bioRxiv Science⌕ Search

Biology subjects

De Martino, F.

Publications and source records attributed to De Martino, F..

26 records · Page 2Linked to original sources

Linguistic modulation of the neural encoding of phonemes

Speech comprehension entails the neural mapping of the acoustic speech signal onto learned linguistic units. This acousto-linguistic transformation is bi-directional, whereby higher-level linguistic processes (e.g., semantics) modulate the acoustic analysis of individual linguistic units. Here, we investigated the cortical topography and linguistic modulation of the most fundamental linguistic unit, the phoneme. We presented natural speech and phoneme quilts (pseudo-randomly shuffled phonemes) in either a familiar (English) or unfamiliar (Korean) language to native English speakers while recording fMRI. This allowed us to dissociate the contribution of acoustic vs. linguistic processes towards phoneme analysis. We show that (1) the acoustic analysis of phonemes is modulated by linguistic analysis and (2) that for this modulation both of acoustic and phonetic information need to be incorporated. These results suggest that the linguistic modulation of cortical sensitivity to phoneme classes minimizes prediction error during natural speech perception, thereby aiding speech comprehension in challenging listening situations.

neuroscience↗

A Paradigm Change in Functional Brain Mapping: Suppressing the Thermal Noise in fMRI

Functional magnetic resonance imaging (fMRI) has become one of the most powerful tools for investigating the human brain. However, virtually all fMRI studies have relatively poor signal-to-noise ratio (SNR). Here we introduce a novel fMRI denoising technique, which suppresses noise that is indistinguishable from zero-mean, Gaussian-distributed noise. Thermal noise, falling in this category, is a major source of noise in fMRI, particularly, but not exclusively, at high spatial and/or temporal resolutions. Using 7-Tesla high-resolution data, we demonstrate improvements in temporal-SNR, the detection of stimulus-induced signal changes, and functional maps, while leaving stimulus-induced signal change amplitudes, image spatial precision, and functional point-spread-function unaltered. We also show that the method is equally applicable when using supra-millimeter resolution 3- and 7-Tesla fMRI data, different cortical regions, stimulation/task paradigms, and acquisition strategies. This denoising approach improves key metrics of functional activation detection while preserving spatial precision.

neuroscience↗

Deep Learning Enables Individual Xenograft Cell Classification in Histological Images by Analysis of Contextual Features

Patient-Derived Xenografts (PDXs) are the preclinical models which best recapitulate inter- and intra-patient complexity of human breast malignancies, and are also emerging as useful tools to study the normal breast epithelium. However, data analysis generated with such models is often confounded by the presence of host cells and can give rise to data misinterpretation. For instance, it is important to discriminate between xenografted and host cells in histological sections prior to performing immunostainings. We developed Single Cell Classifier (SCC), a data-driven deep learning-based computational tool that provides an innovative approach for automated cell species discrimination based on a multi-step process entailing nuclei segmentation and single cell classification. We show that human and murine cells contextual features, more than cell-intrinsic ones, can be exploited to discriminate between cell species in both normal and malignant tissues, yielding up to 96% classification accuracy. SCC will facilitate the interpretation of H&E stained histological sections of xenografted human-in-mouse tissues and it is open to new in-house built models for further applications. SCC is released as an open-source plugin in ImageJ/Fiji available at the following link: https://github.com/Biomedical-Imaging-Group/SingleCellClassifier. Author summaryBreast cancer is the most commonly diagnosed tumor in women worldwide and its incidence in the population is increasing over time. Because our understanding of such disease has been hampered by the lack of adequate human preclinical model, efforts have been made in order to develop better approaches to model the human complexity. Recent advances in this regard were achieved with Patient-Derived Xenografts (PDXs), which entail the implantation of human-derived specimens to recipient immunosuppressed mice and are, thus far, the preclinical system best recapitulating the heterogeneity of both normal and malignant human tissues. However, histological analyses of the resulting tissues are usually confounded by the presence of cells of different species. To circumvent this hurdle and to facilitate the discrimination of human and murine cells in xenografted samples, we developed Single Cell Classifier (SCC), a deep learning-based open-source software, available as a plugin in ImageJ/Fiji, performing automated species classification of individual cells in H&E stained sections. We show that SCC can reach up to 96% classification accuracy to classify cells of different species mainly leveraging on their contextual features in both normal and tumor PDXs. SCC will improve and automate histological analyses of human-in-mouse xenografts and is open to new in-house built models for further classification tasks and applications in image analysis.

systems biology↗

Multivoxel Pattern of Blood Oxygen Level Dependent Activity can be sensitive to stimulus specific fine scale responses

1.At ultra-high field, fMRI voxels can span the sub-millimeter range, allowing the recording of blood oxygenation level dependent (BOLD) responses at the level of fundamental units of neural computation, such as cortical columns and layers. This sub-millimeter resolution, however, is only nominal in nature as a number of factors limit the spatial acuity of functional voxels. Multivoxel Pattern Analysis (MVPA) may provide a means to detect information at finer spatial scales that may otherwise not be visible at the single voxel level due to limitations in sensitivity and specificity. Here, we evaluate the spatial scale of stimuli specific BOLD responses in multivoxel patterns exploited by linear Support Vector Machine, Linear Discriminant Analysis and Naive Bayesian classifiers across cortical depths in V1. To this end, we artificially misaligned the testing relative to the training portion of the data in increasing spatial steps, then investigated the breakdown of the classifiers performances. A one voxel shift led to a significant decrease in decoding accuracy (p<.05) across all cortical depths, indicating that stimulus specific responses in a multivoxel pattern of BOLD activity exploited by multivariate decoders can be as precise as the nominal resolution of single voxels (here .8 mm isotropic). Our results further indicate that large draining vessels, prominently residing in proximity of the pial surface, do not, in this case, hinder the ability of MVPA to exploit fine scale patterns of BOLD signals. We argue that tailored analytical approaches can help overcoming limitations in high-resolution fMRI and permit studying the mesoscale organization of the human brain with higher sensitivities.

