Demo Data from EDBT 2026 / reviewers in the wild / expert
Elizabeth C. Randall
dblp:318/1742
· DBLP profile ↗
1ranked-venue papers
0as first author
1since 2021 · last 2022
—ORCID · none
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 67% Medical and health informatics · 33% |
Topics — the 3 heaviest of 3, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › metabolomics
mass spectrometry imaging |
0.6 | 1 | 2022 | massNet: integrated processing and classification of spatially resolved mass spectrometry data using deep learning for rapid tumor delineation · Bioinform. 2022 |
Bioinformatics and computational biology › epigenomics › ChIP-seq analysis
peak detection |
0.6 | 1 | 2022 | massNet: integrated processing and classification of spatially resolved mass spectrometry data using deep learning for rapid tumor delineation · Bioinform. 2022 |
Medical and health informatics › medical imaging › medical image analysis › medical image segmentation › lesion segmentation
tumor segmentation |
0.6 | 1 | 2022 | massNet: integrated processing and classification of spatially resolved mass spectrometry data using deep learning for rapid tumor delineation · Bioinform. 2022 |
Methods — techniques the papers use, named apart from their topics
deep learning · 0.6cross-validation · 0.6
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2022 | massNet: integrated processing and classification of spatially resolved mass spectrometry data using deep learning for rapid tumor delineationabstractMOTIVATION: Mass spectrometry imaging (MSI) provides rich biochemical information in a label-free manner and therefore holds promise to substantially impact current practice in disease diagnosis. However, the complex nature of MSI data poses computational challenges in its analysis. The complexity of the data arises from its large size, high-dimensionality and spectral nonlinearity. Preprocessing, including peak picking, has been used to reduce raw data complexity; however, peak picking is sensitive to parameter selection that, perhaps prematurely, shapes the downstream analysis for tissue classification and ensuing biological interpretation. RESULTS: We propose a deep learning model, massNet, that provides the desired qualities of scalability, nonlinearity and speed in MSI data analysis. This deep learning model was used, without prior preprocessing and peak picking, to classify MSI data from a mouse brain harboring a patient-derived tumor. The massNet architecture established automatically learning of predictive features, and automated methods were incorporated to identify peaks with potential for tumor delineation. The model's performance was assessed using cross-validation, and the results demonstrate higher accuracy and a substantial gain in speed compared to the established classical machine learning method, support vector machine. AVAILABILITY AND IMPLEMENTATION: https://github.com/wabdelmoula/massNet. The data underlying this article are available in the NIH Common Fund's National Metabolomics Data Repository (NMDR) Metabolomics Workbench under project id (PR001292) with http://dx.doi.org/10.21228/M8Q70T. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Walid M. Abdelmoula, Sylwia Stopka, Elizabeth C. Randall, Michael Regan, Jeffrey N. Agar, Jann N. Sarkaria, William M. Wells III, Tina Kapur, Nathalie Y. R. Agar |
Bioinform. | 3 |