Phenotype driven molecular genetic test recommendation for diagnosing pediatric rare disorders

Patients with rare diseases often experience prolonged diagnostic delays. Ordering appropriate genetic tests is crucial yet challenging, especially for general pediatricians without genetic expertise. Recent American College of Medical Genetics (ACMG) guidelines embrace early use of exome sequencing (ES) or genome sequencing (GS) for conditions like congenital anomalies or developmental delays while still recommend gene panels for patients exhibiting strong manifestations of a specific disease. Recognizing the difficulty in navigating these options, we developed a machine learning model trained on 1005 patient records from Columbia University Irving Medical Center to recommend appropriate genetic tests based on the phenotype information. The model achieved a remarkable performance with an AUROC of 0.823 and AUPRC of 0.918, aligning closely with decisions made by genetic specialists, and demonstrated strong generalizability (AUROC:0.77, AUPRC: 0.816) in an external cohort, indicating its potential value for general pediatricians to expedite rare disease diagnosis by enhancing genetic test ordering.

Authors

Institutions

Publication Details

Journal
npj Digital Medicine
Published
2024-11-21
DOI
https://doi.org/10.1038/s41746-024-01331-1
Citations
11
Primary Topic
Genomics and Rare Diseases
Type
article
Field-Weighted Citation Impact
6.05

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Phenotype driven molecular genetic test recommendation for diagnosing pediatric rare disorders

Chunhua Weng, Wendy K. Chung, Priyanka Ahimaz, Sarah E. Sheppard et al.
11 citations
npj Digital Medicine
Genomics and Rare Diseases
6.05
article

Phenotype driven molecular genetic test recommendation for diagnosing pediatric rare disorders

Chunhua Weng, Wendy K. Chung, Priyanka Ahimaz, Sarah E. Sheppard, Casey Ta, Ian M. Campbell, Fangyi Chen, Cong Liu, Kai Wang, Nga Nguyen, Rachel Lewis, Katherine M. Szigety
article en
11 citations

Abstract

Patients with rare diseases often experience prolonged diagnostic delays. Ordering appropriate genetic tests is crucial yet challenging, especially for general pediatricians without genetic expertise. Recent American College of Medical Genetics (ACMG) guidelines embrace early use of exome sequencing (ES) or genome sequencing (GS) for conditions like congenital anomalies or developmental delays while still recommend gene panels for patients exhibiting strong manifestations of a specific disease. Recognizing the difficulty in navigating these options, we developed a machine learning model trained on 1005 patient records from Columbia University Irving Medical Center to recommend appropriate genetic tests based on the phenotype information. The model achieved a remarkable performance with an AUROC of 0.823 and AUPRC of 0.918, aligning closely with decisions made by genetic specialists, and demonstrated strong generalizability (AUROC:0.77, AUPRC: 0.816) in an external cohort, indicating its potential value for general pediatricians to expedite rare disease diagnosis by enhancing genetic test ordering.

npj Digital MedicineVol. 7(1)
Boston Children's Hospital (US), Children's Hospital of Philadelphia (US), Harvard University (US), Columbia University Irving Medical Center (US), Columbia University (US), University of Pennsylvania (US)
National Institutes of Health, National Human Genome Research Institute, National Center for Advancing Translational Sciences
Openalex Percentile: Top 3%
Genomics and Rare Diseases
6.05
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.