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Co-Authors
- Sudesh Jakhar
- Sunil Makkar
- Aditya Kumar
- Alok Kumar Singh
- Anil Rajak
- Ashish Panna
- M. Sujitha
- P. S. Satsangi
- Sushila Maan
- Anuj Tiwari
- Deepika Chaudhary
- Anita Dalal
- Nitish Bansal
- Vinay Kumar
- Kanisht Batra
- Naresh Kumar Kakker
- Narender Singh Maan
- Dinesh Kumar
- Priydarshi Hem
- Ravindra Kumar Gupta
- U. K. Singh
Journals
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z All
Kumar, Aman
- Distinction between Secret Key and Public Key Cryptography with Existing Glitches
Abstract Views :299 |
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Authors
Affiliations
1 BRCM Bahal Bhiwani, IN
2 Associate Professor, Department of Information technology, BRCM Bahal (Bhiwani), IN
3 Assistant Professor, Department of Information technology, BRCM Bahal (Bhiwani), IN
1 BRCM Bahal Bhiwani, IN
2 Associate Professor, Department of Information technology, BRCM Bahal (Bhiwani), IN
3 Assistant Professor, Department of Information technology, BRCM Bahal (Bhiwani), IN
Source
Indian Journal of Education and Information Management, Vol 1, No 9 (2012), Pagination: 392-395Abstract
Internet use and network size is growing very fast day-by-day. So there is more need to secure the data transmitted through different services. To provide the security to the network and data, different encryption methods are used. Encryption is the process of translating, plain text" unhidden" to a cipher text "hidden" to provide the security again different attacks. So as to provide the security, two wide secret and public key cryptography algorithms are used. Secret key cryptography and public key cryptography is also known as symmetrical and asymmetrical key cryptography. In this paper, we will comprises the brief description of Secret key cryptography and Public key cryptography algorithms Implement the Public Key Cryptography with RSA algorithm.Keywords
Encryption, Decryption, Plaintext, Cipher TextReferences
- Atul Kahte (2008) Cryptography and Network Security, 2nd Ed.
- Dan Boneh and Glenn Durfee (1999) Cryptanalysis of low exponent RSA
- Diffie W, Hellman ME (1976) New Directions in cryptography.
- Eli Biham & Adli Shamir (1990) Differential Cryptanalysis of full DES.
- Ferguson N, Schnier B & Konho T (2010) Cryptography Engineering: Design principles and Practical applications, 1st Ed.
- Himani Agarwal & Manish Sharma (2010) Implementation and analysis of various symmetric cryptosystems, Indian Journal of Science and Technology, 3(11) Dec-2010.
- Piper F (1997) Encryption. Security and Detection, Ecos. European Conference.
- Schweighofer E (1997) Downloading information Information & Communication technology.
- Yogesh Kumar, Rajiv Munjal (2011) Comparision of symmetric and asymmetric cryptography with existing Vulnerabilities IJCMS.
- Dual Tone Multiple Frequency (DTMF) Mobile Control Robot
Abstract Views :212 |
PDF Views:5
Authors
Affiliations
1 Dept. EEE, Dr. MGR Educational and Research Institute, IN
2 Dept. EEE, Dr. MGR Educational and Research Institute, Chennai-95, Tamilnadu, IN
3 Department of EEE, Dr. MGR Educational and Research Institute, Chennai-95, Tamilnadu, IN
1 Dept. EEE, Dr. MGR Educational and Research Institute, IN
2 Dept. EEE, Dr. MGR Educational and Research Institute, Chennai-95, Tamilnadu, IN
3 Department of EEE, Dr. MGR Educational and Research Institute, Chennai-95, Tamilnadu, IN
Source
Automation and Autonomous Systems, Vol 7, No 4 (2015), Pagination: 106-110Abstract
In the age of existing systems it is important to be able to control robots everywhere. Although many methods to remotely control robots have been devised, the methods have the problems such as the need for special devices or software to control the robots. This paper suggests a method for robotic control using the DTMF tone generated when the user pushes mobile phone keypad buttons o when connected with a remote mobile robot. This paper summarizes a the feasibility of implementing Dual-Tone, Multi-Frequency (DTMF) as an alternative mean of robotic communication to Radio Frequency (RF). Our robot is controlled by a cell phone, through this we can make our robot communicate on a large scale over a large distance even from different cities. This robot can also be used to reach the places where humans cannot reach such as small tunnels, etc.Keywords
Atmega 8 Microcontroller, DTMF Mobile.- Magnetic Field Assisted Micro EDM - A Review
Abstract Views :191 |
PDF Views:3
Authors
Aman Kumar
