Synthesis of Digital Microfluidic Biochips with Reconfigurable Operation Execution Elena Maftei Technical University of Denmark DTU Informatics www.dreamstime.com.

Slides:



Advertisements
Similar presentations
Force-Directed List Scheduling for DMFBs Kenneth ONeal, Dan Grissom, Philip Brisk Department of Computer Science and Engineering Bourns College of Engineering.
Advertisements

A Field-Programmable Pin-Constrained Digital Microfluidic Biochip Dan Grissom and Philip Brisk University of California, Riverside Design Automation Conference.
1 An Adaptive GA for Multi Objective Flexible Manufacturing Systems A. Younes, H. Ghenniwa, S. Areibi uoguelph.ca.
NCKU CSIE EDALAB Shang-Tsung Yu, Sheng-Han Yeh, and Tsung-Yi Ho Electronic Design Automation Laboratory.
Solutions for Scheduling Assays. Why do we use laboratory automation? Improve quality control (QC) Free resources Reduce sa fety risks Automatic data.
Optimal Testing of Digital Microfluidic Biochips: A Multiple Traveling Salesman Problem R. Garfinkel 1, I.I. Măndoiu 2, B. Paşaniuc 2 and A. Zelikovsky.
William L. Hwang †, Fei Su ‡, Krishnendu Chakrabarty Department of Electrical & Computer Engineering Duke University, Durham, NC 27708, USA Automated.
Early Days of Circuit Placement Martin D. F. Wong Department of Electrical and Computer Engineering University of Illinois at Urbana-Champaign.
Droplet-Aware Module-Based Synthesis for Fault-Tolerant Digital Microfluidic Biochips Elena Maftei, Paul Pop, and Jan Madsen Technical University of Denmark.
1 of 30 June 14, 2000 Scheduling and Communication Synthesis for Distributed Real-Time Systems Paul Pop Department of Computer and Information Science.
Process Scheduling for Performance Estimation and Synthesis of Hardware/Software Systems Slide 1 Process Scheduling for Performance Estimation and Synthesis.
Supply Voltage Degradation Aware Analytical Placement Andrew B. Kahng, Bao Liu and Qinke Wang UCSD CSE Department {abk, bliu,
Scheduling with Optimized Communication for Time-Triggered Embedded Systems Slide 1 Scheduling with Optimized Communication for Time-Triggered Embedded.
K. Bazargan R. KastnerM. Sarrafzadeh Physical Design for Reconfigurable Computing Systems using Firm Templates Department of Electrical & Computer Engineering.
HW/SW Co-Synthesis of Dynamically Reconfigurable Embedded Systems HW/SW Partitioning and Scheduling Algorithms.
A Scheduling and Routing Algorithm for DMFS Ring Layouts with Bus-phase Addressing Megha Gupta Srinivas Akella.
1 Dot Plots For Time Series Analysis Dragomir Yankov, Eamonn Keogh, Stefano Lonardi Dept. of Computer Science & Eng. University of California Riverside.
Torino (Italy) – June 25th, 2013 Ant Colony Optimization for Mapping, Scheduling and Placing in Reconfigurable Systems Christian Pilato Fabrizio Ferrandi,
Tabu Search-Based Synthesis of Dynamically Reconfigurable Digital Microfluidic Biochips Elena Maftei, Paul Pop, Jan Madsen Technical University of Denmark.
Tradeoff Analysis for Dependable Real-Time Embedded Systems during the Early Design Phases Junhe Gan.
1 electrowetting-driven digital microfluidic devices Frieder Mugele University of Twente Physics of Complex Fluids Fahong Li, Adrian Staicu, Florent Malloggi,
NCKU CSIE EDALAB Department of Computer Science and Information Engineering National Cheng Kung University Tainan, Taiwan Tsung-Wei.
A Field-Programmable Pin-Constrained Digital Microfluidic Biochip Dan Grissom and Philip Brisk University of California, Riverside Design Automation Conference.
Recent Research and Emerging Challenges in the System-Level Design of Digital Microfluidic Biochips Paul Pop, Elena Maftei, Jan Madsen Technical University.
Programmable Microfluidics Using Soft Lithography J.P. Urbanski Advisor: Todd Thorsen Hatsopoulos Microfluidics Lab, MIT January 25/2006.
LOPASS: A Low Power Architectural Synthesis for FPGAs with Interconnect Estimation and Optimization Harikrishnan K.C. University of Massachusetts Amherst.
Energy/Reliability Trade-offs in Fault-Tolerant Event-Triggered Distributed Embedded Systems Junhe Gan, Flavius Gruian, Paul Pop, Jan Madsen.
1 Towards Optimal Custom Instruction Processors Wayne Luk Kubilay Atasu, Rob Dimond and Oskar Mencer Department of Computing Imperial College London HOT.
Path Scheduling on Digital Microfluidic Biochips Dan Grissom and Philip Brisk University of California, Riverside Design Automation Conference San Francisco,
Ping-Hung Yuh, Chia-Lin Yang, and Yao-Wen Chang
