def main(dataset_df, bin=None, start=0, end=None):
"""
Computes character frequencies (0.0 to 1.0) at each position
Arguments:
dataset_df (pd.DataFrame): A dataframe containing a valid dataset.
bin (int): A bin number specifying which counts to use
start (int): An integer specifying the sequence start position
end (int): An integer specifying the sequence end position
Returns:
freq_df (pd.DataFrame): A dataframe containing counts for each nucleotide/amino acid character at each position.
"""
# Validate dataset_df
qc.validate_dataset(dataset_df)
# Compute counts
counts_df = profile_ct.main(dataset_df, bin=bin, start=start, end=end)
# Create columns for profile_freqs table
ct_cols = [c for c in counts_df.columns if qc.is_col_type(c,'ct_')]
freq_cols = ['freq_'+c.split('_')[1] for c in ct_cols]
# Compute frequencies from counts
freq_df = counts_df[ct_cols].div(counts_df['ct'], axis=0)
freq_df.columns = freq_cols
freq_df['pos'] = counts_df['pos']
# Validate as counts dataframe
freq_df = qc.validate_profile_freq(freq_df,fix=True)
return freq_df
def main(filelist_df,tags_df=None,indir='./',seq_type=None):
""" Merges datasets listed in the filelist_df dataframe
"""
# Validate filelist
qc.validate_filelist(filelist_df)
# Read datasets into dictionary indexed by bin number
dataset_df_dict = {}
for item in filelist_df.iterrows():
# Autodetect fasta, fastq, or text file based on file extension
fn = indir+item[1]['file']
b = item[1]['bin']
if re.search(fasta_filename_patterns,fn):
df = io.load_dataset(fn,file_type='fasta',seq_type=seq_type)
elif re.search(fastq_filename_patterns,fn):
df = io.load_dataset(fn,file_type='fastq',seq_type=seq_type)
else:
df = io.load_dataset(fn,file_type='text',seq_type=seq_type)
dataset_df_dict[b] = df
# Merge datasets into one
out_df = merge_datasets(dataset_df_dict)
# Add seqs if given tags_df
if not tags_df is None:
qc.validate_tagkey(tags_df)
tag_col = 'tag'
# Test to make sure all tags in dataset are a subset of tags
data_tags = set(out_df[tag_col])
all_tags = set(tags_df[tag_col])
if not (data_tags <= all_tags):
sys.stderr.write('Some tags probably could not be identified.')
# Get name of seq column
seq_cols = qc.get_cols_from_df(tags_df, 'seqs')
if not len(seq_cols)==1:
raise SortSeqError('Multiple seq columns; exaclty 1 required.')
seq_col = seq_cols[0]
# Set tag to be index column of dataframe
tags_df = tags_df.set_index(tag_col)
# Add seqs corresponding to each tag
tags = out_df[tag_col]
seqs = tags_df[seq_col][tags].values
if not all([type(x)==str for x in seqs]):
raise SortSeqError('Some looked-up seqs are not strings.')
out_df[seq_col] = tags_df[seq_col][tags].values
qc.validate_dataset(out_df)
return out_df
def main(dataset_df, bin=None, start=0, end=None, err=False):
"""
Computes the mutation rate (0.0 to 1.0) at each position. Mutation rate is defined as 1.0 minus the maximum character frequency at a position. Errors are estimated using bionomial uncertainty
Arguments:
dataset_df (pd.DataFrame): A dataframe containing a valid dataset.
bin (int): A bin number specifying which counts to use
start (int): An integer specifying the sequence start position
end (int): An integer specifying the sequence end position
Returns:
freq_df (pd.DataFrame): A dataframe containing results.
