def prok1603_architecture_frequencies():
work_dir = os.path.join(gv.project_data_path, 'UvrD/')
map_file = os.path.join(work_dir, 'prok1603/prok1603_weights.txt')
locus2weight = {l.split()[0]:float(l.split()[1]) for l in open(map_file)}
def_file = os.path.join(gv.project_data_path, 'cas4/profiles/defenseProfiles.tab')
profile2gene={}
profile2def = {}
for l in open(def_file):
terms = l.strip().split('\t')
profile = terms[0]
gene_names = terms[3].split(',')
if len(gene_names)>1:
profile2gene[profile] = gene_names[1]
else:
profile2gene[profile] = gene_names[0]
profile2def[profile] = terms[4]
cdd_profile2gene = t.map_cdd_profile2gene_name()
cdd_profile2gene.update(profile2gene)
cdd_profile2def = t.map_cdd_profile2def()
cdd_profile2def.update(profile2def)
prok1603_loci_file = os.path.join(work_dir, 'prok1603The CRISPR/prok1603_loci.p.bz2')
loci = t.load_compressed_pickle(prok1603_loci_file)
profile2loci = {}
for locus in loci:
for _profile in locus.profiles:
if _profile in profile2loci:
profile2loci[_profile].append(locus)
else:
profile2loci[_profile] = [locus]
for (profile, loci) in sorted(profile2loci.items(), key=lambda x: len(x[1]), reverse=True):
_weight = sum([locus2weight[locus.base_file_name] for locus in loci])
print "%s\t%s\t%d\t%f\t%s" % (profile,
cdd_profile2gene[profile] if profile in cdd_profile2gene else "",
len(loci),
_weight,
cdd_profile2def[profile] if profile in cdd_profile2def else "")
# print 'Dumping to files'
# dump_file = bz2.BZ2File(os.path.join(save_path, 'pentaplets_merged_across.p.bz2'), 'w')
# pickle.dump(pentaplets, dump_file)
# dump_file = bz2.BZ2File(os.path.join(save_path, 'quadruplets_merged_across.p.bz2'), 'w')
# pickle.dump(quadruplets, dump_file)
# dump_file = bz2.BZ2File(os.path.join(save_path, 'triplets_merged_across.p.bz2'), 'w')
# pickle.dump(triplets, dump_file)
# dump_file = bz2.BZ2File(os.path.join(save_path, 'duplets_merged_across.p.bz2'), 'w')
# pickle.dump(duplets, dump_file)
if __name__ == '__main__':
print 'Pre-Loading dictionaries'
target_profiles = t.bacteria_target_profiles()
profile2def = t.map_cdd_profile2def()
gid2arcog_cdd = t.map_gid2arcog_cdd()
neighborhood_files_path = neighborhoods_path()
profile_id2code = map_id2cdd()
# for limit_to, report_dir in zip([300, 500, 1000, 100000],['top_300', 'top_500', 'top_1000', 'top_100000']):
#
# print "Limit_to:", limit_to
# print
# generate_plots(limit_to, report_dir, target_profiles, profile2def, gid2arcog_cdd, neighborhood_files_path, profile_id2code)
# print 'Done'
# print "------------------------"
data_path = os.path.join(gv.project_data_path, 'Bacteria/pickle/')
print 'Generating pickles'
def calculate_profile_based_crispricity(cas1402_loci, cas1402_gis,
cas1402_organisms, prok1402_path_file):
print "Loding global maps"
global_profile2orgs2gis = load_maps_simple(prok1402_path_file, cas1402_gis)
print "Loading weights"
gnm2weight = t.map_genome2weight()
print "Loading CDD definitions"
profile2def = t.map_cdd_profile2def()
print "Counting in CRISPR loci"
profile2orgs2obj = {}
for locus in cas1402_loci:
for gene in locus:
for _cogid in gene.cogid.split():
if _cogid not in profile2orgs2obj:
profile2orgs2obj[_cogid] = {}
for _org in cas1402_organisms:
_orgObj = ProfileInOrganismCount(_org, _cogid)
if _cogid in global_profile2orgs2gis:
_orgObj.outside = len(global_profile2orgs2gis[_cogid][_org]) \
if _org in global_profile2orgs2gis[_cogid] \
else 0
else:
_orgObj.outside = 0
profile2orgs2obj[_cogid][_org] = _orgObj
profile2orgs2obj[_cogid][gene.organism].in_crispr += 1
out_file = os.path.join(gv.project_data_path,
'cas1402/crispricity_count.tab')
in_crispr_all = []
crispricity_all = []
profiles_all = []
print "Writing to file:", out_file