SVM-Based Routability-Driven Chip-Level Design for Voltage-Aware Pin-Constraint EWOD Chips Qin Wang 1, Weiran He, Hailong Yao 1, Tsung-Yi Ho 2, Yici Cai.
ILP-Based Pin-Count Aware Design Methodology for Microfluidic Biochips Chiung-Yu Lin and Yao-Wen Chang Department of EE, NTU DAC 2009.
Exact routing for digital microfluidic biochips with temporary blockages OLIVER KESZOCZE ROBERT WILLE ROLF DRECHSLER ICCAD’14.
1. Placement of Digital Microfluidic Biochips Using the T-tree Formulation Ping-Hung Yuh 1, Chia-Lin Yang 1, and Yao-Wen Chang 2 1 Dept. of Computer Science.
Design of a High-Throughput Low-Power IS95 Viterbi Decoder Xun Liu Marios C. Papaefthymiou Advanced Computer Architecture Laboratory Electrical Engineering.
A SAT-Based Routing Algorithm for Cross-Referencing Biochips Ping-Hung Yuh 1, Cliff Chiung-Yu Lin 2, Tsung- Wei Huang 3, Tsung-Yi Ho 3, Chia-Lin Yang 4,
Task Graph Scheduling for RTR Paper Review By Gregor Scott.
Johnathan Fiske, *Dan Grissom, Philip Brisk
Reliability-Oriented Broadcast Electrode- Addressing for Pin-Constrained Digital Microfluidic Biochips Department of Computer Science and Information Engineering.
NCKU CSIE EDALAB Tsung-Wei Huang, Chun-Hsien Lin, and Tsung-Yi Ho Department of Computer Science and Information Engineering.
Fast Online Synthesis of Generally Programmable Digital Microfluidic Biochips Dan Grissom and Philip Brisk University of California, Riverside CODES+ISSS.
NCKU CSIE EDALAB Tsung-Wei Huang and Tsung-Yi Ho Department of Computer Science and Information Engineering National Cheng.
1 of 16 April 25, 2006 System-Level Modeling and Synthesis Techniques for Flow-Based Microfluidic Large-Scale Integration Biochips Contact: Wajid Hassan.
1 ICC 2013, 9-13 June, Budapest, Hungary Localization packet scheduling for an underwater acoustic sensor network By Hamid Ramezani & Geert Leus.
LEMAR: A Novel Length Matching Routing Algorithm for Analog and Mixed Signal Circuits H. Yao, Y. Cai and Q. Gao EDA Lab, Department of CS, Tsinghua University,
Wajid Minhass, Paul Pop, Jan Madsen Technical University of Denmark
Operating Systems Lecture 31.
Outline Motivation and Contributions Related Works ILP Formulation
Physically Aware HW/SW Partitioning for Reconfigurable Architectures with Partial Dynamic Reconfiguration Sudarshan Banarjee, Elaheh Bozorgzadeh, Nikil.
ILP-Based Synthesis for Sample Preparation Applications on Digital Microfluidic Biochips ABHIMANYU YADAV, TRUNG ANH DINH, DAIKI KITAGAWA AND SHIGERU YAMASHITA.
1 Hardware-Software Co-Synthesis of Low Power Real-Time Distributed Embedded Systems with Dynamically Reconfigurable FPGAs Li Shang and Niraj K.Jha Proceedings.
System-Level Modeling and Simulation of the Cell Culture Microfluidic Biochip ProCell Wajid Hassan Minhass †, Paul Pop †, Jan Madsen † Mette Hemmingsen.
Task Mapping and Partition Allocation for Mixed-Criticality Real-Time Systems Domițian Tămaș-Selicean and Paul Pop Technical University of Denmark.
Synthesis of Reliable Digital Microfluidic Biochips using Monte Carlo Simulation Elena Maftei, Paul Pop, Florin Popenţiu Vlădicescu Technical University.
Routing-Based Synthesis of Digital Microfluidic Biochips Elena Maftei, Paul Pop, Jan Madsen Technical University of Denmark CASES’101Routing-Based Synthesis.
1 Double-Patterning Aware DSA Template Guided Cut Redistribution for Advanced 1-D Gridded Designs Zhi-Wen Lin and Yao-Wen Chang National Taiwan University.
Operating Systems Lecture 31 Syed Mansoor Sarwar.
Optimization of Time-Partitions for Mixed-Criticality Real-Time Distributed Embedded Systems Domițian Tămaș-Selicean and Paul Pop Technical University.
Synthesis of Biochemical Applications on Digital Microfluidic Biochips with Operation Variability Mirela Alistar, Elena Maftei, Paul Pop, Jan Madsen.
1 Placement-Aware Architectural Synthesis of Digital Microfluidic Biochips using ILP Elena Maftei Institute of Informatics and Mathematical Modelling Technical.
Contents Introduction Bus Power Model Related Works Motivation
Introduction | Model | Solution | Evaluation
Architecture Synthesis for Cost Constrained Fault Tolerant Biochips
Elena Maftei Technical University of Denmark DTU Informatics
Nithin Michael, Yao Wang, G. Edward Suh and Ao Tang Cornell University
Class project by Piyush Ranjan Satapathy & Van Lepham
Fault-Tolerant Architecture Design for Flow-Based Biochips
Microfluidic Biochips
A New Hybrid FPGA with Nanoscale Clusters and CMOS Routing Reza M. P
Algorithm Course Algorithms Lecture 3 Sorting Algorithm-1
Presentation transcript:

