Compare outcomes from differential analysis based on different imputation methods#

  • load scores based on 10_1_ald_diff_analysis

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import logging
from pathlib import Path

import matplotlib.pyplot as plt
import pandas as pd
import seaborn as sns
from IPython.display import display

import pimmslearn
import pimmslearn.databases.diseases

logger = pimmslearn.logging.setup_nb_logger()

plt.rcParams['figure.figsize'] = (2, 2)
fontsize = 5
pimmslearn.plotting.make_large_descriptors(fontsize)
logging.getLogger('fontTools').setLevel(logging.ERROR)

# catch passed parameters
args = None
args = dict(globals()).keys()

Parameters#

Default and set parameters for the notebook.

folder_experiment = 'runs/appl_ald_data/plasma/proteinGroups'

target = 'kleiner'
model_key = 'VAE'
baseline = 'RSN'
out_folder = 'diff_analysis'
selected_statistics = ['p-unc', '-Log10 pvalue', 'qvalue', 'rejected']

disease_ontology = 5082  # code from https://disease-ontology.org/
# split diseases notebook? Query gene names for proteins in file from uniprot?
annotaitons_gene_col = 'PG.Genes'
# Parameters
disease_ontology = 10652
folder_experiment = "runs/alzheimer_study"
target = "AD"
baseline = "PI"
model_key = "CF"
out_folder = "diff_analysis"
annotaitons_gene_col = "None"

Add set parameters to configuration

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params = pimmslearn.nb.get_params(args, globals=globals())
args = pimmslearn.nb.Config()
args.folder_experiment = Path(params["folder_experiment"])
args = pimmslearn.nb.add_default_paths(args,
                                 out_root=(
                                     args.folder_experiment
                                     / params["out_folder"]
                                     / params["target"]
                                     / f"{params['baseline']}_vs_{params['model_key']}"))
args.update_from_dict(params)
args.scores_folder = scores_folder = (args.folder_experiment
                                      / params["out_folder"]
                                      / params["target"]
                                      / 'scores')
args.freq_features_observed = args.folder_experiment / 'freq_features_observed.csv'
args
root - INFO     Removed from global namespace: folder_experiment
root - INFO     Removed from global namespace: target
root - INFO     Removed from global namespace: model_key
root - INFO     Removed from global namespace: baseline
root - INFO     Removed from global namespace: out_folder
root - INFO     Removed from global namespace: selected_statistics
root - INFO     Removed from global namespace: disease_ontology
root - INFO     Removed from global namespace: annotaitons_gene_col
root - INFO     Already set attribute: folder_experiment has value runs/alzheimer_study
root - INFO     Already set attribute: out_folder has value diff_analysis
{'annotaitons_gene_col': 'None',
 'baseline': 'PI',
 'data': PosixPath('runs/alzheimer_study/data'),
 'disease_ontology': 10652,
 'folder_experiment': PosixPath('runs/alzheimer_study'),
 'freq_features_observed': PosixPath('runs/alzheimer_study/freq_features_observed.csv'),
 'model_key': 'CF',
 'out_figures': PosixPath('runs/alzheimer_study/figures'),
 'out_folder': PosixPath('runs/alzheimer_study/diff_analysis/AD/PI_vs_CF'),
 'out_metrics': PosixPath('runs/alzheimer_study'),
 'out_models': PosixPath('runs/alzheimer_study'),
 'out_preds': PosixPath('runs/alzheimer_study/preds'),
 'scores_folder': PosixPath('runs/alzheimer_study/diff_analysis/AD/scores'),
 'selected_statistics': ['p-unc', '-Log10 pvalue', 'qvalue', 'rejected'],
 'target': 'AD'}

Excel file for exports#

files_out = dict()
writer_args = dict(float_format='%.3f')

fname = args.out_folder / 'diff_analysis_compare_methods.xlsx'
files_out[fname.name] = fname
writer = pd.ExcelWriter(fname)
logger.info("Writing to excel file: %s", fname)
root - INFO     Writing to excel file: runs/alzheimer_study/diff_analysis/AD/PI_vs_CF/diff_analysis_compare_methods.xlsx

