iderare-pheno 0.5.0

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IDeRare-Pheno

IDeRare or "Indonesia Exome Rare Disease Variant Discovery Pipeline" is a simple and ready to use variant discovery pipeline to discover rare disease variants from exome sequencing data.

This repository is the first part of IDeRare workflow for phenotype analysis. For complete pipeline for phenotype-genotype analysis, kindly refer to IDeRare Github repository.

Authored by

Ivan William Harsono^a, Yulia Ariani^b, Beben Benyamin^c,d,e, Fadilah Fadilah^f,g, Dwi Ari Pujianto^b, Cut Nurul Hafifah^h

^aDoctoral Program in Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.
^bDepartment of Medical Biology, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.
^cAustralian Centre for Precision Health, University of South Australia, Adelaide, SA, 5000, Australia.
^dUniSA Allied Health and Human Performance, University of South Australia, Adelaide, SA, 5000, Australia.
^eSouth Australian Health and Medical Research Institute (SAHMRI), University of South Australia, Adelaide, SA, 5000, Australia.
^fDepartment of Medical Chemistry, Faculty of Medicine, Universitas Indonesia, Jalan Salemba Raya number 4, Jakarta, 10430, Indonesia.
^gBioinformatics Core Facilities - IMERI, Faculty of Medicine, Universitas Indonesia, Jalan Salemba Raya number 6, Jakarta, 10430, Indonesia .
^hDepartment of Child Health, Dr. Cipto Mangunkusumo Hospital, Faculty of Medicine, University of Indonesia, Jakarta, Indonesia.

Note: Currently IDeRare paper is being considered journal submission. The citation will be updated once the paper is published.

Quick links

• Documentation
• PyPI Package
• License
• Interactive Playbook Example
• Interactive Webapps Implementation of at Streamlit

What does it do?

This script is recommended if you would like to do conversion, linkage analysis, similarity scoring, and gene-disease recommendation based on the phenotype data provided at clinical_data.txt. Full feature :

1. Convert the phenotype data to HPO code (accept mixed SNOMED, LOINC, and HPO code)
2. Similarity scoring of differential diagnosis
3. Linkage analysis of differential diagnosis (accept mixed SNOMED, ICD-10, ORPHA, OMIM code), include dendrogram tree visualization.
   • This should help clinician to systematically doing work-up and excluding similar diagnosis together based on the patient's phenotype.
4. Gene and disease recommendation based on the phenotype data similarity scoring between phenotype and OMIM gene and disease databank.
5. Linkage analysis of recommended causative gene and disease based on phenotype data (include dendrogram tree visualization).
   • This should help clinician to explore / enrich their differential diagnosis based on the patient's phenotype.
6. Example of the clinical data provided at Clinical Information Example section

Installation

iderare-pheno requires Python 3.8 or later.

Installing with pip

iderare-pheno is available on PyPI. Just run

pip install iderare-pheno

Installing from source

To install iderare-pheno from source, first clone the repository:

git clone https://github.com/ivanwilliammd/iderare-pheno.git
cd iderare_pheno

Then run

pip install -e .

Importing the library

from iderare_pheno.converter import term2omim, term2orpha, term2hpo, batchconvert
from iderare_pheno.simrec import hpo2omim_similarity, omim_recommendation, hpo2name
from iderare_pheno.utils import linkage_dendrogram, list2tsv, generate_yml

As the complete readthedocs.io is still ongoing, please kindly refer to this Interactive Playbook Example

Team

iderare-pheno is developed and maintained by the author(s), To learn more about who specifically contributed to this codebase, see our contributors page.

License

iderare-pheno license is derived from IDeRare