1,
P. S. Satsangi
1
Affiliations
1 Mechanical Engineering Department, PEC University of Technology, Chandigarh, IN
1 Mechanical Engineering Department, PEC University of Technology, Chandigarh, IN
Source
Research Cell: An International Journal of Engineering Sciences, Vol 18, No 1 (2016), Pagination: 108-114Abstract
Micro Electrical discharge machining commonly called as Micro EDM (μEDM) is a well known non-traditional technology used for machining of very hard and difficult to machine materials which are extensively used in die-production, machining of complex 3D geometrical structures, aerospace now a days. μEDM as the name suggests produces part at micro level but it is very time consuming process with very low MRR. This paper presents a review and insight on Micro EDM, followed by the ongoing research and development using magnetic field (MF) assistance on Micro EDM (MFMEDM). This paper also includes literature review on improvements in performance measures with the application of magnetic field assistance on μEDM. In last section, a summary of the future research directions are also discussed.Keywords
EDM, Micro Electrical discharge machining (μEDM), magnetic field assistance, Material Removal Rate, Tool Wear Rate, Surface Roughness.- A Comprehensive Study on Seroprevalence of Bluetongue Virus in Haryana State of India
Abstract Views :246 |
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Materials and Methods: A total of 803 serum samples, 408 of cattle and 395 of buffalo origin, respectively, were collected from different villages of Haryana. Sampling was done randomly to obtain unbiased results. The samples were evaluated by a competitive enzyme-linked immunosorbent assay for the presence of BTV antibodies.
Results: Overall seroprevalence of BTV antibody in cattle and buffaloes for all 21 districts of Haryana state was found to be 75.49% and 92.91%, respectively. The prevalence of BTV in different agroclimatic zones ranged between 72-77% and 90-94% for cattle and buffalo, respectively. In buffaloes, the BTV seroprevalence was comparatively higher than in cattle.
Conclusion: The study showed that BTV is circulating in cattle and buffalo populations in the Northern part of India.
Authors
Sushila Maan
1,
Anuj Tiwari
2,
Deepika Chaudhary
1,
Anita Dalal
1,
Nitish Bansal
1,
Vinay Kumar
1,
Kanisht Batra
1,
Aman Kumar
1,
Naresh Kumar Kakker
3,
Narender Singh Maan
4
Affiliations
1 Department of Animal Biotechnology, College of Veterinary Sciences, Lala Lajpat Rai University of Veterinary and Animal Sciences, Hisar-125004, Haryana, IN
2 Department of Veterinary Microbiology, G. B. Pant University of Agriculture and Technology, Pantnagar-263145, Uttarakhand, IN
3 Department of Veterinary Microbiology, College of Veterinary Sciences, Lala Lajpat Rai University of Veterinary and Animal Sciences, Hisar-125004, Haryana, IN
4 Department of Animal Nutrition, College of Veterinary Sciences, Lala Lajpat Rai University of Veterinary and Animal Sciences, Hisar-125004, Haryana, IN
1 Department of Animal Biotechnology, College of Veterinary Sciences, Lala Lajpat Rai University of Veterinary and Animal Sciences, Hisar-125004, Haryana, IN
2 Department of Veterinary Microbiology, G. B. Pant University of Agriculture and Technology, Pantnagar-263145, Uttarakhand, IN
3 Department of Veterinary Microbiology, College of Veterinary Sciences, Lala Lajpat Rai University of Veterinary and Animal Sciences, Hisar-125004, Haryana, IN
4 Department of Animal Nutrition, College of Veterinary Sciences, Lala Lajpat Rai University of Veterinary and Animal Sciences, Hisar-125004, Haryana, IN
Source
Veterinary World, Vol 10, No 12 (2017), Pagination: 1464-1470Abstract
Aim: The aim of present study was to determine seroprevalence of bluetongue virus (BTV) in Haryana state of India.Materials and Methods: A total of 803 serum samples, 408 of cattle and 395 of buffalo origin, respectively, were collected from different villages of Haryana. Sampling was done randomly to obtain unbiased results. The samples were evaluated by a competitive enzyme-linked immunosorbent assay for the presence of BTV antibodies.
Results: Overall seroprevalence of BTV antibody in cattle and buffaloes for all 21 districts of Haryana state was found to be 75.49% and 92.91%, respectively. The prevalence of BTV in different agroclimatic zones ranged between 72-77% and 90-94% for cattle and buffalo, respectively. In buffaloes, the BTV seroprevalence was comparatively higher than in cattle.
