• Title/Summary/Keyword: RS coding

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Single Relay Selection for Bidirectional Cooperative Networks with Physical-Layer Network Coding

  • Liu, Yingting;Zhang, Hailin;Hui, Leifang;Liu, Quanyang;Lu, Xiaofeng
    • ETRI Journal
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    • v.34 no.1
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    • pp.102-105
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    • 2012
  • To serve the growing demand of the bidirectional information exchange, we propose a single relay selection (RS) scheme for physical-layer network coding (PNC) in a bidirectional cooperative network consisting of two sources and multiple relays. This RS scheme selects a single best relay by maximizing the bottleneck of the capacity region of both information flows in the bidirectional network. We show that the proposed RS rule minimizes the outage probability and that it can be used as a performance benchmark for any RS rules with PNC. We derive a closed-form exact expression of the outage probability for the proposed RS rule and show that it achieves full diversity gain. Finally, numerical results demonstrate the validity of our analysis.

Association of lnc-LAMC2-1:1 rs2147578 and CASC8 rs10505477 Polymorphisms with Risk of Childhood Acute Lymphoblastic Leukemia

  • Hashemi, Mohammad;Bahari, Gholamreza;Naderi, Majid;Bojd, Simin Sadeghi;Taheri, Mohsen
    • Asian Pacific Journal of Cancer Prevention
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    • v.17 no.11
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    • pp.4985-4989
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    • 2016
  • Long non-coding RNAs (lncRNAs) are a novel class of non-protein coding RNAs that are involved in a wide variety of biological processes. There are limited data regarding the impact of lnc-LAMC2-1:1 rs2147578 as well as CASC8 rs10505477 T>C polymorphisms on cancer development. Here we examined for the first time whether rs2147578 and rs10505477 polymorphisms are associated with childhood acute lymphoblastic leukemia (ALL) in a total of 110 cases and 120 healthy controls. Genotyping was achieved by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. The rs2147578 variant increased the risk of ALL in codominant (OR=4.33, 95%CI=2.00-9.37, p<0.0001, CG vs CC, and OR=5.81, 95%CI=2.30-14.69, p=0.0002, GG vs CC), dominant (OR=4.63, 95%CI=2.18-9.86, p<0.0001, CG+GG vs CC), overdominant (OR=1.74, 95%CI=1.02-2.97, p=0.0444, CG vs CC+GG) and allele (OR=1.91, 95%CI=1.32-2.77, p=0.0008, G vs C) inheritance models tested. No significant association was found between the CASC8 rs10505477 T>C variant and risk of childhood ALL. In conclusion, the present study revealed that the lnc-LAMC2-1:1 rs2147578 polymorphism may be a risk factor for developing childhood ALL. Further studies with larger sample sizes with different ethnicities are now required to confirm our findings.

FPGA Implementation of Reed-Solomon Encoder for image transmission (영상 전송을 위한 Reed-Solomon Encoder의 FPGA 구현)

  • Kim, Dong-Nyeon;Cai, Yu Qing;Byon, Kun-sik
    • Proceedings of the Korean Institute of Information and Commucation Sciences Conference
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    • 2009.05a
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    • pp.907-910
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    • 2009
  • This paper is the FPGA Implementation of Reed-Solomon Encoder that is one of Error control Codes. Reed-Solomon codes are block-based error control codes with a wide range of applications in digital communications. RS codes are strong on burst errors because it process signals as symbol. We simulate this system using Matlab from Mathworks and design it using System Generator from Xilinx. We refer Matlab source in Implementation of Reed-Solomon Error Control Coding for Compressed Images by Simon Anthony Raspa.

