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July 18th, 2025
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National Center of Biotechnology (CSIC)
molecular biology
biorxiv

How many (distinguishable) classes can we identify in Single Particle Analysis?

Lauzirika, O.Open in Google Scholar•Pernica, M.Open in Google Scholar•Herreros, D.Open in Google Scholar•Ramirez, E.Open in Google Scholar•Krieger, J.Open in Google Scholar•Gragera, M.Open in Google Scholar•Iceta, M.Open in Google Scholar•Conesa, P.Open in Google Scholar•Fonseca, Y.Open in Google Scholar•Jimenez, J.Open in Google Scholaret al.

Heterogeneity in cryoEM is essential for capturing macromolecule structural variability, reflecting their functional states and biological significance. However, estimating heterogeneity remains challenging due to particle misclassification and algorithmic biases, which can lead to reconstructions that blend distinct conformations or fail to resolve subtle differences. Furthermore, the low signal-to-noise ratio (SNR) inherent in cryo-EM data makes it nearly impossible to detect minute structural changes, as noise often obscures subtle variations in macromolecular projections. In this paper, we investigate the use of p-values associated with the null hypothesis that the observed classification differs from a random partition of the input dataset, thereby providing a statistical framework for determining the number of distinguishable classes present in a given dataset.

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