Mohammed Tajuddin - Academia.edu (original) (raw)

Papers by Mohammed Tajuddin

Research paper thumbnail of Propagation of waves at the loosely bonded interface of two porous elastic half-spaces

Employing Biot's theory for wave propagation in porous solids, the propagation of waves at the lo... more Employing Biot's theory for wave propagation in porous solids, the propagation of waves at the loosely bonded interface between two poroelastic half-spaces is examined theoretically. The analogous study of Stoneley waves for smooth interface and bonded interface form a limiting case. The results due to classical theory are shown as a special case.

Research paper thumbnail of Low bone mineral density in osteomalacia: does definition of osteoporosis need modification

Osteoporosis International, 1996

Without Abstract

Research paper thumbnail of Spinal osteoporosis of pregnancy

Osteoporosis International, 1996

Without Abstract

Research paper thumbnail of Neisseria Species Identification Assay for the Confirmation of Neisseria gonorrhoeae-Positive Results of the COBAS Amplicor PCR

Journal of Clinical Microbiology, 2007

Screening assays for Neisseria gonorrhoeae exhibit low positive predictive values, particularly i... more Screening assays for Neisseria gonorrhoeae exhibit low positive predictive values, particularly in low-prevalence populations. A new real-time PCR assay that detects and identifies individual Neisseria spp. using melt curve analysis was compared to two previously published supplementary assays. NsppID, a 16S rRNA real-time PCR/melt curve assay developed to distinguish N. gonorrhoeae from other Neisseria spp., was compared to real-time PCR assays targeting genes reportedly specific for N. gonorrhoeae, the cppB gene and the porA pseudogene. A total of 408 clinical specimens (324 female endocervical swabs and 84 male urine or urogenital swab specimens) were screened using the COBAS Amplicor assay for Chlamydia trachomatis and N. gonorrhoeae (CT/NG) (Roche Diagnostics, Indianapolis, IN) followed by confirmatory testing via real-time PCR. The NsppID assay detected Neisseria spp. in 150/181 COBAS-positive specimens (82%), including six dual infections, and identified N. gonorrhoeae in 102 (56%) specimens. Sixty-nine of 181 (38%) specimens were positive for N. gonorrhoeae by porA pseudogene, and 115/181 (64%) were positive for cppB. However, cppB was also positive in 15% of COBAS-negative specimens, more than either NsppID (4%) or porA pseudogene (2%) assays. The porA pseudogene assay had the highest specificity for both genders but the lowest sensitivity, especially in female specimens. NsppID had a slightly lower specificity but greater sensitivity and overall accuracy. The least desirable confirmatory assay was cppB, due to poor specificity. The NsppID assay is an accurate confirmatory assay for N. gonorrhoeae detection. In addition, the NsppID assay can identify the non-N. gonorrhoeae species responsible for the majority of false-positive results from the COBAS Amplicor CT/NG assay.

Research paper thumbnail of Neisseria Species Identification Assay for the Confirmation of Neisseria gonorrhoeae-Positive Results of the COBAS Amplicor PCR

Journal of Clinical Microbiology, 2007

Screening assays for Neisseria gonorrhoeae exhibit low positive predictive values, particularly i... more Screening assays for Neisseria gonorrhoeae exhibit low positive predictive values, particularly in low-prevalence populations. A new real-time PCR assay that detects and identifies individual Neisseria spp. using melt curve analysis was compared to two previously published supplementary assays. NsppID, a 16S rRNA real-time PCR/melt curve assay developed to distinguish N. gonorrhoeae from other Neisseria spp., was compared to real-time PCR assays targeting genes reportedly specific for N. gonorrhoeae, the cppB gene and the porA pseudogene. A total of 408 clinical specimens (324 female endocervical swabs and 84 male urine or urogenital swab specimens) were screened using the COBAS Amplicor assay for Chlamydia trachomatis and N. gonorrhoeae (CT/NG) (Roche Diagnostics, Indianapolis, IN) followed by confirmatory testing via real-time PCR. The NsppID assay detected Neisseria spp. in 150/181 COBAS-positive specimens (82%), including six dual infections, and identified N. gonorrhoeae in 102 (56%) specimens. Sixty-nine of 181 (38%) specimens were positive for N. gonorrhoeae by porA pseudogene, and 115/181 (64%) were positive for cppB. However, cppB was also positive in 15% of COBAS-negative specimens, more than either NsppID (4%) or porA pseudogene (2%) assays. The porA pseudogene assay had the highest specificity for both genders but the lowest sensitivity, especially in female specimens. NsppID had a slightly lower specificity but greater sensitivity and overall accuracy. The least desirable confirmatory assay was cppB, due to poor specificity. The NsppID assay is an accurate confirmatory assay for N. gonorrhoeae detection. In addition, the NsppID assay can identify the non-N. gonorrhoeae species responsible for the majority of false-positive results from the COBAS Amplicor CT/NG assay.

