
#####find score of gene weighted by centrality
gene_centrality = my.Gene_Centrality_func(G, ccs)
cent_weighted_score = my.Product_func(subnet_geneScore,
gene_centrality)
#cent_weighted_score_delta.append((cent_weighted_score,delta))
#####calculate significant test
"""Sum and Size of subnetwork"""
Alpha_sig, Subnetscore_sig, Conponet_sig, count, sig_conponet = my.MyStatistics_func(
subnet_geneScore, gene_degree, permuted_sub_score,
permuted_gene_degree, ccs, 1)
"""Degree weighted sum and size of subnetwork"""
Alpha_sig2, Subnetscore_sig_dwss, Conponet_sig_dwss, count_dwss, sig_conponet_dwss = my.MyStatistics_func(
degree_weighted_score, gene_degree, permuted_degree_weighted_score,
permuted_gene_degree, ccs, 1)
"""Centrality weighted sum and size of subnewtwork"""
Alpha_sig3, Subnetscore_sig_cwss, Conponet_sig_cwss, count_cwss, sig_conponet_cwss = my.MyStatistics_func(
cent_weighted_score, gene_degree,
permuted_centality_weighted_score, permuted_gene_degree, ccs, 1)
"""Sum and Sum of degree of gene within subnetwork"""
Alpha_sig1, Subnetscore_sig_sd, Conponet_sig_sd, count_sd, sig_conponet_sd = my.MyStatistics_func(
subnet_geneScore, gene_degree, permuted_sub_score,
permuted_gene_degree, ccs, 2)
"""Degree weighted sum and Sum of degree of gene within subnetwork"""
Alpha_sig4, Subnetscore_sig_dwsd, Conponet_sig_dwsd, count_dwsd, sig_conponet_dwsd = my.MyStatistics_func(
degree_weighted_score, gene_degree, permuted_degree_weighted_score,
permuted_gene_degree, ccs, 2)
"""Centrality weighted sum and Sum of degree of gene within subnetwork"""
Alpha_sig5, Subnetscore_sig_cwsd, Conponet_sig_cwsd, count_cwsd, sig_conponet_cwsd = my.MyStatistics_func(
cent_weighted_score, gene_degree,
permuted_centality_weighted_score, permuted_gene_degree, ccs, 2)
#####store all the result
####this is My results
My_results.append(
(permuted_sub_score, subnet_geneScore, Alpha_sig, Subnetscore_sig,
Conponet_sig, count, sig_conponet, gene_degree,
permuted_gene_degree, cent_weighted_score, degree_weighted_score,
permuted_centality_weighted_score, permuted_degree_weighted_score,
Subnetscore_sig_sd, Conponet_sig_sd, count_sd, sig_conponet_sd,
Subnetscore_sig_dwss, Conponet_sig_dwss, count_dwss,
sig_conponet_dwss, Subnetscore_sig_cwss, Conponet_sig_cwss,
count_cwss, sig_conponet_cwss, Subnetscore_sig_dwsd,
Conponet_sig_dwsd, count_dwsd, sig_conponet_dwsd,
Subnetscore_sig_cwsd, Conponet_sig_cwsd, count_cwsd,
sig_conponet_cwsd, delta))
#print Subnetscore_sig
"""end here """
results.append((ccs, sizes2stats, delta))
####this is My results
return results, My_results
def run(args):
# create output directory if doesn't exist; warn if it exists and is not empty
if not os.path.exists(args.output_directory):
os.makedirs(args.output_directory)
if len(os.listdir(args.output_directory)) > 0:
print("WARNING: Output directory is not empty. Any conflicting files will be overwritten. ")
print("(Ctrl-c to cancel).")
