• Title/Summary/Keyword: m-Sequence

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Transmission Signal Detection Technique Using Spreading Sequence for Multi-User Cooperative Communication Systems (다중 사용자 간 협력통신에서의 확산코드를 이용한 송신 신호 검출 기법)

  • Kim, Yoon-Hyun;Park, In-Hwan;Kim, Jin-Young
    • The Journal of the Institute of Internet, Broadcasting and Communication
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    • v.10 no.6
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    • pp.257-262
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    • 2010
  • In this paper, we propose an effective method for detecting signals among multi-user in cooperative communication system. Spread sequence is inserted to NULL space of synchronization channel to synchronize between each user among frame formats of the cooperative communication and then transmitted. In the receiver, the wanted signal is detected by using correlation among the inserted spread sequences. As simulation results, correlations among the signals using m-sequence in AWGN, Rician, and Rayleigh channel are shown. Using the simulation results in this paper, we expect a reliable cooperative communication.

INVERSE SYSTEM AND ARTINIAN O-SEQUENCES OF CODIMENSION 4

  • Shin, Dong-Soo
    • Journal of applied mathematics & informatics
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    • v.25 no.1_2
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    • pp.513-518
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    • 2007
  • There is a one to one correspondence between Artinian algebras $k[x_1,...,x_n]/Ann(M)$ and finitely generated $k[x_1,...,x_n]-submodules$ M of $k[y_1,...,y_n]$ by Inverse System. In particular, any Artinian level algebra $k[x_1,...,x_n]/Ann(M)$ can be obtained when M is finitely generated by only maximal degree generators. We prove that H = (1, 4, 8, 13,..., 27, 8, 2) is not a level Artinian O-sequence using this inverse system.

Heterologous Regulation of BCG hsp65 Promoter by M.leprae 18 kDa Transcription Repression Responsive Element

  • Kim, Hyun Bae;You, Ji Chang
    • Genomics & Informatics
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    • v.1 no.2
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    • pp.113-118
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    • 2003
  • Among a number of antigens characterized in M leprae, an etiological agent of Leprosy, the 18 kDa antigen, is unique to M leprae. We have previously determined a sequence specific element in the 18 kDa gene of M leprae, which confers transcriptional repression. In this report, we have examined if the element could be applied to genes other than the 18 kDa gene of M leprae. To identify the roles of the regulatory sequence in heterologous promoter, we have constructed pB3 vector series, which contains BCG hsp65 promoter and the M leprae 18 kDa transcription repression responsive element in tandem using LacZ gene as a reporter gene. Cloning of hsp65 promoters of M bovis BCG or M smegmatis in front of LacZ gene resulted in normal $\beta$­galactosidase activity as expected. However, when the sequence element was placed between the promoter and the LacZ gene, $\beta$-galactosidase activity was reduced 10-fold less. Also we have examined with pB3(-) vector, that harbors the transcription repression responsive element in a reversed orientation, the $\beta$-galactosidase activity was found to be similar to pB3(+) vector. Thus, these results further confirm that M leprae 18 kDa transcription repression responsive element could regulate BCG hsp65 heterologous promoter and that the element could act as an operator for the transcription of mycobacteria.

Molecular Systematics of the Genus Megoura (Hemiptera: Aphididae) Using Mitochondrial and Nuclear DNA Sequences

  • Kim, Hyojoong;Lee, Seunghwan
    • Molecules and Cells
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    • v.25 no.4
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    • pp.510-522
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    • 2008
  • To construct the molecular systematics of the genus Megoura (Hemiptera: Aphididae), DNA based-identification was performed using four mitochondrial and three nuclear DNA regions: partial cytochrome c oxidase I (COI), partial tRNA-leucine + cytochrome c oxidase II (tRNA/COII), cytochrome b (CytB), partial 12S rRNA + tRNA-valine + 16S rRNA (12S/16S), elongation factor-1 alpha ($EF1{\alpha}$), and the internal transcribed spacers 1 and 2 (ITS1, ITS2). Pairwise sequence divergences between taxa were compared, and phylogenetic analyses were performed based on each DNA region separately, and the combined datasets. COI, CytB, $EF1{\alpha}$, ITS1, and ITS2 were relatively effective in determining species and resolving their relationships. By contrast, the sequences of tRNA/COII and 12S/16S were not able to separate the closely related species. CytB and $EF1{\alpha}$ gave better resolution with higher average sequence divergences (4.7% for CytB, 5.2% for $EF1{\alpha}$). The sequence divergence of COI (3.0%) was moderate, and those of the two ITS regions (1.8% for ITS1, 2.0% for ITS2) were very low. Phylogenetic trees were constructed by minimum evolution, maximum parsimony, maximum likelihood, and Bayesian phylogenetic analyses. The results indicated that the phylogenetic relationships between Megoura species were associated with their host preferences. Megoura brevipilosa and M. lespedezae living on Lespedeza were closely related, and M. nigra, monophagous on Vicia venosa, was rather different from M. crassicauda, M. litoralis, and M. viciae, which are oligophagous on Lathyrus and Vicia. The three populations of M. crassicauda formed a clade separated from M. litoralis and M. viciae. Nevertheless M. litoralis and M. viciae, which are morphologically similar, were not separated due to negligible sequence divergence. We discuss the phylogenetic relationships of the Megoura, and the usefulness of the seven DNA regions for determining the species level phylogeny of aphids.

