Hardware Reference
In-Depth Information
which implies that operations
opt
w
and
opt
v
are implemented concurrently.
It is important to note that multiple operations cannot share on-chip resources
(including dispensing ports and electrodes) at the same time. Thus
opt
w
and
opt
v
must satisfy following constraint:
.M
opt
w
.3/; M
opt
w
.3/
C
M
opt
w
.5//
\
.M
opt
v
.3/; M
opt
v
.3/
C
M
opt
v
.5//
D;
;
[
.M
opt
w
.4/; M
opt
w
.4/
C
M
opt
w
.6//
\
.M
opt
v
.4/; M
opt
v
.4/
C
M
opt
v
.6//
D;
;
i.e., their corresponding modules cannot overlap with each other.
2. For any pair of operations
opt
w
and
opt
v
,if
opt
w
is the predecessor of
opt
v
,
then
opt
w
must be completed earlier than the start time of
opt
v
,i.e.M
opt
v
.1/
M
opt
w
(2).
The completion time of the bioassay can be written as:
f
M
opt
i
.2/
g
C
p
D
Max
opt
i
2
P
Thus the synthesis of the biochip can be viewed as an optimization problem. The
inputs are the set of operations
P
and the set of constraints
C
. The target is:
f
M
opt
i
.2/
g
minimize: Max
opt
i
2
P
Previously published computer-aided design methods for digital microfluidic
biochips have several proposed algorithms to solve this optimization problem.
For example, the PRSA-based synthesis algorithms can be used to quickly derive
optimized synthesis results [
23
].
After the optimized synthesis results are derived, the off-line data preparation
step is completed. The bioassay is next executed according to the initial synthesis
result, and the next step is the on-line monitoring of droplets.
2.4.2
On-Line Monitoring of Droplets and Re-synthesis
of the Bioassay
During the execution of the bioassay, the control software must implement the
following steps.