Synthesis of Digital Microfluidic Biochips with Reconfigurable Operation Execution Elena Maftei Technical University of Denmark DTU Informatics

2 Duke University Digital Microfluidic Biochip

3 Applications Sampling and real time testing of air/water for biochemical toxins Food testing DNA analysis and sequencing Clinical diagnosis Point of care devices Drug development

4 Challenges: Design complexity Radically different design and test methods required Integration with microelectronic components in future SoCs ‏ Advantages & Challenges Advantages: High throughput (reduced sample / reagent consumption)‏ Space (miniaturization)‏ Time (parallelism)‏ Automation (minimal human intervention)‏

5 Outline Motivation Architecture Operation Execution Contribution I Module-Based Synthesis with Dynamic Virtual Devices Contribution II Routing-Based Synthesis Contribution III Droplet-Aware Module-Based Synthesis Conclusions & Future Directions

6 Architecture and Working Principles Biochip architecture Cell architecture Electrowetting-on-dielectric Droplet Top plate Ground electrode Control electrodes Insulators Filler fluid Bottom plate S2S2 R2R2 B S3S3 S1S1 W R1R1 Reservoir Detector

7 S2S2 R2R2 B S3S3 S1S1 W R1R1 Dispensing Detection Splitting/Merging Storage Mixing/Dilution Microfluidic Operations

8 Reconfigurability S2S2 R2R2 B S3S3 S1S1 W R1R1 Dispensing Detection Splitting/Merging Storage Mixing/Dilution

9 Reconfigurability S2S2 R2R2 B S3S3 S1S1 W R1R1 Dispensing Detection Splitting/Merging Storage Mixing/Dilution Non-reconfigurable

10 Reconfigurability S2S2 R2R2 B S3S3 S1S1 W R1R1 Dispensing Detection Splitting/Merging Storage Mixing/Dilution Non-reconfigurable Reconfigurable

11 Module-Based Operation Execution S2S2 R2R2 B S3S3 S1S1 W R1R1 2 x 4 module

12 Module-Based Operation Execution S2S2 R2R2 B S3S3 S1S1 W R1R1 OperationArea (cells)Time (s) Mix2 x 43 Mix2 x 24 Dilution2 x 44 Dilution2 x 25 Module library 2 x 4 module

13 Module-Based Operation Execution S2S2 R2R2 B S3S3 S1S1 W R1R1 2 x 4 module segregation cells

14 Module-Based Operation Execution S2S2 R2R2 B S3S3 S1S1 W R1R1 Operations confined to rectangular, fixed modules Positions of droplets inside modules ignored Segregation cells

15 Module-Based Synthesis with Dynamic Virtual Modules

16 Example S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D1D1 tApplication graph In S 1 In B In S 2 In R 1 Dilute Mix In S 3 In B Dilute In BIn R 2 Dilute

17 Example Biochip S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D1D1 Application graph 2 x 2 2 x 4 2 x 2 2 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

18 Example t S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D1D1 D 2 (O 5 ) Application graph 2 x 2 2 x 4 2 x 2 2 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

19 Example S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D 3 (O 12 ) M 1 (O 6 ) D 4 (O 13 ) store O 5 t+4Application graph 2 x 2 2 x 4 2 x 2 2 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

20 Example Application graph S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D 3 (O 12 ) D 4 (O 13 ) M 2 (O 7 ) t+8 2 x 2 2 x 4 2 x 22 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

21 Example Schedule Mixer 1 Mixer 2 Diluter 2 Diluter 3 Diluter 4 O5O5 O6O6 O 12 O 13 O7O7 store tt+8t+11 Allocation Application graph 2 x 2 2 x 4 2 x 2 2 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