"""
# Validate dataset_df
qc.validate_dataset(dataset_df)
# Compute counts
counts_df = profile_ct.main(dataset_df, bin=bin, start=start, end=end)
# Create columns for profile_freqs table
ct_cols = [c for c in counts_df.columns if qc.is_col_type(c, "ct_")]
# Record positions in new dataframe
mut_df = counts_df[["pos"]].copy()
# Compute mutation rate across counts
max_ct = counts_df[ct_cols].max(axis=1)
sum_ct = counts_df[ct_cols].sum(axis=1)
mut = 1.0 - (max_ct / sum_ct)
mut_df["mut"] = mut
# Computation of error rate is optional
if err:
mut_err = np.sqrt(mut * (1.0 - mut) / sum_ct)
mut_df["mut_err"] = mut_err
# Figure out which alphabet the cts dataframe specifies
alphabet = "".join([c.split("_")[1] for c in ct_cols])
seqtype = qc.alphabet_to_seqtype_dict[alphabet]
wt_col = qc.seqtype_to_wtcolname_dict[seqtype]
# Compute WT base at each position
mut_df[wt_col] = "X"
for col in ct_cols:
indices = (counts_df[col] == max_ct).values
mut_df.loc[indices, wt_col] = col.split("_")[1]
# Validate as counts dataframe
mut_df = qc.validate_profile_mut(mut_df, fix=True)
return mut_df
def test_preprocess(self):
""" Test the ability of mpathic.preprocess to collate data in multiple sequence files
"""
print '\nIn test_preprocess...'
file_names = glob.glob(self.input_dir + 'files_*.txt')
# Make sure there are files to test
self.assertTrue(len(file_names) > 0)
for file_name in file_names:
print '\t%s =' % file_name,
description = file_name.split('_')[-1].split('.')[0]
# If fasta or fastq, assume dna
if ('fasta' in file_name) or ('fastq' in file_name):
seq_type = 'dna'
else:
seq_type = None
executable = lambda: preprocess.main(io.load_filelist(file_name),
indir=self.input_dir,
seq_type=seq_type)
# If _good_, then preprocess.main should produce a valid df
if ('_good' in file_name) or ('_fix' in file_name):
try:
df = executable()
qc.validate_dataset(df)
out_file = self.output_dir + 'dataset_%s.txt' % description
io.write(df, out_file) # Test write
io.load_dataset(out_file) # Test loading
print 'good.'
except:
print 'bad (ERROR).'
raise
# If _bad, then preprocess.main should raise SortSeqError
elif '_bad' in file_name:
try:
self.assertRaises(SortSeqError, executable)
print 'badtype.'
except:
print 'good (ERROR).'
raise
# There are no other options
else:
raise SortSeqError('Unrecognized class of file_name.')
def main(dataset_df,model_df,left=None,right=None):
# Validate dataframes
qc.validate_dataset(dataset_df)
qc.validate_model(model_df)
# Detect model type based on columns
seqtype, modeltype = qc.get_model_type(model_df)
seqcol = qc.seqtype_to_seqcolname_dict[seqtype]
# Set start and end based on left or right
if not ((left is None) or (right is None)):
raise SortSeqError('Cannot set both left and right at same time.')
if not (left is None):
start = left
end = start + model_df.shape[0] + (1 if modeltype=='NBR' else 0)
elif not (right is None):
end = right
start = end - model_df.shape[0] - (1 if modeltype=='NBR' else 0)
else:
start = model_df['pos'].values[0]
end = model_df['pos'].values[-1] + (2 if modeltype=='NBR' else 1)
assert start < end
# Validate start and end positions
seq_length = len(dataset_df[seqcol][0])
if start < 0:
raise SortSeqError('Invalid start=%d'%start)
if end > seq_length:
raise SortSeqError('Invalid end=%d for seq_length=%d'%(end,seq_length))
#select target sequence region
out_df = dataset_df.copy()
out_df.loc[:,'seq'] = out_df.loc[:,'seq'].str.slice(start,end)
#Create model object of correct type
if modeltype == 'MAT':
mymodel = Models.LinearModel(model_df)
elif modeltype == 'NBR':
mymodel = Models.NeighborModel(model_df)
else:
raise SortSeqError('Unrecognized model type %s'%modeltype)
# Compute values
out_df['val'] = mymodel.evaluate(out_df)
# Validate dataframe and return
return qc.validate_dataset(out_df,fix=True)
def wrapper(args):
try:
npar = args.noiseparam.strip("[").strip("]").split(",")
except:
npar = []
nbins = args.nbins
# Run funciton
if args.i:
df = pd.io.parsers.read_csv(args.i, delim_whitespace=True, dtype={"seqs": str, "batch": int})
else:
df = pd.io.parsers.read_csv(sys.stdin, delim_whitespace=True, dtype={"seqs": str, "batch": int})
if len(utils.get_column_headers(df)) > 0:
raise SortSeqError("Library already sorted!")
