Compare outcomes from differential analysis based on different imputation methods#

  • load scores based on 10_1_ald_diff_analysis

Hide code cell source

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 = "RF"
out_folder = "diff_analysis"
annotaitons_gene_col = "None"

Add set parameters to configuration

Hide code cell source

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': 'RF',
 'out_figures': PosixPath('runs/alzheimer_study/figures'),
 'out_folder': PosixPath('runs/alzheimer_study/diff_analysis/AD/PI_vs_RF'),
 '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_RF/diff_analysis_compare_methods.xlsx

Load scores#

Load baseline model scores#

Show all statistics, later use selected statistics

Hide code cell source

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#

Hide code cell source

fname = args.scores_folder / f'diff_analysis_scores_{args.model_key}.pkl'
scores_model = pd.read_pickle(fname)
scores_model
model RF
var SS DF F p-unc np2 -Log10 pvalue qvalue rejected
protein groups Source
A0A024QZX5;A0A087X1N8;P35237 AD 1.010 1 7.629 0.006 0.038 2.200 0.019 True
age 0.002 1 0.017 0.896 0.000 0.048 0.934 False
Kiel 0.206 1 1.559 0.213 0.008 0.671 0.339 False
Magdeburg 0.388 1 2.933 0.088 0.015 1.053 0.169 False
Sweden 1.521 1 11.489 0.001 0.057 3.070 0.003 True
... ... ... ... ... ... ... ... ... ...
S4R3U6 AD 1.041 1 2.252 0.135 0.012 0.869 0.238 False
age 0.807 1 1.746 0.188 0.009 0.726 0.308 False
Kiel 1.830 1 3.958 0.048 0.020 1.318 0.103 False
Magdeburg 1.832 1 3.963 0.048 0.020 1.319 0.103 False
Sweden 12.678 1 27.419 0.000 0.126 6.367 0.000 True

7105 rows × 8 columns

Combined scores#

show only selected statistics for comparsion

Hide code cell source

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 PI RF
var p-unc -Log10 pvalue qvalue rejected p-unc -Log10 pvalue qvalue rejected
protein groups Source
A0A024QZX5;A0A087X1N8;P35237 AD 0.240 0.620 0.397 False 0.006 2.200 0.019 True
Kiel 0.045 1.347 0.112 False 0.213 0.671 0.339 False
Magdeburg 0.005 2.274 0.020 True 0.088 1.053 0.169 False
Sweden 0.000 3.574 0.002 True 0.001 3.070 0.003 True
age 0.620 0.207 0.750 False 0.896 0.048 0.934 False
... ... ... ... ... ... ... ... ... ...
S4R3U6 AD 0.469 0.328 0.623 False 0.135 0.869 0.238 False
Kiel 0.961 0.017 0.976 False 0.048 1.318 0.103 False
Magdeburg 0.105 0.978 0.218 False 0.048 1.319 0.103 False
Sweden 0.000 3.878 0.001 True 0.000 6.367 0.000 True
age 0.185 0.734 0.328 False 0.188 0.726 0.308 False

7105 rows × 8 columns

Models in comparison (name mapping)

Hide code cell source

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

Describe scores#

Hide code cell source

scores.describe()
model PI RF
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 0.261 2.476 0.338 0.233 3.079 0.291
std 0.303 5.328 0.331 0.295 5.788 0.323
min 0.000 0.000 0.000 0.000 0.000 0.000
25% 0.004 0.335 0.016 0.001 0.388 0.003
50% 0.121 0.916 0.243 0.071 1.149 0.142
75% 0.463 2.411 0.617 0.409 3.086 0.546
max 0.999 146.241 0.999 1.000 84.835 1.000