22 Example S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D 2 (O 5 ) D1D1 tApplication graph 2 x 2 2 x 4 2 x 22 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

23 Example S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D 2 (O 5 ) tApplication graph 2 x 2 2 x 4 2 x 22 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

24 Example S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D 2 (O 5 ) tApplication graph 2 x 2 2 x 4 2 x 22 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

25 Example S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D 2 (O 5 ) tApplication graph 2 x 2 2 x 4 2 x 22 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

26 Example S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D 2 (O 5 ) t Application graph 2 x 2 2 x 4 2 x 22 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

27 Example S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D 2 (O 5 ) t Application graph 2 x 2 2 x 4 2 x 22 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

28 Example S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D 2 (O 5 ) t Application graph 2 x 2 2 x 4 2 x 22 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

29 Example S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D 2 (O 5 ) t Application graph 2 x 2 2 x 4 2 x 22 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

30 Example S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D 2 (O 5 ) t Application graph 2 x 2 2 x 4 2 x 22 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

31 Example S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D 2 (O 5 ) t Application graph 2 x 2 2 x 4 2 x 22 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

32 Example S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D 2 (O 5 ) t Application graph 2 x 2 2 x 4 2 x 22 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

33 Example S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D 2 (O 5 ) D1D1 t Application graph 2 x 2 2 x 4 2 x 22 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

34 Example S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 D 2 (O 5 ) D1D1 t M 1 (O 6 ) Application graph 2 x 2 2 x 4 2 x 22 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

35 Example t+4 D 3 (O 12 ) S1S1 S2S2 S3S3 B1B1 R2R2 R1R1 W B2B2 M 2 (O 7 ) D 4 (O 13 ) Application graph 2 x 2 2 x 4 2 x 22 x 4 S1 S1 B1 B1 S2 S2 R1 R1 R2 R2 B2 B2 B1 B1 S3 S

36 Example Schedule – operation execution with dynamic virtual modules O6O6 Mixer 1 Mixer 2 Diluter 2 Diluter 3 Diluter 4 O5O5 t t+9 O 12 O 13 O7O7 t+4 Allocation Mixer 1 Mixer 2 Diluter 2 Diluter 3 Diluter 4 O5O5 O6O6 O 12 O 13 O7O7 store tt+8 t+11 Allocation Schedule – operation execution with fixed virtual modules

37 Solution Tabu Search List Scheduling Maximal Empty Rectangles Binding of modules to operations Schedule of the operations Placement of modules performed inside scheduling Placement of the modules Free space manager based on [Bazargan et al. 2000] that divides free space on the chip into overlapping rectangles

38 Dynamic Placement Algorithm S1S1 S2S2 S3S3 B1B1 R1R1 R2R2 W B2B2 Rect 2 Rect 1 Rect 3 (0,0) (7,0) (0,4) (3,8) (8,8) D1D1

39 Dynamic Placement Algorithm S1S1 S2S2 S3S3 B1B1 R1R1 R2R2 W B2B2 D1D1 Rect 2 Rect 1 Rect 3 (0,0) D 2 (O 5 ) (6,4) (3,4) (8,8) (7,0)

40 Dynamic Placement Algorithm Rect 2 (4,0) Rect 1 (8,4) (6,0) S1S1 S2S2 S3S3 B1B1 R1R1 R2R2 W B2B2 D 2 (O 5 ) D1D1 (8,8)

41 Experimental Evaluation Tabu Search-based algorithm implemented in Java Benchmarks Real-life applications Colorimetric protein assay In-vitro diagnosis Polymerase chain reaction – mixing stage Synthetic benchmarks 10 TGFF-generated benchmarks with 10 to 100 operations Comparison between: Module-based synthesis with fixed modules (MBS) T-Tree [Yuh et al. 2007] Module-based synthesis with dynamic modules (DMBS)

42 Experimental Evaluation Best-, average schedule length and standard deviation out of 50 runs for MBS AreaTime limit (min) Best (s)Average (s)Standard dev. (%) 13 x x Colorimetric protein assay

43 Experimental Evaluation Colorimetric protein assay Best schedule length out of 50 runs for MBS vs. T-Tree Colorimetric protein assay % improvement for 9 x 9

44 Experimental Evaluation Average schedule length out of 50 runs for DMBS vs. MBS Colorimetric protein assay 7.68 % improvement for 11 x 12

45 Routing-Based Operation Execution

46 Module-Based vs. Routing-Based Operation Execution S2S2 R2R2 B S3S3 S1S1 W R1R1 S2S2 R2R2 B S3S3 S1S1 W R1R1 c2c2 c1c1

