Difference between revisions of "Walkthrough on manual marker clicking"
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= Data set =
= Data set =
During the ''Dynamo'' workshop you will find the
During the ''Dynamo'' workshop you will find the tilt series in your data folder. Outside the workshop we suggest to follow this tutorial wit h the data set from the public EMPIAR database (entry number 10064, data item VPP_tomo4.mrc), which can be accessed through an ftp server:
Revision as of 17:23, 27 August 2019
Reconstruction of a tomogram implies the availability of a set of alignment parameters that bring the tilt series delivered by the microscopio onto a compatible reference. Fiducial markers can be located using automated methods. In this walkthrough, we describe the tools that Dynamo offers to locate them manually through graphical interaction with the tilt series.
- 1 Data set
- 2 The dmarkers GUI
- 3 Fitting to an alignment model
- 4 Reconstruction through the command line
During the Dynamo workshop you will find the needed tilt series in your data folder. Outside the workshop we suggest to follow this tutorial wit h the data set from the public EMPIAR database (entry number 10064, data item VPP_tomo4.mrc), which can be accessed through an ftp server:
in linux, or, in Mac:
The dmarkers GUI
This GUI is the basic tool for exploring tilt series and annotating on it using Dynamo. It allows to edit manually positions of markers, to fit them to a projection model, and to create an aligned data stack and a reconstruction based on this fitting.
Loading the data
Opening the dmarkers GUI on a tilt series:
It is convenient to first read the tilt series:
ts = dread('VPP_tomo4.mrc');
and then pass the variable to the gui dmarkers:
gui = dmarkers(ts,'tiltAngles',-60:2:60);
here, gui is just a handle to the GUI. This handle can be used on a later point to operate on it. Note that we also need to pass the tilt angles, as they will be needed for fitting a projection model.
Basic visualization controls
Slide on micrographs
- Use the slide bar to view a transition of the micrographs (lower resolution images will be shown during the transition, full resolution images will be shown )
- left and right arrows move the previous or next micrograph in the tilt series.
- You can zoom into a point by using the wheel.
- The small red window in the tool bar can be used as magnifying-glass to zoom in into a hand-draw a region.
- The tool with the four arrows pointing into the corners zooms out of the scene totally.
The scene gets dragged by moving the mouse while keeping pressed the primary mouse button.
Elimination of defective tilts
Some micrographs may be defective because of errors during acquisition. They can be markers as invalid by the key x. If you want to undo the marking of a micrograph as invalid, use shift+x.
Initiating a trace
A three-dimensional gold bead is represented by a trace. A trace is a set of observations, where we call observation to the location of the projection of a gold bead in a given micrograph.
The tool with a black point and a red edge starts the trace initiator. The cursor in the GUI becomes a cross; while this cursor is active, clicking on the screen will create a new gold bead.
Following a trace
To select a gold bead, click on it with the mouse, a green box will appear on the observation corresponding to the selected markers in the current micrograph. Important to add observations into a trace that you have just created, you need to select it, otherwise your next clicks on the screen will be assigned to the trace that is currently under selection.
Once you have selected a gold bead, you should switch off the tool for adding gold beads, and switch on the tool for adding observations to the gold bead currently under selection. The icon represents a point being tracked across several micrographs.
You can use the arrows to move to the next or previous micrograph after clicking the gold bead.
Additionally, you can connect the click and right or click and left tools. When they are switched on, after a click on the screen, the GUI will automatically move to the next micrograph.
Key controls during clicking
- d will delete the closest observation (point in currently shown micrograph).
- shift + d will delete a full trace.
- m will move the observation of the currently selected shape to the location of the cursor.
Auxiliar views during clicking
There are two auxiliary GUIs that can be used to control the growth of the traces based as you click the points. The occupancy window updates as a new observation is added into a gold bead, showing the current content of each trace. And additional control shows the content of each trace as new points are clicked inside.
Saving the marker set
We want to save current set of markers into disk, by using the save to disk option in the Tracks menu. This will create the file Tracks.dms in disk.
Fitting to an alignment model
When you have enough observations, you can proceed to fitting the location of your gold beads to a projection model. The tool with the icon Fit will compute a set of shifts and a single angle psi of rotation for the tilt axis.
In the Fit menu on the GUI, you can find the current error, i.e., the mean residual between each observation and the projection estimated by the fitting model.
Extended fitting models
In a coarse fitting, Dynamo only tries to solve for shifts and a single rotation angle for all micrographs. It is possible to refine this fitting allowing a different rotation of the tilt axis for each micrograph. You can select for a richer model that computes for one different rotation angle on each micrograph by checking the option eachTilt on the parameter psi (default is single).
Although you will get a lower error value, this might be due to overfitting. Thus, richer parametric models should not be used if you don't have enough markers on each micrograph (in the order of the tens.)
Reconstruction through the command line
Creating reconstructions through the command line is convenient when organizing the processing of batches of tilt series. Automatic selection of markers is explored in a different walkthrough, here we describe the command line tools for creating reconstructions once a marker set is available. The steps are:
- Fitting of the available markers (using a fitter object).
- Extraction of alignment parameters (using an aligner object).
- Creation of an aligned tilt series.
- Weighting the tilt series appropriately for a weighted-back-projection or Sirt-like reconstruction.
- Creation of the tomogram through back projecting the filtered aligned stack.
If you have a set of markers saved in a file in disk, you can load it to memory through:
markers = dread('Tracks.dms');
Then, you can create a fitter object:
fitter = dfitter(markers);
This object needs to know where to put the rotation center of the aligned tilt series.
and prepare it to run with standard parameters:
will then compute the best psi angle for the rotation of the tilt axis together with the shifts. They can be gathered into an stack alignment object
stackAligner = fitter.getStackAligner();
that gets then applied onto the original tilt series in the variable ts.
tsAligned = stackAligner.applyOnStack(ts);
This aligned stack can be visualized through:
A reconstruction with a bigger pixel size can be computed by resizing both tilt series and markers. A marker object can be resized through:
markersBinned = markers.math.bin(2);
Here, the factor 2 indicates that the coordinates of the markers get halved twice. This factor needs to be applied also to the tilt series:
tsBinned = dpktilt.bin(ts,2);
Now, we can refit the binned markers, proceeding as above:
binnedFitter = dfitter(markersBinned); binnedFitter.setCenter(tsBinned); binnedFitter.physical.defaultInitialization(); binnedFitter.linearScan(); binnedAligner = binnedFitter.getStackAligner(); tsBinnedAligned = binnedAligner.applyOnStack(tsBinned);
To create a weighted back projection reconstruction, this stack needs to be weighted with a ramp function in the Fourier space.
tsBinnedRamp = dpktomo.rec.applyRampFilter(tsBinnedAligned);
Then, we can use the command dpktilt.math.backproject to create a reconstruction.
fbp = dpktilt.math.backproject([600,600,600],tsBinnedRamp,-60:2:60,'mw','*'); .
Here, the flag 'mw' is merely instructing Dynamo to use all available cores.
The reconstruction object fbp contains the reconstructed tomogram in its property .rec, which can be visualized through: