Counting Cells with ImageJ

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  • Опубліковано 17 лис 2024

КОМЕНТАРІ • 75

  • @vercas.1664
    @vercas.1664 4 роки тому

    Thank you for explaining how to process an image through ImageJ and uploading a video about it!
    and I believe you need to revisit your video whenever there are new comments to answer them...again thanks!

  • @GautamGawande24
    @GautamGawande24 5 років тому

    Thanks Kevin. It made my job a lot easier.

  • @majestia19
    @majestia19 11 років тому +2

    Thanks! Trying out image J for the first time.

  • @davideduardoabadcontreras5566
    @davideduardoabadcontreras5566 4 роки тому

    You saved my master degree

  • @andrewvirtual
    @andrewvirtual 9 років тому

    thanks this makes measurements so much easier

  • @michaelb2211
    @michaelb2211 3 роки тому

    Thanks alot! Fill holes doesn't work well for my particular images - the middle area of cells disappears completely and the outer cells don't change. Eh. It still is working well - I used the 'record' feature to make a macro to automate it and it works like a charm

    • @michaelb2211
      @michaelb2211 3 роки тому

      edit, I see you included macro code - yep. any luck running this in batch?

  • @HaploMaster
    @HaploMaster 9 років тому

    Thank you very much for that quick tutorial that helped me a lot !

  • @conglu5497
    @conglu5497 4 роки тому

    Thanks very much for sharing! this is very helpful!!!!

  • @alejandroprieto9212
    @alejandroprieto9212 10 років тому

    Thanks! That's great, I'm trying for geological material!

  • @rizwanurrahmanabeer1429
    @rizwanurrahmanabeer1429 4 роки тому

    Outstanding Tutorial! It just solved my problem. Thanks a lot, Kevin. :)

  • @vidakarimnia6971
    @vidakarimnia6971 5 років тому

    Thank you very much for the great video

  • @mzulfadh
    @mzulfadh 7 років тому

    This is what I looking for.. Thank you

  • @anaghaa6894
    @anaghaa6894 3 роки тому

    Thank you so much! ❤️ This really helped me a lot ☺️

  • @oo-nah
    @oo-nah 7 років тому +1

    That's sooooooo useful!! Thanks A LOT!!

  • @qianzhu2746
    @qianzhu2746 9 років тому

    Thanks very much! It's really helpful.

  • @claudiaespinosagarcia546
    @claudiaespinosagarcia546 9 років тому

    WONDERFUL!
    Thanks very helpful

  • @canadasolarandacademics1759
    @canadasolarandacademics1759 3 роки тому

    Thanks so much. Please I do I calibrate my sample. Please how do I record my my values

  • @isoagyeman1
    @isoagyeman1 6 років тому

    It was really useful. Thanks a lot!

  • @RobertaBraga_
    @RobertaBraga_ 6 років тому

    Thank you very much! Very useful

  • @alainareagan7364
    @alainareagan7364 10 років тому

    Thank you! This was very helpful!

  • @sau002
    @sau002 3 роки тому

    Nice video.

  • @LikesStrokes
    @LikesStrokes 2 роки тому

    Thanks for the video! It's excellent!
    I have one question: I have to quantify some PI (propidium iodide) images of hippocampal slices... how do I get the percentage of dead cells for the total tissue area? For that, how do I get a sum of the area of ​​all dead cells and divide by the total area of ​​the slice?
    Preferably in a quick way without having to mark all dead cells.
    Thank you!

  • @DanNguyen-hu6pt
    @DanNguyen-hu6pt 5 років тому

    Many thanks for the video, it helps me a lot. I wonder that if I have cells stained with Hoechst, and I want to count dividing cells with 2 nuclei close to each other (at anaphase or telophase) as 1 cell, what should I do?

  • @zingo94
    @zingo94 9 років тому +1

    Does this work for 3D images as well? As in if i have several slices of pictures?
    Thank you for this!

  • @chethanaraj1589
    @chethanaraj1589 2 роки тому

    Nice video, I want to count spherical shape cells. But the sizes vary from each other might be small as 10um diameter to too big diameter. Can you help me to count all the cells

  • @irishguy200007
    @irishguy200007 3 роки тому

    Kevin, How does someone acquire the photograph of a sample that is stand. I mean if I want to count cells per ml, how do I know how much sample is in the photo.
    I know people say use a hemocytometer but is there a glass slide with a groove that takes a desired amount of sample or something other than a hemocytometer. I would have thought a hemocytometers lines would mess up the image taken from a microscope.