Load scores#

Load baseline model scores#

Show all statistics, later use selected statistics

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fname = args.scores_folder / f'diff_analysis_scores_{args.baseline}.pkl'
scores_baseline = pd.read_pickle(fname)
scores_baseline
model PI
var SS DF F p-unc np2 -Log10 pvalue qvalue rejected
protein groups Source
A0A024QZX5;A0A087X1N8;P35237 AD 0.833 1 1.390 0.240 0.007 0.620 0.397 False
age 0.147 1 0.246 0.620 0.001 0.207 0.750 False
Kiel 2.439 1 4.072 0.045 0.021 1.347 0.112 False
Magdeburg 4.762 1 7.949 0.005 0.040 2.274 0.020 True
Sweden 8.268 1 13.800 0.000 0.067 3.574 0.002 True
... ... ... ... ... ... ... ... ... ...
S4R3U6 AD 0.531 1 0.525 0.469 0.003 0.328 0.623 False
age 1.792 1 1.774 0.185 0.009 0.734 0.328 False
Kiel 0.002 1 0.002 0.961 0.000 0.017 0.976 False
Magdeburg 2.675 1 2.648 0.105 0.014 0.978 0.218 False
Sweden 15.376 1 15.221 0.000 0.074 3.878 0.001 True

7105 rows × 8 columns

Load selected comparison model scores#

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fname = args.scores_folder / f'diff_analysis_scores_{args.model_key}.pkl'
scores_model = pd.read_pickle(fname)
scores_model
model CF
var SS DF F p-unc np2 -Log10 pvalue qvalue rejected
protein groups Source
A0A024QZX5;A0A087X1N8;P35237 AD 1.070 1 7.461 0.007 0.038 2.161 0.020 True
age 0.005 1 0.038 0.846 0.000 0.073 0.898 False
Kiel 0.324 1 2.260 0.134 0.012 0.872 0.231 False
Magdeburg 0.606 1 4.223 0.041 0.022 1.385 0.088 False
Sweden 2.063 1 14.383 0.000 0.070 3.699 0.001 True
... ... ... ... ... ... ... ... ... ...
S4R3U6 AD 1.832 1 3.644 0.058 0.019 1.238 0.117 False
age 0.856 1 1.703 0.193 0.009 0.713 0.307 False
Kiel 2.730 1 5.430 0.021 0.028 1.681 0.050 False
Magdeburg 3.283 1 6.528 0.011 0.033 1.943 0.030 True
Sweden 18.244 1 36.280 0.000 0.160 8.065 0.000 True

7105 rows × 8 columns

Combined scores#

show only selected statistics for comparsion

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scores = scores_model.join(scores_baseline, how='outer')[[args.baseline, args.model_key]]
scores = scores.loc[:, pd.IndexSlice[scores.columns.levels[0].to_list(),
                                     args.selected_statistics]]
scores
model CF PI
var p-unc -Log10 pvalue qvalue rejected p-unc -Log10 pvalue qvalue rejected
protein groups Source
A0A024QZX5;A0A087X1N8;P35237 AD 0.007 2.161 0.020 True 0.240 0.620 0.397 False
Kiel 0.134 0.872 0.231 False 0.045 1.347 0.112 False
Magdeburg 0.041 1.385 0.088 False 0.005 2.274 0.020 True
Sweden 0.000 3.699 0.001 True 0.000 3.574 0.002 True
age 0.846 0.073 0.898 False 0.620 0.207 0.750 False
... ... ... ... ... ... ... ... ... ...
S4R3U6 AD 0.058 1.238 0.117 False 0.469 0.328 0.623 False
Kiel 0.021 1.681 0.050 False 0.961 0.017 0.976 False
Magdeburg 0.011 1.943 0.030 True 0.105 0.978 0.218 False
Sweden 0.000 8.065 0.000 True 0.000 3.878 0.001 True
age 0.193 0.713 0.307 False 0.185 0.734 0.328 False

7105 rows × 8 columns

Models in comparison (name mapping)