Research paper thumbnail of The I1307K APC polymorphism in Ashkenazi Jews with colorectal cancer: clinical and pathologic features

Cancer Genetics and Cytogenetics, 2006

Colorectal cancer is common in Ashkenazi Jews. The I1307K APC mutation occurs in 6-7% of Ashkenaz... more Colorectal cancer is common in Ashkenazi Jews. The I1307K APC mutation occurs in 6-7% of Ashkenazi Jews and increases the risk of colorectal cancer. This study aimed to describe the clinical, pathologic and epidemiologic features of colorectal cancer in I1307K carriers to determine whether there were any features which might warrant individual screening for the mutation. In all, 215 Ashkenazi Jews with a personal history of colorectal cancer were enrolled. Clinical and family history, pathology reports, and slides were obtained and blood drawn for I1307K determination. The presence of the mutation was determined by PCR from white blood cell DNA. Colorectal cancer pathology slides were read in a blinded fashion. Of the 215 enrolled patients, 26 (12.1%) tested positive for I1307K. There was no difference in the pathologic features between colorectal cancers in Ashkenazi carriers compared to noncarriers. There was no difference in the age at diagnosis or history of second or other primaries. Carriers had an increased likelihood of having a first-degree relative with colorectal cancer (50%) compared to noncarriers (28%, P < 0.04). We could find no distinguishing feature other than family history that characterizes I1307K positive colorectal cancers. We could find no group of Ashkenazi Jews with colorectal cancer for whom screening for I1307K would be clinically useful.

Research paper thumbnail of Neisseria Species Identification Assay for the Confirmation of Neisseria gonorrhoeae-Positive Results of the COBAS Amplicor PCR

Screening assays for Neisseria gonorrhoeae exhibit low positive predictive values, particularly i... more Screening assays for Neisseria gonorrhoeae exhibit low positive predictive values, particularly in low-prevalence populations. A new real-time PCR assay that detects and identifies individual Neisseria spp. using melt curve analysis was compared to two previously published supplementary assays. NsppID, a 16S rRNA real-time PCR/melt curve assay developed to distinguish N. gonorrhoeae from other Neisseria spp., was compared to real-time PCR assays targeting genes reportedly specific for N. gonorrhoeae, the cppB gene and the porA pseudogene. A total of 408 clinical specimens (324 female endocervical swabs and 84 male urine or urogenital swab specimens) were screened using the COBAS Amplicor assay for Chlamydia trachomatis and N. gonorrhoeae (CT/NG) (Roche Diagnostics, Indianapolis, IN) followed by confirmatory testing via real-time PCR. The NsppID assay detected Neisseria spp. in 150/181 COBAS-positive specimens (82%), including six dual infections, and identified N. gonorrhoeae in 102 (56%) specimens. Sixty-nine of 181 (38%) specimens were positive for N. gonorrhoeae by porA pseudogene, and 115/181 (64%) were positive for cppB. However, cppB was also positive in 15% of COBAS-negative specimens, more than either NsppID (4%) or porA pseudogene (2%) assays. The porA pseudogene assay had the highest specificity for both genders but the lowest sensitivity, especially in female specimens. NsppID had a slightly lower specificity but greater sensitivity and overall accuracy. The least desirable confirmatory assay was cppB, due to poor specificity. The NsppID assay is an accurate confirmatory assay for N. gonorrhoeae detection. In addition, the NsppID assay can identify the non-N. gonorrhoeae species responsible for the majority of false-positive results from the COBAS Amplicor CT/NG assay.

