def hasAllele(subject, allele, locus, i):
fieldName = alleleFieldNames[locus][i]
admissibles = [
mhctools.MhcObject(a) for a in subject[fieldName].split(';')
]
in_adms = [adm_allele in allele for adm_allele in admissibles]
return any(in_adms)
def parseHLAstring(hlastring, censor_code, locus=None):
## parse the HLA based on the censor code
if censor_code == missing_code:
return mhctools.MhcObject(locus=locus)
loc = hlastring[0]
if locus is not None and loc != locus:
raise Exception("the passed locus does not correspond to locus inferred from the HLA string")
elif censor_code == one_field_code:
field1 = hlastring[1:3]
return mhctools.MhcObject(locus=loc, field1=field1)
elif censor_code == uncensored_code:
field1 = hlastring[1:3]
field2 = hlastring[3:5]
return mhctools.MhcObject(locus=loc, field1=field1, field2=field2)
else:
raise Exception("invalid censor code.")
def addLeafBars(tree, hlaAlleles, counts, represDict=None):
"""
input:
- tree -- an ete object with hlaAlleles in the leafs
- hlaAlleles -- ordered HLA alleles, indexed by locus
- counts -- counts in the same order as hlaAlleles
- represDict -- if some of the hlaAlleles are not in the tree,
then they must be represented by another alleles. (default: None)
output: None, the tree is modified
"""
## loop over leaves of the tree
if represDict is not None:
equivClassDict = aux.invertRepresDict(represDict)
for leaf in tree:
## find the index of the HLA allele
mhc = mhctools.MhcObject(leaf.hla)
if represDict is not None:
## note that the represDict can contain more alleles than listed in hlaAlleles
mhcs = [
x for x in equivClassDict[mhc] if x in hlaAlleles[mhc.locus]
]
else:
mhcs = [mhc]
total_count = 0
for mhc in mhcs:
hlaIdx = hlaAlleles[mhc.locus].index(mhc)
total_count += counts[mhc.locus][hlaIdx]
## add a bar to the leaf
F = ete3.RectFace(width=total_count * 2.5,
height=10,
fgcolor='k',
bgcolor='k')
leaf.add_face(F, 0)
def funFitPMM(subjectFileName,
hlaFileName,
pSeqFileName,
aaCovFileName,
summaryFileName,
parDict,
chain_len=1000,
chain_thin=10,
num_chains=4,
dry_run=False,
use_cache=False,
name_base="anon",
sampler="jags",
cross_val=None,
parallel=True):
"""Todo: implement cross_val, PMM could also be used for many other situations..."""
traitFieldName = parDict["traitFieldName"]
alleleFieldNames = parDict["alleleFieldNames"]
dataDict = fetcher.importSubjectData(subjectFileName,
traitFieldName,
alleleFieldNames,
verbose=True,
traitTransform=np.log10)
hlaAlleles = dataDict["Alleles"]
## define models by their HLA tree
pSeqDict = mhcclus.mkPseqDict(pSeqFileName)
## restrict the pSeqDict to alleles in the dataset
loci = sorted(hlaAlleles.keys())
pSeqDictRestr = dict(
(hla, pSeqDict[hla]) for X in loci for hla in hlaAlleles[X])
## choose distances between amino-acids
aaDistDict = sequences.mkAaDistDict(aaCovFileName,
rescale=True,
ignore_aas=sequences.ambiguous_aas)
## use the data to make a tree (in Newick format)
## using representatives for NetMHCpan equivalence classes
newick_str_pseq, represDict = mhcclus.mkNewickTree(pSeqDictRestr,
aaDistDict=aaDistDict,
collapse=True)
hlaCovMat, alleleList = mhcclus.treeToCovmat(newick_str_pseq)
hlaCovMatHeader = [
mhctools.MhcObject(allele, fmt="Newick") for allele in alleleList
]
## run the model
result = fittrees.fitPMMweights(dataDict,
parDict,
hlaFileName,
hlaCovMat,
hlaCovMatHeader,
represDict=represDict,
chain_len=chain_len,
chain_thin=chain_thin,
num_chains=num_chains,
modelName=name_base,
verbose=True,
dry_run=dry_run,
use_cache=use_cache,
parallel=parallel)
return result
def importNetMhcOutput(fileName, version="3.0"):
"""
Import binding predictions produced by NetMHCpan and
store them in a dictionary.