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A new syndrome check error estimation algorithm and its concatenated coding for wireless communication

  • 이문호;장진수;최승배
    • The Journal of Korean Institute of Communications and Information Sciences
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    • v.22 no.7
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    • pp.1419-1426
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    • 1997
  • A new SCEE(Syndrome Check Error Estimation) decoding method for convolutional code and concatenated SCEE/RS (Reed-Solomon) conding scheme are proposed. First, we describe the operation of the decoding steps in the proposed algorithm. Then deterministic values on the decoding operation are drived when some combination of predecoder-reencoder is used. Computer simulation results show that the compuatational complexity of the proposed SCEE decoder is significantly reduced compared to that of conventional Viterbi-decoder without degratation of the $P_{e}$ performance. Also, the concatenated SCEE/RS decoder has almost the same complexity of a RS decoder and its coding gain is higher than that of soft decision Viterbi or RS decoder respectively.

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Performance Analysis of Multimedia CDMA Network with Concatenated Coding and RAKE Receiver

  • Roh Jae-Sung;Kim Choon-Gil;Cho Sung-Joon
    • Journal of information and communication convergence engineering
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    • v.2 no.3
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    • pp.139-144
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    • 2004
  • In order to transmit various types of multimedia data (i.e. voice, video, and data) over a wireless channel, the coding and modulation scheme needs to be flexible and capable of providing a variable quality of service, data rates, and latency. In this paper, we study a mobile multimedia COMA network combined with the concatenated Reed-Solomon/Rate Compatible Punctured Convolution code (RS/RCPC). Also, this paper propose the combination of concatenated RS/RCPC coder and COMA RAKE receiver for multimedia COMA traffic which can be sent over wireless channels. From the results, using a frequency selective Rayleigh fading channel model, it is shown that concatenated RS/RCPC coder at the wireless physical layer can be effective in providing reliable wireless multimedia CDMA network. And the proposed scheme that combine concatenated RS/RCPC coder and CDMA RAKE receiver provides a significant gain in the BER performance over multi-user interference and multipath frequency selective fading channels.

Sequence Variations in the Non-Coding Sequence of CTX Phages in Vibrio cholerae

  • Kim, Eun Jin;Yu, Hyun Jin;Kim, Dong Wook
    • Journal of Microbiology and Biotechnology
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    • v.26 no.8
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    • pp.1473-1480
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    • 2016
  • This study focused on the variations in the non-coding sequences between ctxB and rstR of various CTX phages. The non-coding sequences of CTX-1 and CTX-cla are phage type-specific. The length of the non-coding region of CTX-1 and CTX-cla is 601 and 730 nucleotides, respectively. The non-coding sequence of CTX phage could be divided into three regions. There is a phage type-specific Variable region between two homologous Common regions (Common regions 1 and 2). The non-coding sequence of RS1 element is similar to CTX-1 except that Common region 1 is replaced by a short RS1-specific sequence. The non-coding sequences of CTX-2 and CTX-cla are homologous, indicating the non-coding sequence of CTX-2 is derived from CTX-cla. The non-coding region of CTX-O139 is similar to CTX-cla and CTX-2; however, it contains an extra phage type-specific sequence between Common region 2 and rstR. The variations in the non-coding sequences of CTX phages might be associated with the difference in the replication efficiency and the directionality in the integration into the V. cholerae chromosome.

The Study about Channel code to Overcome Multipath of Underwater Channel (수중통신채널에서 다중경로 극복을 위한 오류정정부호에 대한 연구)

  • Kim, Nam-Soo;Kim, Min-Hyuk;Park, Tae-Doo;Kim, Chul-Seung;Jung, Ji-Won
    • Journal of Advanced Marine Engineering and Technology
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    • v.33 no.5
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    • pp.738-745
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    • 2009
  • Underwater acoustic communication has multipath error because of reflection by sea-level and sea-bottom. The multipath of underwater channel causes receive signal to make error floor. In this paper, we propose the underwater communication system using various channel coding schemes such as RS coding, convolutional code, turbo code and concatenated code for overcoming the multipath effect in underwater channel. As shown in simulation results, characteristic of multipath error is similar to that of random error. So interleaver has not effect on error correcting. For correcting of error floor by multipath, it is necessary to use strong channel codes like turbo code. Turbo code is one of the iterative codes. And the performance of concatenated codes including RS code has better performance than using singular channel codes.

