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b
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Fig. 2.1
( a ) Initial sequencing graph; ( b ) operations 12, 13, and 14 are added for error-recovery
1. The first drawback is the over-simplification of fault detection and the associated
assumptions. It is impractical to use a uniform “expected value” for the cali-
bration of each detection operation. Note that the concentration of intermediate
product droplets vary in a dynamic manner at various stages during bioassay
execution. Hence the calibration needs to be repeated and carried out dynamically
as well.
2. In [ 11 ], all recovery operations are carried out in a stand-alone manner. All
other ongoing bioassay-related fluidic operations are interrupted when an error is
detected. The potential long waiting times introduced by recovery operations will
lead to sample degradation and erroneous assay outcomes [ 14 ]. Some operations,
such as colorimetric enzyme-kinetic reactions, require precise durations as spec-
ified by the reaction protocol, and they cannot be elongated without introducing
unpredictability in the experiment outcome [ 15 ].
3. The error-recovery approach in [ 11 ] cannot handle situations when multiple
errors occur during a bioassay. For example, [ 11 ] assumes that all error-recovery
operations will be executed successfully and it does not consider the likelihood
that errors can also occur during recovery.
4. The error-recovery strategy in [ 11 ] does not consider reliability issues. Errors
such as the generation of droplets with abnormal volumes are usually caused by
the accumulation of charge on the surface of certain electrodes [ 7 , 8 ]. If the use
of such electrodes is continued, it is likely that they will introduce more errors
[ 7 , 8 ]. Thus, in order to ensure the reliability of biochips, we must minimize the
utilization of these electrodes.
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