47 Operation Execution Characterization S2S2 R2R2 B S3S3 S1S1 W R1R1 c2c2 90 ◦ 0◦0◦ 180 ◦ c1c1 p 90, p 180, p 0 ?

48 Operation Execution Characterization Type Area (cells) Time (s) Mix/Dlt2 x 42.9 Mix/Dlt1 x 44.6 Mix/Dlt2 x 36.1 Mix/Dlt2 x 29.9 Input-2 Detect1 x 130 0◦0◦ 0◦0◦ 0◦0◦ 0◦0◦ 90 ◦ 0◦0◦ 0◦0◦ 0◦0◦ 180 ◦ 0◦0◦ 0◦0◦ 0◦0◦ 90 ◦ p 90, p 180, p 0 Electrode pitch size = 1.5 mm, gap spacing = 0.3 mm, average velocity rate = 20 cm/s.

49 Operation Execution Characterization Type Area (cells) Time (s) Mix/Dlt2 x 42.9 Mix/Dlt1 x 44.6 Mix/Dlt2 x 36.1 Mix/Dlt2 x 29.9 Input-2 Detect1 x 130 p 90 = 0.1 % p 180 = % p 0 = 0.29 % p 0 = 0.58 % Electrode pitch size = 1.5 mm, gap spacing = 0.3 mm, average velocity rate = 20 cm/s. 1 2

50 Example In S 1 In R 1 Mix In R 2 3 In S 2 8 Mix Dilute 9 56 In S 3 In B Waste In R Mix Application graphBiochip S2S2 R2R2 B R1R1 S1S1 W S3S3

51 Example Application graph S2S2 R2R2 B R1R1 S1S1 W S3S3 M 2 (O 7 ) M 1 (O 8 ) t = 2.04 s 1 x 4 2 x 4 1 x 4 W R 1 R 2 S 3 B S 2 R 1 S 1

52 Example t = 6.67 s S2S2 R2R2 B R1R1 S1S1 W S3S3 M 3 (O 10 ) D 1 (O 9 ) Application graph x 4 2 x 4 1 x 4 W R 1 R 2 S 3 B S 2 R 1 S 1

53 Example t = 9.5 s S2S2 R2R2 B R1R1 S1S1 W S3S3 M 4 (O 12 ) M 3 (O 10 ) Application graph x 4 2 x 4 1 x 4 W R 1 R 2 S 3 B S 2 R 1 S 1

54 Example Mixer 1 Mixer 3 Mixer 2 O8O8 O9O O 12 O 10 Diluter 1 Mixer 4 O7O7 ScheduleApplication graph x 4 2 x 4 1 x 4 W R 1 R 2 S 3 B S 2 R 1 S 1

55 Example t = 2.03 s S2S2 R2R2 R1R1 S1S1 B W Application graph x 4 2 x 4 1 x 4 W R 1 R 2 S 3 B S 2 R 1 S 1

56 Example t = 4.20 s S2S2 R2R2 S1S1 W S3S3 R1R1 B times Application graph x 4 2 x 4 1 x 4 W R 1 R 2 S 3 B S 2 R 1 S 1

57 Example t = 4.28 s R2R2 W S1S1 R1R1 S3S3 B S2S e e Application graph x 4 2 x 4 1 x 4 W R 1 R 2 S 3 B S 2 R 1 S 1

58 Example t = 6.34 s R2R2 W S1S1 R1R1 S3S3 B S2S times Application graph x 4 2 x 4 1 x 4 W R 1 R 2 S 3 B S 2 R 1 S 1

59 Example Schedule – module-based operation execution Schedule – routing-based operation execution Mixer 1 Mixer 3 Mixer 2 O8O8 O9O O 12 O 10 Diluter 1 Mixer 4 O7O O 10 O7O7 O8O8 O9O9 O 12

60 Solution In S 1 In R 1 Mix In R 2 SourceSource 3 In S 2 8 Mix Dilute SinkSink 9 56 In S 3 In B Waste In R Mix Merge Mix

61 Solution In S 1 In R 1 Mix In R 2 SourceSource 3 In S 2 8 Mix Dilute SinkSink 9 56 In S 3 In B Waste In R Mix Merge Mix Minimize the completion time for the operation Minimize the time until the droplets meet

62 Solution Greedy Randomized Adaptive Search Procedure (GRASP) S2S2 R2R2 S3S3 R1R1 S1S1 B W

63 Solution Greedy Randomized Adaptive Search Procedure (GRASP) S2S2 R2R2 S3S3 R1R1 S1S1 B W For each droplet: Determine possible moves Evaluate each move Merge: minimize Manhattan distance Mix: maximize operation execution Make a list of the best N moves Perform a random move from N