Identification of volterra kernal of nonlinear systems by use of M-sequence

  • Kashiwagi, Hiroshi;Yeping, Sun;Nishiyama, Eiji
    • 제어로봇시스템학회:학술대회논문집
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    • 1993.10b
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    • pp.150-154
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    • 1993
  • A new method is proposed for obtaining Volterra kernals of a nonlinear system by use of a nonlinear systems by use of pseudorandom M-sequences and correlation technique. M-sequence is applied to a nonlinear technique. M-sequence is applied to a nonlinear system and the crosscorrelation function between the input and the output displays not only the linear impulse response of the linear part of the system, but also crosssections of the Volterra kernals of nonlinear system. Simulations are carried out for up to 3rd order Volterra kernal, and the results show a good agreement with the theoretical considerations.

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ESSENTIAL EXACT SEQUENCES

  • Akray, Ismael;Zebari, Amin
    • Communications of the Korean Mathematical Society
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    • v.35 no.2
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    • pp.469-480
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    • 2020
  • Let R be a commutative ring with identity and M a unital R-module. We give a new generalization of exact sequences called e-exact sequences. A sequence $0{\rightarrow}A{\longrightarrow[20]^f}B{\longrightarrow[20]^g}C{\rightarrow}0$ is said to be e-exact if f is monic, Imf ≤e Kerg and Img ≤e C. We modify many famous theorems including exact sequences to one includes e-exact sequences like 3 × 3 lemma, four and five lemmas. Next, we prove that for torsion-free module M, the contravariant functor Hom(-, M) is left e-exact and the covariant functor M ⊗ - is right e-exact. Finally, we define e-projective module and characterize it. We show that the direct sum of R-modules is e-projective module if and only if each summand is e-projective.

New Constructions of Binary LCZ Sequence Sets With Flexible LCZ and Set Size (유연한 LCZ와 집합 크기를 갖는 새로운 이진 LCZ 수열 집합의 생성)

  • Kim, Young-Sik;Jang, Ji-Woong;No, Jong-Seon;Chung, Ha-Bong
    • The Journal of Korean Institute of Communications and Information Sciences
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    • v.32 no.3C
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    • pp.226-233
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    • 2007
  • In this paper, we construct new LCZ sequence sets with parameters $(2^{n+1}-2,M,L,2)$. In this scheme, we can relatively freely choose the LCZ length L and the resulting LCZ sequence set has the size in which is nearly optimal with respect to Tang, Fan, and Matsufuji bound.

Spliced leader sequences detected in EST data of the dinoflagellates Cochlodinium polykrikoides and Prorocentrum minimum

  • Guo, Ruoyu;Ki, Jang-Seu
    • ALGAE
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    • v.26 no.3
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    • pp.229-235
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    • 2011
  • Spliced leader (SL) trans-splicing is a mRNA processing mechanism in dinoflagellate nuclear genes. Although studies have identified a short, conserved dinoflagellate SL (dinoSL) sequence (22-nt) in their nuclear-encoded transcripts, whether the majority of nuclear-coded transcripts in dinoflagellates have the dinoSL sequence remains doubtful. In this study, we investigated dinoSL-containing gene transcripts using 454 pyrosequencing data (Cochlodinium polykrikoides, 93 K sequence reads, 31 Mb; Prorocentrum minimum, 773 K sequence reads, 291 Mb). After making comparisons and performing local BLAST searches, we identified dinoSL for one C. polykrikoides gene transcript and eight P. minimum gene transcripts. This showed transcripts containing the dinoSL sequence were markedly fewer in number than the total expressed sequence tag (EST) transcripts. In addition, we found no direct evidence to prove that most dinoflagellate nuclear-coded transcripts have this dinoSL sequence.

Helicobacter pylori vacA Mosaicism and New Primers for vacA Signal Sequence Indigenous to Korea (Helicobacter pylori vacA 대립유전자의 Mosaicism과 Signal Sequence의 한국고유 시발체)

  • Ahn, Yeon-Hwa;Kim, Heung-Ryel;Lee, Ji-Eun;Hwang, Tae-Sook;Choe, Yon-Ho
    • Pediatric Gastroenterology, Hepatology & Nutrition
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    • v.4 no.2
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    • pp.155-160
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    • 2001
  • Purpose: Helicobacter pylori has been known to have diverse vacA allelic types. The purpose of the study was to identify vacA diversity in Korea and design new primers for signal sequence alleles indigenous to Korea. Methods: Fifty antral biopsy specimens, which had been proven to be H. pylori-positive, were examined for vacA status; signal sequence and mid-region. After PCR amplification and DNA sequencing, vacA alleles of Korean H. pylori strains were compared with those from other countries. Results: Among Korean H. pylori strains vacA alleles with all combinations of signal sequence and mid-region were found, with the exception of s1b or s2. vacA genotype s1c/m1 was predominant in Korea. We found that GGGAGCGTTR in s1a and GGGGYTATTG in s1c were the indigenous sequences to Korea and constructed the new Korean specific primers for the vacA signal sequence; VASK-F, VASK-R, S1AK-F, and S1CK-F. Conclusion: This study showed that s1c/m1 is the predominant type of vacA allele in Korea. We designed new primers for the vacA signal sequence.

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