Biomedical Engineering Reference
In-Depth Information
NOP
S
1
: Urine
S
2
: Plasma
S
3
: Serum
R
1
: Glucose oxidase
R
2
: Lactate oxidase
B
: Buffer fluid
S
1
S
1
R
2
R
1
l
2
S
2
S
3
B
B
l
4
l
5
l
6
t
7
l
8
l
1
l
3
R
2
R
1
B
M
1
M
2
Dl
1
l
10
Dl
2
l
11
l
9
R
1
R
2
l
13
Dt
1
Dt
2
M
3
M
4
l
12
Dl
3
Dt
3
Dt
4
M
5
M
6
l
1: Dispensing operation
Dl
1: Diluting operation
M
1: Mixing operation
Dt
1: Optical detection
Dt
5
Dt
6
NOP
Figure 3.24
Sequencing graph model of bioassay example.
S
1
l
1
S
2
S
3
R
1
R
2
B
D
1
D
2
0
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
l
7
l
2
l
8
Sub-problem
1
Sub-problem
2
l
3
l
5
l
4
l
6
M
1
Dl
2
Dl
1
M
2
l
9
l
10
l
11
Sub-problem
3
Sub-problem
4
M
3
M
4
Dl
3
l
12
l
13
Dt
1
Dt
2
Sub-problem
5
SS
Sub-problem
6
M
5
M
6
Sub-problem
7
Dt
4
Dt
3
S
S
Sub-problem
8
Sub-problem
9
Dt
6
Dt
5
Sub-problem
10
Sub-problem
11
Figure 3.25
Schedule obtained via architectural-level synthesis.
protocol, based on Trinder's reaction, can be modeled by a sequencing graph,
as shown in Figure 3.24. We assume that the schedule for assay operations
and resource binding have been obtained via architectural-level synthe-
sis (e.g., through the modified list-scheduling algorithm [16]), as shown in
Figure 3.25. Note that one time unit in this schedule is set to 2 s. Moreover,
