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Michael A Jacobs

Publications and source records attributed to Michael A Jacobs.

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Cross-Domain Federated Learning in Medical Imaging

Federated learning is increasingly being explored in the field of medical imaging to train deep learning models on large scale datasets distributed across different data centers while preserving privacy by avoiding the need to transfer sensitive patient information. In this manuscript, we explore federated learning in a multi-domain, multi-task setting wherein different participating nodes may contain datasets sourced from different domains and are trained to solve different tasks. We evaluated cross-domain federated learning for the tasks of object detection and segmentation across two different experimental settings: multi-modal and multi-organ. The result from our experiments on cross-domain federated learning framework were very encouraging with an overlap similarity of 0.79 for organ localization and 0.65 for lesion segmentation. Our results demonstrate the potential of federated learning in developing multi-domain, multi-task deep learning models without sharing data from different domains.

eess.IV

Estimating the Number of Essential Genes in Random Transposon Mutagenesis Libraries

Biologists use random transposon mutagenesis to construct knockout libraries for bacteria. Random mutagenesis offers cost and efficiency benefits over the standard site directed mutagenesis, but one can no longer ensure that all the nonessential genes will appear in the library. In random libraries for haploid organisms, there is always a class of genes for which knockout clones have not been made, and the members of this class are either essential or nonessential. One requires statistical methods to estimate the number of essential genes. Two groups of researchers, Blades and Broman and Jacobs et al., independently and simultaneously developed methods to do this. Blades and Broman used a Gibbs sampler and Jacobs et al. used a parametric bootstrap. We compare the performance of these two methods and find that they both depend on having an accurate probabilistic model for transposon insertion or on having a library with a large number of clones. At this point, we do not have good enough probabilistic models so we must build libraries that have at least five clones per open reading frame to accurately estimate the number of essential genes.

q-bio.OT