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Sarah Alamdari

dblp:279/4752 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2025
—ORCID · unresolved

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 · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
protein function prediction
0.912025
ProtNote: a multimodal method for protein-function annotation · Bioinform. 2025
Bioinformatics and computational biology › protein function prediction
zero-shot protein function prediction
0.912025
ProtNote: a multimodal method for protein-function annotation · Bioinform. 2025
Bioinformatics and computational biology › protein sequence analysis
sequence-function relationship
0.312025
ProtNote: a multimodal method for protein-function annotation · Bioinform. 2025

Methods — techniques the papers use, named apart from their topics

zero-shot learning · 0.9multimodal deep learning · 0.9free-form text representation · 0.9
YearPublicationVenuePosition
2025 ProtNote: a multimodal method for protein-function annotation
abstract
MOTIVATION: Understanding the protein sequence-function relationship is essential for advancing protein biology and engineering. However, <1% of known protein sequences have human-verified functions. While deep-learning methods have demonstrated promise for protein-function prediction, current models are limited to predicting only those functions on which they were trained. RESULTS: Here, we introduce ProtNote, a multimodal deep-learning model that leverages free-form text to enable both supervised and zero-shot protein-function prediction. ProtNote not only maintains near state-of-the-art performance for annotations in its training set but also generalizes to unseen and novel functions in zero-shot test settings. ProtNote demonstrates superior performance in the prediction of novel Gene Ontology annotations and Enzyme Commission numbers compared to baseline models by capturing nuanced sequence-function relationships that unlock a range of biological use cases inaccessible to prior models. We envision that ProtNote will enhance protein-function discovery by enabling scientists to use free text inputs without restriction to predefined labels-a necessary capability for navigating the dynamic landscape of protein biology. AVAILABILITY AND IMPLEMENTATION: The code is available on GitHub: https://github.com/microsoft/protnote; model weights, datasets, and evaluation metrics are provided via Zenodo: https://zenodo.org/records/13897920.
Samir Char, Nathaniel Corley, Sarah Alamdari, Kevin K. Yang, Ava P. Amini
Bioinform.3