64 Solution Greedy Randomized Adaptive Search Procedure (GRASP) S2S2 R2R2 S3S3 R1R1 S1S1 B W For each droplet: Determine possible moves Evaluate each move Merge: minimize Manhattan distance Mix: maximize operation execution Make a list of the best N moves Perform a random move from N

65 Solution Greedy Randomized Adaptive Search Procedure (GRASP) S2S2 R2R2 S3S3 R1R1 S1S1 B W For each droplet: Determine possible moves Evaluate each move Merge: minimize Manhattan distance Mix: maximize operation execution Make a list of the best N moves Perform a random move from N

66 Solution Greedy Randomized Adaptive Search Procedure (GRASP) S2S2 R2R2 S3S3 R1R1 S1S1 B W For each droplet: Determine possible moves Evaluate each move Merge: minimize Manhattan distance Mix: maximize operation execution Make a list of the best N moves Perform a random move from N

67 Experimental Evaluation GRASP-based algorithm implemented in Java Benchmarks Real-life applications Colorimetric protein assay Synthetic benchmarks 10 TGFF-generated benchmarks with 10 to 100 operations Comparison between: Routing-based synthesis (RBS) Module-based synthesis with fixed modules (MBS)

68 Experimental Evaluation Colorimetric protein assay 44.95% improvement for 10 x 10 Colorimetric protein assay Average schedule length out of 50 runs for RBS vs. MBS Colorimetric protein assay % improvement for 10 x 10

69 Routing-Based Operation Execution - Conclusions Improved completion time compared to module-based synthesis Challenge: contamination

70 Routing-Based Operation Execution - Conclusions Improved completion time compared to module-based synthesis Challenge: contamination S1S1 R1R1 W S3S3 B1B1 B2B2 S2S2 R3R3 R2R2 1 residues

71 Routing-Based Operation Execution - Conclusions Improved completion time compared to module-based synthesis Challenge: contamination S1S1 R1R1 S3S3 B1B1 B2B2 S2S2 R2R2 W R3R3 1 w1w1

72 Routing-Based Operation Execution - Conclusions Improved completion time compared to module-based synthesis Challenge: contamination S1S1 R1R1 S3S3 B1B1 B2B2 S2S2 R2R2 W R3R3 1 w1w1

73 Routing-Based Operation Execution - Conclusions Improved completion time compared to module-based synthesis Challenge: contamination S1S1 R1R1 S3S3 B1B1 B2B2 S2S2 R2R2 W R3R3 1 w1w1

74 Routing-Based Operation Execution - Conclusions Improved completion time compared to module-based synthesis Challenge: contamination S1S1 R1R1 S3S3 B1B1 B2B2 S2S2 R2R2 W R3R3 1 w1w1 Partition 1 Partition 2 w2w2

75 Routing-Based Operation Execution - Conclusions Improved completion time compared to module-based synthesis Challenge: contamination S1S1 R1R1 S3S3 B1B1 B2B2 S2S2 R2R2 W R3R3 1 w1w1 Partition 1 Partition 2 w2w2 S1S1 R1R1 S3S3 B1B1 B2B2 S2S2 R2R2 1 W R3R3

76 Routing-Based Operation Execution - Conclusions Improved completion time compared to module-based synthesis Challenge: contamination S1S1 R1R1 S3S3 B1B1 B2B2 S2S2 R2R2 W R3R3 1 w1w1 Partition 1 Partition 2 w2w2 S1S1 R1R1 S3S3 B1B1 B2B2 S2S2 R2R2 1 W R3R3 w2w2 w1w1

77 Droplet-Aware Operation Execution without Contamination

78 Example Biochip In S 1 In B 8 In S In R In B In R 2 Dilute Mix Dilute In S 2 Mix In B Application graph S1S1 R2R2 W S3S3 B1B1 S2S2 R1R1 B2B2

79 Example S1S1 R2R2 W S3S3 B1B1 S2S2 R1R1 B2B In S 1 8 In S In R Dilute Mix Dilute In S 2 Mix 2 x 4 1 x 4 R2R2 B2B2 2 x 3 S3S3 B1B1 S1S1 S2S2 Application graphBiochip B1B1 R1R1

80 Example S1S1 R2R2 W S3S3 B1B1 S2S2 R1R1 B2B2 t = 2 s Application graph In S 1 8 In S In R Dilute Mix Dilute In S 2 Mix 2 x 4 1 x 4 R2R2 B2B2 2 x 3 S3S3 B1B1 S1S1 S2S2 B1B1 R1R1

81 Example t = 4.9 s M 2 (O 7 ) S1S1 R2R2 W S3S3 B1B1 S2S2 R1R1 B2B2 Application graph In S 1 8 In S In R Dilute Mix Dilute In S 2 Mix 2 x 4 1 x 4 R2R2 B2B2 2 x 3 S3S3 B1B1 S1S1 S2S2 B1B1 R1R1

