|
|
(15 intermediate revisions by one user not shown) |
Line 1: |
Line 1: |
| [[Category:Spring 2012]] | | [[Category:Spring 2012]] |
− | {{Template:Leanna20.345}} | + | {{Template:Leanna20.345LFM}} |
| | | |
| + | = Light Field Microscope Final Reports = |
| + | == Presentation == |
| + | [http://web.mit.edu/leanna/Public/LFPresentation.pdf Presentation] |
| | | |
− | | + | == Poster == |
− | = Light Field Microscope = | + | Coming soon. |
− | <h3>Vincent Lee & Leanna Morinishi</h3>
| + | |
− | == Introduction and Motivation ==
| + | |
− | A light field microscope (LFM) is capable of producing a 3-dimensional rendering of a sample using information from a single image. The addition of a microlens array, a grid of lenses with diameters on the microscale, to a traditional illumination microscope grants this capability. Here we propose integrating a Lytro™ camera into a basic wide field and epifluorescence microscope, associated code and recommended experiments for use in a teaching undergraduate laboratory.
| + | |
− | | + | |
− | | + | |
− | == Microscope Design ==
| + | |
− | | + | |
− | == Reverse engineering the Lytro™ images ==
| + | |
− | | + | |
− | == Dealing with the hexagonal microarray ==
| + | |
− | | + | |
− | == Acknowledgments ==
| + | |
− | # Nirav Patel, for reverse engineering the Lytro image and lfpsplitter.
| + | |
− | # Frank Warmerdam, Andrey Kiselev, Bob Friesenhahn, Joris Van Damme and Lee Howard for raw2tiff tools.
| + | |
− | | + | |
| | | |
| {{Template:20.345 bottom}} | | {{Template:20.345 bottom}} |