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models = pimmslearn.nb.Config.from_dict(
    pimmslearn.pandas.index_to_dict(scores.columns.get_level_values(0)))
vars(models)
{'CF': 'CF', 'PI': 'PI'}

Describe scores#

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scores.describe()
model CF PI
var p-unc -Log10 pvalue qvalue p-unc -Log10 pvalue qvalue
count 7,105.000 7,105.000 7,105.000 7,105.000 7,105.000 7,105.000
mean 0.225 3.283 0.278 0.261 2.476 0.338
std 0.292 6.223 0.319 0.303 5.328 0.331
min 0.000 0.000 0.000 0.000 0.000 0.000
25% 0.001 0.408 0.002 0.004 0.335 0.016
50% 0.062 1.209 0.124 0.121 0.916 0.243
75% 0.391 3.272 0.521 0.463 2.411 0.617
max 1.000 86.405 1.000 0.999 146.241 0.999

One to one comparison of by feature:#

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scores = scores.loc[pd.IndexSlice[:, args.target], :]
scores.to_excel(writer, 'scores', **writer_args)
scores
/tmp/ipykernel_88830/3761369923.py:2: FutureWarning: Starting with pandas version 3.0 all arguments of to_excel except for the argument 'excel_writer' will be keyword-only.
  scores.to_excel(writer, 'scores', **writer_args)
model CF PI
var p-unc -Log10 pvalue qvalue rejected p-unc -Log10 pvalue qvalue rejected
protein groups Source
A0A024QZX5;A0A087X1N8;P35237 AD 0.007 2.161 0.020 True 0.240 0.620 0.397 False
A0A024R0T9;K7ER74;P02655 AD 0.035 1.460 0.077 False 0.059 1.228 0.139 False
A0A024R3W6;A0A024R412;O60462;O60462-2;O60462-3;O60462-4;O60462-5;Q7LBX6;X5D2Q8 AD 0.380 0.420 0.510 False 0.040 1.393 0.103 False
A0A024R644;A0A0A0MRU5;A0A1B0GWI2;O75503 AD 0.251 0.600 0.376 False 0.420 0.377 0.580 False
A0A075B6H7 AD 0.004 2.389 0.013 True 0.027 1.567 0.075 False
... ... ... ... ... ... ... ... ... ...
Q9Y6R7 AD 0.175 0.756 0.284 False 0.175 0.756 0.316 False
Q9Y6X5 AD 0.189 0.724 0.301 False 0.070 1.155 0.159 False
Q9Y6Y8;Q9Y6Y8-2 AD 0.083 1.079 0.158 False 0.083 1.079 0.182 False
Q9Y6Y9 AD 0.628 0.202 0.733 False 0.348 0.459 0.512 False
S4R3U6 AD 0.058 1.238 0.117 False 0.469 0.328 0.623 False

1421 rows × 8 columns

And the descriptive statistics of the numeric values:

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scores.describe()
model CF PI
var p-unc -Log10 pvalue qvalue p-unc -Log10 pvalue qvalue
count 1,421.000 1,421.000 1,421.000 1,421.000 1,421.000 1,421.000
mean 0.239 1.580 0.299 0.252 1.411 0.334
std 0.293 1.831 0.315 0.291 1.654 0.316
min 0.000 0.000 0.000 0.000 0.001 0.000
25% 0.007 0.385 0.020 0.013 0.368 0.041
50% 0.089 1.052 0.165 0.121 0.917 0.242
75% 0.412 2.161 0.542 0.428 1.899 0.588
max 0.999 20.851 1.000 0.999 25.104 0.999

and the boolean decision values

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scores.describe(include=['bool', 'O'])
model CF PI
var rejected rejected
count 1421 1421
unique 2 2
top False False
freq 952 1031

