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Samuel F. Feng

Publications and source records attributed to Samuel F. Feng.

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Benchmarking end-to-end genotype-to-phenotype prediction workflows across 80 openSNP phenotypes

Genotype-to-phenotype prediction is a central goal of statistical genetics, yet practical comparisons of prediction workflows remain limited in small, heterogeneous, participant-shared genomic datasets. Here, we benchmarked end-to-end case-control prediction across 80 curated binary phenotypes from openSNP using machine learning, deep learning, and polygenic score workflows. We evaluated 29 machine-learning algorithms, 80 deep-learning model variants, and 3 polygenic score tools across 675 clumping and pruning configurations. No workflow family dominated universally. Polygenic score workflows achieved the highest observed discrimination for 53 phenotypes, whereas machine-learning or deep-learning workflows achieved the highest for 27. However, many apparent phenotype-level wins were modest, with 41.2\% of comparisons representing practical ties within five discrimination points. Performance was strongly phenotype-dependent and sensitive to modeling and preprocessing choices. Distinct workflow-specific failure modes were also observed, including unstable behaviour in PRSice and non-informative collapse in lassosum for 13 phenotypes. Higher peak performance was concentrated in smaller phenotypes, reinforcing the need for cautious interpretation in limited-data settings. The cohort was predominantly of European ancestry, restricting generalisability. Together, these results position openSNP as a useful stress-test environment for genomic prediction and support benchmark-guided workflow selection under realistic conditions of data scarcity, phenotype heterogeneity, and ancestry imbalance.

q-bio.GN

Deep learning pipeline for image classification on mobile phones

This article proposes and documents a machine-learning framework and tutorial for classifying images using mobile phones. Compared to computers, the performance of deep learning model performance degrades when deployed on a mobile phone and requires a systematic approach to find a model that performs optimally on both computers and mobile phones. By following the proposed pipeline, which consists of various computational tools, simple procedural recipes, and technical considerations, one can bring the power of deep learning medical image classification to mobile devices, potentially unlocking new domains of applications. The pipeline is demonstrated on four different publicly available datasets: COVID X-rays, COVID CT scans, leaves, and colorectal cancer. We used two application development frameworks: TensorFlow Lite (real-time testing) and Flutter (digital image testing) to test the proposed pipeline. We found that transferring deep learning models to a mobile phone is limited by hardware and classification accuracy drops. To address this issue, we proposed this pipeline to find an optimized model for mobile phones. Finally, we discuss additional applications and computational concerns related to deploying deep-learning models on phones, including real-time analysis and image preprocessing. We believe the associated documentation and code can help physicians and medical experts develop medical image classification applications for distribution.

eess.IV

A martingale analysis of first passage times of time-dependent Wiener diffusion models

Research in psychology and neuroscience has successfully modeled decision making as a process of noisy evidence accumulation to a decision bound. While there are several variants and implementations of this idea, the majority of these models make use of a noisy accumulation between two absorbing boundaries. A common assumption of these models is that decision parameters, e.g., the rate of accumulation (drift rate), remain fixed over the course of a decision, allowing the derivation of analytic formulas for the probabilities of hitting the upper or lower decision threshold, and the mean decision time. There is reason to believe, however, that many types of behavior would be better described by a model in which the parameters were allowed to vary over the course of the decision process. In this paper, we use martingale theory to derive formulas for the mean decision time, hitting probabilities, and first passage time (FPT) densities of a Wiener process with time-varying drift between two time-varying absorbing boundaries. This model was first studied by Ratcliff (1980) in the two-stage form, and here we consider the same model for an arbitrary number of stages (i.e. intervals of time during which parameters are constant). Our calculations enable direct computation of mean decision times and hitting probabilities for the associated multistage process. We also provide a review of how martingale theory may be used to analyze similar models employing Wiener processes by re-deriving some classical results. In concert with a variety of numerical tools already available, the current derivations should encourage mathematical analysis of more complex models of decision making with time-varying evidence.

math.PR