infmat = scipy.io.loadmat(args.infmat_file)[INFMAT_NAME]
infmat_index = hnio.load_index(args.infmat_index_file)
heat = hnio.load_heat_tsv(args.heat_file)
# filter out genes with heat score less than min_heat_score
heat, addtl_genes, args.min_heat_score = hnheat.filter_heat(heat, args.min_heat_score)
# find delta that maximizes # CCs of size >= MIN_SIZE for each permuted data set
deltas = ft.get_deltas_for_heat(infmat, infmat_index, heat, addtl_genes, args.num_permutations,
args.parallel)
#find the multiple of the median delta s.t. the size of the largest CC in the real data
#is <= MAX_CC_SIZE
medianDelta = np.median(deltas[MIN_CC_SIZE])
M, gene_index = hn.induce_infmat(infmat, infmat_index, sorted(heat.keys()), quiet=False)
h = hn.heat_vec(heat, gene_index)
sim = hn.similarity_matrix(M, h)
for i in range(1, 11):
G = hn.weighted_graph(sim, gene_index, i*medianDelta)
max_cc_size = max([len(cc) for cc in hn.connected_components(G)])
if max_cc_size <= MAX_CC_SIZE:
break
# load interaction network edges and determine location of static HTML files for visualization
edges = hnio.load_ppi_edges(args.edge_file) if args.edge_file else None
index_file = '%s/viz_files/%s' % (os.path.realpath(__file__).rsplit('/', 1)[0], VIZ_INDEX)
subnetworks_file = '%s/viz_files/%s' % (os.path.realpath(__file__).rsplit('/', 1)[0], VIZ_SUBNETWORKS)
gene2index = dict([(gene, index) for index, gene in list(infmat_index.items())])
#and run HotNet with that multiple and the next 4 multiples
run_deltas = [i*medianDelta for i in range(i, i+5)]
for delta in run_deltas:
# create output directory
delta_out_dir = args.output_directory + "/delta_" + str(delta)
if not os.path.isdir(delta_out_dir):
os.mkdir(delta_out_dir)
# find connected components
G = hn.weighted_graph(sim, gene_index, delta)
ccs = hn.connected_components(G, args.min_cc_size)
# calculate significance (using all genes with heat scores)
print("* Performing permuted heat statistical significance...")
heat_permutations = p.permute_heat(heat, args.num_permutations, addtl_genes, args.parallel)
sizes = list(range(2, 11))
print("\t- Using no. of components >= k (k \\in")
print("[%s, %s]) as statistic" % (min(sizes), max(sizes)))
sizes2counts = stats.calculate_permuted_cc_counts(infmat, infmat_index, heat_permutations,
delta, sizes, args.parallel)
real_counts = stats.num_components_min_size(G, sizes)
size2real_counts = dict(list(zip(sizes, real_counts)))
sizes2stats = stats.compute_statistics(size2real_counts, sizes2counts, args.num_permutations)
# sort ccs list such that genes within components are sorted alphanumerically, and components
# are sorted first by length, then alphanumerically by name of the first gene in the component
ccs = [sorted(cc) for cc in ccs]
ccs.sort(key=lambda comp: comp[0])
ccs.sort(key=len, reverse=True)
# write output
heat_dict = {"heat": heat, "parameters": {"heat_file": args.heat_file}}
heat_out = open(os.path.abspath(delta_out_dir) + "/" + HEAT_JSON, 'w')
json.dump(heat_dict, heat_out, indent=4)
heat_out.close()
args.heat_file = os.path.abspath(delta_out_dir) + "/" + HEAT_JSON
args.delta = delta
output_dict = {"parameters": vars(args), "sizes": hn.component_sizes(ccs),
"components": ccs, "statistics": sizes2stats}
hnio.write_significance_as_tsv(os.path.abspath(delta_out_dir) + "/" + SIGNIFICANCE_TSV,
sizes2stats)
json_out = open(os.path.abspath(delta_out_dir) + "/" + JSON_OUTPUT, 'w')
json.dump(output_dict, json_out, indent=4)
json_out.close()
hnio.write_components_as_tsv(os.path.abspath(delta_out_dir) + "/" + COMPONENTS_TSV, ccs)
# write visualization output if edge file given
if args.edge_file:
viz_data = {"delta": delta, 'subnetworks': list()}
for cc in ccs:
viz_data['subnetworks'].append(viz.get_component_json(cc, heat, edges, gene2index, args.network_name))
delta_viz_dir = '%s/viz/delta%s' % (args.output_directory, delta)
if not os.path.isdir(delta_viz_dir):
os.makedirs(delta_viz_dir)
viz_out = open('%s/subnetworks.json' % delta_viz_dir, 'w')
json.dump(viz_data, viz_out, indent=4)
viz_out.close()
shutil.copy(subnetworks_file, delta_viz_dir)
if args.edge_file:
viz.write_index_file(index_file, '%s/viz/%s' % (args.output_directory, VIZ_INDEX), run_deltas)
def run_helper(args,
infmat,
full_index2gene,
G,
nname,
pnp,
heat,
hname,
addtl_genes,
get_deltas_fn,
infmat_name="PPR",
max_cc_sizes=[5, 10, 15, 20],
verbose=0):
"""Helper shared by runHotNet2 and runClassicHotNet.