with open(out_file, 'w') as outf:
outf.write(
"Profile\tOccurrence in CRISPR loci\tCrispricity\tDefinition\n")
for profile in profile2orgs2obj:
in_crispr = 0
everywhere = 0
# for org in profile2orgs2obj[profile]:
# _org = profile2orgs2obj[profile][org]
# in_crispr += _org.in_crispr * gnm2weight[org]
# everywhere += (_org.in_crispr + _org.outside) * gnm2weight[org]
for org in profile2orgs2obj[profile]:
_org = profile2orgs2obj[profile][org]
in_crispr += _org.in_crispr
everywhere += (_org.in_crispr + _org.outside)
crispricity = in_crispr / everywhere
in_crispr_all.append(in_crispr)
crispricity_all.append(crispricity)
profiles_all.append(profile)
outf.write("%s\t%f\t%f\t%s\n" %
(profile, in_crispr, crispricity, profile2def[profile]))
in_crispr_all = np.asarray(in_crispr_all)
in_crispr_all = np.log10(in_crispr_all)
crispricity_all = np.asarray(crispricity_all)
# crispricity_all = np.log(crispricity_all)
plt.ioff()
fig, ax = plt.subplots()
ax.scatter(in_crispr_all, crispricity_all, s=1)
plt.xlabel("Effective orcurrence in CRISPR loci (log10)")
plt.ylabel("X-axis / Effective occurrences")
# fig.savefig('first.png')
plt.savefig('first_count.png')
def calculate_profile_based_baiticity(bacteria_loci, loci_gis, loci_organisms,
arcog_path_file, bait_profiles,
filter_threshold, save_path):
print "Loding global maps"
global_profile2orgs2gis = load_maps_simple(arcog_path_file, loci_gis)
print "Loading weights"
gnm2weight = t.map_genome2weight()
print "Loading CDD definitions"
profile2def = t.map_cdd_profile2def()
profile2def.update(t.map_profile2def())
print "Counting in loci"
profile2orgs2obj = {}
gi_checklist = set()
for locus in bacteria_loci:
for gene in locus:
if gene.gid in gi_checklist:
continue
for _cogid in gene.cogid.split():
if _cogid in bait_profiles:
continue
if _cogid not in profile2orgs2obj:
profile2orgs2obj[_cogid] = {}
for _org in loci_organisms:
_orgObj = ProfileInOrganismCount(_org, _cogid)
if _cogid in global_profile2orgs2gis:
_orgObj.outside = len(global_profile2orgs2gis[_cogid][_org]) \
if _org in global_profile2orgs2gis[_cogid] \
else 0
else:
_orgObj.outside = 0
profile2orgs2obj[_cogid][_org] = _orgObj
profile2orgs2obj[_cogid][gene.organism].in_locus += 1
gi_checklist.update([gene.gid])
print len(profile2orgs2obj['arCOG08578'])
# print profile2orgs2obj['arCOG08578'].keys()
for org, obj in profile2orgs2obj['arCOG08578'].items():
if obj.in_locus + obj.outside > 0:
print org, obj.in_locus, obj.outside
sys.exit()
out_file = os.path.join(save_path, 'baiticity.tab')
profiles = []
in_loci_count = []
baiticity_count = []
in_loci_weight = []
baiticity_weight = []
rare_profiles_file = open(os.path.join(save_path, 'rare_profiles.tab'),
'w')
rare_profiles_file.write(
"Profile\tOccurence everywhere\tOccurrence in loci\tBaiticity\tDefinition\n"
)
print "Writing to file:", out_file
with open(out_file, 'w') as outf:
outf.write(
"Profile\tOccurrence in loci(count)\tBaiticity(count)\tOccurrence in loci(weight)\tBaiticity(weight)\tDefinition\n"
)
for profile in profile2orgs2obj:
if profile == 'arCOG14077':
continue
in_locus_count = 0
everywhere_count = 0
in_locus_weight = 0
everywhere_weight = 0
for org in profile2orgs2obj[profile]:
if org in [
'Nitrosoarchaeum_koreensis_MY1_MY1',
'Nitrosoarchaeum_limnia_SFB1'
]:
continue
_org = profile2orgs2obj[profile][org]
in_locus_count += _org.in_locus
everywhere_count += (_org.in_locus + _org.outside)
in_locus_weight += _org.in_locus * gnm2weight[org]
everywhere_weight += (_org.in_locus +
_org.outside) * gnm2weight[org]
_baiticity_count = 1.0 * in_locus_count / everywhere_count
_baiticity_weight = in_locus_weight / everywhere_weight
if everywhere_weight < filter_threshold:
rare_profiles_file.write(
"%s\t%f\t%f\t%f\t%s\n" %
