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Samuel J. Yang

Publications and source records attributed to Samuel J. Yang.

5 recordsLinked to original sources

SpeechCompass: Enhancing Mobile Captioning with Diarization and Directional Guidance via Multi-Microphone Localization

Speech-to-text capabilities on mobile devices have proven helpful for hearing and speech accessibility, language translation, note-taking, and meeting transcripts. However, our foundational large-scale survey (n=263) shows that the inability to distinguish and indicate speaker direction makes them challenging in group conversations. SpeechCompass addresses this limitation through real-time, multi-microphone speech localization, where the direction of speech allows visual separation and guidance (e.g., arrows) in the user interface. We introduce efficient real-time audio localization algorithms and custom sound perception hardware running on a low-power microcontroller and four integrated microphones, which we characterize in technical evaluations. Informed by a large-scale survey (n=494), we conducted an in-person study of group conversations with eight frequent users of mobile speech-to-text, who provided feedback on five visualization styles. The value of diarization and visualizing localization was consistent across participants, with everyone agreeing on the value and potential of directional guidance for group conversations.

cs.HC

Accurate Prediction of Experimental Band Gaps from Large Language Model-Based Data Extraction

Machine learning is transforming materials discovery by providing rapid predictions of material properties, which enables large-scale screening for target materials. However, such models require training data. While automated data extraction from scientific literature has potential, current auto-generated datasets often lack sufficient accuracy and critical structural and processing details of materials that influence the properties. Using band gap as an example, we demonstrate Large language model (LLM)-prompt-based extraction yields an order of magnitude lower error rate. Combined with additional prompts to select a subset of experimentally measured properties from pure, single-crystalline bulk materials, this results in an automatically extracted dataset that's larger and more diverse than the largest existing human-curated database of experimental band gaps. Compared to the existing human-curated database, we show the model trained on our extracted database achieves a 19% reduction in the mean absolute error of predicted band gaps. Finally, we demonstrate that LLMs are able to train models predicting band gap on the extracted data, achieving an automated pipeline of data extraction to materials property prediction.

cond-mat.mtrl-sci

Speech Intelligibility Classifiers from 550k Disordered Speech Samples

We developed dysarthric speech intelligibility classifiers on 551,176 disordered speech samples contributed by a diverse set of 468 speakers, with a range of self-reported speaking disorders and rated for their overall intelligibility on a five-point scale. We trained three models following different deep learning approaches and evaluated them on ~94K utterances from 100 speakers. We further found the models to generalize well (without further training) on the TORGO database (100% accuracy), UASpeech (0.93 correlation), ALS-TDI PMP (0.81 AUC) datasets as well as on a dataset of realistic unprompted speech we gathered (106 dysarthric and 76 control speakers,~2300 samples).

eess.AS

Physics-enhanced machine learning for virtual fluorescence microscopy

This paper introduces a new method of data-driven microscope design for virtual fluorescence microscopy. Our results show that by including a model of illumination within the first layers of a deep convolutional neural network, it is possible to learn task-specific LED patterns that substantially improve the ability to infer fluorescence image information from unstained transmission microscopy images. We validated our method on two different experimental setups, with different magnifications and different sample types, to show a consistent improvement in performance as compared to conventional illumination methods. Additionally, to understand the importance of learned illumination on inference task, we varied the dynamic range of the fluorescent image targets (from one to seven bits), and showed that the margin of improvement for learned patterns increased with the information content of the target. This work demonstrates the power of programmable optical elements at enabling better machine learning algorithm performance and at providing physical insight into next generation of machine-controlled imaging systems.

eess.IV

Correcting Nuisance Variation using Wasserstein Distance

Profiling cellular phenotypes from microscopic imaging can provide meaningful biological information resulting from various factors affecting the cells. One motivating application is drug development: morphological cell features can be captured from images, from which similarities between different drug compounds applied at different doses can be quantified. The general approach is to find a function mapping the images to an embedding space of manageable dimensionality whose geometry captures relevant features of the input images. An important known issue for such methods is separating relevant biological signal from nuisance variation. For example, the embedding vectors tend to be more correlated for cells that were cultured and imaged during the same week than for those from different weeks, despite having identical drug compounds applied in both cases. In this case, the particular batch in which a set of experiments were conducted constitutes the domain of the data; an ideal set of image embeddings should contain only the relevant biological information (e.g. drug effects). We develop a general framework for adjusting the image embeddings in order to `forget' domain-specific information while preserving relevant biological information. To achieve this, we minimize a loss function based on distances between marginal distributions (such as the Wasserstein distance) of embeddings across domains for each replicated treatment. For the dataset we present results with, the only replicated treatment happens to be the negative control treatment, for which we do not expect any treatment-induced cell morphology changes. We find that for our transformed embeddings (i) the underlying geometric structure is not only preserved but the embeddings also carry improved biological signal; and (ii) less domain-specific information is present.

stat.ML