One to one comparison of by feature:#

Hide code cell source

scores = scores.loc[pd.IndexSlice[:, args.target], :]
scores.to_excel(writer, 'scores', **writer_args)
scores
/tmp/ipykernel_88901/3761369923.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 PI RF
var p-unc -Log10 pvalue qvalue rejected p-unc -Log10 pvalue qvalue rejected
protein groups Source
A0A024QZX5;A0A087X1N8;P35237 AD 0.240 0.620 0.397 False 0.006 2.200 0.019 True
A0A024R0T9;K7ER74;P02655 AD 0.059 1.228 0.139 False 0.031 1.511 0.072 False
A0A024R3W6;A0A024R412;O60462;O60462-2;O60462-3;O60462-4;O60462-5;Q7LBX6;X5D2Q8 AD 0.040 1.393 0.103 False 0.403 0.395 0.540 False
A0A024R644;A0A0A0MRU5;A0A1B0GWI2;O75503 AD 0.420 0.377 0.580 False 0.257 0.591 0.390 False
A0A075B6H7 AD 0.027 1.567 0.075 False 0.009 2.051 0.026 True
... ... ... ... ... ... ... ... ... ...
Q9Y6R7 AD 0.175 0.756 0.316 False 0.175 0.756 0.292 False
Q9Y6X5 AD 0.070 1.155 0.159 False 0.203 0.692 0.327 False
Q9Y6Y8;Q9Y6Y8-2 AD 0.083 1.079 0.182 False 0.083 1.079 0.162 False
Q9Y6Y9 AD 0.348 0.459 0.512 False 0.328 0.484 0.468 False
S4R3U6 AD 0.469 0.328 0.623 False 0.135 0.869 0.238 False

1421 rows × 8 columns

And the descriptive statistics of the numeric values:

Hide code cell source

scores.describe()
model PI RF
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 0.252 1.411 0.334 0.246 1.519 0.311
std 0.291 1.654 0.316 0.293 1.759 0.317
min 0.000 0.001 0.000 0.000 0.001 0.000
25% 0.013 0.368 0.041 0.009 0.374 0.027
50% 0.121 0.917 0.242 0.101 0.997 0.188
75% 0.428 1.899 0.588 0.423 2.030 0.559
max 0.999 25.104 0.999 0.998 18.758 0.998

and the boolean decision values

Hide code cell source

scores.describe(include=['bool', 'O'])
model PI RF
var rejected rejected
count 1421 1421
unique 2 2
top False False
freq 1031 961

Load frequencies of observed features#

Hide code cell source

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#

Hide code cell source

scores_common = (scores
                 .dropna()
                 .reset_index(-1, drop=True)
                 ).join(
    freq_feat, how='left'
)
scores_common
PI RF data
p-unc -Log10 pvalue qvalue rejected p-unc -Log10 pvalue qvalue rejected frequency
protein groups
A0A024QZX5;A0A087X1N8;P35237 0.240 0.620 0.397 False 0.006 2.200 0.019 True 186
A0A024R0T9;K7ER74;P02655 0.059 1.228 0.139 False 0.031 1.511 0.072 False 195
A0A024R3W6;A0A024R412;O60462;O60462-2;O60462-3;O60462-4;O60462-5;Q7LBX6;X5D2Q8 0.040 1.393 0.103 False 0.403 0.395 0.540 False 174
A0A024R644;A0A0A0MRU5;A0A1B0GWI2;O75503 0.420 0.377 0.580 False 0.257 0.591 0.390 False 196
A0A075B6H7 0.027 1.567 0.075 False 0.009 2.051 0.026 True 91
... ... ... ... ... ... ... ... ... ...
Q9Y6R7 0.175 0.756 0.316 False 0.175 0.756 0.292 False 197
Q9Y6X5 0.070 1.155 0.159 False 0.203 0.692 0.327 False 173
Q9Y6Y8;Q9Y6Y8-2 0.083 1.079 0.182 False 0.083 1.079 0.162 False 197
Q9Y6Y9 0.348 0.459 0.512 False 0.328 0.484 0.468 False 119
S4R3U6 0.469 0.328 0.623 False 0.135 0.869 0.238 False 126

1421 rows × 9 columns

Annotate decisions in Confusion Table style:#

Hide code cell source

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
PI (no)  - RF (no)    896
PI (yes) - RF (yes)   325
PI (no)  - RF (yes)   135
PI (yes) - RF (no)     65
Name: count, dtype: int64

