Comments (5)
Very good point. I would say it is also necessary to inspect a down-sampled and zero-mean version of the movie to be sure that spikes are not missed and/or that overlapping neurons are properly segmented.
cc @marius10p @agiovann @epnev @Selmaan @aaronkerlin @sofroniewn @svoboda314 @boazmohar @syncrostone
from neurofinder.
@agiovann agreed - a great way to draw rois would be to have a mode where such a movie could be made to play in loop in the background as you are drawing on top of it
from neurofinder.
I'd agree with the idea about actually playing the (heavily temporally down-sampled) movie in the background, or some other means to check hand circling against the timeseries data. I don't think the mean or a local correlation image are a replacement for this if we want ground truth.
The ROIs will probably have some relatively inactive neurons selected because of a mean image, and active neurons not visible in the mean image. It would be useful in evaluating an algorithm's performance to do some minimal processing of the traces (e.g. %frames above 1 dF/F) to classify cells as active or inactive for this purpose.
from neurofinder.
@Selmaan great point, if we do this redo of the ground truth, we could compute some measure of activity as you suggest, and then add a toggle for two versions of the results table, one for all neurons, and one for all neurons with activity above some threshold, @marius10p had suggested something similar.
from neurofinder.
@freeman-lab sounds like a great plan to me, and definitely worth it for understanding the behavior of the algorithms. It would also allow you to compare the algorithms to inter-human agreement, which is useful information.
Not sure how you compute the local correlation map, but we find it useful to highpass filter the images at ~50um (like a background subtraction), and bandpass filter the timecourses of each pixel between 0.1 and 2 Hz (or something like that).
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Related Issues (20)
- color themes
- ignore case on search
- fix links HOT 1
- Add Data Explanation HOT 3
- have a switch between 1) results as currently displayed, and 2) results ONLY on active cells HOT 1
- full-length datasets HOT 7
- The tested algorithms have not been developed for 1-2 minute long recordings
- what are the performance measures? HOT 1
- add durations to data section HOT 2
- scale detection distance threshold by pixels? HOT 4
- registration artifacts in 00 series due to line-by-line registration HOT 3
- show mean images
- 04.00 erroneous/inconsistent labels HOT 2
- Neurofinder website not connecting
- Website gives connection error HOT 6
- License for datasets?
- Codeneuro website not working HOT 1
- The dataset can't be download correctly.
- Citation?
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