"""
# Perform delta selection (if necessary)
if args.deltas:
deltas = args.deltas
else:
deltas = get_deltas_fn(full_index2gene, heat,
args.network_permutations, args.num_cores,
infmat, addtl_genes, pnp, infmat_name,
max_cc_sizes, verbose)
sim, index2gene = hn.similarity_matrix(infmat,
full_index2gene,
heat,
True,
verbose=verbose)
results = []
for delta in deltas:
# find connected components
G = hn.weighted_graph(sim, index2gene, delta, directed=True)
ccs = hn.connected_components(G, args.min_cc_size)
# calculate significance (using all genes with heat scores)
if verbose > 4:
print "* Performing permuted heat statistical significance..."
print "\t- Using no. of components >= k (k \\in",
print "[%s, %s]) as statistic" % (min(HN2_STATS_SIZES),
max(HN2_STATS_SIZES))
heat_permutations = p.permute_heat(heat, full_index2gene.values(),
args.heat_permutations, addtl_genes,
args.num_cores)
sizes2counts = stats.calculate_permuted_cc_counts(
infmat, full_index2gene, heat_permutations, delta, HN2_STATS_SIZES,
True, args.num_cores)
real_counts = stats.num_components_min_size(G, HN2_STATS_SIZES)
size2real_counts = dict(zip(HN2_STATS_SIZES, real_counts))
sizes2stats = stats.compute_statistics(size2real_counts, sizes2counts,
args.heat_permutations)
# sort ccs list such that genes within components are sorted alphanumerically, and components
# are sorted first by length, then alphanumerically by name of the first gene in the component
ccs = [sorted(cc) for cc in ccs]
ccs.sort(key=lambda comp: comp[0])
ccs.sort(key=len, reverse=True)
# Record the results for this delta
results.append((ccs, sizes2stats, delta))
return results
def run(args):
# create output directory if doesn't exist; warn if it exists and is not empty
if not os.path.exists(args.output_directory):
os.makedirs(args.output_directory)
if len(os.listdir(args.output_directory)) > 0:
print("WARNING: Output directory is not empty. Any conflicting files will be overwritten. "
"(Ctrl-c to cancel).")