"""
assert (version in supportedNetMHCpanVersions)
fileHandle = open(fileName, 'r')
csvReader = csv.reader(fileHandle, delimiter='\t', quotechar='\n')
predictionTable = [line for line in csvReader]
fileHandle.close()
header1PredictionTable = predictionTable[0]
header2PredictionTable = predictionTable[1]
predictionTable = predictionTable[2:]
## TODO: infer form header
if version == "2.8":
fstMhcCol = 3
numMhcCols = 3 ## aff, nM, rank
peptideCol = 1
posCol = 0
proteinCol = 2
affCol = 0
nMCol = 1
rankCol = 2
elif version == "3.0":
fstMhcCol = 3
numMhcCols = 4 ## core, aff, nM, rank
peptideCol = 1
posCol = 0
proteinCol = 2
coreCol = 0
affCol = 1
nMCol = 2
rankCol = 3
mhc_names = [x for x in header1PredictionTable if x != '']
predPerMhcDict = {}
for row in predictionTable:
for i, mhc_name in enumerate(mhc_names):
## put hla in proper format
mhc = mhctools.MhcObject(mhctools.fromNetMhcFormat(mhc_name))
predDict = {}
pos = predDict["pos"] = int(row[posCol])
pep = predDict["pep"] = row[peptideCol]
prot = predDict["prot"] = row[proteinCol]
pepid = "{0:s}_{1:d}_{2:s}".format(prot, pos, pep)
predDict["aff"] = float(row[fstMhcCol + i * numMhcCols + affCol])
predDict["nM"] = float(row[fstMhcCol + i * numMhcCols + nMCol])
predDict["rank"] = float(row[fstMhcCol + i * numMhcCols + rankCol])
if version == "3.0":
predDict["core"] = row[fstMhcCol + i * numMhcCols + coreCol]
if mhc in list(predPerMhcDict.keys()):
predPerMhcDict[mhc][pepid] = predDict
else:
predPerMhcDict[mhc] = {pepid: predDict}
return predPerMhcDict
def mkPseqDict(pSeqFileName): ## MHC_pseudo.dat
"""
input:
- pSeqFileName -- name of file with pseudo sequences
output:
- pSeqDict -- dictionary with HLA alleles -> pseudo sequences
"""
classic_human_loci = ["HLA-A", 'HLA-B', "HLA-C"]
with open(pSeqFileName, 'r') as pSeqFileHandle:
pSeqDict = pSeqFileHandle.read().split('\n')
pSeqDict = [row.split(' ') for row in pSeqDict]
pSeqDict = dict((mhctools.MhcObject(mhctools.fromNetMhcFormat(row[0])), row[1])
for row in pSeqDict if any([x in row[0] for x in classic_human_loci]))
return pSeqDict
def compareModels(modelname1, modelname2, deltalpd_threshold=0.1):
"""
Compare two cross-validated models.
