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import streamlit as st |
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import pandas as pd |
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from os import listdir |
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import plotly.graph_objects as go |
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gene_names_eve = [file.split('_')[0] for file in listdir('./CPT1_score_EVE_set/')] |
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gene_names_no_eve1 = [file.split('_')[0] for file in listdir('./CPT1_score_no_EVE_set_1/')] |
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gene_names_no_eve2 = [file.split('_')[0] for file in listdir('./CPT1_score_no_EVE_set_2/')] |
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st.subheader('CPT-1') |
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st.markdown('Cross-protein transfer learning for variant effect prediction') |
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st.markdown('This is a lookup tool for the variant effect preditions of CPT-1 for 18,602 human proteins, initially released with the manuscript "Cross-protein transfer learning substantially improves zero-shot prediction of disease variant effects (2022)".') |
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gene = st.selectbox( |
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'Which gene/protein are you interested in?', |
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gene_names_eve + gene_names_no_eve1 + gene_names_no_eve2) |
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if st.button('Show results'): |
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if gene in gene_names_eve: |
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pred = pd.read_csv('./CPT1_score_EVE_set/' + gene + '_HUMAN.csv.gz', compression = 'gzip') |
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elif gene in gene_names_no_eve1: |
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pred = pd.read_csv('./CPT1_score_no_EVE_set_1/' + gene + '_HUMAN.csv.gz', compression = 'gzip') |
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else: |
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pred = pd.read_csv('./CPT1_score_no_EVE_set_2/' + gene + '_HUMAN.csv.gz', compression = 'gzip') |
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mat = pred.copy() |
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mat['Mutant amino acid'] = mat['mutant'].str[-1] |
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mat['Position on protein sequence'] = mat['mutant'].str[:-1] |
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mat = mat.set_index('mutant') |
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mat['Position on protein sequence'] = pd.Categorical( |
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mat['Position on protein sequence'], |
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categories = mat['Position on protein sequence'].unique(), |
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ordered = True) |
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mat = mat.pivot(index='Mutant amino acid', columns='Position on protein sequence', values = mat.columns[0]) |
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fig = go.Figure() |
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fig.add_trace( |
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go.Heatmap(z = mat, y = mat.index, x = mat.columns, |
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colorbar = dict(title='Variant effect'), |
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colorscale=[[0, '#6FA8DC'], |
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[0.3, '#CFE2F3'], |
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[0.5, '#FFFFFF'], |
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[0.7, '#F4CCCC'], |
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[1.0, '#BA1111']], |
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hovertemplate='Wild-type amino acid and position: %{x}\ |
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<br>Mutant amino acid: %{y}\ |
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<br>Prediction: %{z}<extra></extra>') |
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) |
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fig.update_layout( |
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title_text = "CPT-1 variant effect prediction for " + gene + " (red: pathogenic, blue: benign)", |
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xaxis = dict( |
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title = 'Position on protein sequence', |
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rangeslider = dict(visible=True) |
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), |
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yaxis = dict( |
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title = 'Mutant amino acid' |
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), |
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yaxis_nticks = mat.shape[0], |
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height = 600 |
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) |
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st.plotly_chart(fig, theme = "streamlit", use_container_width = True, height = 600) |
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st.download_button('Download CSV', |
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pred.set_index('mutant').to_csv().encode('utf-8'), |
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gene + '_CPT_score.csv', |
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'text/csv') |
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st.markdown('</br>' |
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'<h5> Citation </h5>' |
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'Jagota, M.\*, Ye, C.\*, Rastogi, R., Albors, C., Koehl, A., Ioannidis, N., and Song, Y.S.†' |
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'"Cross-protein transfer learning substantially improves zero-shot prediction of disease variant effects", ' |
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'bioRxiv (2022) </br>' |
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'\*These authors contributed equally to this work. </br>' |
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'† To whom correspondence should be addressed: yss@berkeley.edu </br>' |
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'DOI: https://doi.org/10.1101/2022.11.15.516532', |
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unsafe_allow_html = True) |
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