  • @Mirula
    @Mirula 9 років тому

    Does anyone know why images are first converted to binary images before analysing them? Why is it not possible to do it on the grayscale picture?

  • @irishguy200007
    @irishguy200007 3 роки тому

    Do I buy a glass slide with a well and inject my stained sample into this well prior to taking photo.

  • @kater329
    @kater329 8 років тому

    You are amazing thanks a million!!

  • @tom87731
    @tom87731 8 років тому +2

    Hi Kevin, good job, I was wondering if it is possible to count cells in more than one image at once.
    for example, I have 200 images and I want to cell counts from each image at once.
    Thank you in advance!

  • @DrsJacksonn
    @DrsJacksonn 6 років тому +1

    Hi there. I'm looking for a program to count cells, but this program doesn't seem to do the trick. I have images of a micro-array covered with wells and I only want to count cells _inside_ those wells (which are regularly interspaced as if located on the vertices of a grid). In other words, I need the program to only count cells on particular pre-selected locations of the picture. Any advice there?

  • @DoryAbelman
    @DoryAbelman 5 років тому

    Thank you for the informative video. Is there any way to batch this if we have many samples to count?

  • @ratnakaur5287
    @ratnakaur5287 10 років тому +1

    I am interested in counting pollen grains and also pollen types differentiated using staining dye for viability. However using the methodology as shown I am still not able to get the exact results and colour differentiation not possible. can you describe the steps if I mail you a sample pic. I shall be highly obliged.

    • @johntialcungling5661
      @johntialcungling5661 10 років тому

      why don't you try with MTT dude? (Dafni's method) it's nice and easy....but i also have a problem of how to count :(

  • @mauroccm
    @mauroccm 9 років тому +3

    Hi. Thank you for showing this. it's very good. However this is good for counting round cells. Cells in culture with different morphology are more complicated. Does anyone have a clue how to count fibroblasts?

    • @XellosWizz
      @XellosWizz 9 років тому +5

      +Mauro Cafundó de Morais Use DAPI and count nuclei

  • @ahmedauwal4913
    @ahmedauwal4913 6 років тому

    Hi. Thanks for the video.
    How can I use imagej to count islets of langerhan?

  • @nari_journey
    @nari_journey 4 роки тому

    Thank you so much for your woderful tutorial.
    I have a question. How I can know the exactly threshold?

    • @nari_journey
      @nari_journey 4 роки тому

      and how many pixel I should use for subtract background in each photo? Is it the same?

  • @melinaoliveira2018
    @melinaoliveira2018 5 років тому

    Hi! Thanks for the video. When I put the watershed part my software is just binding black points... Its not working as the video said.. can you help me?

  • @zahraahmadi2234
    @zahraahmadi2234 3 місяці тому

    Hello I have a question
    I want to count hair graft with imageJ
    ( i have numbers of grafts but when I use this app the results is not correct )
    Would you please help me ?

  • @yasiralshebib6626
    @yasiralshebib6626 4 роки тому

    Hello Kevin
    Thanks for the video. It is very informative.
    Do you think the image file must be (tif) in order to use the watershed function and subsequently you can count the objects using the analyze particle command?

  • @blahapavel
    @blahapavel 10 років тому

    Thanks for the video!
    In the results table - how did you manage to get the Perim., Circ., AR columns? I have just Area, Mean, Min, Max. (also I don't see the center of a cell - just the borders). Thanks for any help

    • @TT-iz2ps
      @TT-iz2ps 5 років тому +1

      On Results window press the button "Results" and then choose "set measurements".
      It's been 5 years since your question but maybe I will help someone else.

  • @leoilegal5478
    @leoilegal5478 4 роки тому

    What exactly does the image show?What kind of cells?I am writing my thesis and it could be very helpful to have more information about the picture.Thanks a lot in advance.

  • @geetasowmya2819
    @geetasowmya2819 6 років тому

    hi, could you please give me the link of microscopic blood image..