"""
modelnames = [modelname1, modelname2]
filenames = ["cv_alleles_summary.{}.tsv".format(modelname) for modelname in modelnames]
work_folder = os.getcwd()
fullfilenames = [os.path.join(work_folder, "data", filename) for filename in filenames]
lpdDicts = [{}, {}]
for filename, lpdDict in zip(fullfilenames, lpdDicts):
with open(filename, 'r') as f:
reader = csv.DictReader(f, delimiter='\t')
for record in reader:
allele = mhctools.MhcObject(record["allele"])
lpd = float(record["lpd"]) ## NB: using weighted lpd
lpdDict[allele] = lpd
alleles = sorted(lpdDicts[0].keys())
loci = aux.unique([allele.locus for allele in alleles])
alleles = dict((X, [allele for allele in alleles if allele.locus == X]) for X in loci)
fig, axs = plt.subplots(1, len(loci), figsize=(15,10))
height = np.max([len(alleles[locus]) for locus in loci])
maxabsdiff = 0 ## used for x-limits of the axes
for locus, ax in zip(loci, axs):
selected_diffs = []
selected_alleles = []
for allele in alleles[locus]:
vals = [lpdDict[allele] for lpdDict in lpdDicts]
diff = vals[1] - vals[0]
if np.abs(diff) >= deltalpd_threshold:
selected_diffs.append(diff)
selected_alleles.append(allele)
maxabsdiff = max(np.abs(diff), maxabsdiff)
pos = np.argsort(np.abs(selected_diffs))[::-1]
ax.grid(axis='y')
ax.barh(range(len(pos)), [selected_diffs[p] for p in pos], 0.3,
color=defn.locusColorDict[locus])
ax.set_yticks(range(len(pos)))
ax.set_yticklabels([selected_alleles[p].short_str() for p in pos])
ax.axvline(x=0, color='k')
ax.set_xlabel("$\\Delta lpd$ HLA-{}".format(locus))
## do some basic statistics
positive = np.sum(1 for x in selected_diffs if x > 0)
total = len(selected_diffs)
pval = sts.binom_test(positive, total)
print("HLA-{0}: positive = {1}, total = {2}, P = {3}".format(locus, positive, total, pval))
## additional formatting...
for ax in axs:
ax.set_xlim((-maxabsdiff, maxabsdiff))
fig.tight_layout()
fig.savefig("compare.{0}.{1}.png".format(modelname1, modelname2), dpi=300, bbox_inches='tight')
def importAlleleFrequencyData(
fileName): ## "mhc-top0.99counts-ncbi-Sub-Saharan-Africa.tsv"
"""
input: name of the file with frequency data.
output: a dictionary with HLA counts, of the form
MhcObject -> int
"""
with open(fileName, 'r') as fileHandle:
table = [
row.split('\t') for row in fileHandle.read().split('\n')
if row != ''
]
header = table[0]
table = table[1:]
countDict = dict(
(mhctools.MhcObject(row[0]), int(row[1])) for row in table)
return countDict
def mkEteHlaTree(newick_str, midpoint=False, colorfun=(lambda x: 'black')):
"""
Transform a Newick tree into the ETE format.
Args:
newick_str (str): a string representing the tree in the Newick format
Kwargs:
midpoint (bool): if True, find the midpoint of the tree and re-root.
colorfun (function): a rule for coloring faces (TODO)
Returns:
A tuple consisting of an ete3.Tree object and a list of integer node names
"""
tree = ete3.Tree(newick_str)
if midpoint:
tree.set_outgroup(
tree.get_leaves()[0]) ## make arbitrary leaf the outgroup
outgrp_node = tree.get_midpoint_outgroup() ## now use ete algorithm
tree.set_outgroup(outgrp_node) ## and re-define the outgroup
## give nodes a name to be used in Bayesian model
nodeNames = []
for i, node in enumerate(tree.traverse()):
if node.name != '':
hla = mhctools.MhcObject(node.name, fmt="Newick")
node.add_feature('hla', str(hla)) ## FIXME: use MhcObject
node.name = str(i)
nodeNames.append(i)
## set width and color of edges
size = 10
nstyle = ete3.treeview.NodeStyle()
nstyle["vt_line_width"] = size
nstyle[
"hz_line_width"] = size ## FIXME make sure that ultrametric trees are rendered properly
## make sure that ultrametric trees are rendered correctly
nstyle["size"] = 0 ## do not render nodes
node.set_style(nstyle)
## NB: colorEteTree overrides set_style
## set colors of the HLA tags
for leaf in tree:
N = ete3.AttrFace("hla", fsize=50, fgcolor=colorfun(leaf.hla))
leaf.add_face(N, 0)
return (tree, nodeNames)
def mkSubSeqNewickTree(hlaAlleles, positions, start=0, aaDistDict=None, verbose=False):
"""
make a tree using particular positions in the MHC sequence.