Load frequencies of observed features#

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freq_feat = pd.read_csv(args.freq_features_observed, index_col=0)
freq_feat.columns = pd.MultiIndex.from_tuples([('data', 'frequency'),])
freq_feat
data
frequency
protein groups
A0A024QZX5;A0A087X1N8;P35237 186
A0A024R0T9;K7ER74;P02655 195
A0A024R3W6;A0A024R412;O60462;O60462-2;O60462-3;O60462-4;O60462-5;Q7LBX6;X5D2Q8 174
A0A024R644;A0A0A0MRU5;A0A1B0GWI2;O75503 196
A0A075B6H7 91
... ...
Q9Y6R7 197
Q9Y6X5 173
Q9Y6Y8;Q9Y6Y8-2 197
Q9Y6Y9 119
S4R3U6 126

1421 rows × 1 columns

Compare shared features#

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scores_common = (scores
                 .dropna()
                 .reset_index(-1, drop=True)
                 ).join(
    freq_feat, how='left'
)
scores_common
CF PI data
p-unc -Log10 pvalue qvalue rejected p-unc -Log10 pvalue qvalue rejected frequency
protein groups
A0A024QZX5;A0A087X1N8;P35237 0.007 2.161 0.020 True 0.240 0.620 0.397 False 186
A0A024R0T9;K7ER74;P02655 0.035 1.460 0.077 False 0.059 1.228 0.139 False 195
A0A024R3W6;A0A024R412;O60462;O60462-2;O60462-3;O60462-4;O60462-5;Q7LBX6;X5D2Q8 0.380 0.420 0.510 False 0.040 1.393 0.103 False 174
A0A024R644;A0A0A0MRU5;A0A1B0GWI2;O75503 0.251 0.600 0.376 False 0.420 0.377 0.580 False 196
A0A075B6H7 0.004 2.389 0.013 True 0.027 1.567 0.075 False 91
... ... ... ... ... ... ... ... ... ...
Q9Y6R7 0.175 0.756 0.284 False 0.175 0.756 0.316 False 197
Q9Y6X5 0.189 0.724 0.301 False 0.070 1.155 0.159 False 173
Q9Y6Y8;Q9Y6Y8-2 0.083 1.079 0.158 False 0.083 1.079 0.182 False 197
Q9Y6Y9 0.628 0.202 0.733 False 0.348 0.459 0.512 False 119
S4R3U6 0.058 1.238 0.117 False 0.469 0.328 0.623 False 126

1421 rows × 9 columns

Annotate decisions in Confusion Table style:#

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def annotate_decision(scores, model, model_column):
    return scores[(model_column, 'rejected')].replace({False: f'{model} (no) ', True: f'{model} (yes)'})


annotations = None
for model, model_column in models.items():
    if annotations is not None:
        annotations += ' - '
        annotations += annotate_decision(scores_common,
                                         model=model, model_column=model_column)
    else:
        annotations = annotate_decision(
            scores_common, model=model, model_column=model_column)
annotations.name = 'Differential Analysis Comparison'
annotations.value_counts()
Differential Analysis Comparison
CF (no)  - PI (no)    891
CF (yes) - PI (yes)   329
CF (yes) - PI (no)    140
CF (no)  - PI (yes)    61
Name: count, dtype: int64

List different decisions between models#

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mask_different = (
    (scores_common.loc[:, pd.IndexSlice[:, 'rejected']].any(axis=1))
    & ~(scores_common.loc[:, pd.IndexSlice[:, 'rejected']].all(axis=1))
)
_to_write = scores_common.loc[mask_different]
_to_write.to_excel(writer, 'differences', **writer_args)
logger.info("Writen to Excel file under sheet 'differences'.")
_to_write
/tmp/ipykernel_88830/1417621106.py:6: FutureWarning: Starting with pandas version 3.0 all arguments of to_excel except for the argument 'excel_writer' will be keyword-only.
  _to_write.to_excel(writer, 'differences', **writer_args)
root - INFO     Writen to Excel file under sheet 'differences'.
CF PI data
p-unc -Log10 pvalue qvalue rejected p-unc -Log10 pvalue qvalue rejected frequency
protein groups
A0A024QZX5;A0A087X1N8;P35237 0.007 2.161 0.020 True 0.240 0.620 0.397 False 186
A0A075B6H7 0.004 2.389 0.013 True 0.027 1.567 0.075 False 91
A0A075B6I0 0.001 3.142 0.003 True 0.023 1.641 0.066 False 194
A0A075B6Q5 0.009 2.040 0.025 True 0.891 0.050 0.936 False 104
A0A075B6R2 0.000 3.313 0.002 True 0.259 0.587 0.419 False 164
... ... ... ... ... ... ... ... ... ...
Q9UKB5 0.069 1.164 0.135 False 0.014 1.861 0.044 True 148
Q9ULZ9 0.042 1.372 0.091 False 0.003 2.460 0.014 True 171
Q9UNW1 0.719 0.143 0.800 False 0.016 1.803 0.049 True 171
Q9UP79 0.000 3.674 0.001 True 0.316 0.501 0.480 False 135
Q9UQ52 0.000 3.373 0.002 True 0.034 1.473 0.089 False 188

