title	emoji	sdk	sdk_version	app_file	python_version	pinned
PhenoGenius	genie	streamlit	1.25.0	phenogenius_app.py	3.8	true

PhenoGenius

Symptom interaction modeling for precision medicine

Overview

Symptom interaction model provide a method to standardize clinical descriptions and fully exploit phenotypic data in precision medicine.

This repository contains scripts and files to use PhenoGenius, the phenotype matching system for genetic disease based on this model. Please try PhenoGenius in the cloud at https://huggingface.co/spaces/kyauy/PhenoGenius.

If you use PhenoGenius, please cite:

Yauy et al., Learning phenotypic patterns in genetic disease by symptom interaction modeling. medrXiv (2023). https://doi.org/10.1101/2022.07.29.22278181

Install

• Requirements

python == 3.8 #(pyenv install 3.8)
poetry #(https://python-poetry.org/docs/#installation)

• Install dependencies

poetry install

Use streamlit webapp in your desktop

Run

poetry shell
streamlit run phenogenius_app.py

Use command-line client

Run

poetry shell
python phenogenius_cli.py --hpo_list HP:0000107,HP:0000108,HP:0001407,HP:0005562 --result_file PKD1.tsv

Usage: phenogenius_cli.py [OPTIONS]

Options:
  --version           Show the version and exit.
  --result_file TEXT  Output file name, default = match.tsv
  --hpo_list TEXT     (Mandatory) List of HPO terms to match, separated with
                      commas
  --gene_list TEXT    (Optional) List of genes in NCBI ID format to match,
                      separated with commas

Field	Description
gene_id	NCBI gene identifier
gene_symbol	HGNC gene symbol
rank	Output line position, from the most to the less "phenotype matching" (integer)
score	“Phenotype matching”: confidence of the symptoms gene association. The higher it is, the higher this confidence (float)
hpo_implicated	List of HPO IDs associated to the gene (scores correspond to confidence to each HPO gene association)
hpo_description_implicated	List of HPO names associated to the gene
phenotype_specificity	Phenotype specificity into one of "A", "B", "C" or "D"
	A - Highly specific and relatively unique to the gene (top 40, 50% of diagnosis in PhenoGenius cohort)
	B - Consistent with the gene, highly specific, but not unique (top 250, 75% of diagnosis in PhenoGenius cohort)
	C - Limited association, not highly specific or with high genetic heterogeneity
	D - Not consistent with what is expected for the gene/genomic region or not consistent in general

Explore interactive graphs of symptoms interactions

Human Phenotype Ontology

Click on the image!

Groups of interacting symptoms

Click on the image!

Enjoy !

License

PhenoGenius is licensed under the Apache License, Version 2.0. See LICENSE for the full license text.

Misc

PhenoGenius is a collaboration of :