82 Example Diluter 1 O5O5 O O7O7 O6O6 O 13 Diluter 2 Diluter 3 Mixer 1 Mixer 2 ScheduleApplication graph In S 1 8 In S In R Dilute Mix Dilute In S 2 Mix 2 x 4 1 x 4 R2R2 B2B2 2 x 3 S3S3 B1B1 S1S1 S2S2 B1B1 R1R1

83 Example S1S1 R2R2 W S3S3 B1B1 S2S2 R1R1 B2B2 t = 2 sApplication graph In S 1 8 In S In R Dilute Mix Dilute In S 2 Mix 2 x 4 1 x 4 R2R2 B2B2 2 x 3 S3S3 B1B1 S1S1 S2S2 B1B1 R1R1

84 Example t = 2 s S1S1 R2R2 W S3S3 B1B1 S2S2 R1R1 B2B2 65 Application graph In S 1 8 In S In R Dilute Mix Dilute In S 2 Mix 2 x 4 1 x 4 R2R2 B2B2 2 x 3 S3S3 B1B1 S1S1 S2S2 B1B1 R1R1

85 Example t = 4.17 s S1S1 R2R2 W S3S3 B1B1 S2S2 R1R1 B2B Application graph In S 1 8 In S In R Dilute Mix Dilute In S 2 Mix 2 x 4 1 x 4 R2R2 B2B2 2 x 3 S3S3 B1B1 S1S1 S2S2 B1B1 R1R1

86 Example Schedule Diluter 1 O5O5 O O7O7 O6O6 O 13 Diluter 2 Diluter 3 Mixer 1 Mixer Application graph In S 1 8 In S In R Dilute Mix Dilute In S 2 Mix 2 x 4 1 x 4 R2R2 B2B2 2 x 3 S3S3 B1B1 S1S1 S2S2 B1B1 R1R1

87 Example Schedule – module-based operation execution Schedule – droplet-aware operation execution Diluter 1 O5O5 O O7O7 O6O6 O 13 Diluter 2 Diluter 3 Mixer 1 Mixer Diluter 1 O5O5 O O7O7 O6O6 O 13 Diluter 2 Diluter 3 Mixer 1 Mixer 2

88 Solution Location of modules determined using Tabu Search Greedy movement of droplets inside modules Routing of droplets between modules and between modules and I/O ports determined using GRASP

89 Droplet-Aware Operation Execution S1S1 R2R2 W S3S3 B1B1 S2S2 B2B2 R1R1 M 2 (O 7 ) D 3 (O 13 ) D 2 (O 12 )

90 Droplet-Aware Operation Execution S1S1 R2R2 W S3S3 B1B1 S2S2 B2B2 R1R

91 Droplet-Aware Operation Execution S1S1 R2R2 W S3S3 B1B1 S2S2 B2B2 R1R

92 Droplet-Aware Operation Execution S1S1 R2R2 W S3S3 B1B1 S2S2 B2B2 R1R

93 Experimental Evaluation Algorithm implemented in Java Benchmarks Real-life applications In-vitro diagnosis Colorimetric protein assay Synthetic benchmarks 3 TGFF-generated benchmarks with 20, 40, 60 operations Comparison between: Droplet-aware module-based synthesis (DAS) Module-based synthesis (MBS)

94 Experimental Evaluation 21.55% improvement for 13 x 13 Colorimetric protein assay Average schedule length out of 50 runs for DAS vs. MBS Colorimetric protein assay % improvement for 13 x 13 Colorimetric protein assay

95 Experimental Evaluation Algorithm implemented in Java Benchmarks Real-life applications Colorimetric protein assay Synthetic benchmarks 3 TGFF-generated benchmarks with 20, 40, 60 operations Comparison between: Droplet-aware module-based synthesis (DASC) Routing-based synthesis (RBSC) with contamination avoidance

96 Experimental Evaluation 11.19% improvement for 14 x 14 Colorimetric protein assay Average schedule length out of 50 runs for DASC vs. RBSC Colorimetric protein assay % improvement for 14 x 14 Colorimetric protein assay

97 Contributions Tabu Search-based algorithm for the module-based synthesis with fixed devices [CASES09] Module-based synthesis with virtual devices [CASES09] Module-based synthesis with non-rectangular virtual devices [DAEM10] Analytical method for operation execution characterization [CASES10] ‏Routing-based synthesis [CASES10] + contamination [DAEM, submitted] Droplet-aware module based synthesis [JETC, submitted] ILP formulation for the synthesis of digital biochips [VLSI- SoC08]

98 Conclusions Proposed several synthesis techniques for DMBs Considered the reconfigurability characteristic of DMBs Shown that by considering reconfigurability during operation execution improvements in the completion time of applications can be obtained