201 rows × 9 columns

Plot qvalues of both models with annotated decisions#

Prepare data for plotting (qvalues)

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var = 'qvalue'
to_plot = [scores_common[v][var] for v in models.values()]
for s, k in zip(to_plot, models.keys()):
    s.name = k.replace('_', ' ')
to_plot.append(scores_common['data'])
to_plot.append(annotations)
to_plot = pd.concat(to_plot, axis=1)
to_plot
CF PI frequency Differential Analysis Comparison
protein groups
A0A024QZX5;A0A087X1N8;P35237 0.020 0.397 186 CF (yes) - PI (no)
A0A024R0T9;K7ER74;P02655 0.077 0.139 195 CF (no) - PI (no)
A0A024R3W6;A0A024R412;O60462;O60462-2;O60462-3;O60462-4;O60462-5;Q7LBX6;X5D2Q8 0.510 0.103 174 CF (no) - PI (no)
A0A024R644;A0A0A0MRU5;A0A1B0GWI2;O75503 0.376 0.580 196 CF (no) - PI (no)
A0A075B6H7 0.013 0.075 91 CF (yes) - PI (no)
... ... ... ... ...
Q9Y6R7 0.284 0.316 197 CF (no) - PI (no)
Q9Y6X5 0.301 0.159 173 CF (no) - PI (no)
Q9Y6Y8;Q9Y6Y8-2 0.158 0.182 197 CF (no) - PI (no)
Q9Y6Y9 0.733 0.512 119 CF (no) - PI (no)
S4R3U6 0.117 0.623 126 CF (no) - PI (no)

1421 rows × 4 columns

List of features with the highest difference in qvalues

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# should it be possible to run not only RSN?
to_plot['diff_qvalue'] = (to_plot[str(args.baseline)] - to_plot[str(args.model_key)]).abs()
to_plot.loc[mask_different].sort_values('diff_qvalue', ascending=False)
CF PI frequency Differential Analysis Comparison diff_qvalue
protein groups
P17302 0.000 0.942 135 CF (yes) - PI (no) 0.941
A0A087WU43;A0A087WX17;A0A087WXI5;P12830;P12830-2 0.000 0.931 134 CF (yes) - PI (no) 0.931
O60565 0.006 0.920 81 CF (yes) - PI (no) 0.914
A0A075B6Q5 0.025 0.936 104 CF (yes) - PI (no) 0.911
P48745 0.006 0.913 180 CF (yes) - PI (no) 0.907
... ... ... ... ... ...
F5GY80;F5H7G1;P07358 0.047 0.057 197 CF (yes) - PI (no) 0.010
Q9NX62 0.045 0.056 197 CF (yes) - PI (no) 0.010
P00740;P00740-2 0.043 0.053 197 CF (yes) - PI (no) 0.010
K7ERG9;P00746 0.042 0.052 197 CF (yes) - PI (no) 0.009
Q16706 0.052 0.046 195 CF (no) - PI (yes) 0.006