infmat = scipy.io.loadmat(args.infmat_file)[INFMAT_NAME]
infmat_index = hnio.load_index(args.infmat_index_file)
heat = hnio.load_heat_tsv(args.heat_file)
#filter out genes with heat score less than min_heat_score
heat, addtl_genes, args.min_heat_score = hnheat.filter_heat(heat, args.min_heat_score)
#find delta that maximizes # CCs of size >= MIN_SIZE for each permuted data set
deltas = ft.get_deltas_for_heat(infmat, infmat_index, heat, addtl_genes, args.num_permutations,
args.parallel)
#find the multiple of the median delta s.t. the size of the largest CC in the real data
#is <= MAX_CC_SIZE
medianDelta = np.median(deltas[MIN_CC_SIZE])
M, gene_index = hn.induce_infmat(infmat, infmat_index, sorted(heat.keys()), quiet=False)
h = hn.heat_vec(heat, gene_index)
sim = hn.similarity_matrix(M, h)
for i in range(1, 11):
G = hn.weighted_graph(sim, gene_index, i*medianDelta)
max_cc_size = max([len(cc) for cc in hn.connected_components(G)])
if max_cc_size <= MAX_CC_SIZE:
break
#and run HotNet with that multiple and the next 4 multiples
run_deltas = [i*medianDelta for i in range(i, i+5)]
for delta in run_deltas:
#create output directory
delta_out_dir = args.output_directory + "/delta_" + str(delta)
if not os.path.isdir(delta_out_dir):
os.mkdir(delta_out_dir)
#find connected components
G = hn.weighted_graph(sim, gene_index, delta)
ccs = hn.connected_components(G, args.min_cc_size)
# calculate significance (using all genes with heat scores)
print "* Performing permuted heat statistical significance..."
heat_permutations = p.permute_heat(heat, args.num_permutations, addtl_genes, args.parallel)
sizes = range(2, 11)
print "\t- Using no. of components >= k (k \\in",
print "[%s, %s]) as statistic" % (min(sizes), max(sizes))
sizes2counts = stats.calculate_permuted_cc_counts(infmat, infmat_index, heat_permutations,
delta, sizes, args.parallel)
real_counts = stats.num_components_min_size(G, sizes)
size2real_counts = dict(zip(sizes, real_counts))
sizes2stats = stats.compute_statistics(size2real_counts, sizes2counts, args.num_permutations)
#sort ccs list such that genes within components are sorted alphanumerically, and components
#are sorted first by length, then alphanumerically by name of the first gene in the component
ccs = [sorted(cc) for cc in ccs]
ccs.sort(key=lambda comp: comp[0])
ccs.sort(key=len, reverse=True)
# write output
output_dict = {"parameters": vars(args), "sizes": hn.component_sizes(ccs),
"components": ccs, "statistics": sizes2stats}
hnio.write_significance_as_tsv(os.path.abspath(delta_out_dir) + "/" + SIGNIFICANCE_TSV,
sizes2stats)
json_out = open(os.path.abspath(delta_out_dir) + "/" + JSON_OUTPUT, 'w')
json.dump(output_dict, json_out, indent=4)
json_out.close()
hnio.write_components_as_tsv(os.path.abspath(delta_out_dir) + "/" + COMPONENTS_TSV, ccs)
def run(args):
# create output directory if doesn't exist; warn if it exists and is not empty
if not os.path.exists(args.output_directory):
os.makedirs(args.output_directory)
if len(os.listdir(args.output_directory)) > 0:
print("WARNING: Output directory is not empty. Any conflicting files will be overwritten. "
"(Ctrl-c to cancel).")
