How to track multiple particles or bacteria in ImageJ?
I am using multitracker in imageJ but unable to track many particles and bacteria. please help and give valuable suggestions.
Try using Kalman filter plugin
https://imagej.nih.gov/ij/plugins/kalman.html
@Aparna Sathya Murthy Can you say how do perform Kalman Filter plugin?. I have tried once but there is no option for multi tracking
Have you tried this : https://imagej.nih.gov/ij/plugins/multitracker.html
Aparna Sathya Murthy yes I have tried but unable to track so if u know something please share
I used ImageJ long ago !!! it is very effective tool !!
I use Matlab : https://www.mathworks.com/help/vision/examples/motion-based-multiple-object-tracking.html
This link is motion detection and tracking . You can try
You can try neuron j also
Follow
Not my soecilization
Could someone suggests which MW of FITC-Dextran is used for chemotaxis of bacteria? Also, if I make a FITC-dextran solution in PBS then how long can we store this solution at 4 degree Celsius?
31 December 2019 3,700 1 View
Can anybody say which calcium binding agent (which either fluoroscence or give colours) are use to measure calcium level outside the cell or in extracellular media ?
07 August 2019 6,057 2 View
If photoresist is coated over first alignment marks then how will I do 2nd alignment through MJB4 mask aligner?
07 August 2019 7,641 4 View
I want 1000 bacteria (numbers) to begin my experiments .How will i get these numbers? Any specific methods? please give suggestions.
07 August 2019 3,828 12 View
Could anybody say what is the general porosity of PDMS , i mean pore size ? can we use PDMS for DNA run?? one more thing what is the pore size of Whatmann filter paper??
03 April 2019 2,710 2 View
I got a agar stabs of bacterial strains, how will i use for this for my experiment i.e how to subculture or revive from stored strains in agar stab?
01 February 2019 3,249 4 View
How do make a glycerol stock of bacteria for future use? I need valuable suggestions for that.Please put here and share your experience.
01 February 2019 3,841 3 View
Fluorescent intensity of cytosolic GFP of bacterial cell is assumed to be equal to their cell volume? what does it mean?. could anybody explain it why cytosolic GFP? and their intensity...
01 February 2019 7,971 5 View
What is L-Form of Bacteria. How can we make E.coli L-form i mean what is the protocol to make it L-form. How can i maintain this L-form to longer time. If not , from where can we order simple...
08 September 2018 8,013 0 View
Everytime i found different OD data which was fluctuating and sometimes continue increase of OD .Though growth curve and colony under microscope dont tell wheather it is contaminated or not.If...
08 September 2018 593 15 View
average particle size calculation from TEM
04 August 2024 2,921 1 View
TEP presentation caption (The Environmental Project) Re: Why should Washington’s DC, or any country government point of location think of as nowadays of as to being 'tomorrow as to come! if it...
03 August 2024 2,484 1 View
Dear Researchers I need to know, how to load and plot 2D-PIV (particle image velocimetry) recorded velocity vector field data in Tecplot? Thank You
02 August 2024 3,615 1 View
The delta function seems produce logical contradictions when analyzed on a fundamental level. I would be curious if anyone else agrees.
31 July 2024 10,109 3 View
I have images of film formed on the bottom of a 50mL beaker, and I have been trying to figure out the surface area. I could easily use features on imageJ to do that, but I want to know which area...
23 July 2024 4,461 1 View
Some of the techniques I am familiar with are standard. I would like to know which of the two methods under study is preferable, as well as the cost and list of particles and devices needed in...
22 July 2024 1,921 3 View
Hi everyone, I experienced some moving particles in my mouse hippocampal slices. The media looks clear. Any idea what these moving particles might be? Thanks you!
22 July 2024 3,734 0 View
Dear All: I have to quantify the fluorescence intensity of cells that are fluorescent to two different markers, so i'm interested in finding out if this is possible. Previously I have...
22 July 2024 8,770 1 View
Is it reasonable to exclude all trials with a blink or saccade in the 150 ms before stimulus onset? As an alternative, would it be better to exclude blinks (after extending them by about 100 ms...
19 July 2024 3,838 0 View
I am a beginner with ImageJ and would like to know how to quantify fluorescence images of platelets taken with a fluorescence microscope at 40x and 100x magnification. If you could provide...
11 July 2024 1,464 7 View