Learn how to use Fiji to analyze biology images

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  • Опубліковано 9 лис 2024

КОМЕНТАРІ • 11

  • @rommelviloan
    @rommelviloan Рік тому +1

    Really nice and useful tutorial! Thanks!

  • @ramnageenasingh7465
    @ramnageenasingh7465 2 роки тому

    Hi Erick, It is a nice tutorial. I am trying to use Fiji for for my image analysis Confocal laser images. But facing issues. Unable to set scale bar and other things. Could you help me to that? Thanks
    Ram

  • @yasiralshebib6626
    @yasiralshebib6626 3 роки тому +2

    hi there
    thanks for the tutorial.
    could you please upload the link for StarDist jar file. I could not find it!
    thanks in advance

  • @Yousef1364
    @Yousef1364 2 роки тому

    Hi Erick, It is a useful tutorial. Would you please tell me how I can contact you to ask my questions regarding Fiji program?

  • @ЗагрузиЛося
    @ЗагрузиЛося 8 місяців тому

    THANK YOU!!

  • @katiewarren3422
    @katiewarren3422 8 місяців тому

    THANK YOU

  • @ivankuzko7037
    @ivankuzko7037 3 роки тому

    Thank you very much for the tutorial. 1LF, Charles University in Prague.

  • @sunsite15
    @sunsite15 3 роки тому

    Thank you so much!

  • @chigozieofoedu1731
    @chigozieofoedu1731 Рік тому

    I downloaded StarDIst and tried to use it on my image and I got an error message "[Thu Jan 12 11:16:16 ACDT 2023] [ERROR] [] net.imagej.DefaultDataset: Input axis of type Channel should have size 1 but has size 3" Please what do I do?

    • @Schrodingy
      @Schrodingy 8 місяців тому

      Hi! Pretty sure you've solved the issue, so leaving a comment for others. The image, of which you're creating a mask, should be single channel. (Image --> Color --> Split Channels) is one way to separate channels.

  • @zahraahmadi2234
    @zahraahmadi2234 3 місяці тому

    hello. I have a question.would you please help me?I want to count the number of grafts inside the plates with the Fiji (filament detector). how can i do that(can i have your email address i want to send photos of analysis)