model_df = io.load_model(args.model)
output_df = main(df, model_df, args.noisemodel, npar, nbins, start=args.start, end=args.end)
if args.out:
outloc = open(args.out, "w")
else:
outloc = sys.stdout
pd.set_option("max_colwidth", int(1e8))
# Validate dataframe for writting
output_df = qc.validate_dataset(output_df, fix=True)
io.write(output_df, outloc)
def wrapper(args):
T_LibCounts = args.totallibcounts
T_mRNACounts = args.totalmRNAcounts
if T_LibCounts <=0 or T_mRNACounts <= 0:
raise SortSeqError('Counts must be greater than zero')
model_df = io.load_model(args.model)
if args.i:
df = pd.io.parsers.read_csv(args.i,delim_whitespace=True)
else:
df = pd.io.parsers.read_csv(sys.stdin,delim_whitespace=True)
#make sure the library is not already sorted
if len(utils.get_column_headers(df)) > 0:
raise SortSeqError('Library already sorted!')
header = df.columns
libcounts,expcounts = main(df,model_df,T_LibCounts,T_mRNACounts,start=args.start,end=args.end)
#add these counts to input dataframe
lc = pd.Series(libcounts,name='ct_0')
ec = pd.Series(expcounts,name='ct_1')
df['ct_0'] = lc
df['ct_1'] = ec
df['ct'] = df[['ct_0','ct_1']].sum(axis=1)
if args.out:
outloc = open(args.out,'w')
else:
outloc = sys.stdout
pd.set_option('max_colwidth',int(1e8))
# Validate dataframe for writting
df = qc.validate_dataset(df,fix=True)
io.write(df,outloc)
def test_preprocess(self):
""" Test the ability of mpathic.preprocess to collate data in multiple sequence files
"""
print '\nIn test_preprocess...'
file_names = glob.glob(self.input_dir+'files_*.txt')
# Make sure there are files to test
self.assertTrue(len(file_names)>0)
for file_name in file_names:
print '\t%s ='%file_name,
description = file_name.split('_')[-1].split('.')[0]
# If fasta or fastq, assume dna
if ('fasta' in file_name) or ('fastq' in file_name):
seq_type = 'dna'
else:
seq_type = None
executable = lambda: preprocess.main(io.load_filelist(file_name),indir=self.input_dir, seq_type=seq_type)
# If _good_, then preprocess.main should produce a valid df
if ('_good' in file_name) or ('_fix' in file_name):
try:
df = executable()
qc.validate_dataset(df)
out_file = self.output_dir+'dataset_%s.txt'%description
io.write(df,out_file) # Test write
io.load_dataset(out_file) # Test loading
print 'good.'
except:
print 'bad (ERROR).'
raise
# If _bad, then preprocess.main should raise SortSeqError
elif '_bad' in file_name:
try:
self.assertRaises(SortSeqError,executable)
print 'badtype.'
except:
print 'good (ERROR).'
raise
# There are no other options
else:
raise SortSeqError('Unrecognized class of file_name.')
def merge_datasets(dataset_df_dict):
"""
Merges multiple datasets into one. Data from disparate files is merged via values in 'tag', seq', 'seq_rna', or 'seq_pro' columns (in order of preference, chosen according to availability). Each value in the 'ct' column of each dataset is recorded in the 'ct_[bin]' column of the final dataset. A total 'ct' column is then computed, and rows in the final dataset are sorted in descending order according to this.
