emilyalsentzer commited on
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5b2b768
1 Parent(s): d042411

Update app.py

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Files changed (1) hide show
  1. app.py +1 -13
app.py CHANGED
@@ -3,18 +3,6 @@ import pandas as pd
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  from pathlib import Path
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  import ast
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- '''
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- Causal Gene Discovery Model
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- /home/ema30/zaklab/rare_disease_dx/checkpoints/aligner/04_30_22:13:29:55_lr_1e-05_val_simulated_pats.disease_split_val_sim_pats_kg_8.9.21_kg_losstype_gene_multisimilarity/all_udn_patients_kg_8.9.21_kgsolved_manual_baylor_nobgm_distractor_genes_5_candidates_mapped_only_genes
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-
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- Patients-Like-Me Model
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- /home/ema30/zaklab/rare_disease_dx/checkpoints/patient_NCA/04_26_22:17:38:30_lr_5e-05_val_simulated_pats.disease_split_val_sim_pats_kg_8.9.21_kg_losstype_patient_patient_NCA/mygene2_all_sim_all_udn_patients_kg_8.9.21_kgsolved_with_phenotypes
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-
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- Disease Characterization Model
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- /home/ema30/zaklab/rare_disease_dx/checkpoints/patient_NCA/05_13_22:08:00:32_lr_1e-05_val_simulated_pats.disease_split_val_sim_pats_kg_8.9.21_kg_losstype_pd_NCA/mygene2_all_sim_all_udn_patients_kg_8.9.21_kgsolved_with_phenotypes
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- '''
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-
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-
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  gene_scores_df = pd.read_csv('gene_discovery_scores.csv')
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  exomiser_gene_scores_df = pd.read_csv('exomiser_gene_discovery_scores.csv')
@@ -25,7 +13,7 @@ dx_attn_df = pd.read_csv('dx_characterization_scores_attn.csv')
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  gene_attn_df = pd.read_csv('gene_discovery_scores_attn.csv')
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  exomiser_gene_attn_df = pd.read_csv('exomiser_gene_discovery_scores_attn.csv')
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- diseases_map = {'UDN-P1': 'POLR3-releated leukodystrophy', 'UDN-P2': 'Novel Syndrome', 'UDN-P3':'Coffin-Lowry syndrome' ,
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  'UDN-P4': 'automsomal recessive spastic paraplegia type 76', 'UDN-P5': 'atypical presentation of familial cold autoinflammatory syndrome',
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  'UDN-P6': '*GATAD2B*-associated syndrome', 'UDN-P7': 'AR limb-girdle muscular atrophy type 2D', 'UDN-P8': '*ATP5PO*-related Leigh syndrome', 'UDN-P9': 'Spondyloepimetaphyseal dysplasia, Isidor-Toutain type'}
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  genes_map = {'UDN-P3': 'RPS6KA3', 'UDN-P4': 'CAPN1', 'UDN-P5': 'NLRP12, RAPGEFL1', 'UDN-P6': 'GATAD2B', 'UDN-P7': 'SGCA', 'UDN-P8': 'ATP5P0', 'UDN-P9': 'RPL13'}
 
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  from pathlib import Path
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  import ast
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  gene_scores_df = pd.read_csv('gene_discovery_scores.csv')
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  exomiser_gene_scores_df = pd.read_csv('exomiser_gene_discovery_scores.csv')
 
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  gene_attn_df = pd.read_csv('gene_discovery_scores_attn.csv')
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  exomiser_gene_attn_df = pd.read_csv('exomiser_gene_discovery_scores_attn.csv')
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+ diseases_map = {'UDN-P1': 'POLR3-releated leukodystrophy', 'UDN-P2': 'Novel PRKAR1B-Related Neurodevelopmental Disorder', 'UDN-P3':'Coffin-Lowry syndrome' ,
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  'UDN-P4': 'automsomal recessive spastic paraplegia type 76', 'UDN-P5': 'atypical presentation of familial cold autoinflammatory syndrome',
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  'UDN-P6': '*GATAD2B*-associated syndrome', 'UDN-P7': 'AR limb-girdle muscular atrophy type 2D', 'UDN-P8': '*ATP5PO*-related Leigh syndrome', 'UDN-P9': 'Spondyloepimetaphyseal dysplasia, Isidor-Toutain type'}
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  genes_map = {'UDN-P3': 'RPS6KA3', 'UDN-P4': 'CAPN1', 'UDN-P5': 'NLRP12, RAPGEFL1', 'UDN-P6': 'GATAD2B', 'UDN-P7': 'SGCA', 'UDN-P8': 'ATP5P0', 'UDN-P9': 'RPL13'}