Abstract
This paper presents a solution to the difficulty and confusion one suffers in direct viewing of confocal optical sections in 3D by means of manually contouring cell nucleus in 3D. Discussed also are the advantages as well as ways to overcome the disadvantages of this method.
| Original language | English |
|---|---|
| Pages (from-to) | 158-159 |
| Number of pages | 2 |
| Journal | Proceedings - Annual Meeting, Microscopy Society of America |
| State | Published - 1993 |
| Event | Proceedings of the 51st Annual Meeting Microscopy Society of America - Cincinnati, OH, USA Duration: Aug 1 1993 → Aug 6 1993 |
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