Error Control Coding and Space-Time MMSE Multiuser Detection in DS-CDMA Systems

  • Hamouda, Walaa;McLane, Peter J.
    • Journal of Communications and Networks
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    • v.5 no.3
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    • pp.187-196
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    • 2003
  • We consider the use of error control coding in direct sequence-code-division multiple access (OS-COMA) systems that employ multiuser detection (MUO) and space diversity. The relative performance gain between Reed-Solomon (RS) code and convolutional code (CC) is well known in [1] for the single user, additive white Gaussian noise (AWGN) channel. In this case, RS codes outperform CC's at high signal-to-noise ratios. We find that this is not the case for the multiuser interference channel mentioned above. For useful error rates, we find that soft-decision CC's to be uniformly better than RS codes when used with DS-COMA modulation in multiuser space-time channels. In our development, we use the Gaussian approximation on the interference to determine performance error bounds for systems with low number of users. Then, we check their accuracy in error rate estimation via system's simulation. These performance bounds will in turn allow us to consider a large number of users where we can estimate the gain in user-capacity due to channel coding. Lastly, the use of turbo codes is considered where it is shown that they offer a coding gain of 2.5 dB relative to soft-decision CC.

Mutation Screening and Association Study of the Folylpolyglutamate Synthetase (FPGS) Gene with Susceptibility to Childhood Acute Lymphoblastic Leukemia

  • Piwkham, Duangjai;Siriboonpiputtana, Teerapong;Beuten, Joke;Pakakasama, Samart;Gelfond, Jonathan AL;Paisooksantivatana, Karan;Tomlinson, Gail E;Rerkamnuaychoke, Budsaba
    • Asian Pacific Journal of Cancer Prevention
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    • v.16 no.11
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    • pp.4727-4732
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    • 2015
  • Background: Folylpolyglutamate synthetase (FPGS), an important enzyme in the folate metabolic pathway, plays a central role in intracellular accumulation of folate and antifolate in several mammalian cell types. Loss of FPGS activity results in decreased cellular levels of antifolates and consequently to polyglutamatable antifolates in acute lymphoblastic leukemia (ALL). Materials and Methods: During May 1997 and December 2003, 134 children diagnosed with ALL were recruited from one hospital in Thailand. We performed a mutation analysis in the coding regions of the FPGS gene and the association between single nucleotide polymorphisms (SNPs) within FPGS in a case-control sample of childhood ALL patients. Mutation screening was conducted by polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) and subsequently with direct sequencing (n=72). Association analysis between common FPGS variants and ALL risk was done in 98 childhood ALL cases and 95 healthy volunteers recruited as controls. Results: Seven SNPs in the FPGS coding region were identified by mutation analysis, 3 of which (IVS13+55C>T, g.1297T>G, and g.1508C>T) were recognized as novel SNPs. Association analysis revealed 3 of 6 SNPs to confer significant increase in ALL risk these being rs7039798 (p=0.014, OR=2.14), rs1544105 (p=0.010, OR= 2.24), and rs10106 (p=0.026, OR=1.99). Conclusions: These findings suggested that common genetic polymorphisms in the FPGS coding region including rs7039789, rs1544105, and rs10106 are significantly associated with increased ALL risk in Thai children.

Design of a (204, 188) Reed-Solomon Decoder ((204,188) Read-Solomon 복호기 설계)

  • 김진규;강성태;유영갑;조경록
    • The Journal of Korean Institute of Communications and Information Sciences
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    • v.25 no.5B
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    • pp.966-973
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    • 2000
  • In this paper, we propose a novel RS decoder design yielding smallr circuit size shorter coding latency. The proposed architecture of RS decoder has the following two features. First, circuit size reduced by using Euclid algorithm with mutual operation between cells. Second, coding latency is reduced by using higher frequency than syndrome and error value calculation block. We performed simulation with C language and MATLAB in order to verify the decoding algorithm and implemented using FPGA chips in VHDL.

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