infmat = scipy.io.loadmat(args.infmat_file)[INFMAT_NAME]
infmat_index = hnio.load_index(args.infmat_index_file)
heat = hnio.load_heat_tsv(args.heat_file)
# filter out genes with heat score less than min_heat_score
heat, addtl_genes, args.min_heat_score = hnheat.filter_heat(heat, args.min_heat_score)
# find delta that maximizes # CCs of size >= MIN_SIZE for each permuted data set
deltas = ft.get_deltas_for_heat(infmat, infmat_index, heat, addtl_genes, args.num_permutations,
args.parallel)
#find the multiple of the median delta s.t. the size of the largest CC in the real data
#is <= MAX_CC_SIZE
medianDelta = np.median(deltas[MIN_CC_SIZE])
M, gene_index = hn.induce_infmat(infmat, infmat_index, sorted(heat.keys()), quiet=False)
h = hn.heat_vec(heat, gene_index)
sim = hn.similarity_matrix(M, h)
for i in range(1, 11):
G = hn.weighted_graph(sim, gene_index, i*medianDelta)
max_cc_size = max([len(cc) for cc in hn.connected_components(G)])
if max_cc_size <= MAX_CC_SIZE:
break
# load interaction network edges and determine location of static HTML files for visualization
edges = hnio.load_ppi_edges(args.edge_file) if args.edge_file else None
index_file = '%s/viz_files/%s' % (os.path.realpath(__file__).rsplit('/', 1)[0], VIZ_INDEX)
subnetworks_file = '%s/viz_files/%s' % (os.path.realpath(__file__).rsplit('/', 1)[0], VIZ_SUBNETWORKS)
gene2index = dict([(gene, index) for index, gene in infmat_index.iteritems()])
#and run HotNet with that multiple and the next 4 multiples
run_deltas = [i*medianDelta for i in range(i, i+5)]
for delta in run_deltas:
# create output directory
delta_out_dir = args.output_directory + "/delta_" + str(delta)
if not os.path.isdir(delta_out_dir):
os.mkdir(delta_out_dir)
# find connected components
G = hn.weighted_graph(sim, gene_index, delta)
ccs = hn.connected_components(G, args.min_cc_size)
# calculate significance (using all genes with heat scores)
print "* Performing permuted heat statistical significance..."
heat_permutations = p.permute_heat(heat, args.num_permutations, addtl_genes, args.parallel)
sizes = range(2, 11)
print "\t- Using no. of components >= k (k \\in",
print "[%s, %s]) as statistic" % (min(sizes), max(sizes))
sizes2counts = stats.calculate_permuted_cc_counts(infmat, infmat_index, heat_permutations,
delta, sizes, args.parallel)
real_counts = stats.num_components_min_size(G, sizes)
size2real_counts = dict(zip(sizes, real_counts))
sizes2stats = stats.compute_statistics(size2real_counts, sizes2counts, args.num_permutations)
# sort ccs list such that genes within components are sorted alphanumerically, and components
# are sorted first by length, then alphanumerically by name of the first gene in the component
ccs = [sorted(cc) for cc in ccs]
ccs.sort(key=lambda comp: comp[0])
ccs.sort(key=len, reverse=True)
# write output
heat_dict = {"heat": heat, "parameters": {"heat_file": args.heat_file}}
heat_out = open(os.path.abspath(delta_out_dir) + "/" + HEAT_JSON, 'w')
json.dump(heat_dict, heat_out, indent=4)
heat_out.close()
args.heat_file = os.path.abspath(delta_out_dir) + "/" + HEAT_JSON
args.delta = delta
output_dict = {"parameters": vars(args), "sizes": hn.component_sizes(ccs),
"components": ccs, "statistics": sizes2stats}
hnio.write_significance_as_tsv(os.path.abspath(delta_out_dir) + "/" + SIGNIFICANCE_TSV,
sizes2stats)
json_out = open(os.path.abspath(delta_out_dir) + "/" + JSON_OUTPUT, 'w')
json.dump(output_dict, json_out, indent=4)
json_out.close()
hnio.write_components_as_tsv(os.path.abspath(delta_out_dir) + "/" + COMPONENTS_TSV, ccs)
# write visualization output if edge file given
if args.edge_file:
viz_data = {"delta": delta, 'subnetworks': list()}
for cc in ccs:
viz_data['subnetworks'].append(viz.get_component_json(cc, heat, edges, gene2index,
args.network_name))
delta_viz_dir = '%s/viz/delta%s' % (args.output_directory, delta)
if not os.path.isdir(delta_viz_dir):
os.makedirs(delta_viz_dir)
viz_out = open('%s/subnetworks.json' % delta_viz_dir, 'w')
json.dump(viz_data, viz_out, indent=4)
viz_out.close()
shutil.copy(subnetworks_file, delta_viz_dir)
if args.edge_file:
viz.write_index_file(index_file, '%s/viz/%s' % (args.output_directory, VIZ_INDEX), run_deltas)