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	<updated>2026-09-27T23:46:24Z</updated>
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		<id>https://3demmethods.i2pc.es/index.php?title=2026Kassab&amp;diff=5289&amp;oldid=prev</id>
		<title>Vilas: Created page with &quot;== Citation == Mohamad Kassab, Chengzhi Cao, Vincent Yao, Xiangrui Zeng, Qirong Ho, Min Xu, Semi-supervised clustering with knowledge-guided representation learning in cryo-electron tomography, PLOS Digital Health, 5, 8, 1-22, (2026).  == Abstract == The automated discovery of structural patterns in macromolecular complexes remains a central challenge in cryo-electron tomography, particularly in highly heterogeneous datasets. Although fully unsupervised clustering method...&quot;</title>
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		<updated>2026-09-27T21:39:53Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Citation == Mohamad Kassab, Chengzhi Cao, Vincent Yao, Xiangrui Zeng, Qirong Ho, Min Xu, Semi-supervised clustering with knowledge-guided representation learning in cryo-electron tomography, PLOS Digital Health, 5, 8, 1-22, (2026).  == Abstract == The automated discovery of structural patterns in macromolecular complexes remains a central challenge in cryo-electron tomography, particularly in highly heterogeneous datasets. Although fully unsupervised clustering method...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;== Citation ==&lt;br /&gt;
Mohamad Kassab, Chengzhi Cao, Vincent Yao, Xiangrui Zeng, Qirong Ho, Min Xu, Semi-supervised clustering with knowledge-guided representation learning in cryo-electron tomography, PLOS Digital Health, 5, 8, 1-22, (2026).&lt;br /&gt;
&lt;br /&gt;
== Abstract ==&lt;br /&gt;
The automated discovery of structural patterns in macromolecular complexes remains a central challenge in cryo-electron tomography, particularly in highly heterogeneous datasets. Although fully unsupervised clustering methods have shown promise in grouping subtomograms by structural similarity, they often ignore a crucial source of information: the partial ground truth routinely available to structural biologists from prior studies or manual annotations. In this work, we propose a semi-supervised structural discovery framework that utilizes partial supervision to guide clustering without compromising the ability to uncover previously unknown structures. At the core of our method is a label-anchored probabilistic clustering mechanism that seeds the latent space using a small subset of labeled examples and refines it through a multi-resolution consensus strategy based on PCA-space voting. This is complemented by an entropy-based confidence scoring scheme that attenuates the influence of ambiguous samples, as well as a feature propagation procedure that extends structural labels to low-confidence regions using local similarity in feature space. Together, these components create a stable and adaptive pipeline capable of discovering both known and novel structures. Our approach is efficient, requires as little as 1% of labeled data per class, and consistently produces clearer, more interpretable feature embeddings compared to fully unsupervised methods, with well-separated clusters from the very first iterations. Extensive experiments on simulated and realistic tomographic datasets demonstrate that this semi-supervised strategy significantly improves clustering performance, robustness, and biological relevance in cryo-electron tomography analysis. These methods are integrated as extensions to the existing Deep Iterative Subtomogram Clustering Approach pipeline, enhancing its capability for guided structural discovery.&lt;br /&gt;
&lt;br /&gt;
== Keywords ==&lt;br /&gt;
cryo-electron tomography, semi-supervised clustering, representation learning, structural discovery, macromolecular complexes, subtomogram clustering, deep learning&lt;br /&gt;
&lt;br /&gt;
== Links ==&lt;br /&gt;
https://doi.org/10.1371/journal.pdig.0001619&lt;/div&gt;</summary>
		<author><name>Vilas</name></author>
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