How to process a z-stack image into a 2D image in ImageJ | How to process confocal microscope images

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  • Опубликовано: 24 авг 2024

Комментарии • 12

  • @johnalexis8819
    @johnalexis8819 3 месяца назад +1

    Madam, thank you a lot a lot for this video! It's so useful for my image selection and merging, thumbs up👍🏻

  • @joaopauloferreirarodrigues5576
    @joaopauloferreirarodrigues5576 Год назад +1

    Fantastic!!!! Thank you Alicerita

  • @mahsamodareszadeh519
    @mahsamodareszadeh519 8 месяцев назад +2

    Thank you for the video, would you please explain in comments how to make a 3d image (not max intensity) which we can turn like the window you showed in 1:43 (projection of organelles)?

    • @AliceritaE
      @AliceritaE  8 месяцев назад +1

      I'll make a video to show you

  • @eduardoduarte1968
    @eduardoduarte1968 11 месяцев назад +1

    Very nice! Thanks!

  • @917xyz
    @917xyz 5 месяцев назад +1

    very informative and useful. how to do the reverse, i.e. converting single 2D image into 3D?

    • @AliceritaE
      @AliceritaE  5 месяцев назад

      I don't think a single 2D image can be project led into 3D. You will need more images at different depth to construct a 3D.

    • @917xyz
      @917xyz 5 месяцев назад +1

      @@AliceritaE is it possible to assess depth on the basis of pixel contrast ?

    • @AliceritaE
      @AliceritaE  5 месяцев назад

      Depth here is about capturing the image at different focus point. Just like different slices of a bread makes a loaf.