example: re-create netMHCpan pseudo sequences.
input:
- hlaAlleles -- the alleles at the leafs of the tree
- fastaFileName -- aligned MHC protein sequences
- positions -- the positions of interest
- start -- the alignment could start at a different position
(see the function sequences.mkPseudoSequence)
- verbose -- print comments (default: False) TODO: unused
output:
- newick_str -- the resulting tree in Newick format
- represDict -- a dictionary mapping the alleles to the chosen representative
"""
## import IMGT sequences
imgtSeqDict = {}
work_folder = os.getcwd() ## FIXME pass path and name of fasta files?
loci = sorted(hlaAlleles.keys())
for locus in loci:
imgtFileName = os.path.join(work_folder, "data/hla/HLA-{}-IMGT-protein-alignment.fasta".format(locus))
imgtSeqDict.update(sequences.readFastaFile(imgtFileName))
## get sub-sequences
subSeqDict = {}
imgtKeys = sorted(imgtSeqDict.keys())
for locus in loci:
for hla in hlaAlleles[locus]:
## find a key in imgtSeqDict containing the HLA allele
key = next(filter(lambda k: mhctools.MhcObject(k) in hla, imgtKeys), None)
## NB: changed behavior: previously hla.subtype_str() in key
if key is None:
raise Exception("HLA allele {} not present in IMGT database".format(hla))
seq = imgtSeqDict[key]
subSeq = sequences.mkPseudoSequence(seq, positions, start)
subSeqDict[hla] = subSeq
## make a newick tree, collapsing equivalence classes into one representative in the tree
newick_str, represDict = mkNewickTree(subSeqDict, aaDistDict=aaDistDict, collapse=True)
if verbose:
print("representative alleles:")
for repres in aux.unique(list(represDict.values())):
print(repres, subSeqDict[repres])
return (newick_str, represDict)
cohortHlaAlleles = {}
for X in "ABC":
uniques = [mustGetUnique(recordsByID[ID][key]) for key in hlaLocusKeyDict[X] for ID in subjectIDs]
censors = [getHLAcensor(hlastring) for hlastring in uniques]
## only use uncensored values
alleles = [parseHLAstring(x, c, X) for x, c in censors if c == uncensored_code]
cohortHlaAlleles[X] = aux.unique(alleles)
## import HLA alleles from another cohort
with open(rootFolder + "hla/mhc-top0.99counts-ncbi-Sub-Saharan-Africa.tsv", 'r') as f:
hla_table = [row.split('\t') for row in f.read().split('\n') if row != '']
hla_header = hla_table[0]
hla_table = hla_table[1:]
hlaCountDict = dict((mhctools.MhcObject(row[0]), int(row[1])) for row in hla_table)
popHlaAlleles = {
X : sorted(filter(lambda x: x.locus == X, hlaCountDict.keys()),
key=lambda x: hlaCountDict[x], reverse=True)
for X in "ABC"
}
## make a combined list of admissible alleles
admHlaAlleles = {
X : aux.unique(cohortHlaAlleles[X] + popHlaAlleles[X])
for X in "ABC"
}
## import alleles belonging to serotypes
with open(os.path.join(data_folder, "HLA_serotypes.tsv"), 'r') as f:
def compareModelsSEM(modelname1, modelname2, deltalpd_threshold=0.1):
"""
Compare two cross-validated models, also calculate the (scaled) SEMs
"""
modelnames = [modelname1, modelname2]
filenames = ["cv_alleles_summary.{}.tsv".format(modelname) for modelname in modelnames]
work_folder = os.getcwd()
fullfilenames = [os.path.join(work_folder, "data", filename) for filename in filenames]
subjectDicts = [{}, {}]
