<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Joseph West | NeuroEng@Usach</title><link>https://neuroeng-usach.cl/author/joseph-west/</link><atom:link href="https://neuroeng-usach.cl/author/joseph-west/index.xml" rel="self" type="application/rss+xml"/><description>Joseph West</description><generator>Hugo Blox Builder (https://hugoblox.com)</generator><language>en-us</language><lastBuildDate>Tue, 01 Sep 2026 00:00:00 +0000</lastBuildDate><image><url>https://neuroeng-usach.cl/media/icon_hu2350702243547591566.png</url><title>Joseph West</title><link>https://neuroeng-usach.cl/author/joseph-west/</link></image><item><title>Interpretable machine learning of micro-ERG reveals muted retinal gain tracking in 5xFAD mice</title><link>https://neuroeng-usach.cl/publication/medina-2026-interpretable-ml/</link><pubDate>Tue, 01 Sep 2026 00:00:00 +0000</pubDate><guid>https://neuroeng-usach.cl/publication/medina-2026-interpretable-ml/</guid><description>&lt;h3 id="funding">Funding&lt;/h3>
&lt;p>Becas Chile de Postdoctorado en el Extranjero; ANID Exploración 13220082; Fondecyt Regular 1241202.&lt;/p></description></item><item><title>Interpretable machine learning of micro-ERG reveals muted retinal gain tracking in 5xFAD mice</title><link>https://neuroeng-usach.cl/event/falan2026/</link><pubDate>Mon, 31 Aug 2026 09:00:00 -0400</pubDate><guid>https://neuroeng-usach.cl/event/falan2026/</guid><description>&lt;p>&lt;strong>Background.&lt;/strong> Inexpensive, scalable biomarkers of early Alzheimer&amp;rsquo;s disease (AD) remain an unmet need, and the retina, as a developmental enlargement of the central nervous system, may offer such a window. The 5xFAD mouse exhibits electrophysiologically detectable retinal alterations. We ask whether multi-electrode micro-electroretinogram (μERG) signals can discriminate wild-type (WT) from 5xFAD retinas, and whether deep-learning interpretability may guide the discovery of mechanistic features.&lt;/p>
&lt;p>&lt;strong>Methods.&lt;/strong> We recorded μERG from 23 WT and 23 5xFAD, across young and adult cohorts, using a 16x16 multi-electrode array under a 35-second chirp (flash, frequency, and amplitude sweeps) and a 10-second natural-image video. Under subject-disjoint 5-fold cross-validation with age-blind inputs, we compared three strategies: 1) 1-D convolutional neural networks (CNNs), 2) classical machine learning on hand-crafted (HC) features, and 3) multiscale-entropy complexity features.&lt;/p>
&lt;p>&lt;strong>Results.&lt;/strong> For chirp, HC with logistic regression reached a pooled area under the curve (AUC) of 0.735, complexity features 0.729, and CNN 0.590; for natural images, the values were 0.782, 0.736, and 0.752. Further, interpretability analyses, i.e., Grad-CAM, integrated gradients, virtual band blockade, and Bayesian input optimization, localized the CNN&amp;rsquo;s cue to the amplitude-sweep fundamental-frequency gain trajectory, a pattern we term &amp;ldquo;muted gain tracking&amp;rdquo; in 5xFAD; encoding it as four additional features raised chirp AUC to 0.834, thereby surpassing the network.&lt;/p>
&lt;p>&lt;strong>Conclusions.&lt;/strong> Taken together, μERG signals carry a robust 5xFAD signature recoverable by machine learning, with compact, biologically-grounded features matching end-to-end deep learning; nevertheless, CNN interpretability translates modest performance into mechanistic markers, namely, retinal gain tracking, with promising translational potential as AD biomarkers.&lt;/p>
&lt;p>&lt;strong>Financiamiento/Funding.&lt;/strong> Becas Chile de Postdoctorado en el Extranjero; ANID Exploración 13220082; Fondecyt Regular 1241202.&lt;/p></description></item></channel></rss>