Abstract
AbstractWhile structured illumination microscopy (SIM) is a widely used super‐resolution microscopy technique for densely labelled samples, we apply a modified version of the matrix pencil method to single molecule imaging. We prove that under reasonable conditions we can recover up to two times more molecule positions compared to conventional microscopy exactly from noiseless data and include numerical examples illustrating benefits as well as limitations of the algorithm.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