201 rows × 5 columns

Differences plotted with created annotations#

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figsize = (4, 4)
size = 5
fig, ax = plt.subplots(figsize=figsize)
x_col = to_plot.columns[0]
y_col = to_plot.columns[1]
ax = sns.scatterplot(data=to_plot,
                     x=x_col,
                     y=y_col,
                     s=size,
                     hue='Differential Analysis Comparison',
                     ax=ax)
_ = ax.legend(fontsize=fontsize,
              title_fontsize=fontsize,
              markerscale=0.4,
              title='',
              )
ax.set_xlabel(f"qvalue for {x_col}")
ax.set_ylabel(f"qvalue for {y_col}")
ax.hlines(0.05, 0, 1, color='grey', linestyles='dotted')
ax.vlines(0.05, 0, 1, color='grey', linestyles='dotted')
sns.move_legend(ax, "upper right")
files_out[f'diff_analysis_comparision_1_{args.model_key}'] = (
    args.out_folder /
    f'diff_analysis_comparision_1_{args.model_key}')
fname = files_out[f'diff_analysis_comparision_1_{args.model_key}']
pimmslearn.savefig(fig, name=fname)
pimmslearn.plotting - INFO     Saved Figures to runs/alzheimer_study/diff_analysis/AD/PI_vs_CF/diff_analysis_comparision_1_CF
../../../_images/14c3debddf670465aaf5d1ff4bd133635b75a3acec4177ade5b53c2542dea15b.png
  • also showing how many features were measured (“observed”) by size of circle

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fig, ax = plt.subplots(figsize=figsize)
ax = sns.scatterplot(data=to_plot,
                     x=to_plot.columns[0],
                     y=to_plot.columns[1],
                     size='frequency',
                     s=size,
                     sizes=(5, 20),
                     hue='Differential Analysis Comparison')
_ = ax.legend(fontsize=fontsize,
              title_fontsize=fontsize,
              markerscale=0.6,
              title='',
              )
ax.set_xlabel(f"qvalue for {x_col}")
ax.set_ylabel(f"qvalue for {y_col}")
ax.hlines(0.05, 0, 1, color='grey', linestyles='dotted')
ax.vlines(0.05, 0, 1, color='grey', linestyles='dotted')
sns.move_legend(ax, "upper right")
files_out[f'diff_analysis_comparision_2_{args.model_key}'] = (
    args.out_folder / f'diff_analysis_comparision_2_{args.model_key}')
pimmslearn.savefig(
    fig, name=files_out[f'diff_analysis_comparision_2_{args.model_key}'])
pimmslearn.plotting - INFO     Saved Figures to runs/alzheimer_study/diff_analysis/AD/PI_vs_CF/diff_analysis_comparision_2_CF
../../../_images/627f56bc709cabeb46a723c78e33cac858c8e2e05436b0c072ad94c8d1219617.png

Only features contained in model#

  • this block exist due to a specific part in the ALD analysis of the paper

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scores_model_only = scores.reset_index(level=-1, drop=True)
_diff = scores_model_only.index.difference(scores_common.index)
if not _diff.empty:
    scores_model_only = (scores_model_only
                         .loc[
                             _diff,
                             args.model_key]
                         .sort_values(by='qvalue', ascending=True)
                         .join(freq_feat.squeeze().rename(freq_feat.columns.droplevel()[0])
                               )
                         )
    display(scores_model_only)
else:
    scores_model_only = None
    logger.info("No features only in new comparision model.")

if not _diff.empty:
    scores_model_only.to_excel(writer, 'only_model', **writer_args)
    display(scores_model_only.rejected.value_counts())
    scores_model_only_rejected = scores_model_only.loc[scores_model_only.rejected]
    scores_model_only_rejected.to_excel(
        writer, 'only_model_rejected', **writer_args)
root - INFO     No features only in new comparision model.

DISEASES DB lookup#

Query diseases database for gene associations with specified disease ontology id.