Arguments:
dataset_df_dict (dict): Keys are bin numbers, values are dataset dataframes
Returns:
out_df (pd.DataFrame): A validated dataset dataframe
"""
# Make sure datasets were loaded
if not len(dataset_df_dict)>=1:
raise SortSeqError('No datasets were loaded')
# Determine index column. Must be same for all files
df = dataset_df_dict.values()[0]
if 'tag' in df.columns:
index_col = 'tag'
elif 'seq' in df.columns:
index_col = 'seq'
elif 'seq_rna' in df.columns:
index_col = 'seq_rna'
elif 'seq_pro' in df.columns:
index_col = 'seq_pro'
# Concatenate dataset dataframes
out_df = pd.DataFrame()
for b in dataset_df_dict.keys():
df = dataset_df_dict[b]
# Verify that dataframe has correct column
if not index_col in df.columns:
raise SortSeqError('\
Dataframe does not contain index_col="%s"'%index_col)
if not 'ct' in df.columns:
raise SortSeqError('\
Dataframe does not contain a "ct" column')
# Delete "ct_X" columns
for col in df.columns:
if qc.is_col_type(col,'ct_'):
del df[col]
# Add bin number to name of counts column.
df = df.rename(columns={'ct':'ct_%d'%b})
# Index dataset by index_col
df = df.groupby(index_col).sum()
# Concatenate
out_df = pd.concat([out_df,df],axis=1)
# Rename index as tag
out_df.reset_index(inplace=True)
out_df.rename(columns = {'index':index_col},inplace=True)
# Fill undefined counts with zero
out_df.fillna(value=0,inplace=True)
# Add 'ct' column, with proper counts
out_df['ct'] = 0
for col in out_df.columns:
if qc.is_col_type(col,'ct_'):
out_df['ct'] += out_df[col]
# Sort by 'ct' column
out_df.sort('ct',ascending=False,inplace=True)
out_df.reset_index(drop=True,inplace=True)
# Validate out_df as dataset and return it
out_df = qc.validate_dataset(out_df,fix=True)
return out_df
def main(dataset_df, err=False, method="naive", pseudocount=1.0, start=0, end=None):
"""
Computes the mutual information (in bits), at each position, between the character and the bin number.
Arguments:
dataset_df (pd.DataFrame): A dataframe containing a valid dataset.
start (int): An integer specifying the sequence start position
end (int): An integer specifying the sequence end position
method (str): Which method to use to estimate mutual information
Returns:
info_df (pd.DataFrame): A dataframe containing results.
"""
# Validate dataset_df
qc.validate_dataset(dataset_df)
# Get number of bins
bin_cols = [c for c in dataset_df.columns if qc.is_col_type(c, "ct_")]
if not len(bin_cols) >= 2:
raise SortSeqError("Information profile requires at least 2 bins.")
bins = [int(c.split("_")[1]) for c in bin_cols]
num_bins = len(bins)
# Get number of characters
seq_cols = [c for c in dataset_df.columns if qc.is_col_type(c, "seqs")]
if not len(seq_cols) == 1:
raise SortSeqError("Must be only one seq column.")
