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.
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