neuroscience↗

Motion displaces population receptive fields in the direction opposite to motion

Motion signals can bias the perceived position of visual stimuli. While the apparent position of a stimulus is biased in the direction of motion, electro-physiological studies have shown that the receptive field (RF) of neurons is shifted in the direction opposite to motion, at least in cats and macaque monkeys. In humans, it remains unclear how motion signals affect population RF (pRF) estimates. We addressed this question using psychophysical measurements and functional magnetic resonance imaging (fMRI) at 7 Tesla. We systematically varied two factors: the motion direction of the carrier pattern (inward, outward and flicker motion) and the contrast of the mapping stimulus (low and high stimulus contrast). We observed that while physical positions were identical across all conditions, presence of low-contrast motion, but not high-contrast motion, shifted perceived stimulus position in the direction of motion. Correspondingly, we found that pRF estimates in early visual cortex were shifted against the direction of motion for low-contrast stimuli but not for high stimulus contrast. We offer an explanation in form of a model for why apertures are perceptually shifted in the direction of motion even though pRFs shift in the opposite direction.

neuroscience↗

Methods for computing the maximum performance of computational models of fMRI responses

Computational neuroimaging methods aim to predict brain responses (measured e.g. with functional magnetic resonance imaging [fMRI]) on the basis of stimulus features obtained through computational models. The accuracy of such prediction is used as an indicator of how well the model describes the computations underlying the brain function that is being considered. However, the prediction accuracy is bounded by the proportion of the variance of the brain response which is related to the measurement noise and not with the stimuli (or cognitive functions). The bound to the performance of a computational model to the prediction of brain responses has been referred to as the noise ceiling. In previous neuroimaging applications two methods have been proposed for estimating the noise ceiling based on either a split-half procedure or Monte Carlo simulations. These methods make different assumptions over the nature of the effects underlying the data, and, importantly, their relation has not been clarified yet. Here, we use a two-level generative framework to formally describe the partition between the variance of measurement noise and the stimulus related variance. In this framework we derive an analytical form for the noise ceiling that does not require computationally expensive simulations or a splitting procedure that reduce the amount of data. We describe the relation between the newly introduced noise ceiling estimator and the previous methods for variable levels of measurements noise using simulated data. Additionally, as the relation to the noise ceiling is used to make conclusions on the validity of a model with respect to others, we evaluate the effect the interplay between regularization (often used to estimate model fits to the data when the number of computational features in the model is large) and model complexity on the performance with respect to the noise ceiling. Finally, we show the differences between the methods on real fMRI data acquired at 7 Tesla. We demonstrate that while the split half estimator provides a pessimistic estimate of the noise ceiling due to the small amount of data available in conventional fMRI datasets, the parametric nature of the Monte Carlo estimator results in overly optimistic estimates. For this reason, for real data, we propose a robust procedure to the estimation of the noise ceiling based on bootstraps.\n\nAuthor SummaryEncoding computational models in brain responses measured with fMRI allows testing the algorithmic representations carried out by the neural population within voxels. The accuracy of a model in predicting new responses is used as a measure of the brain validity of this model, but the result of this analysis is determined not only by how precisely the model describes the responses but also by the quality of the data. In this article, we validate existing approaches to estimate the best possible accuracy that any computational model can achieve conditioned to the amount of measurement noise that is present in the experimental data (i.e. the noise ceiling). Additionally we introduce a close form estimation of the noise ceiling that does not require computationally or data expensive procedures. All the methods are compared using simulated and real fMRI data. We draw conclusions over the impact of regularisation procedures and model complexity and make practical recommendations on how to report the results of computational models in neuroimaging.

neuroscience↗

A scalable method to improve gray matter segmentation at ultra high field MRI

High-resolution (functional) magnetic resonance imaging (MRI) at ultra high magnetic fields (7 Tesla and above) enables researchers to study how anatomical and functional properties change within the cortical ribbon, along surfaces and across cortical depths. These studies require an accurate delineation of the gray matter ribbon, which often suffers from inclusion of blood vessels, dura mater and other non-brain tissue. Residual segmentation errors are commonly corrected by browsing the data slice-by-slice and manually changing labels. This task becomes increasingly laborious and prone to error at higher resolutions since both work and error scale with the number of voxels. Here we show that many mislabeled, non-brain voxels can be corrected more efficiently and semi-automatically by representing three-dimensional anatomical images using two-dimensional histograms. We propose both a uni-modal (based on first spatial derivative) and multi-modal (based on compositional data analysis) approach to this representation and quantify the benefits in 7 Tesla MRI data of nine volunteers. We present an openly accessible Python implementation of these approaches and demonstrate that editing cortical segmentations using two-dimensional histogram representations as an additional post-processing step aids existing algorithms and yields improved gray matter borders. By making our data and corresponding expert (ground truth) segmentations openly available, we facilitate future efforts to develop and test segmentation algorithms on this challenging type of data.

neuroscience↗