Research paper thumbnail of Species-Level Identification of Staphylococcal Isolates by Real-Time PCR and Melt Curve Analysis

A real-time PCR assay was developed to identify common staphylococcal species. A single set of co... more A real-time PCR assay was developed to identify common staphylococcal species. A single set of consensus primers was designed to amplify a portion of the 16S rRNA gene, and a pair of fluorescence resonance energy transfer probes was used to identify species based on the unique melt properties of the probes resulting from sequence variations in the amplicons from each species. Nine common staphylococcal strains (S. aureus, S. capitis, S. epidermidis, S. haemolyticus, S. hominis, S. lugdunensis, S. schleiferi, S. simulans, and S. warneri) were used for assay development. The species-specific melting profiles were validated by correctly identifying 36 of 37 coagulase-negative staphylococcal (CoNS) isolates identified by ribotyping. In a study of clinical isolates, the PCR/melt curve approach correctly identified 56/56 S. aureus isolates identified by coagulase/protein A latex agglutination. Fifty-four CoNS clinical isolates characterized using the API Staph assay were studied, with the PCR/melt curve approach yielding matching identifications for 32/54 (59%). The API Staph assay was unable to identify 18 CoNS isolates, and differing results were obtained for 4 isolates. Sequencing of the 22 discrepant or unidentified CoNS samples revealed that the PCR/melt curve results were correct for all but one isolate. Thus, PCR/melt curve analysis achieved a nearly 100% accuracy and performed better than biochemical testing. Performance of the PCR/melt curve approach requires less than 2 h after colony selection. This method thus provides a rapid and accurate approach to the identification of staphylococcal species in the clinical laboratory.

Research paper thumbnail of Species-Level Identification of Staphylococcal Isolates by Real-Time PCR and Melt Curve Analysis

Journal of Clinical Microbiology, 2005

A real-time PCR assay was developed to identify common staphylococcal species. A single set of co... more A real-time PCR assay was developed to identify common staphylococcal species. A single set of consensus primers was designed to amplify a portion of the 16S rRNA gene, and a pair of fluorescence resonance energy transfer probes was used to identify species based on the unique melt properties of the probes resulting from sequence variations in the amplicons from each species. Nine common staphylococcal strains (S. aureus, S. capitis, S. epidermidis, S. haemolyticus, S. hominis, S. lugdunensis, S. schleiferi, S. simulans, and S. warneri) were used for assay development. The species-specific melting profiles were validated by correctly identifying 36 of 37 coagulase-negative staphylococcal (CoNS) isolates identified by ribotyping. In a study of clinical isolates, the PCR/melt curve approach correctly identified 56/56 S. aureus isolates identified by coagulase/protein A latex agglutination. Fifty-four CoNS clinical isolates characterized using the API Staph assay were studied, with the PCR/melt curve approach yielding matching identifications for 32/54 (59%). The API Staph assay was unable to identify 18 CoNS isolates, and differing results were obtained for 4 isolates. Sequencing of the 22 discrepant or unidentified CoNS samples revealed that the PCR/melt curve results were correct for all but one isolate. Thus, PCR/melt curve analysis achieved a nearly 100% accuracy and performed better than biochemical testing. Performance of the PCR/melt curve approach requires less than 2 h after colony selection. This method thus provides a rapid and accurate approach to the identification of staphylococcal species in the clinical laboratory.

Research paper thumbnail of TMS320F2812 Digital Signal Processor (DSP) implementation of DPWM

This paper presents the programming and use of TMS320F2812 digital signal processor (DSP) in gene... more This paper presents the programming and use of TMS320F2812 digital signal processor (DSP) in generating the digital pulse width modulation (DPWM). The structure and functions of eZdsp 2812 board used in this work is explained briefly and the steps need to be taken for the programming is explain in detail to control the frequency, the duty cycle and dead band of the generated PWM. The PWM generated by DSP from programming can be used to control and regulate power electronic converters.