  • @Fer-hh7ii
    @Fer-hh7ii 7 років тому

    Thanks so much!!

  • @darkychangaming3236
    @darkychangaming3236 2 роки тому

    nice info, but how to cite in journal?

  • @VashTheTyphonicStampede
    @VashTheTyphonicStampede 9 років тому

    Nice tutorial video, it's very informative. I have a question if you don't mind. Is there a functionality or option in ImageJ that allows the user to count the number of pixels of a particular color and/or get its percentage from the total number of pixels?
    For example, I have an image with color A and B, I want to get the total number of pixels of color A, or color B. (For simplicity, we can let color A = black, and color B = white)
    I would really appreciate if you could respond to my queries, it will be a great help. Thanks in advance.

    • @TT-iz2ps
      @TT-iz2ps 5 років тому

      You can paint B color as red in histogram menu and then count the area of red color in Results table.

  • @hoopermolly910
    @hoopermolly910 5 років тому +1

    Hi. Thanks for your sharing. It's so helpful! I have a question about watershed. I can't separate cell one by one. Are there some better method to separate cells?

  • @sau002
    @sau002 3 роки тому

    How does the "Fill holes" algorithm at 2:07 work?

  • @dominikka3030
    @dominikka3030 2 роки тому

    I would like to count just pairs of cells (2 cells that are close to each other and no cells which are standing single) Do you have any clue how to do that with ImageJ?

  • @johntialcungling5661
    @johntialcungling5661 10 років тому

    many thxs for the share

  • @mansourehmohseni1810
    @mansourehmohseni1810 4 роки тому

    Hi, I have a question and hope to get my answer from you.
    Actually, I have some pictures (with green florescent dots as cells) randomly taken from my sample. I counted the cells/picture by ImageJ and I was wondering how to extrapolate these certain number of cells counted as it's very hard to take lots of pictures from my samples by a florescent microscope.

    • @psmanici4
      @psmanici4 4 роки тому

      You shouldn't really extrapolate like that because you're assuming even growth across the plate/well. If you have to, then you really should take 5 random images and take the average of those 5 images. After this, divide the total size of the well/plate by the frame size of the image then multiply this factor by your cell-count. Ie:
      Image frame size = 2mm^2,
      well size = 100mm^2
      Average cell count across 5 images= 200
      Total cell count = 200 * (100/ 2)
      = 10000 cells

  • @songohan393
    @songohan393 Рік тому

    Thanks

  • @PaolaRamirez-wi5gr
    @PaolaRamirez-wi5gr 4 роки тому

    if I want to erase something, how do I do that?

  • @gengpan
    @gengpan 9 років тому

    hi Kevin, may I ask if I can choose the area I am interested in to count the cell number? do I have to count all the cells in the figure?

  • @gnusnomis
    @gnusnomis 4 роки тому

    And how do you actually count the number of cells??

  • @BASSCYH
    @BASSCYH 9 років тому

    good!! thanks

  • @thestella2241
    @thestella2241 Рік тому

    Hi what magnification did you get your image on?

  • @malatestaaa
    @malatestaaa 3 роки тому

    Gracias!!

  • @aanggoro00
    @aanggoro00 5 років тому

    thx for the tutorial. btw, i have an image that consisting of dirt. if dirt > 0.04 mm need to count, if below 0.04 mm not count. where i can put this parameter? thx

  • @marcoarnulfomatagomez4521
    @marcoarnulfomatagomez4521 4 роки тому

    What is the size of the cells? I mean, the diameter.

  • @calixtepelo9146
    @calixtepelo9146 6 років тому

    Hey guys! Wish this message finds you well. Is there anyone here have the text tutorial of this software so he could share it with me via my e-mail please? I need it a lot to estimate the severity of bean anthracnose for my thesis. Thank you in advance!

  • @rudolfgyorkei9558
    @rudolfgyorkei9558 6 років тому

    Thanks ..................

  • @cncbilly14
    @cncbilly14 9 років тому

    Thanks so much for posting this! Is this method attached to any publication that I could cite?

  • @mohammadhdaib3300
    @mohammadhdaib3300 5 років тому

    thanks...

  • @pabloramos1022
    @pabloramos1022 7 років тому

    If someone can tell me how to count stomata; that'd make my life waaaayyyy easier! ;)