for filename, subjDict in zip(fullfilenames, subjectDicts):
with open(filename, 'r') as f:
reader = csv.DictReader(f, delimiter='\t')
for record in reader:
allele = mhctools.MhcObject(record["allele"])
subject_line = record["subjects"]
subject_table = [row.split(",") for row in subject_line.split(";")]
subject_dict = {int(row[0]) : (float(row[1]), float(row[2])) for row in subject_table}
subjDict[allele] = subject_dict
alleles = sorted(subjectDicts[0].keys())
## compute Delta lpd and scaled sems
deltaLpdDict = {}
semDict = {}
for allele in alleles:
subject_dicts = [subjDict[allele] for subjDict in subjectDicts]
idxs = list(subject_dicts[0].keys())
diffs = []
weights = []
for idx in idxs:
clpd0, ppc0 = subject_dicts[0][idx]
clpd1, ppc1 = subject_dicts[1][idx]
if ppc0 != 0 and ppc1 != 0:
diffs.append(clpd1 - clpd0)
weights.append(ppc1 * ppc0)
if len(diffs) > 0:
deltaLpdDict[allele] = np.sum([d*w for d, w in zip(diffs, weights)])
if len(diffs) > 1:
mu = deltaLpdDict[allele] / np.sum(weights)
semDict[allele] = np.sqrt(np.sum([w*(d-mu)**2 for d, w in zip(diffs, weights)]))
else:
semDict[allele] = np.nan
else:
deltaLpdDict[allele] = np.nan
semDict[allele] = np.nan
## make figure
loci = aux.unique([allele.locus for allele in alleles])
alleles = dict((X, [allele for allele in alleles if allele.locus == X]) for X in loci)
fig, axs = plt.subplots(1, len(loci), figsize=(10,6.67))
height = np.max([len(alleles[locus]) for locus in loci])
for locus, ax in zip(loci, axs):
maxabsdiff = 0 ## used for x-limits of the axes
selected_diffs = []
selected_alleles = []
selected_errs = []
for allele in alleles[locus]:
diff = deltaLpdDict[allele]
if diff is not None and np.abs(diff) >= deltalpd_threshold:
selected_diffs.append(diff)
selected_alleles.append(allele)
selected_errs.append(semDict[allele])
maxabsdiff = max(np.abs(diff), maxabsdiff)
## revert order to get a "christmas tree plot"
pos = np.argsort(np.abs(selected_diffs))[::-1]
ax.grid(axis='y')
ax.barh(range(len(pos)), [selected_diffs[p] for p in pos], 0.3,
color=defn.locusColorDict[locus],
xerr=np.array([selected_errs[p] for p in pos]),
#ecolor=defn.locusColorDict[locus],
capsize=5)
ax.set_yticks(range(len(pos)))
ax.set_yticklabels([selected_alleles[p].short_str() for p in pos])
ax.axvline(x=0, color='k')
ax.set_xlabel("$\\Delta {{\\rm lpd}}$ HLA-{}".format(locus))
## do some basic statistics
positive = np.sum(1 for x in selected_diffs if x > 0)
total = len(selected_diffs)
pval_binom = sts.binom_test(positive, total)
print("HLA-{0}: positive = {1}, total = {2}, P = {3} (binomial)".format(locus, positive, total, pval_binom))
W, pval_wilcox = sts.wilcoxon(selected_diffs)
print("HLA-{0}: W = {1}, total = {2}, P = {3} (wilcoxon)".format(locus, W, total, pval_wilcox))
ax.set_xlim((-1.05*maxabsdiff, 1.05*maxabsdiff))
## additional formatting...
fig.tight_layout()
fig.savefig("compare.{0}.{1}.png".format(modelname1, modelname2), dpi=300, bbox_inches='tight')
def importSubjectData(fileName,
traitFieldName,
alleleFieldNames,
covariateFieldNames=None,
traitCensFieldName=None,
subset=None,
verbose=False,
traitTransform=(lambda x: x),
categorical=False):
"""
Import MHC data and continuous disease traits.