Research paper thumbnail of State space averaging technique of power converter with digital PID controller

This paper describes a digital proportional-integral-derivative (PID) controller technique applie... more This paper describes a digital proportional-integral-derivative (PID) controller technique applied to the DC-DC buck converter. The converter is modelled using a state space averaging technique. Due to the non-linear of the power converter, the PID controller is designed to simplify the compensation of the DC-DC converter. The control algorithm is implemented in digital signal processor (DSP) TMS320F2812. The steady state and dynamic response performances of the controller are demonstrated. Experimental results are provided to demonstrate the effectiveness of the design.

Research paper thumbnail of Implementation of Fuzzy Logic controller for permanent magnet brushless DC motor drives

This paper presents the analysis of Fuzzy Logic controller for permanent magnet brushless DC moto... more This paper presents the analysis of Fuzzy Logic controller for permanent magnet brushless DC motor drive. The brushless direct current (BLDC) motor is efficiently controlled by Fuzzy logic controller compare to the other type of controllers. The dynamic characteristics of the brushless dc motor such as speed, torque, currents and voltages of the inverter components are easily observed and analyzed by using the developed Matlab model. To verify the effectiveness of the controller the simulation results are compared with experimental results.

Research paper thumbnail of webresource for composite materials

The World Wide Web can be a valuable source of information and being able to use modern tools to ... more The World Wide Web can be a valuable source of information and being able to use modern tools to find information is essential for practicing engineers. The web can be used effectively in a class dealing with composite materials to find information about material properties,manufacturing processes, applications for composite materials, and other things that are not found in a textbook. This article discusses how to find information about books, journal articles, and conference papers but also materials that are available only on the web. We explore both the type of information that can be found and the techniques that can be used for effective searches. It is also important to establish the credibility of the material retrieved and distinguish between what is produced by established publishers, well-known journals, or professional societies and material published by individuals or commercial entities without peer review. Issues such as plagiarism and proper ways to cite information found on the web are discussed. In order to enable students to use this tool, some preparation is required. We discuss hardware and software issues as well as what needs to be taught in order for them to perform some of these tasks as part of a class assignment.

Research paper thumbnail of Propagation of waves at the loosely bonded interface of two porous elastic half-spaces

Employing Biot's theory for wave propagation in porous solids, the propagation of waves at the lo... more Employing Biot's theory for wave propagation in porous solids, the propagation of waves at the loosely bonded interface between two poroelastic half-spaces is examined theoretically. The analogous study of Stoneley waves for smooth interface and bonded interface form a limiting case. The results due to classical theory are shown as a special case.

Research paper thumbnail of Low bone mineral density in osteomalacia: does definition of osteoporosis need modification

Osteoporosis International, 1996

Without Abstract

Research paper thumbnail of Spinal osteoporosis of pregnancy

Osteoporosis International, 1996

Without Abstract

Research paper thumbnail of Neisseria Species Identification Assay for the Confirmation of Neisseria gonorrhoeae-Positive Results of the COBAS Amplicor PCR

Journal of Clinical Microbiology, 2007

Screening assays for Neisseria gonorrhoeae exhibit low positive predictive values, particularly i... more Screening assays for Neisseria gonorrhoeae exhibit low positive predictive values, particularly in low-prevalence populations. A new real-time PCR assay that detects and identifies individual Neisseria spp. using melt curve analysis was compared to two previously published supplementary assays. NsppID, a 16S rRNA real-time PCR/melt curve assay developed to distinguish N. gonorrhoeae from other Neisseria spp., was compared to real-time PCR assays targeting genes reportedly specific for N. gonorrhoeae, the cppB gene and the porA pseudogene. A total of 408 clinical specimens (324 female endocervical swabs and 84 male urine or urogenital swab specimens) were screened using the COBAS Amplicor assay for Chlamydia trachomatis and N. gonorrhoeae (CT/NG) (Roche Diagnostics, Indianapolis, IN) followed by confirmatory testing via real-time PCR. The NsppID assay detected Neisseria spp. in 150/181 COBAS-positive specimens (82%), including six dual infections, and identified N. gonorrhoeae in 102 (56%) specimens. Sixty-nine of 181 (38%) specimens were positive for N. gonorrhoeae by porA pseudogene, and 115/181 (64%) were positive for cppB. However, cppB was also positive in 15% of COBAS-negative specimens, more than either NsppID (4%) or porA pseudogene (2%) assays. The porA pseudogene assay had the highest specificity for both genders but the lowest sensitivity, especially in female specimens. NsppID had a slightly lower specificity but greater sensitivity and overall accuracy. The least desirable confirmatory assay was cppB, due to poor specificity. The NsppID assay is an accurate confirmatory assay for N. gonorrhoeae detection. In addition, the NsppID assay can identify the non-N. gonorrhoeae species responsible for the majority of false-positive results from the COBAS Amplicor CT/NG assay.