(profile, everywhere_count, in_locus_count,
_baiticity_count, profile2def[profile]))
continue
in_loci_count.append(in_locus_count)
baiticity_count.append(_baiticity_count)
in_loci_weight.append(in_locus_weight)
baiticity_weight.append(_baiticity_weight)
profiles.append(profile)
outf.write(
"%s\t%f\t%f\t%f\t%f\t%s\n" %
(profile, in_locus_count, _baiticity_count, in_locus_weight,
_baiticity_weight, profile2def[profile]))
in_loci_weight = np.asarray(in_loci_weight)
in_loci_weight = np.log10(in_loci_weight)
baiticity_weight = np.asarray(baiticity_weight)
plt.ioff()
fig, ax = plt.subplots()
ax.scatter(in_loci_weight, baiticity_weight, s=1)
plt.xlabel("Effective orcurrence in loci (log10)")
plt.ylabel("Baiticity")
image_file = os.path.join(save_path, 'baiticity.png')
plt.savefig(image_file)
# for i, profile in enumerate(profiles_all):
# ax.annotate(profile, (in_loci_all[i], crispricity_all[i]))
# fig.savefig('second.png')
# plt.savefig('second.png')
rare_profiles_file.close()
for j, kplet_sublist in enumerate(kplet_pool):
cur_reports_folder = os.path.join(report_files_dir, str(i))
if not os.path.exists(cur_reports_folder):
os.mkdir(cur_reports_folder)
xls_file_name = os.path.join(cur_reports_folder, "%d_%d.xls" % (j+1, i))
r.write_to_xls(xls_file_name,kplet_sublist,target_profiles,profile2def,gid2arcog_cdd,neighborhood_files_path,file2src_src2org_map)
if __name__ == '__main__':
import cPickle
import bz2
print 'Pre-Loading dictionaries'
target_profiles = t.bacteria_target_profiles()
profile2def = t.map_cdd_profile2def()
gid2arcog_cdd = t.map_gid2arcog_cdd()
neighborhood_files_path = neighborhoods_path()
# profile_id2code = map_id2cdd()
# pickle.dump(profile_id2code, open('profile_id2code.p','w'))
profile_id2code = cPickle.load(open('/Users/hudaiber/Projects/NewSystems/code/Bacteria/profile_id2code.p'))
fname = '/Users/hudaiber/Projects/NewSystems/data/Bacteria/pickle/100000/pentaplets_merged_across.p.bz2'
f = bz2.BZ2File(fname, 'rb')
buffer = ""
while 1:
data = f.read()
if data == "":
break
buffer += data
def calculate_profile_based_baiticity(bacteria_loci, loci_gis,
loci_organisms,
prok1402_path_file,
bait_profiles,
filter_threshold,
save_path):
print "Loding global maps"
global_profile2orgs2gis = load_maps_simple(prok1402_path_file, loci_gis)
print "Loading weights"
gnm2weight = t.map_genome2weight()
print "Loading CDD definitions"
profile2def = t.map_cdd_profile2def()
print "Counting in loci"
profile2orgs2obj = {}
gi_checklist = set()
for locus in bacteria_loci:
for gene in locus:
if gene.gid in gi_checklist:
continue
for _cogid in gene.cogid.split():
if _cogid in bait_profiles:
continue
if _cogid not in profile2orgs2obj:
profile2orgs2obj[_cogid] = {}
for _org in loci_organisms:
_orgObj = ProfileInOrganismCount(_org, _cogid)
if _cogid in global_profile2orgs2gis:
_orgObj.outside = len(global_profile2orgs2gis[_cogid][_org]) \
if _org in global_profile2orgs2gis[_cogid] \
else 0
else:
_orgObj.outside = 0
profile2orgs2obj[_cogid][_org] = _orgObj
profile2orgs2obj[_cogid][gene.organism].in_locus += 1
gi_checklist.update([gene.gid])
out_file = os.path.join(save_path, 'baiticity.tab')
profiles = []
in_loci_count = []
baiticity_count = []
in_loci_weight = []
baiticity_weight = []
rare_profiles_file = open(os.path.join(save_path, 'rare_profiles.tab'), 'w')
rare_profiles_file.write("Profile\tOccurence everywhere\tOccurrence in loci\tBaiticity\tDefinition\n")
print "Writing to file:", out_file
with open(out_file, 'w') as outf:
outf.write("Profile\tOccurrence in loci(count)\tBaiticity(count)\tOccurrence in loci(weight)\tBaiticity(weight)\tDefinition\n")
for profile in profile2orgs2obj:
in_locus_count = 0
everywhere_count = 0
in_locus_weight = 0