List different decisions between models#

Hide code cell source

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_88901/1417621106.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'.
PI RF data
p-unc -Log10 pvalue qvalue rejected p-unc -Log10 pvalue qvalue rejected frequency
protein groups
A0A024QZX5;A0A087X1N8;P35237 0.240 0.620 0.397 False 0.006 2.200 0.019 True 186
A0A075B6H7 0.027 1.567 0.075 False 0.009 2.051 0.026 True 91
A0A075B6I0 0.023 1.641 0.066 False 0.001 3.146 0.003 True 194
A0A075B6J9 0.028 1.552 0.077 False 0.019 1.713 0.049 True 156
A0A075B6R2 0.259 0.587 0.419 False 0.002 2.734 0.007 True 164
... ... ... ... ... ... ... ... ... ...
Q9UKB5 0.014 1.861 0.044 True 0.474 0.324 0.606 False 148
Q9ULZ9 0.003 2.460 0.014 True 0.071 1.150 0.142 False 171
Q9UNW1 0.016 1.803 0.049 True 0.920 0.036 0.950 False 171
Q9UP79 0.316 0.501 0.480 False 0.000 3.777 0.001 True 135
Q9UQ52 0.034 1.473 0.089 False 0.001 3.082 0.003 True 188

200 rows × 9 columns

Plot qvalues of both models with annotated decisions#

Prepare data for plotting (qvalues)

Hide code cell source

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
PI RF frequency Differential Analysis Comparison
protein groups
A0A024QZX5;A0A087X1N8;P35237 0.397 0.019 186 PI (no) - RF (yes)
A0A024R0T9;K7ER74;P02655 0.139 0.072 195 PI (no) - RF (no)
A0A024R3W6;A0A024R412;O60462;O60462-2;O60462-3;O60462-4;O60462-5;Q7LBX6;X5D2Q8 0.103 0.540 174 PI (no) - RF (no)
A0A024R644;A0A0A0MRU5;A0A1B0GWI2;O75503 0.580 0.390 196 PI (no) - RF (no)
A0A075B6H7 0.075 0.026 91 PI (no) - RF (yes)
... ... ... ... ...
Q9Y6R7 0.316 0.292 197 PI (no) - RF (no)
Q9Y6X5 0.159 0.327 173 PI (no) - RF (no)
Q9Y6Y8;Q9Y6Y8-2 0.182 0.162 197 PI (no) - RF (no)
Q9Y6Y9 0.512 0.468 119 PI (no) - RF (no)
S4R3U6 0.623 0.238 126 PI (no) - RF (no)

1421 rows × 4 columns

List of features with the highest difference in qvalues

Hide code cell source

# 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)
PI RF frequency Differential Analysis Comparison diff_qvalue
protein groups
P55268 0.999 0.049 194 PI (no) - RF (yes) 0.949
F6VDH7;P50502;Q3KNR6 0.011 0.958 175 PI (yes) - RF (no) 0.946
P17302 0.942 0.002 135 PI (no) - RF (yes) 0.939
A0A087X1Z2;C9JTV4;H0Y4Y4;Q8WYH2;Q96C19;Q9BUP0;Q9BUP0-2 0.004 0.939 66 PI (yes) - RF (no) 0.935
A0A087WU43;A0A087WX17;A0A087WXI5;P12830;P12830-2 0.931 0.001 134 PI (no) - RF (yes) 0.929
... ... ... ... ... ...
O15354 0.059 0.050 197 PI (no) - RF (yes) 0.009
Q9NX62 0.056 0.047 197 PI (no) - RF (yes) 0.009
P00740;P00740-2 0.053 0.044 197 PI (no) - RF (yes) 0.008
K7ERG9;P00746 0.052 0.044 197 PI (no) - RF (yes) 0.008
Q16706 0.046 0.054 195 PI (yes) - RF (no) 0.008

200 rows × 5 columns

Differences plotted with created annotations#

Hide code cell source

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_RF/diff_analysis_comparision_1_RF
../../../_images/4dea7fb7a99fb55ce8797d28767d861301cc51b3ef3587e8a83906eb268be4c6.png
  • also showing how many features were measured (“observed”) by size of circle

Hide code cell source

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_RF/diff_analysis_comparision_2_RF
../../../_images/a3de51cf84c5b05154a894a5c31452e23cd575af5c88054eb7ff338fd8ffb27d.png

Only features contained in model#

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

Hide code cell source

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.

Hide code cell source

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

Hide code cell source

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

Hide code cell source

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()

Hide code cell source

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

only by model#

Hide code cell source

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)

Hide code cell source

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

Only by model which were significant#

Hide code cell source

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)

Hide code cell source

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()

Hide code cell source

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)

Hide code cell source

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()

Hide code cell source

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)

Hide code cell source

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#

Hide code cell source

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#

Hide code cell source

writer.close()
files_out