Evidence map›Paper›PMID 38835075›Full record

ArticleGenome medicine2024

Optimizing clinico-genomic disease prediction across ancestries: a machine learning strategy with Pareto improvement.

Yan Gao, Yan Cui

Abstract read
In one paragraph

Article in Genome medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Yan GaoDepartment of Genetics, Genomics and Informatics, University of Tennessee Health Science Center, Memphis, TN, 38163, USA.
Yan CuiDepartment of Genetics, Genomics and Informatics, University of Tennessee Health Science Center, Memphis, TN, 38163, USA. ycui2@uthsc.edu.ORCID 0000-0002-7577-6845

Funding

Algorithm-based prevention and reduction of differences in cancer outcomes arising from data imbalanceR01CA262296 · NCI · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI CUI, YAN · 2021 to 2025
$1.7M
Division of Cancer Epidemiology and Genetics, National Cancer Institute R01CA262296NCI NIH HHS R01 CA262296
6 · The paper itself

Abstract

backgroundAccurate prediction of an individual's predisposition to diseases is vital for preventive medicine and early intervention. Various statistical and machine learning models have been developed for disease prediction using clinico-genomic data. However, the accuracy of clinico-genomic prediction of diseases may vary significantly across ancestry groups due to their unequal representation in clinical genomic datasets.

methodsWe introduced a deep transfer learning approach to improve the performance of clinico-genomic prediction models for data-disadvantaged ancestry groups. We conducted machine learning experiments on multi-ancestral genomic datasets of lung cancer, prostate cancer, and Alzheimer's disease, as well as on synthetic datasets with built-in data inequality and distribution shifts across ancestry groups.

resultsDeep transfer learning significantly improved disease prediction accuracy for data-disadvantaged populations in our multi-ancestral machine learning experiments. In contrast, transfer learning based on linear frameworks did not achieve comparable improvements for these data-disadvantaged populations.

conclusionsThis study shows that deep transfer learning can enhance fairness in multi-ancestral machine learning by improving prediction accuracy for data-disadvantaged populations without compromising prediction accuracy for other populations, thus providing a Pareto improvement towards equitable clinico-genomic prediction of diseases.

Indexed as

GenomicsMachine LearningAlzheimer DiseaseGenetic Predisposition to DiseaseHumansLung NeoplasmsMaleProstatic NeoplasmsDeep neural networkDisease predictionHealth equityTransfer learning

Identifiers

PMID38835075
PMCPMC11149372

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.