everywhere_weight = 0
for org in profile2orgs2obj[profile]:
_org = profile2orgs2obj[profile][org]
in_locus_count += _org.in_locus
everywhere_count += (_org.in_locus + _org.outside)
in_locus_weight += _org.in_locus * gnm2weight[org]
everywhere_weight += (_org.in_locus + _org.outside) * gnm2weight[org]
_baiticity_count = 1.0 * in_locus_count / everywhere_count
_baiticity_weight = in_locus_weight / everywhere_weight
if everywhere_weight < filter_threshold:
rare_profiles_file.write("%s\t%f\t%f\t%f\t%s\n"%(profile, everywhere_count, in_locus_count, _baiticity_count, profile2def[profile]))
continue
in_loci_count.append(in_locus_count)
baiticity_count.append(_baiticity_count)
in_loci_weight.append(in_locus_weight)
baiticity_weight.append(_baiticity_weight)
profiles.append(profile)
outf.write("%s\t%f\t%f\t%f\t%f\t%s\n"%(profile,
in_locus_count,
_baiticity_count,
in_locus_weight,
_baiticity_weight,
profile2def[profile]))
in_loci_weight = np.asarray(in_loci_weight)
in_loci_weight = np.log10(in_loci_weight)
baiticity_weight = np.asarray(baiticity_weight)
plt.ioff()
fig, ax = plt.subplots()
ax.scatter(in_loci_weight, baiticity_weight, s=1)
plt.xlabel("Effective orcurrence in loci (log10)")
plt.ylabel("Baiticity")
image_file = os.path.join(save_path, 'baiticity.png')
plt.savefig(image_file)
# for i, profile in enumerate(profiles_all):
# ax.annotate(profile, (in_loci_all[i], crispricity_all[i]))
# fig.savefig('second.png')
# plt.savefig('second.png')
rare_profiles_file.close()
def calculate_profile_based_crispricity(cas1402_loci, cas1402_gis, cas1402_organisms, prok1402_path_file):
print "Loding global maps"
global_profile2orgs2gis = load_maps_simple(prok1402_path_file, cas1402_gis)
print "Loading weights"
gnm2weight = t.map_genome2weight()
print "Loading CDD definitions"
profile2def = t.map_cdd_profile2def()
print "Counting in CRISPR loci"
profile2orgs2obj = {}
for locus in cas1402_loci:
for gene in locus:
for _cogid in gene.cogid.split():
if _cogid not in profile2orgs2obj:
profile2orgs2obj[_cogid] = {}
for _org in cas1402_organisms:
_orgObj = ProfileInOrganismCount(_org, _cogid)
if _cogid in global_profile2orgs2gis:
_orgObj.outside = len(global_profile2orgs2gis[_cogid][_org]) \
if _org in global_profile2orgs2gis[_cogid] \
else 0
else:
_orgObj.outside = 0
profile2orgs2obj[_cogid][_org] = _orgObj
profile2orgs2obj[_cogid][gene.organism].in_crispr += 1
out_file = os.path.join(gv.project_data_path, 'cas1402/crispricity_count.tab')
in_crispr_all = []
crispricity_all = []
profiles_all = []
print "Writing to file:", out_file
with open(out_file, 'w') as outf:
outf.write("Profile\tOccurrence in CRISPR loci\tCrispricity\tDefinition\n")
for profile in profile2orgs2obj:
in_crispr = 0
everywhere = 0
# for org in profile2orgs2obj[profile]:
# _org = profile2orgs2obj[profile][org]
# in_crispr += _org.in_crispr * gnm2weight[org]
# everywhere += (_org.in_crispr + _org.outside) * gnm2weight[org]
for org in profile2orgs2obj[profile]:
_org = profile2orgs2obj[profile][org]
in_crispr += _org.in_crispr
everywhere += (_org.in_crispr + _org.outside)
crispricity = in_crispr / everywhere
in_crispr_all.append(in_crispr)
crispricity_all.append(crispricity)
profiles_all.append(profile)
outf.write("%s\t%f\t%f\t%s\n"%(profile, in_crispr, crispricity, profile2def[profile]))
in_crispr_all = np.asarray(in_crispr_all)
in_crispr_all = np.log10(in_crispr_all)
crispricity_all = np.asarray(crispricity_all)
# crispricity_all = np.log(crispricity_all)
plt.ioff()
fig, ax = plt.subplots()
ax.scatter(in_crispr_all, crispricity_all, s=1)
plt.xlabel("Effective orcurrence in CRISPR loci (log10)")
plt.ylabel("X-axis / Effective occurrences")
# fig.savefig('first.png')
plt.savefig('first_count.png')
