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Biology subjects

Merz, S.

Publications and source records attributed to Merz, S..

4 recordsLinked to original sources

Machine learning on magnetoencephalography data yields generalizable low-dimensional neural fingerprints that distinguish individuals across task conditions

Individual brains are unique in structure and function. Functional differences are captured by neural fingerprints, which reflect individual differences in behavior and cognition as well as group-level changes related to neurodegenerative diseases. Most research efforts so far have focused on fingerprints com-prising full functional connectomes. However, the high dimensionality of the connectomes can increase computational load and impede performance of machine learning methods in potential applications. A low-dimensional alternative that retains individual features of the full connectomes would thus be beneficial. The present study employed latent-noise Bayesian Reduced Rank Regression (lnBRRR) to learn low-dimensional latent spaces that capture individual features in functional connectivity and power spectral density data derived from MEG recordings. LnBRRR performance was assessed with low training set sizes (N=20-44), and against principal component analysis and linear discriminant analysis. Model performance was also assessed with task data, and the solutions were compared across task conditions with cosine similarity to establish whether individual features are altered by different cognitive processes. LnBRRR captured generalizable individual patterns already at N=20 but N=30-35 was needed to reach optimal test accuracies and to prevent potential overfitting. The model also achieved comparable performance to the alternative models. Latent fingerprints derived from task data attained comparable performance to resting-state latent fingerprints, and lnBRRR solutions were shown to generalize across conditions. Additionally, the model solutions for power spectral density data were discovered to be notably similar, yet differently rotated, over task conditions, suggesting that similar patterns of individual features were captured by the model regardless of the task condition. Altogether, the present results highlight lnBRRR as a potential tool for neuroimaging data analysis and demonstrate that individual differences in power spectral density are largely intrinsic and unaffected by varying cognitive processes.

neuroscience↗

Capturing individual variation in children's oscillatory brain activity during nREM sleep

Human brain dynamics are highly unique between individuals: functional neuroimaging studies have recently described functional features that can be used as neural fingerprints. As such studies have generally been performed on adults, it is unclear if the results are applicable during brain development. Here we applied Bayesian reduced-rank regression (BRRR), to extract low-dimensional representations of electroencephalography (EEG) power spectra measured from normally developing children at different ages. The clinical EEG recordings represented different sleep stages in a pediatric population (N=782) of ages varying from 6 weeks to 19 years. The representations learned within specific sleep stages successfully separated between the subjects. Furthermore, a model trained with data across sleep stages generalized to unseen data, suggesting that informative neural fingerprints could be extracted. Fingerprint stability increased with the age of the subjects. In comparison to correlation-based measures in differentiating individuals from each other, the BRRR model performed better, highlighting the usefulness of the dimensionality reduction for data obtained in demanding clinical settings. While further studies are needed to address the possible non-linear maturation effects over developmental periods, our results demonstrate, for the first time, the existence of stable within-session neurofunctional fingerprints in pediatric populations.

neuroscience↗

Spatiotemporal biases in localization and interception: common underlying mechanisms?

Human perception of space, time and motion is subject to several biases. Lab studies showed such effects in psychophysical judgements of location, but also in action-tasks, like predicting motion and intercepting. Given that similar underlying processes have been proposed for some of these biases, we tested for a shared mechanism by correlating them across observers. Using the classical implied motion sequence, participants either indicated the remembered location of an intermittently presented dot consistently moving from one location to the next, or intercepted a predicted future location of the same intermittently presented dot. We examined whether the errors in those tasks are associated by correlating i) the overall amount of overshooting, and ii) the effect of temporal manipulations of the jump duration on these biases across participants. We found two medium correlations indicating that these two biases are indeed related to each other. Participants who show a larger effect in one task also show a larger effect in the other task, and participants with larger proneness to temporal features show them consistently across both tasks. This suggests a shared underlying mechanism, and theoretical implications are discussed.

neuroscience↗

Computer-Assisted Mitotic Count Using a Deep Learning-based Algorithm Improves Inter-Observer Reproducibility and Accuracy in canine cutaneous mast cell tumors

The mitotic count (MC) is an important histological parameter for prognostication of malignant neoplasms. However, it has inter- and intra-observer discrepancies due to difficulties in selecting the region of interest (MC-ROI) and in identifying/classifying mitotic figures (MFs). Recent progress in the field of artificial intelligence has allowed the development of high-performance algorithms that may improve standardization of the MC. As algorithmic predictions are not flawless, the computer-assisted review by pathologists may ensure reliability. In the present study we have compared partial (MC-ROI preselection) and full (additional visualization of MF candidate proposal and display of algorithmic confidence values) computer-assisted MC analysis to the routine (unaided) MC analysis by 23 pathologists for whole slide images of 50 canine cutaneous mast cell tumors (ccMCTs). Algorithmic predictions aimed to assist pathologists in detecting mitotic hotspot locations, reducing omission of MF and improving classification against imposters. The inter-observer consistency for the MC significantly increased with computer assistance (interobserver correlation coefficient, ICC = 0.92) compared to the unaided approach (ICC = 0.70). Classification into prognostic stratifications had a higher accuracy with computer assistance. The algorithmically preselected MC-ROIs had a consistently higher MCs than the manually selected MC-ROIs. Compared to a ground truth (developed with immunohistochemistry for phosphohistone H3), pathologist performance in detecting individual MF was augmented when using computer assistance (F1-score of 0.68 increased to 0.79) with a reduction in false negatives by 38%. The results of this study prove that computer assistance may lead to a more reproducible and accurate MCs in ccMCTs.

pathology↗