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adaptive file read+merge
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import os | |
import pandas as pd | |
import platform | |
import re | |
import parmap | |
from tcrdist.swap_gene_name import adaptive_to_imgt | |
path= "" #path to key file | |
key = "" #list of adaptive files to include | |
files=pd.read_csv(os.path.join(path, key), sep="\t") | |
files=sorted(files['file']) | |
print(files) | |
count=1 | |
vzv_list=list() | |
for file in files: | |
if not file.endswith(".tsv"): | |
continue | |
df = pd.read_csv(os.path.join(path, file), | |
sep="\t") | |
df['file']=file | |
df.dropna(subset = ["aminoAcid"], inplace=True) | |
df.dropna(subset = ['vMaxResolved'], inplace=True) | |
print(df.head(2)) | |
vzv_list.append(df) | |
count=count+1 | |
# if count>5: break | |
vzv_tcrs = pd.concat(vzv_list, axis=0) | |
vzv_tcrs = vzv_tcrs[vzv_tcrs['sequenceStatus']=='In'].reset_index(drop = True) | |
vzv_tcrs.columns | |
cols = {'nucleotide': 'cdr3_b_nucseq', | |
'aminoAcid': 'cdr3_b_aa', | |
'count (templates/reads)': 'templates', | |
'frequencyCount (%)': 'freq', | |
'vMaxResolved': 'vMaxResolved', | |
'jMaxResolved': 'jMaxResolved', | |
'file': 'file'} | |
vzv_tcrs = vzv_tcrs[cols].rename(columns = cols) | |
vzv_tcrs['file'] = vzv_tcrs['file'].str.replace("gE_CD4","gE") | |
vzv_tcrs[['person', 'cell', 'type', 'TCR']] = vzv_tcrs.file.str.split('_', n=3, expand =True) | |
vzv_tcrs['source'] = vzv_tcrs['cell'] + "_" + vzv_tcrs['type'] | |
vzv_tcrs['v_b_gene'] = vzv_tcrs['vMaxResolved'].apply(lambda x: adaptive_to_imgt['human'].get(x.split("*")[0]) if isinstance(x,str) else None) | |
vzv_tcrs['j_b_gene'] = vzv_tcrs['jMaxResolved'].apply(lambda x: adaptive_to_imgt['human'].get(x.split("*")[0]) if isinstance(x,str) else None) | |
cols = {'cdr3_b_nucseq': 'cdr3_b_nucseq', | |
'cdr3_b_aa': 'cdr3_b_aa', | |
'templates': 'count', | |
'freq': 'freq', | |
'person': 'person', | |
'source': 'source', | |
'v_b_gene': 'v_b_gene', | |
'j_b_gene': 'j_b_gene'} | |
vzv_tcrs = vzv_tcrs[cols].rename(columns = cols) | |
## frequency wide version | |
dfp = vzv_tcrs.pivot(index=['cdr3_b_nucseq', 'cdr3_b_aa', 'v_b_gene', 'j_b_gene', 'person'], | |
columns='source', values='freq') | |
dfp = dfp.reset_index(drop = False) | |
## counts wide version | |
dft = vzv_tcrs.pivot(index=['cdr3_b_nucseq', 'cdr3_b_aa', 'v_b_gene', 'j_b_gene', 'person'], | |
columns='source', values='count') | |
dft = dft.reset_index(drop = False) |
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