seq_col = seq_cols[0]
seqtype = qc.colname_to_seqtype_dict[seq_col]
alphabet = qc.seqtype_to_alphabet_dict[seqtype]
ct_cols = ["ct_" + a for a in alphabet]
num_chars = len(alphabet)
# Get sequence length and check start, end numbers
num_pos = len(dataset_df[seq_col][0])
if not (0 <= start < num_pos):
raise SortSeqError("Invalid start==%d, num_pos==%d" % (start, num_pos))
if end is None:
end = num_pos
elif end > num_pos:
raise SortSeqError("Invalid end==%d, num_pos==%d" % (end, num_pos))
elif end <= start:
raise SortSeqError("Invalid: start==%d >= end==%d" % (start, end))
# Record positions in new dataframe
counts_df = profile_ct.main(dataset_df)
info_df = counts_df.loc[start : (end - 1), ["pos"]].copy() # rows from start:end
info_df["info"] = 0.0
if err:
info_df["info_err"] = 0.0
# Fill in 3D array of counts
ct_3d_array = np.zeros([end - start, num_chars, num_bins])
for i, bin_num in enumerate(bins):
# Compute counts
counts_df = profile_ct.main(dataset_df, bin=bin_num)
# Fill in counts table
ct_3d_array[:, :, i] = counts_df.loc[start : (end - 1), ct_cols].astype(float)
# Compute mutual information for each position
for i in range(end - start): # i only from start:end
# Get 2D counts
nxy = ct_3d_array[i, :, :]
assert len(nxy.shape) == 2
# Compute mutual informaiton
if err:
mi, mi_err = info.estimate_mutualinfo(nxy, err=True, method=method, pseudocount=pseudocount)
info_df.loc[i + start, "info"] = mi
info_df.loc[i + start, "info_err"] = mi_err
else:
mi = info.estimate_mutualinfo(nxy, err=False, method=method, pseudocount=pseudocount)
info_df.loc[i + start, "info"] = mi
# Validate info dataframe
info_df = qc.validate_profile_info(info_df, fix=True)
return info_df
def main(wtseq=None, mutrate=0.10, numseq=10000,dicttype='dna',probarr=None,
tags=False,tag_length=10):
#generate sequence dictionary
seq_dict,inv_dict = utils.choose_dict(dicttype)
mutrate = float(mutrate)
if (mutrate < 0.0) or (mutrate > 1.0):
raise SortSeqError('Invalid mutrate==%f'%mutrate)
numseq = int(numseq)
if (numseq <= 0):
raise SortSeqError('numseq must be positive. Is %d'%numseq)
tag_length = int(tag_length)
if (tag_length <= 0):
raise SortSeqErorr('tag_length must be positive. Is %d'%tag_length)
if isinstance(probarr,np.ndarray):
L = probarr.shape[1]
#Generate bases according to provided probability matrix
letarr = np.zeros([numseq,L])
for z in range(L):
letarr[:,z] = np.random.choice(
range(len(seq_dict)),numseq,p=probarr[:,z])
else:
parr = []
wtseq = wtseq.upper()
L = len(wtseq)
letarr = np.zeros([numseq,L])
#Check to make sure the wtseq uses the correct bases.
