A cell
does not contribute to MIP from any viewing direction (and
therefore should not to be considered for rendering), if all rays
passing through it collect a higher value by passing through other
cells
either before or after
is processed.
The first approach is to investigate direct
neighbors
of a cell
only.
does not contribute to
any ray through it if
. As we
assume continuous rays to be traced through the volume, only
face-connected neighbors of
have to be considered (A ray entering
through an edge or vertex at least ``touches'' some face-connected
neighbors).
Applying such a unified relevance detection for cell elimination, which considers the whole domain of viewing directions, is very ineffective and leads to low cell removal rates. Significantly better results can be achieved if several distinct clusters of similar viewing directions are distinguished. For rendering, the set of cells corresponding to the cluster which contains the current viewing-direction is selected and used for MIP. To minimize the number of neighbors which have to be checked for elimination, a decomposition of all viewing directions into 24 clusters is performed first (in the same way as for the voxel-based MIP). Each cluster of viewing directions corresponds to a quarter-face of the directional cube as depicted in figure 4.12b. Considering just viewing directions out of one cluster, a cell's relevance to MIP depends on just three neighbors (figure 4.12c) instead of six as in the case of viewpoint-independent preprocessing (figure 4.12a).
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As the direction of ray traversal is not relevant for MIP and a MIP generated from a certain viewing direction produces exactly the same image as a MIP from the opposite direction, sets of possibly contributing cells have only to be calculated for 12 of the 24 clusters of viewing directions. Furthermore, as can be seen in figures 4.12b and c, three clusters of viewing directions around each corner of the directional cube result in the same set of direct neighbors on which a cell's relevance depends (for example clusters 1, 11 and 20). Unfortunately, the clusters differ in the way in which the estimations for rays entering through cell faces combine to the estimations for exiting faces. As the removal algorithm uses face estimations for determining non-contributing cells, the clusters can not be combined without sacrificing removal efficiency.
To achieve effective cell elimination, not only the influence of direct neighbors, but also the influence of more distant cells on rays has to be investigated. This can be done by applying a simple two-pass scheme for each cluster of viewing directions. For reasons of simplicity, the procedure will be explained in 2D. The extension to 3D is straight-forward.
For cell removal in 2D, the viewing domain is decomposited into 8
clusters, each one covering a range of viewing directions spanning
45 degrees (figure 4.13a). Rays within cluster 1 can
enter cell
only through edge
or
. Considering
just the values at the cell's vertices, cell
has no influence on
the maximum of rays through
, if
- in this case,
the maximum contribution of the cell to any
ray entering through
and leaving through
or
is
located on the edge
. As this edge is shared
with cell
which is traversed by the rays earlier,
does not
contribute to the rays. Similarly, the cell has no influence on
rays through
if
due to the contribution of cell
- the condition for
has to consider the influence of
, as a
large data value at
may influence the data gradient within the
cell in a way that rays through
obtain
a larger value within the cell than at
or
.
By preprocessing the volume in a spatially consecutive order, the
influence of cells on ray maxima
can be propagated with an advancing front approach. In the example in
figure 4.13b, cells
and
are processed before cell
is
reached. For both of them, lower-bound estimations of the maximum for rays
which leave the cells have been calculated (for this cluster, rays leave
cells either through face
or through face
). This means, that
at the time
is processed, lower-bound estimations
for rays
entering through
and
for rays entering through
are
available, which already include the influence of more distant (preceding)
cells and the influence of the edges themselves (
and
). Thus, the revised test for the irrelevance of cell
is
and
. If both
conditions are true,
is removed and never ever considered for
MIP anymore. After classifying the
cell, the lower-bound estimations for the maxima of rays leaving the
cell have to be computed. As for the investigated cluster of viewing
directions only rays which have entered the cell
through
can leave through
, the
estimation for rays
through
is
. As rays
entering through both,
and
can
leave through
, the estimation for
.
While the first sweep allows to identify and remove low-valued cells located behind higher-valued parts of the volume, a second sweep in the opposite direction is required to propagate the influence of high-valued cells to cells reached earlier by the rays of this cluster. The second sweep is identical with the first sweep with the exception of the inverted orientation of the rays and thus an inverted volume scan order. Cells which have been removed during the first sweep do not influence ray values during the second sweep. Considering also cells removed during the first sweep would result in mutual elimination of cells and would lead to holes in the volume.
The two-pass method presented above can be extended to 3D in a straight-forward way. For a decomposition of the viewing domain into 24 (12) clusters, rays may enter and leave cells through three faces for each cluster. Lower-bound estimations have to be propagated for faces instead of edges.
To even further increase the efficiency of removal and to compensate for noise which is usually present in MR data sets, the removal process can be modified to remove also cells which violate the exact criteria by a factor which does not exceed a user specified threshold (removal tolerance). After the preprocessing with a 1% tolerance, on average only about 30% of all cells remain as possibly contributing for a single view-set. For detailed results please refer to section 4.2.4 and table 4.5.