To uncover the circuit-level alterations that underlie atypical sensory processing associated with autism, we adopted a symptom-to-circuit approach in the Fmr1-knockout (Fmr1) mouse model of Fragile X syndrome. Using a go/no-go task and in vivo two-photon calcium imaging, we find that impaired visual discrimination in Fmr1 mice correlates with marked deficits in orientation tuning of principal neurons and with a decrease in the activity of parvalbumin interneurons in primary visual cortex. Restoring visually evoked activity in parvalbumin cells in Fmr1 mice with a chemogenetic strategy using designer receptors exclusively activated by designer drugs was sufficient to rescue their behavioral performance. Strikingly, human subjects with Fragile X syndrome exhibit impairments in visual discrimination similar to those in Fmr1 mice. These results suggest that manipulating inhibition may help sensory processing in Fragile X syndrome.

Digital holographic microscopy enables the 3D reconstruction of volumetric samples from a single-snapshot hologram. However, unlike a conventional bright-field microscopy image, the quality of holographic reconstructions is compromised by interference fringes as a result of twin images and out-of-plane objects. Here, we demonstrate that cross-modality deep learning using a generative adversarial network (GAN) can endow holographic images of a sample volume with bright-field microscopy contrast, combining the volumetric imaging capability of holography with the speckle- and artifact-free image contrast of incoherent bright-field microscopy. We illustrate the performance of this “bright-field holography” method through the snapshot imaging of bioaerosols distributed in 3D, matching the artifact-free image contrast and axial sectioning performance of a high-NA bright-field microscope. This data-driven deep-learning-based imaging method bridges the contrast gap between coherent and incoherent imaging, and enables the snapshot 3D imaging of objects with bright-field contrast from a single hologram, benefiting from the wave-propagation framework of holography.

No abstract

Fast and affordable solutions for COVID-19 testing are necessary to contain the spread of the global pandemic and help relieve the burden on medical facilities. Currently, limited testing locations and expensive equipment pose difficulties for individuals trying to be tested, especially in low-resource settings. Researchers have successfully presented models for detecting COVID-19 infection status using audio samples recorded in clinical settings [5, 15], suggesting that audio-based Artificial Intelligence models can be used to identify COVID-19. Such models have the potential to be deployed on smartphones for fast, widespread, and low-resource testing. However, while previous studies have trained models on cleaned audio samples collected mainly from clinical settings, audio samples collected from average smartphones may yield suboptimal quality data that is different from the clean data that models were trained on. This discrepancy may add a bias that affects COVID-19 status predictions. To tackle this issue, we propose a multi-branch deep learning network that is trained and tested on crowdsourced data where most of the data has not been manually processed and cleaned. Furthermore, the model achieves state-of-art results for the COUGHVID dataset [16]. After breaking down results for each category, we have shown an AUC of 0.99 for audio samples with COVID-19 positive labels.

No abstract