Human GeneticsGeneticsPeer-reviewed journal article
Evaluation of enzyme activity predictions for variants of unknown significance in Arylsulfatase A
Shantanu JainiD, Marena I. TrinidadiD, Thanh NguyeniD, Kaiya Jones, Santiago Diaz Neto, Fang GeiD, Ailin Glagovsky, Cameron Jones, Giankaleb Moran, Boqi Wang, Kobra Rahimi, Sümeyra Zeynep ÇalıcıiD, Luis R. CedilloiD, Silvia BerardelliiD, Buse ÖzdeniD, Ken CheniD, Panagiotis KatsonisiD, Amanda M. WilliamsiD, Olivier LichtargeiD, Sadhna RanaiD, Swatantra Pradhan, Rajgopal Srinivasan, Rakshanda Sajeed, Dinesh Joshi, Eshel FaraggiiD, , Wyatt Travis ClarkiD
Abstract
Continued advances in variant effect prediction are necessary to demonstrate the ability of machine learning methods to accurately determine the clinical impact of variants of unknown significance (VUS). Towards this goal, the ARSA Critical Assessment of Genome Interpretation (CAGI) challenge was designed to characterize progress by utilizing 219 experimentally assayed missense VUS in the Arylsulfa-tase A (ARSA) gene to assess the performance of community-submitted predictions of variant functional effects. The challenge involved 15 teams, and evaluated additional predictions from established and recently released models. Notably, a model developed by participants of a genetics and coding bootcamp, trained with standard machine-learning tools in Python, demonstrated superior performance among sub-missions. Furthermore, the study observed that state-of-the-art deep learning methods provided small but statistically significant improvement in predictive performance compared to less elaborate techniques. These findings underscore the utility of variant effect prediction, and the potential for models trained with modest resources to accurately classify VUS in genetic and clinical research.
- organism: human
- assay: whole-exome sequencing
- research focus: variant effect prediction
- approach: machine learning (classical)
- approach: deep learning
- Citations
- 4
- FWCI
- 1.18
- Field percentile
- top 28%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Predicting the impact of rare variants on RNA splicing in CAGI6
Jenny Lord, Carolina Jaramillo Oquendo, … Diana Baralle·Human GeneticsPeer-reviewed·Jan 3, 2024
- Critical assessment of missense variant effect predictors on disease-relevant variant data
Ruchir Rastogi, Ryan Chung, … Nilah M. Ioannidis·Human GeneticsPeer-reviewed·Mar 1, 2025
- Variant pathogenic prediction models VSRFM and VSRFM-s, the importance of splicing and allele frequency.
José Luis Cabrera-Alarcón, Jorge García–Martínez·bioRxiv·Oct 3, 2018
- Assessment of variant effect predictors unveils variants difficulty as a critical performance indicator
Ragousandirane Radjasandirane, Julien Diharce, … Alexandre G. de Brevern·GenomicsPeer-reviewed·Mar 22, 2025
- Genome-wide prediction of disease variants with a deep protein language model
Nadav Brandes, Grant Goldman, … Vasilis Ntranos·bioRxiv·Aug 25, 2022
- Prediction of the functional impact of missense variants in BRCA1 and BRCA2 with BRCA-ML
Steven N. Hart, Eric C. Polley, … Fergus J. Couch·npj Breast CancerPeer-reviewed·Apr 29, 2020