Automated Shared Phenotype Discovery in Undiagnosed Cohorts for Rare Disease Research

Rare disease diagnosis is challenging in large part due to incomplete knowledge of gene-to-phenotype associations. One way to address this is to adopt a gene-to-patient paradigm wherein one selects an in-silico predicted pathogenic variant, identifies individuals with the variant, and then determines if the individuals have a shared phenotype. Most studies following this paradigm determine presence of a shared phenotype through manual review of ontology terms in the patient record. We propose a novel automated method to identify the shared phenotype via genetic search using a fitness function that compares the similarity of phenotype term embeddings generated by advanced NLP models applied to the term's text descriptions. Leveraging Human Phenotype Ontology resources, we generated a library of simulated patients across 5,076 Mendelian diseases. Applying our approach to these simulated disease cohorts, we found that the solution phenotypes included a closely matching term for the majority of terms in the disease phenotype under variable conditions of annotation imprecision and noise. We anticipate these methods can aid gene-to-phenotype association discovery for rare diseases by enabling a scalable gene-to-patient research paradigm.

Authors

Institutions

Publication Details

Published
2024-12-18
DOI
https://doi.org/10.1109/icmla61862.2024.00154
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Automated Shared Phenotype Discovery in Undiagnosed Cohorts for Rare Disease Research

Aaron J. Masino, Ranga Baminiwatte
Genomics and Rare Diseases
article

Automated Shared Phenotype Discovery in Undiagnosed Cohorts for Rare Disease Research

Aaron J. Masino, Ranga Baminiwatte
article en

Abstract

Rare disease diagnosis is challenging in large part due to incomplete knowledge of gene-to-phenotype associations. One way to address this is to adopt a gene-to-patient paradigm wherein one selects an in-silico predicted pathogenic variant, identifies individuals with the variant, and then determines if the individuals have a shared phenotype. Most studies following this paradigm determine presence of a shared phenotype through manual review of ontology terms in the patient record. We propose a novel automated method to identify the shared phenotype via genetic search using a fitness function that compares the similarity of phenotype term embeddings generated by advanced NLP models applied to the term's text descriptions. Leveraging Human Phenotype Ontology resources, we generated a library of simulated patients across 5,076 Mendelian diseases. Applying our approach to these simulated disease cohorts, we found that the solution phenotypes included a closely matching term for the majority of terms in the disease phenotype under variable conditions of annotation imprecision and noise. We anticipate these methods can aid gene-to-phenotype association discovery for rare diseases by enabling a scalable gene-to-patient research paradigm.

Vol. 2024
Clemson University (US)
Openalex Percentile: Top 72%
Genomics and Rare Diseases
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.