lin_seq_dict,lin_inv_dict = utils.choose_dict(dicttype,modeltype='MAT')
def check_sequences(s):
return set(s).issubset(lin_seq_dict)
if not check_sequences(wtseq):
raise SortSeqError(
'wtseq can only contain bases in ' + str(lin_seq_dict.keys()))
#find wtseq array
wtarr = seq2arr(wtseq,seq_dict)
mrate = mutrate/(len(seq_dict)-1) #prob of non wildtype
#Generate sequences by mutating away from wildtype
'''probabilities away from wildtype (0 = stays the same, a 3 for
example means a C becomes an A, a 1 means C-> G)'''
parr = np.array(
[1-(len(seq_dict)-1)*mrate]
+ [mrate for i in range(len(seq_dict)-1)])
#Generate random movements from wtseq
letarr = np.random.choice(
range(len(seq_dict)),[numseq,len(wtseq)],p=parr)
#Find sequences
letarr = np.mod(letarr + wtarr,len(seq_dict))
seqs= []
#Convert Back to letters
for i in range(numseq):
seqs.append(arr2seq(letarr[i,:],inv_dict))
seq_col = qc.seqtype_to_seqcolname_dict[dicttype]
seqs_df = pd.DataFrame(seqs, columns=[seq_col])
# If simulating tags, each generated seq gets a unique tag
if tags:
tag_seq_dict,tag_inv_dict = utils.choose_dict('dna')
tag_alphabet_list = tag_seq_dict.keys()
# Make sure tag_length is long enough for the number of tags needed
if len(tag_alphabet_list)**tag_length < 2*numseq:
raise SortSeqError(\
'tag_length=%d is too short for num_tags_needed=%d'%\
(tag_length,numseq))
# Generate a unique tag for each unique sequence
tag_set = set([])
while len(tag_set) < numseq:
num_tags_left = numseq - len(tag_set)
new_tags = [''.join(choice(tag_alphabet_list,size=tag_length)) \
for i in range(num_tags_left)]
tag_set = tag_set.union(new_tags)
df = seqs_df.copy()
df.loc[:,'ct'] = 1
df.loc[:,'tag'] = list(tag_set)
# If not simulating tags, list only unique seqs w/ corresponding counts
else:
seqs_counts = seqs_df[seq_col].value_counts()
df = seqs_counts.reset_index()
df.columns = [seq_col,'ct']
# Convert into valid dataset dataframe and return
return qc.validate_dataset(df,fix=True)
def main(dataset_df,
bin=None,
start=0,
end=None,
bins_df=None,
pseudocounts=1,
return_profile=False):
"""
Computes character frequencies (0.0 to 1.0) at each position
Arguments:
dataset_df (pd.DataFrame): A dataframe containing a valid dataset.
bin (int): A bin number specifying which counts to use
start (int): An integer specifying the sequence start position
end (int): An integer specifying the sequence end position
Returns:
freq_df (pd.DataFrame): A dataframe containing counts for each
nucleotide/amino acid character at each position.
"""
seq_cols = qc.get_cols_from_df(dataset_df, 'seqs')
if not len(seq_cols) == 1:
raise SortSeqError('Dataframe has multiple seq cols: %s' %
str(seq_cols))
dicttype = qc.colname_to_seqtype_dict[seq_cols[0]]
seq_dict, inv_dict = utils.choose_dict(dicttype)
# Validate dataset_df
qc.validate_dataset(dataset_df)
#for each bin we need to find character frequency profile, then sum over all
#bins to get activity.
#first make sure we have activities of each bin:
if not bins_df:
bins = utils.get_column_headers(dataset_df)
#in this case no activity was specified so just assume the activity
#equals bin number
activity = [float(b.split('_')[-1]) for b in bins]
else:
bins = list(bins_df['bins'])
activity = list(bins_df['activity'])
#initialize dataframe for total counts in all bins
output_ct_df = pd.DataFrame()
#initialize dataframe for running activity calculation
output_activity_df = pd.DataFrame()
for i, b in enumerate(bins):
bin_num = int(b.split('_')[-1])
# Compute counts
counts_df = profile_ct.main(dataset_df,
bin=bin_num,
start=start,
end=end)
# Create columns for profile_freqs table
ct_cols = utils.get_column_headers(counts_df)
#add_pseudocounts
counts_df[ct_cols] = counts_df[ct_cols] + pseudocounts
#add to all previous bin counts
#print output_activity_df
if i == 0:
output_ct_df = counts_df[ct_cols]
