This paper proposes an object oriented model scheduling for parallel computing in media MultiProcessors System on Chip(MPSoC).Firstly,the Coarse Grain Data Flow Graph(CGDFG) parallel programming model is used in this ...This paper proposes an object oriented model scheduling for parallel computing in media MultiProcessors System on Chip(MPSoC).Firstly,the Coarse Grain Data Flow Graph(CGDFG) parallel programming model is used in this approach.Secondly,this approach has the feature of unified abstraction for software objects implementing in processor and hardware objects implementing in ASICs,easy for mapping CGDFG programming on MPSoC.This approach cuts down the kernel overhead and reduces the code size effectively.The principle of the oriented object model,the method of scheduling,and how to map a parallel programming through CGDFG to the MPSoC are analyzed in this approach.This approach also compares the code size and execution cycles with conventional control flow scheduling,and presents respective management overhead for one application in me-dia-SoC.展开更多
Porous silicon(PSi)was applied as a supporting substrate for stepwise covalent derivatization of undecylenic acid, N-hydroxysuccinimidyl ester(NHS-ester)and nitrilotriacetic acid(NTA).By taking the advantages of porou...Porous silicon(PSi)was applied as a supporting substrate for stepwise covalent derivatization of undecylenic acid, N-hydroxysuccinimidyl ester(NHS-ester)and nitrilotriacetic acid(NTA).By taking the advantages of porous silicon as a supporting matrix such as high surface area to volume ratio,infrared transparency,porous semiconductors for laser desorption/ionization mass spectroscopy,and low fluorescence background,a multi-mode detection biochip prototype can be realized. We prepared such a protein microarray by spotting NTA microarray dots on NHS-ester derivatized PSi,converting the rest of chip area into poly(ethylene glycol)background,loading NiII,and finally affinity-binding histidine-tagged(His-tagged)proteins.With the multi-mode analyses of infrared spectroscopy,X-ray photoelectron spectroscopy(XPS),atomic force microscopy(AFM),matrix-assisted laser desorption/ionization mass spectroscopy(MALDI-MS),and fluorescence scanning,two example proteins,His-tagged thioredoxin-urodilatin and His-tagged aprotinin,were well qualified and quantified.展开更多
基金Supported by National Natural Science Foundation ofChina (No.60873112)
文摘This paper proposes an object oriented model scheduling for parallel computing in media MultiProcessors System on Chip(MPSoC).Firstly,the Coarse Grain Data Flow Graph(CGDFG) parallel programming model is used in this approach.Secondly,this approach has the feature of unified abstraction for software objects implementing in processor and hardware objects implementing in ASICs,easy for mapping CGDFG programming on MPSoC.This approach cuts down the kernel overhead and reduces the code size effectively.The principle of the oriented object model,the method of scheduling,and how to map a parallel programming through CGDFG to the MPSoC are analyzed in this approach.This approach also compares the code size and execution cycles with conventional control flow scheduling,and presents respective management overhead for one application in me-dia-SoC.
基金the financial support of the National Basic Research Program of China(2007CB925101)the National Natural Science Foundation of China(20721002&20827001)an open research fund of State Key Laboratory of Bioelectronics,Southeast University
文摘Porous silicon(PSi)was applied as a supporting substrate for stepwise covalent derivatization of undecylenic acid, N-hydroxysuccinimidyl ester(NHS-ester)and nitrilotriacetic acid(NTA).By taking the advantages of porous silicon as a supporting matrix such as high surface area to volume ratio,infrared transparency,porous semiconductors for laser desorption/ionization mass spectroscopy,and low fluorescence background,a multi-mode detection biochip prototype can be realized. We prepared such a protein microarray by spotting NTA microarray dots on NHS-ester derivatized PSi,converting the rest of chip area into poly(ethylene glycol)background,loading NiII,and finally affinity-binding histidine-tagged(His-tagged)proteins.With the multi-mode analyses of infrared spectroscopy,X-ray photoelectron spectroscopy(XPS),atomic force microscopy(AFM),matrix-assisted laser desorption/ionization mass spectroscopy(MALDI-MS),and fluorescence scanning,two example proteins,His-tagged thioredoxin-urodilatin and His-tagged aprotinin,were well qualified and quantified.
