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David A Clifton

Publications and source records attributed to David A Clifton.

2 recordsLinked to original sources

Preserving Patient Privacy while Training a Predictive Model of In-hospital Mortality

Machine learning models can be used for pattern recognition in medical data in order to improve patient outcomes, such as the prediction of in-hospital mortality. Deep learning models, in particular, require large amounts of data for model training. However, the data is often collected at different hospitals and sharing is restricted due to patient privacy concerns. In this paper, we aimed to demonstrate the potential of distributed training in achieving state-of-the-art performance while maintaining data privacy. Our results show that training the model in the federated learning framework leads to comparable performance to the traditional centralised setting. We also suggest several considerations for the success of such frameworks in future work.

cs.LG

Identifying lineage effects when controlling for population structure improves power in bacterial association studies

Bacteria pose unique challenges for genome-wide association studies (GWAS) because of strong structuring into distinct strains and substantial linkage disequilibrium across the genome. While methods developed for human studies can correct for strain structure, this risks considerable loss- of-power because genetic differences between strains often contribute substantial phenotypic variability. Here we propose a new method that captures lineage-level associations even when locus-specific associations cannot be fine-mapped. We demonstrate its ability to detect genes and genetic variants underlying resistance to 17 antimicrobials in 3144 isolates from four taxonomically diverse clonal and recombining bacteria: Mycobacterium tuberculosis, Staphylococcus aureus, Escherichia coli and Klebsiella pneumoniae. Strong selection, recombination and penetrance confer high power to recover known antimicrobial resistance mechanisms, and reveal a candidate association between the outer membrane porin nmpC and cefazolin resistance in E. coli. Hence our method pinpoints locus-specific effects where possible, and boosts power by detecting lineage-level differences when fine-mapping is intractable.

q-bio.GN