Research paper thumbnail of Neisseria Species Identification Assay for the Confirmation of Neisseria gonorrhoeae-Positive Results of the COBAS Amplicor PCR

Journal of Clinical Microbiology, 2007

Screening assays for Neisseria gonorrhoeae exhibit low positive predictive values, particularly i... more Screening assays for Neisseria gonorrhoeae exhibit low positive predictive values, particularly in low-prevalence populations. A new real-time PCR assay that detects and identifies individual Neisseria spp. using melt curve analysis was compared to two previously published supplementary assays. NsppID, a 16S rRNA real-time PCR/melt curve assay developed to distinguish N. gonorrhoeae from other Neisseria spp., was compared to real-time PCR assays targeting genes reportedly specific for N. gonorrhoeae, the cppB gene and the porA pseudogene. A total of 408 clinical specimens (324 female endocervical swabs and 84 male urine or urogenital swab specimens) were screened using the COBAS Amplicor assay for Chlamydia trachomatis and N. gonorrhoeae (CT/NG) (Roche Diagnostics, Indianapolis, IN) followed by confirmatory testing via real-time PCR. The NsppID assay detected Neisseria spp. in 150/181 COBAS-positive specimens (82%), including six dual infections, and identified N. gonorrhoeae in 102 (56%) specimens. Sixty-nine of 181 (38%) specimens were positive for N. gonorrhoeae by porA pseudogene, and 115/181 (64%) were positive for cppB. However, cppB was also positive in 15% of COBAS-negative specimens, more than either NsppID (4%) or porA pseudogene (2%) assays. The porA pseudogene assay had the highest specificity for both genders but the lowest sensitivity, especially in female specimens. NsppID had a slightly lower specificity but greater sensitivity and overall accuracy. The least desirable confirmatory assay was cppB, due to poor specificity. The NsppID assay is an accurate confirmatory assay for N. gonorrhoeae detection. In addition, the NsppID assay can identify the non-N. gonorrhoeae species responsible for the majority of false-positive results from the COBAS Amplicor CT/NG assay.

Research paper thumbnail of The I1307K APC polymorphism in Ashkenazi Jews with colorectal cancer: clinical and pathologic features

Cancer Genetics and Cytogenetics, 2006

Colorectal cancer is common in Ashkenazi Jews. The I1307K APC mutation occurs in 6-7% of Ashkenaz... more Colorectal cancer is common in Ashkenazi Jews. The I1307K APC mutation occurs in 6-7% of Ashkenazi Jews and increases the risk of colorectal cancer. This study aimed to describe the clinical, pathologic and epidemiologic features of colorectal cancer in I1307K carriers to determine whether there were any features which might warrant individual screening for the mutation. In all, 215 Ashkenazi Jews with a personal history of colorectal cancer were enrolled. Clinical and family history, pathology reports, and slides were obtained and blood drawn for I1307K determination. The presence of the mutation was determined by PCR from white blood cell DNA. Colorectal cancer pathology slides were read in a blinded fashion. Of the 215 enrolled patients, 26 (12.1%) tested positive for I1307K. There was no difference in the pathologic features between colorectal cancers in Ashkenazi carriers compared to noncarriers. There was no difference in the age at diagnosis or history of second or other primaries. Carriers had an increased likelihood of having a first-degree relative with colorectal cancer (50%) compared to noncarriers (28%, P < 0.04). We could find no distinguishing feature other than family history that characterizes I1307K positive colorectal cancers. We could find no group of Ashkenazi Jews with colorectal cancer for whom screening for I1307K would be clinically useful.

