Improving the resolution of microscope by deconvolution after dense scan
preprint
OA: closed
Abstract
Super-resolution microscopes (such as STED) illuminate samples with a tiny spot, and achieve very high resolution. But structures smaller than the spot cannot be resolved in this way. Therefore, we propose a technique to solve this problem. It is termed “Deconvolution after Dense Scan (DDS)”. First, a preprocessing stage is introduced to eliminate the optical uncertainty of the peripheral areas around the sample’s ROI (Region of Interest). Then, the ROI is scanned densely together with its peripheral areas. Finally, the high resolution image is recovered by deconvolution. The proposed technique does not need to modify the apparatus much, and is mainly performed by algorithm. Simulation experiments show that the technique can further improve the resolution of super-resolution microscopes.
My notes (saved in your browser only)
Citation neighborhood (no data yet)
We don't have any in-corpus citations linked to this paper yet. The paper's references may be in our DB but unresolved to ``paper_id`` (resolution happens at ingest when the cited DOI matches a row we already have). Run the cross-source citation reconcile pass to retry.
Source provenance
- europepmc
- last seen: 2026-05-19T01:45:01.086888+00:00