Cassie S. Mitchell

dblp:222/3800 · DBLP profile ↗
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6ranked-venue papers
0as first author
6since 2021 · last 2026
0000-0002-5472-6355ORCID · verified

Domains — the database's venue-derived domains; a paper can count in several

Artificial intelligence and machine learning · 3 · 3 since 2021Databases, data management, data science and information retrieval · 3 · 3 since 2021Applied, interdisciplinary, general and emerging computing · 2 · 2 since 2021Graphics, computer vision, multimedia, augmented reality and games · 1 · 1 since 2021
YearPublicationVenuePosition
2026 Integrating curation into scientific publishing to train AI models
abstract
MOTIVATION: High-throughput extraction and structured labeling of data from academic articles are crucial for enabling downstream machine learning applications and secondary analyses. Current approaches lack integration with the publishing process and comprehensive annotation of experimental roles and methodologies alongside bioentity recognition. RESULTS: We embedded multimodal data curation into the academic publishing process to annotate segmented figure panels and captions, combining natural language processing with authors' feedback to increase annotation accuracy. The resulting dataset, SourceData-NLP, comprises over 620 000 annotated biomedical entities, curated from 18 689 figures in 3223 articles in molecular and cell biology. Annotations include eight classes of bioentities (small molecules, gene products, subcellular components, cell lines, cell types, tissues, organisms, and diseases), plus additional classes that delineate the entities' roles in experimental designs and methodologies. We evaluate the utility of the dataset for training AI models using named-entity recognition, segmentation of figure captions into their constituent panels, and a novel context-dependent semantic task that assesses whether an entity is a controlled intervention target or a measurement object. We also demonstrate multi-modal applications for segmenting figures into panel images and their corresponding captions. AVAILABILITY AND IMPLEMENTATION: Trained models are available at https://huggingface.co/EMBO. The SourceData-NLP dataset and code are available at https://github.com/source-data/soda-data, https://github.com/source-data/soda-model, and https://github.com/source-data/soda_image_segmentation.
Jorge Abreu-Vicente, Hannah Sonntag, Thomas Eidens, Cassie S. Mitchell, Thomas Lemberger 0001
Bioinform.4
2023 A Comprehensive Evaluation of Biomedical Entity Linking Models
abstract
Biomedical entity linking (BioEL) is the process of connecting entities referenced in documents to entries in biomedical databases such as the Unified Medical Language System (UMLS) or Medical Subject Headings (MeSH). The study objective was to comprehensively evaluate nine recent state-of-the-art biomedical entity linking models under a unified framework. We compare these models along axes of (1) accuracy, (2) speed, (3) ease of use, (4) generalization, and (5) adaptability to new ontologies and datasets. We additionally quantify the impact of various preprocessing choices such as abbreviation detection. Systematic evaluation reveals several notable gaps in current methods. In particular, current methods struggle to correctly link genes and proteins and often have difficulty effectively incorporating context into linking decisions. To expedite future development and baseline testing, we release our unified evaluation framework and all included models on GitHub at https://github.com/davidkartchner/biomedical-entity-linking.
David Kartchner, Jennifer Deng, Shubham Lohiya, Tejasri Kopparthi, Prasanth Bathala, Daniel Domingo-Fernández, Cassie S. Mitchell
EMNLP7
2023 Towards Interpretable Seizure Detection Using Wearables
abstract
Seizure detection using machine learning is a critical problem for the timely intervention and management of epilepsy. We propose SeizFt, a robust seizure detection framework using EEG from a wearable device. It uses features paired with an ensemble of trees, thus enabling further interpretation of the model's results. The efficacy of the underlying augmentation and class-balancing strategy is also demonstrated. This study was performed for the Seizure Detection Challenge 2023, an ICASSP Grand Challenge.
Irfan Al-Hussaini, Cassie S. Mitchell
ICASSP2
2023 BioSift: A Dataset for Filtering Biomedical Abstracts for Drug Repurposing and Clinical Meta-Analysis
abstract
This work presents a new, original document classification dataset, BioSift, to expedite the initial selection and labeling of studies for drug repurposing. The dataset consists of 10,000 human-annotated abstracts from scientific articles in PubMed. Each abstract is labeled with up to eight attributes necessary to perform meta-analysis utilizing the popular patient-intervention-comparator-outcome (PICO) method: has human subjects, is clinical trial/cohort, has population size, has target disease, has study drug, has comparator group, has a quantitative outcome, and an "aggregate" label. Each abstract was annotated by 3 different annotators (i.e., biomedical students) and randomly sampled abstracts were reviewed by senior annotators to ensure quality. Data statistics such as reviewer agreement, label co-occurrence, and confidence are shown. Robust benchmark results illustrate neither PubMed advanced filters nor state-of-the-art document classification schemes (e.g., active learning, weak supervision, full supervision) can efficiently replace human annotation. In short, BioSift is a pivotal but challenging document classification task to expedite drug repurposing. The full annotated dataset is publicly available and enables research development of algorithms for document classification that enhance drug repurposing.
David Kartchner, Irfan Al-Hussaini, Haydn Turner, Jennifer Deng, Shubham Lohiya, Prasanth Bathala, Cassie S. Mitchell
SIGIR7
2022 CCS Explorer: Relevance Prediction, Extractive Summarization, and Named Entity Recognition from Clinical Cohort Studies
abstract
Clinical Cohort Studies (CCS), such as randomized clinical trials, are a great source of documented clinical research. Ideally, a clinical expert inspects these articles for exploratory analysis ranging from drug discovery for evaluating the efficacy of existing drugs in tackling emerging diseases to the first test of newly developed drugs. However, more than 100 articles are published daily on a single prevalent disease like COVID-19 in PubMed. As a result, it can take days for a physician to find articles and extract relevant information. Can we develop a system to sift through these articles faster and document the crucial takeaways from each of these articles? In this work, we propose CCS Explorer, an end-to-end system for relevance prediction of sentences, extractive summarization, and patient, outcome, and intervention entity detection from CCS. CCS Explorer is packaged in a web-based graphical user interface where the user can provide any disease name. CCS Explorer then extracts and aggregates all relevant information from articles on PubMed based on the results of an automatically generated query produced on the back-end. For each task, CCS Explorer fine-tunes pre-trained language representation models based on transformers with additional layers. The models are evaluated using two publicly available datasets. CCS Explorer obtains a recall of 80.2%, AUC-ROC of 0.843, and an accuracy of 88.3% on sentence relevance prediction using BioBERT and achieves an average Micro F1-Score of 77.8% on Patient, Intervention, Outcome detection (PIO) using PubMedBERT. Thus, CCS Explorer can reliably extract relevant information to summarize articles, saving time by ~660×.
Irfan Al-Hussaini, Davi Nakajima An, Albert J. Lee, Sarah Bi, Cassie S. Mitchell
IEEE Big Data5
2022 SERF: Interpretable Sleep Staging using Embeddings, Rules, and Features
abstract
The accuracy of recent deep learning based clinical decision support systems is promising. However, lack of model interpretability remains an obstacle to widespread adoption of artificial intelligence in healthcare. Using sleep as a case study, we propose a generalizable method to combine clinical interpretability with high accuracy derived from black-box deep learning.
Irfan Al-Hussaini, Cassie S. Mitchell
CIKM2