Args:
fileName (str): name of the tsv/csv file with allele and trait data
per subject
traitFieldName (str): the name of the trait of interest in the header
of the tsv file
alleleFieldNames (dict): a dictionary with the field names for the
alleles.
Kwargs:
covariateFieldNames (list of str): list with covariate names
to be imported from the data file.
traitCensFieldName (str or bool): title of the column with censoring values.
If False, all data is assumed to be uncensored.
If True (default) the key is assumed to be X_censoring,
where X is the traitFieldName.
subset (int): take a sample from the complete data.
If None (default), use all data.
verbose (bool): print some basic statistics on the imported data.
traitTransform (function): a funcion to transform the trait value.
For instance numpy.log, or the identity (default)
categorical (bool): True if the trait is categorical, False otherwise (default).
Use traitTransform to map string to required values (e.g. 0/1)
Returns:
A dictionary containing
- TraitValues: the trait values
- CensCodes: censoring codes for the TraitValues
- CensBounds: upper (or lower) bounds for left (or right) censored Trait
Only included if not categorical
- Categories: a list of possible traitValues
Only included if categorical
- AlleleVecs: admissible alleles
- Alleles: the alleles in the dataset, in the right order for the allele vectors
Todo:
- Intelligently handle censoring codes
- Give a good discription of the expected file format
- Allow for covariates
"""
## detect if the file is tsv or csv
file_base, file_extension = os.path.splitext(fileName)
if file_extension == ".csv":
delim = ','
elif file_extension == ".tsv":
delim = '\t'
elif file_extension == ".xlsx":
## @todo: implement excel files
raise Exception("xlsx file format not yet implemented")
else:
raise Exception("invalid file format (csv or tsv expected)")
## read the contents of the file
with open(fileName, 'r') as fileHandle:
reader = csv.DictReader(fileHandle, delimiter=delim)
data = [row for row in reader]
## take a sub-sample
if subset is not None:
idxs = np.random.choice(len(data), size=subset, replace=False)
data = [data[i] for i in idxs]
## find data in the table
Ploidy = 2
loci = sorted(alleleFieldNames.keys())
Alleles = {}
for locus in loci:
alls = [
row[alleleFieldNames[locus][i]].split(';') for i in range(Ploidy)
for row in data
]
## make MhcObject-s
alls = [mhctools.MhcObject(a) for a in aux.unique(aux.flatten(alls))]
## remove non-expressed alleles and reduce to 2-field
alls = [a.protein for a in alls] ## include Null alleles etc.