output_activity_df = counts_df[ct_cols] * activity[i]
else:
output_ct_df = output_ct_df + counts_df[ct_cols]
output_activity_df = output_activity_df + counts_df[
ct_cols] * activity[i]
#now normalize by each character at each position, this is the activity
#profile
output_activity_df = output_activity_df[ct_cols].div(output_ct_df[ct_cols])
mut_rate = profile_mut.main(dataset_df, bin=bin)
freq = profile_freq.main(dataset_df, bin=bin)
freq_cols = [x for x in freq.columns if 'freq_' in x]
#now normalize by the wt activity
wtseq = ''.join(mut_rate['wt'])
wtarr = utils.seq2mat(wtseq, seq_dict)
wt_activity = np.transpose(wtarr) * (np.array(output_activity_df[ct_cols]))
#sum this to get total
wt_activity2 = wt_activity.sum(axis=1)
delta_activity = output_activity_df.subtract(pd.Series(wt_activity2),
axis=0)
if return_profile:
#first find mutation rate according to formula in SI text
profile_delta_activity = mut_rate['mut']*np.sum(
(1-np.transpose(wtarr))*np.array(\
freq[freq_cols])*np.array(delta_activity),axis=1)
#format into dataframe
output_df = pd.DataFrame()
output_df['pos'] = range(start,
start + len(profile_delta_activity.index))
output_df['mut_activity'] = profile_delta_activity
return output_df
else:
#just add pos column and rename counts columns to activity columns
output_df = pd.DataFrame(delta_activity)
output_df.insert(0, 'pos',
range(start, start + len(delta_activity.index)))
#reorder columns
activity_col_dict = {x:'activity_' + x.split('_')[-1] \
for x in delta_activity.columns if 'ct_' in x}
output_df = output_df.rename(columns=activity_col_dict)
return output_df
def main(dataset_df, bin=None, start=0, end=None):
"""
Computes character counts at each position
Arguments:
dataset_df (pd.DataFrame): A dataframe containing a valid dataset.
bin (int): A bin number specifying which counts to use
start (int): An integer specifying the sequence start position
end (int): An integer specifying the sequence end position
Returns:
counts_df (pd.DataFrame): A dataframe containing counts for each nucleotide/amino acid character at each position.
"""
# Validate dataset_df
qc.validate_dataset(dataset_df)
# Retrieve type of sequence
seq_cols = [c for c in dataset_df.columns if qc.is_col_type(c,'seqs')]
if not len(seq_cols)==1:
raise SortSeqError('Dataset dataframe must have only one seq colum.')
colname = seq_cols[0]
seqtype = qc.colname_to_seqtype_dict[colname]
alphabet = qc.seqtype_to_alphabet_dict[seqtype]
num_chars = len(alphabet)
# Retrieve sequence length
if not dataset_df.shape[0] > 1:
raise SortSeqError('Dataset dataframe must have at least one row.')
total_seq_length = len(dataset_df[colname].iloc[0])
# Validate start and end
if start<0:
raise SortSeqError('start=%d is negative.'%start)
elif start>=total_seq_length:
raise SortSeqError('start=%d >= total_seq_length=%d'%\
(start,total_seq_length))
if end is None:
end=total_seq_length
elif end<=start:
raise SortSeqError('end=%d <= start=%d.'%(end,start))
elif end>total_seq_length:
raise SortSeqError('end=%d > total_seq_length=%d'%\
(start,total_seq_length))
# Set positions
poss = pd.Series(range(start,end),name='pos')
num_poss = len(poss)
# Retrieve counts
if bin is None:
ct_col = 'ct'
else:
ct_col = 'ct_%d'%bin
if not ct_col in dataset_df.columns:
raise SortSeqError('Column "%s" is not in columns=%s'%\
(ct_col,str(dataset_df.columns)))
counts = dataset_df[ct_col]
# Compute counts profile
counts_array = np.zeros([num_poss,num_chars])
counts_cols = ['ct_'+a for a in alphabet]
for i,pos in enumerate(range(start,end)):
char_list = dataset_df[colname].str.slice(pos,pos+1)
counts_array[i,:] = [np.sum(counts[char_list==a]) for a in alphabet]
temp_df = pd.DataFrame(counts_array,columns=counts_cols)
counts_df = pd.concat([poss,temp_df],axis=1)
# Validate as counts dataframe
counts_df = qc.validate_profile_ct(counts_df,fix=True)
return counts_df