Research paper thumbnail of Neisseria Species Identification Assay for the Confirmation of Neisseria gonorrhoeae-Positive Results of the COBAS Amplicor PCR

Screening assays for Neisseria gonorrhoeae exhibit low positive predictive values, particularly i... more Screening assays for Neisseria gonorrhoeae exhibit low positive predictive values, particularly in low-prevalence populations. A new real-time PCR assay that detects and identifies individual Neisseria spp. using melt curve analysis was compared to two previously published supplementary assays. NsppID, a 16S rRNA real-time PCR/melt curve assay developed to distinguish N. gonorrhoeae from other Neisseria spp., was compared to real-time PCR assays targeting genes reportedly specific for N. gonorrhoeae, the cppB gene and the porA pseudogene. A total of 408 clinical specimens (324 female endocervical swabs and 84 male urine or urogenital swab specimens) were screened using the COBAS Amplicor assay for Chlamydia trachomatis and N. gonorrhoeae (CT/NG) (Roche Diagnostics, Indianapolis, IN) followed by confirmatory testing via real-time PCR. The NsppID assay detected Neisseria spp. in 150/181 COBAS-positive specimens (82%), including six dual infections, and identified N. gonorrhoeae in 102 (56%) specimens. Sixty-nine of 181 (38%) specimens were positive for N. gonorrhoeae by porA pseudogene, and 115/181 (64%) were positive for cppB. However, cppB was also positive in 15% of COBAS-negative specimens, more than either NsppID (4%) or porA pseudogene (2%) assays. The porA pseudogene assay had the highest specificity for both genders but the lowest sensitivity, especially in female specimens. NsppID had a slightly lower specificity but greater sensitivity and overall accuracy. The least desirable confirmatory assay was cppB, due to poor specificity. The NsppID assay is an accurate confirmatory assay for N. gonorrhoeae detection. In addition, the NsppID assay can identify the non-N. gonorrhoeae species responsible for the majority of false-positive results from the COBAS Amplicor CT/NG assay.

Research paper thumbnail of Species-Level Identification of Staphylococcal Isolates by Real-Time PCR and Melt Curve Analysis

A real-time PCR assay was developed to identify common staphylococcal species. A single set of co... more A real-time PCR assay was developed to identify common staphylococcal species. A single set of consensus primers was designed to amplify a portion of the 16S rRNA gene, and a pair of fluorescence resonance energy transfer probes was used to identify species based on the unique melt properties of the probes resulting from sequence variations in the amplicons from each species. Nine common staphylococcal strains (S. aureus, S. capitis, S. epidermidis, S. haemolyticus, S. hominis, S. lugdunensis, S. schleiferi, S. simulans, and S. warneri) were used for assay development. The species-specific melting profiles were validated by correctly identifying 36 of 37 coagulase-negative staphylococcal (CoNS) isolates identified by ribotyping. In a study of clinical isolates, the PCR/melt curve approach correctly identified 56/56 S. aureus isolates identified by coagulase/protein A latex agglutination. Fifty-four CoNS clinical isolates characterized using the API Staph assay were studied, with the PCR/melt curve approach yielding matching identifications for 32/54 (59%). The API Staph assay was unable to identify 18 CoNS isolates, and differing results were obtained for 4 isolates. Sequencing of the 22 discrepant or unidentified CoNS samples revealed that the PCR/melt curve results were correct for all but one isolate. Thus, PCR/melt curve analysis achieved a nearly 100% accuracy and performed better than biochemical testing. Performance of the PCR/melt curve approach requires less than 2 h after colony selection. This method thus provides a rapid and accurate approach to the identification of staphylococcal species in the clinical laboratory.