## find unique elements again
Alleles[locus] = aux.unique(alls)
## for each subject, make a vector with zeros and ones
## indicating whether the allele is present
def hasAllele(subject, allele, locus, i):
fieldName = alleleFieldNames[locus][i]
admissibles = [
mhctools.MhcObject(a) for a in subject[fieldName].split(';')
]
in_adms = [adm_allele in allele for adm_allele in admissibles]
return any(in_adms)
AlleleVecs = {}
for locus in sorted(alleleFieldNames.keys()):
AlleleVecs[locus] = [[[
hasAllele(subject, allele, locus, i) for allele in Alleles[locus]
] for i in range(Ploidy)] for subject in data]
## get the trait values and censoring information
if type(traitCensFieldName) is bool and traitCensFieldName == True:
## use the default key, based on the traitFieldName
traitCensFieldName = "{0}_censoring".format(traitFieldName)
## now, get censoring from data set if traitCensFieldName is str
if type(traitCensFieldName) is str:
CensCodes = np.array([
subject[traitCensFieldName]
if traitCensFieldName in subject.keys() else
defn.uncensored_code ## FIXME, make sure that this is consistant
for subject in data
])
else: ## assume everything is uncensored
CensCodes = np.array([defn.uncensored_code for _ in data])
## get trait values
if not categorical:
TraitValues = np.array([
traitTransform(float(subject[traitFieldName]))
if cens_code == defn.uncensored_code else np.nan
for cens_code, subject in zip(CensCodes, data)
])
## find the upper or lower bound for the left and (resp.) right censored values
## FIXME For the non-interval-censored data, use an arbitrary (low) Trait value as lower bound
CensBounds = np.array([
traitTransform(float(subject[traitFieldName]))
if cens_code == defn.left_censored_code or cens_code
== defn.right_censored_code else defn.auxiliaryLowerCensBound
for cens_code, subject in zip(CensCodes, data)
])
else: ## the trait is categorical: Censoring can only be missing or uncensored
TraitValues = np.array([
traitTransform(subject[traitFieldName])
if cens_code == defn.uncensored_code else np.nan
for cens_code, subject in zip(CensCodes, data)
])
## make a list of possible trait values
Categories = aux.unique([
x for x, c in zip(TraitValues, CensCodes) if c == defn.uncensored_code
])
## import covariates
if covariateFieldNames is None:
covariateFieldNames = [] ## empty list
Covariates = {
} ## dictionary indexed by covariate name, empty if no covariates
for cfn in covariateFieldNames:
ccfn = "{0}_censoring".format(cfn)
covVals, covCCs, covCBs = fetchContinuousValue(cfn, ccfn, data)
Covariates[cfn] = {
"Values": covVals,
"CensCodes": covCCs,
"CensBounds": covCBs
}
## do some printing...
if verbose:
## number op subjects
print("number of subjects: {0}".format(len(data)))
## Trait statistics
if not categorical:
mtrait = np.nanmedian(TraitValues)
ltrait = np.nanpercentile(TraitValues, 2.5)
htrait = np.nanpercentile(TraitValues, 97.5)
print(
"median trait value: {0:0.2f}, 2.5 - 97.5 percentiles: {1:0.2f} - {2:0.2f}"
.format(mtrait, ltrait, htrait))
else:
catcounts = {
cat: len([x for x in TraitValues if x == cat])
for cat in Categories
}
print("category histogram:")
for cat in Categories:
print(f"\t{cat}:\t{catcounts[cat]}")
## allele statistics
print("total number of alleles:",
np.sum([len(Alleles[locus]) for locus in loci]))
for locus in sorted(Alleles.keys()):
print(f"number of {locus} alleles: {len(Alleles[locus])}")
numCompleteHaplotypes = 0
for idx in range(len(data)):
compl = [
sum(1 for x in alleleVec if x) == 1
for locus in sorted(Alleles.keys())
for alleleVec in AlleleVecs[locus][idx]
]
if all(compl):
## subject has with 2-field typed haplotype
numCompleteHaplotypes += 1
print(
"number of complete haplotypes: {0}".format(numCompleteHaplotypes))
## Covariates
if len(covariateFieldNames) > 0:
print("covariate statistics:")
for cfn in covariateFieldNames:
mcov = np.nanmean(Covariates[cfn]["Values"])
lcov = np.nanpercentile(Covariates[cfn]["Values"], 2.5)
hcov = np.nanpercentile(Covariates[cfn]["Values"], 97.5)
print(
f"\t'{cfn}' mean value: {mcov:0.2f}, 2.5 - 97.5 percentiles: {lcov:0.2f} - {hcov:0.2f}"
)
## return relevant data in a dictionary
dataDict = {
"TraitValues": TraitValues,
"CensCodes": CensCodes,
"AlleleVecs": AlleleVecs,
"Alleles": Alleles,
"Covariates": Covariates
}
## include censoring bounds if the trait value is a real number
if not categorical:
dataDict.update({"CensBounds": CensBounds})
else:
dataDict.update({"Categories": Categories})
return dataDict