99 Future Directions S1S1 R2R2 W S3S3 B1B1 S2S2 R1R1 B2B2

100 Future Directions S1S1 R2R2 W S3S3 B1B1 S2S2 R1R1 B2B2 S1S1 R2R2 W S3S3 B1B1 S2S2 R1R1 B2B2 Module-Based Synthesis with Overlapping Devices

101 Future Directions S1S1 R2R2 W S3S3 B1B1 S2S2 R1R1 B2B2 Fault-Tolerant Module-Based Synthesis M 1 (O 1 ) M 2 (O 2 ) Faulty cell S1S1 R2R2 W S3S3 B1B1 S2S2 R1R1 B2B2 M 1 (O 1 ) M 2 (O 2 ) M 3 (O 3 )

102 Future Directions S1S1 R2R2 W S3S3 B1B1 S2S2 R1R1 B2B2 Fault-Tolerant Module-Based Synthesis Faulty cell S1S1 R2R2 W S3S3 B1B1 S2S2 R1R1 B2B2 M 1 (O 1 ) M 2 (O 2 ) M 3 (O 3 ) M 2 (O 2 ) M 1 (O 1 ) M 3 (O 3 )

103

104 Back-up slides

105 Electrowetting

106 Surface Tension Imbalance of forces between molecules at an interface (gas/liquid, liquid/liquid, gas/solid, liquid/solid)

107 Dispensing

108 Dispensing

109 Dispensing

110 Splitting

111 Mixing

112 Capacitive sensor

113 Design Tasks OperationArea(cells)Time(s) Mix 2 x 210 Mix1 x 35 Dilute1 x 38 Dilute2 x 53

114 Design Tasks OperationArea(cells)Time(s) Mix 2 x 210 Mix1 x 35 Dilute1 x 38 Dilute2 x 53 S1S1 S2S2 S3S3 B R1R1 R2R2

115 Experimental Evaluation Quality of the solution compared to classical operation execution Best out of 50 Colorimetric protein assay 9.73% improvement for 11 x 12 Colorimetric protein assay

116 Experimental Evaluation Quality of the solution compared to classical operation execution Best out of 50 Colorimetric protein assay 44.63% improvement for 10 x 10

117 Experimental Evaluation Quality of the solution compared to classical operation execution Best out of 50 Colorimetric protein assay 15.76% improvement for 13 x 13

118 Future Directions S1S1 R2R2 W S3S3 B1B1 S2S2 B2B2 R1R Pin-Constrained Routing-Based Synthesis

119 Future Directions S1S1 R2R2 W S3S3 B1B1 S2S2 B2B2 R1R Pin-Constrained Routing-Based Synthesis

120 Future Directions S1S1 R2R2 W S3S3 B1B1 S2S2 B2B2 R1R Pin-Constrained Routing-Based Synthesis

121 Microfluidic Operations S2S2 R2R2 B S3S3 S1S1 W R1R1 Dispensing

122 Microfluidic Operations S2S2 R2R2 B S3S3 S1S1 W R1R1 Dispensing Detection

123 S2S2 R2R2 B S3S3 S1S1 W R1R1 Dispensing Detection Splitting/Merging Microfluidic Operations

124 S2S2 R2R2 B S3S3 S1S1 W R1R1 Dispensing Detection Splitting/Merging Microfluidic Operations

125 S2S2 R2R2 B S3S3 S1S1 W R1R1 Dispensing Detection Splitting/Merging Storage Microfluidic Operations

126 Motivational Example (for the first contrib) Application graph OperationArea(cells)Time(s) Mix2 x 43 Mix2 x 24 Dilution2 x 44 Dilution2 x 25 Dispense - 2 Module library In S 1 In B 8 In S In R In B In R 2 Dilute Mix Dilute In S 2 Mix In B

127 Motivational Example(for the 2 nd contrib) In S 1 In R 1 Mix In R 2 SourceSource 3 In S 2 8 Mix Dilute SinkSink 9 56 In S 3 In B Waste In R Mix Application graph TypeArea (cells) Time (s) Mix/Dlt2 x 42.9 Mix/Dlt1 x 44.6 Mix/Dlt2 x 36.1 Mix/Dlt2 x 29.9 Input-2 Detect1 x 130 Module library

128 Example(for the 3 rd contrib) TypeArea (cells) Time (s) Mix/Dlt2 x 42.9 Mix/Dlt1 x 44.6 Mix/Dlt2 x 36.1 Mix/Dlt2 x 29.9 Input-2 Detect1 x 130 Module libraryApplication graph In S 1 In B 8 In S In R In B In R 2 Dilute Mix Dilute In S 2 Mix In B