Conclusion: The study showed that BTV is circulating in cattle and buffalo populations in the Northern part of India.
Keywords
Bluetongue, Bluetongue Virus, Buffalo, Cattle, Competitive Enzyme-Linked Immunosorbent Assay, Haryana, India, Serology.- Molecular Analysis of Genome Segment-3 of Bluetongue Virus Serotype 12 Isolates From Haryana
Abstract Views :152 |
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Materials and Methods: Blood and swab samples were collected from goat and sheep suspected to be suffering of BT from different outbreaks from Gurugram, Sirsa, Hisar, and Karnal districts of Haryana. The samples were grown in insect and mammalian cell lines. After preliminary identification, serotyping was done using BTV type-specific quantitative reverse transcription-polymerase chain reaction (qRT-PCR) assays. Sequencing was performed using terminal and walking internal primers specific for Seg-3 on ABI Capillary Sequencer 3130 using a “BigDye cycle sequencing kit.” The obtained sequence data were analyzed with various bioinformatic tools.
Results: Real-time PCR results confirmed the samples to be positive for BTV-12. The Seg-3 of Indian isolates was most closely related to that of a south Indian isolate of BTV-12 from Andhra Pradesh (KC662614) with 97% nucleotide identity.
Conclusion: The study confirmed the circulation of BTV-12 in Haryana, India. The variations shown in genome Seg-3 of BTV-12 isolates may have some significance and need to be further explored.
Authors
Anita Dalal
1,
Sushila Maan
2,
Nitish Bansal
2,
Vinay Kumar
2,
Aman Kumar
2,
Narender Singh Maan
3,
Naresh Kumar Kakker
1
Affiliations
1 Department of Veterinary Microbiology, College of Veterinary Sciences, Lala Lajpat Rai University of Veterinary and Animal Sciences, Hisar-125004, Haryana, IN
2 Department of Animal Biotechnology, College of Veterinary Sciences, Lala Lajpat Rai University of Veterinary and Animal Sciences, Hisar-125004, Haryana, IN
3 Department of Animal Nutrition, College of Veterinary Sciences, Lala Lajpat Rai University of Veterinary and Animal Sciences, Hisar-125004, Haryana, IN
1 Department of Veterinary Microbiology, College of Veterinary Sciences, Lala Lajpat Rai University of Veterinary and Animal Sciences, Hisar-125004, Haryana, IN
2 Department of Animal Biotechnology, College of Veterinary Sciences, Lala Lajpat Rai University of Veterinary and Animal Sciences, Hisar-125004, Haryana, IN
3 Department of Animal Nutrition, College of Veterinary Sciences, Lala Lajpat Rai University of Veterinary and Animal Sciences, Hisar-125004, Haryana, IN
Source
Veterinary World, Vol 10, No 11 (2017), Pagination: 1389-1393Abstract
Aim: The present study was designed to characterize the genome segment 3 (Seg-3) of bluetongue virus (BTV) serotype 12 isolates from different outbreaks of Bluetongue disease in Haryana, India.Materials and Methods: Blood and swab samples were collected from goat and sheep suspected to be suffering of BT from different outbreaks from Gurugram, Sirsa, Hisar, and Karnal districts of Haryana. The samples were grown in insect and mammalian cell lines. After preliminary identification, serotyping was done using BTV type-specific quantitative reverse transcription-polymerase chain reaction (qRT-PCR) assays. Sequencing was performed using terminal and walking internal primers specific for Seg-3 on ABI Capillary Sequencer 3130 using a “BigDye cycle sequencing kit.” The obtained sequence data were analyzed with various bioinformatic tools.
Results: Real-time PCR results confirmed the samples to be positive for BTV-12. The Seg-3 of Indian isolates was most closely related to that of a south Indian isolate of BTV-12 from Andhra Pradesh (KC662614) with 97% nucleotide identity.
Conclusion: The study confirmed the circulation of BTV-12 in Haryana, India. The variations shown in genome Seg-3 of BTV-12 isolates may have some significance and need to be further explored.
Keywords
Bluetongue, Bluetongue Virus-12, Genome Segment-3, Haryana, Real Time, Serotype, Sequencing.- Design of Underhand Cut and Fill Method for Extraction of Friable Chromite Ore Left in Open Pit Benches
Abstract Views :146 |
PDF Views:0
Authors
Affiliations
1 Dept of Mining Engineering, IIT/ISM, Dhanbad, IN
1 Dept of Mining Engineering, IIT/ISM, Dhanbad, IN