arXiv:2610.22840v1 Announce Type: new Abstract: Single-particle cryogenic electron microscopy (cryo-EM) is an imaging technique capable of reconstructing high-resolution three-dimensional (3D) structure of biological macromolecules from a set of noisy projection images taken at random viewing directions. The mathematical model for cryo-EM images typically assumes that each image contains exactly one particle, which is centered at the origin. However, many experimental datasets contain particle images which include multiple particles: one central particle and a few crowding particles. This deviation from the model leads to inaccurate estimation of image statistics, such as the low-order image moments. To account for this, we propose a method to estimate image moments while correcting for the effect of crowding particles. This method can be run directly from a set of cryo-EM micrographs with picked particles, and we demonstrate its efficacy on a wide array of synthetic data.