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data = pimmslearn.databases.diseases.get_disease_association(
    doid=args.disease_ontology, limit=10000)
data = pd.DataFrame.from_dict(data, orient='index').rename_axis('ENSP', axis=0)
data = data.rename(columns={'name': args.annotaitons_gene_col}).reset_index(
).set_index(args.annotaitons_gene_col)
data
pimmslearn.databases.diseases - WARNING  There are more associations available
ENSP score
None
APP ENSP00000284981 5.000
PSEN2 ENSP00000355747 5.000
PSEN1 ENSP00000326366 5.000
APOE ENSP00000252486 5.000
TREM2 ENSP00000362205 4.825
... ... ...
PTTG1 ENSP00000377536 0.682
ISL2 ENSP00000290759 0.682
hsa-miR-4433b-3p hsa-miR-4433b-3p 0.682
NEURL1B ENSP00000358815 0.681
SLC26A4 ENSP00000494017 0.681

10000 rows × 2 columns

Shared features#

ToDo: new script -> DISEASES DB lookup

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feat_name = scores.index.names[0]  # first index level is feature name
if args.annotaitons_gene_col in scores.index.names:
    logger.info(f"Found gene annotation in scores index:  {scores.index.names}")
else:
    logger.info(f"No gene annotation in scores index:  {scores.index.names}"
                " Exiting.")
    import sys
    sys.exit(0)
root - INFO     No gene annotation in scores index:  ['protein groups', 'Source'] Exiting.
/home/runner/work/pimms/pimms/project/.snakemake/conda/43fbe714d68d8fe6f9b0c93f5652adb3_/lib/python3.12/site-packages/IPython/core/interactiveshell.py:3756: UserWarning: To exit: use 'exit', 'quit', or Ctrl-D.
  warn("To exit: use 'exit', 'quit', or Ctrl-D.", stacklevel=1)
An exception has occurred, use %tb to see the full traceback.

SystemExit: 0

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gene_to_PG = (scores.droplevel(
    list(set(scores.index.names) - {feat_name, args.annotaitons_gene_col})
)
    .index
    .to_frame()
    .reset_index(drop=True)
    .set_index(args.annotaitons_gene_col)
)
gene_to_PG.head()

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disease_associations_all = data.join(
    gene_to_PG).dropna().reset_index().set_index(feat_name).join(annotations)
disease_associations_all

only by model#

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idx = disease_associations_all.index.intersection(scores_model_only.index)
disease_assocications_new = disease_associations_all.loc[idx].sort_values(
    'score', ascending=False)
disease_assocications_new.head(20)

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mask = disease_assocications_new.loc[idx, 'score'] >= 2.0
disease_assocications_new.loc[idx].loc[mask]

Only by model which were significant#

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idx = disease_associations_all.index.intersection(
    scores_model_only_rejected.index)
disease_assocications_new_rejected = disease_associations_all.loc[idx].sort_values(
    'score', ascending=False)
disease_assocications_new_rejected.head(20)

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mask = disease_assocications_new_rejected.loc[idx, 'score'] >= 2.0
disease_assocications_new_rejected.loc[idx].loc[mask]

Shared which are only significant for by model#

mask = (scores_common[(str(args.model_key), 'rejected')] & mask_different)
mask.sum()

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idx = disease_associations_all.index.intersection(mask.index[mask])
disease_assocications_shared_rejected_by_model = (disease_associations_all.loc[idx].sort_values(
    'score', ascending=False))
disease_assocications_shared_rejected_by_model.head(20)

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mask = disease_assocications_shared_rejected_by_model.loc[idx, 'score'] >= 2.0
disease_assocications_shared_rejected_by_model.loc[idx].loc[mask]

Only significant by RSN#

mask = (scores_common[(str(args.baseline), 'rejected')] & mask_different)
mask.sum()

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idx = disease_associations_all.index.intersection(mask.index[mask])
disease_assocications_shared_rejected_by_RSN = (
    disease_associations_all
    .loc[idx]
    .sort_values('score', ascending=False))
disease_assocications_shared_rejected_by_RSN.head(20)

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mask = disease_assocications_shared_rejected_by_RSN.loc[idx, 'score'] >= 2.0
disease_assocications_shared_rejected_by_RSN.loc[idx].loc[mask]

Write to excel#

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disease_associations_all.to_excel(
    writer, sheet_name='disease_assoc_all', **writer_args)
disease_assocications_new.to_excel(
    writer, sheet_name='disease_assoc_new', **writer_args)
disease_assocications_new_rejected.to_excel(
    writer, sheet_name='disease_assoc_new_rejected', **writer_args)

Outputs#

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writer.close()
files_out