Biologically Enhanced Machine Learning Model to uncover Novel Gene-Drug Targets for Alzheimer’s Disease

Given the complexity and multifactorial nature of Alzheimer's disease, investigating potential drug-gene targets is imperative for developing effective therapies and advancing our understanding of the underlying mechanisms driving the disease. We present an explainable ML model that integrates the role and impact of gene interactions to drive the genomic variant feature selection. The model leverages both the Alzheimer's knowledge base and the Drug-Gene interaction database (DGIdb) to identify a list of biologically plausible novel gene-drug targets for further investigation. Model validation is performed on an ethnically diverse study sample obtained from the Alzheimer's Disease Sequencing Project (ADSP), a multi-ancestry multi-cohort genomic study. To mitigate population stratification and spurious associations from ML analysis, we implemented novel data curation methods. The study outcomes include a set of possible gene targets for further functional follow-up and drug repurposing.

Authors

Institutions

Publication Details

Published
2024-11-21
DOI
https://doi.org/10.1142/9789819807024_0032
Citations
2
Primary Topic
Genetics, Bioinformatics, and Biomedical Research
Type
article
Field-Weighted Citation Impact
0.47
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Biologically Enhanced Machine Learning Model to uncover Novel Gene-Drug Targets for Alzheimer’s Disease

Jason H. Moore, Alena Orlenko, Tayo Obafemi-Ajayi, Mythreye Venkatesan et al.
2 citations
Genetics, Bioinformatics, and Biomedical Research
0.47
article

Biologically Enhanced Machine Learning Model to uncover Novel Gene-Drug Targets for Alzheimer’s Disease

Jason H. Moore, Alena Orlenko, Tayo Obafemi-Ajayi, Mythreye Venkatesan, Zhiping Paul Wang, Li Shen, Marylyn DeRiggi Ritchie
article en
2 citations

Abstract

Given the complexity and multifactorial nature of Alzheimer's disease, investigating potential drug-gene targets is imperative for developing effective therapies and advancing our understanding of the underlying mechanisms driving the disease. We present an explainable ML model that integrates the role and impact of gene interactions to drive the genomic variant feature selection. The model leverages both the Alzheimer's knowledge base and the Drug-Gene interaction database (DGIdb) to identify a list of biologically plausible novel gene-drug targets for further investigation. Model validation is performed on an ethnically diverse study sample obtained from the Alzheimer's Disease Sequencing Project (ADSP), a multi-ancestry multi-cohort genomic study. To mitigate population stratification and spurious associations from ML analysis, we implemented novel data curation methods. The study outcomes include a set of possible gene targets for further functional follow-up and drug repurposing.

Vol. 30
Missouri State University (US), Cedars-Sinai Medical Center (US), University of Pennsylvania (US)
Openalex Percentile: Top 34%
Genetics, Bioinformatics, and Biomedical Research
0.47
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.