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SUMMARY:Multi-messenger optical microscopy
DTSTART:20190529T130000
DTEND:20190529T133000
DTSTAMP:20260407T091607Z
UID:4a5c8d3f4ab006dcd098642555269b5c58228d8a96a0724e2ed90d73
CATEGORIES:Conferences - Seminars
DESCRIPTION:Prof. Alberto Diaspro\nThe possibility of integrating differen
 t light-matter interactions to form images and to correlate image data in 
 optical microscopy is the starting point for the design and implementation
  of a brand new multi-messenger optical microscope. The multi-messenger mi
 croscope could represent a new paradigm in data collection and image forma
 tion with a potential high impact in biophysics exploiting the possibility
  to “tune” the microscope across a large\, almost unlimited\, range of
  spatial and temporal resolution. Confocal\, multiphoton\, image scanning 
 and super resolved fluoresce microscopy can be comined with label free app
 roaches\, including multiphoton\, SHG and Mueller matrix microscopy. The "
 field of battle" is related to for answering an open universal question in
  cellular and molecular biology: what are the local and global four-dimens
 ional (x\,y\,z\,t) chromatin structures in the nucleus that rule the compa
 ction and function of the human genome in the interphase of cells and mito
 tic chromosomes? Within this scenario\, expansion and light sheet microsco
 py will be considered as part of the multi-messenger approach. Liquid lens
 es\, SPAD arrays and enforced deep learning approaches and brand new orien
 ted detectors are key components for the development. The final “destina
 tion”of the multimodal collection of data is oriented to a “liquitopy
 ” (liquid tunable microscopy) development [1]. [1] R. Won\, “The super
 -resolution debate\,” Nature Photonics\, vol. 12\, no. 5\, pp. 259–260
 \, Apr. 2018.
LOCATION:BSP 231 https://plan.epfl.ch/?room==BSP%20231
STATUS:CONFIRMED
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