Research paper thumbnail of Species-Level Identification of Staphylococcal Isolates by Real-Time PCR and Melt Curve Analysis

Journal of Clinical Microbiology, 2005

A real-time PCR assay was developed to identify common staphylococcal species. A single set of co... more A real-time PCR assay was developed to identify common staphylococcal species. A single set of consensus primers was designed to amplify a portion of the 16S rRNA gene, and a pair of fluorescence resonance energy transfer probes was used to identify species based on the unique melt properties of the probes resulting from sequence variations in the amplicons from each species. Nine common staphylococcal strains (S. aureus, S. capitis, S. epidermidis, S. haemolyticus, S. hominis, S. lugdunensis, S. schleiferi, S. simulans, and S. warneri) were used for assay development. The species-specific melting profiles were validated by correctly identifying 36 of 37 coagulase-negative staphylococcal (CoNS) isolates identified by ribotyping. In a study of clinical isolates, the PCR/melt curve approach correctly identified 56/56 S. aureus isolates identified by coagulase/protein A latex agglutination. Fifty-four CoNS clinical isolates characterized using the API Staph assay were studied, with the PCR/melt curve approach yielding matching identifications for 32/54 (59%). The API Staph assay was unable to identify 18 CoNS isolates, and differing results were obtained for 4 isolates. Sequencing of the 22 discrepant or unidentified CoNS samples revealed that the PCR/melt curve results were correct for all but one isolate. Thus, PCR/melt curve analysis achieved a nearly 100% accuracy and performed better than biochemical testing. Performance of the PCR/melt curve approach requires less than 2 h after colony selection. This method thus provides a rapid and accurate approach to the identification of staphylococcal species in the clinical laboratory.

Research paper thumbnail of TMS320F2812 Digital Signal Processor (DSP) implementation of DPWM

This paper presents the programming and use of TMS320F2812 digital signal processor (DSP) in gene... more This paper presents the programming and use of TMS320F2812 digital signal processor (DSP) in generating the digital pulse width modulation (DPWM). The structure and functions of eZdsp 2812 board used in this work is explained briefly and the steps need to be taken for the programming is explain in detail to control the frequency, the duty cycle and dead band of the generated PWM. The PWM generated by DSP from programming can be used to control and regulate power electronic converters.

Research paper thumbnail of State space averaging technique of power converter with digital PID controller

This paper describes a digital proportional-integral-derivative (PID) controller technique applie... more This paper describes a digital proportional-integral-derivative (PID) controller technique applied to the DC-DC buck converter. The converter is modelled using a state space averaging technique. Due to the non-linear of the power converter, the PID controller is designed to simplify the compensation of the DC-DC converter. The control algorithm is implemented in digital signal processor (DSP) TMS320F2812. The steady state and dynamic response performances of the controller are demonstrated. Experimental results are provided to demonstrate the effectiveness of the design.

Research paper thumbnail of Implementation of Fuzzy Logic controller for permanent magnet brushless DC motor drives

This paper presents the analysis of Fuzzy Logic controller for permanent magnet brushless DC moto... more This paper presents the analysis of Fuzzy Logic controller for permanent magnet brushless DC motor drive. The brushless direct current (BLDC) motor is efficiently controlled by Fuzzy logic controller compare to the other type of controllers. The dynamic characteristics of the brushless dc motor such as speed, torque, currents and voltages of the inverter components are easily observed and analyzed by using the developed Matlab model. To verify the effectiveness of the controller the simulation results are compared with experimental results.

Research paper thumbnail of webresource for composite materials

The World Wide Web can be a valuable source of information and being able to use modern tools to ... more The World Wide Web can be a valuable source of information and being able to use modern tools to find information is essential for practicing engineers. The web can be used effectively in a class dealing with composite materials to find information about material properties,manufacturing processes, applications for composite materials, and other things that are not found in a textbook. This article discusses how to find information about books, journal articles, and conference papers but also materials that are available only on the web. We explore both the type of information that can be found and the techniques that can be used for effective searches. It is also important to establish the credibility of the material retrieved and distinguish between what is produced by established publishers, well-known journals, or professional societies and material published by individuals or commercial entities without peer review. Issues such as plagiarism and proper ways to cite information found on the web are discussed. In order to enable students to use this tool, some preparation is required. We discuss hardware and software issues as well as what needs to be taught in order for them to perform some of these tasks as part of a class assignment.