• 응용통계연구
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• 제20권2호
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• pp.345-355
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• 2007

PLS 회귀는 q-변량의 Y 변수에 대한 회귀에서 p-변량의 X 변수가 다중공선성의 문제를 갖는 경우에도 적용 가능한 방법이다. 특히 X 변수의 수 p가 관측개체 수 n보다 큰 경우에 적용 가능하여 계량화학(chemometrics) 분야에서 근적외선 분광기(near-infrared spectroscopy) 자료에 대한 표준적 분석 방법으로 활용되고 있다. 이 연구에서 우리는 PLS회귀의 방법론을 정리하고 이를 활용한 p개의 X 변수들과 q개의 Y 변수들의 동시 시각화를 위한 두 가지의 수량화 방법을 제안한다.

• 대한수학회지
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• 제46권4호
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• pp.733-746
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• 2009

For any integer k $\geq$ 2, let P(c, k + 1;q) be the number of all k+1-tuples with positive integer coordinates ($a_1,a_2,...,a_{k+1}$) such that $1{\leq}a_i{\leq}q$, ($a_i,q$) = 1, $a_1a_2...a_{k+1}{\equiv}$ c (mod q) and 2 $\nmid$ ($a_1+a_2+...+a_{k+1}$), and E(c, k+1; q) = P(c, k+1;q) - $\frac{{\phi}^k(q)}{2}$. The main purpose of this paper is using the properties of Gauss sums, primitive characters and the mean value theorems of Dirichlet L-functions to study the hybrid mean value of the r-th hyper-Kloosterman sums Kl(h,k+1,r;q) and E(c,k+1;q), and give an interesting mean value formula.

• 한국인터넷방송통신학회논문지
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• 제12권5호
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• pp.185-189
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• 2012

큰 반소수 n=pq의 소인수 p,q를 직접 찾는 것은 현실적으로 거의 불가능하여 대부분의 소인수분해 알고리즘은 $a^2{\equiv}b^2$(mod n)의 제곱합동을 찾아 p=GCD(a-b,n),q=GCD(a+b,n)의 소인수를 찾는 간접 방법을 적용하고 있다. 제곱합동 a,b을 찾는 다양한 방법이 제안되었지만 100자리 이상인 RSA 수에 대해서는 적용이 쉽지 않다. 본 논문에서는 $xa={\lceil}\sqrt{zn}{\rceil}\;or\;{\lceil}\sqrt{zn}{\rceil}+z+z=1,2,{\cdots}$로 설정하고 $(xa)^2{\equiv}(yb)^2$(mod n)을 찾는 간단한 방법을 제안한다. 제안된 알고리즘은 19 자리 수 까지는 제곱합동을 빠르게 찾는데 성공하였으나 39 자리 수에 대해서는 실패하였다.

• Journal of Ginseng Research
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• 제22권3호
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• pp.168-172
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• 1998

Systematic electrophoretic analysis of alcohol-soluble proteins and salt-soluble proteins of 247 Panax ginseng (P.g) and Panax quinquefolium (P.q) germplasms seed was carried out on an improved lactate-polyacrylamide gel electrophoresis, a method with high resolving power, good reproducibility and stability. The electrophoregrams of proteins, according to their migration rate, were classified into four groups such as ${\alpha}$, ${\beta}$, ${\gamma}$ and $\omega$ for the alcohol-soluble proteins and three such as I, II and III for the salt-soluble ones. Panax ginseng or Panax quinquefolium had their own unique band pattern distinguishable from each other, regarding as their specific "fingerprint". In this study, 3 of 168 (1.8%) P.g germplasms and 1 of 79 (1.3%) P.q germplasms had their own unique band pattern, showing that P.g and P.q germplasms have poor genetic diversity in species. The band patterns of dry seed and stratified seed (embryo rate=60%) were basically the same. The band number of the F, hybrid of p.gx p.q was exactly equivalent to the number of the common bands plus the specific bands of the two parents, indicating that the difference of band patterns was a genetic trait con- trolled by the nuclear genes. The electrophoregram of F1 of P.g x P.q could be predicted by that of the two parents and the band pattern of the F1 hybrids could be demnonstrated by that of the mixed seed extract from the two parents.

• 대한수학회보
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• 제59권3호
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• pp.685-695
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• 2022

The minimum number of complete bipartite subgraphs needed to partition the edges of a graph G is denoted by b(G). A known lower bound on b(G) states that b(G) ≥ max{p(G), q(G)}, where p(G) and q(G) are the numbers of positive and negative eigenvalues of the adjacency matrix of G, respectively. When equality is attained, G is said to be eigensharp and when b(G) = max{p(G), q(G)} + 1, G is called an almost eigensharp graph. In this paper, we investigate the eigensharpness and almost eigensharpness of lexicographic products of some graphs.

• 대한수학회보
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• 제47권2호
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• pp.319-339
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• 2010

In this paper, we prove that if $f^nf'\;-\;P$ and $g^ng'\;-\;P$ share 0 CM, where f and g are two distinct transcendental meromorphic functions, $n\;{\geq}\;11$ is a positive integer, and P is a nonzero polynomial such that its degree ${\gamma}p\;{\leq}\;11$, then either $f\;=\;c_1e^{cQ}$ and $g\;=\;c_2e^{-cQ}$, where $c_1$, $c_2$ and c are three nonzero complex numbers satisfying $(c_1c_2)^{n+1}c^2\;=\;-1$, Q is a polynomial such that $Q\;=\;\int_o^z\;P(\eta)d{\eta}$, or f = tg for a complex number t such that $t^{n+1}\;=\;1$. The results in this paper improve those given by M. L. Fang and H. L. Qiu, C. C. Yang and X. H. Hua, and other authors.

• 한국인터넷방송통신학회논문지
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• 제13권3호
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• pp.93-101
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• 2013

본 논문은 경쟁업체 $F_B$가 q개의 상점을 운영하고 있는 상황에서 신규 업체 $F_A$가 시장 점유율을 최대로 하는 p,(p$V=V{\backslash}F_B$ 후보 노드들 중 최단거리를 기준으로 최대로 확보한 상위 노드들 q개를 선택하였다. q개 노드에 대해 포함-배제 원리를 적용하여 p개의 확보 고객수 합을 구해 경쟁을 통해 최대 값을 가진 노드 집합을 $F_A$의 상점 위치로 결정하는 경쟁 알고리즘이다. 제안된 경쟁 알고리즘은 q=5에 대해 p1,2,3,4의 상점 위치를 최적으로 간단히 결정하였으며, 시장 점유율도 최대로 높일 수 있음을 보였다.

• Korean Journal of Mathematics
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• 제25권2호
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• pp.201-209
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• 2017

There exists already mass formula which is the number of self orthogonal codes in $GF(q)^n$, but not proof of it. In this paper we described some theories about finite geometry and by using them proved the mass formula when $q=p^m$, p is odd prime.

• The Korean Journal of Ecology
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• 제27권2호
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• pp.115-120
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• 2004

Coarse woody debris (CWD, $\ge$ 5 cm in maximum diameter) is an important functional component, especially to nutrient cycling in forest ecosystems. To compare mass and nutrient dynamics of CWD in natural oak forests, a two-year study was conducted at Quercus serrata and Q. variabilis stands in Yangpyeong, Kyonggi Province. Total CWD (snag, stump, log and large branch) and annual decomposition mass (Mg/ha) were 1.9 and 0.4 for the Q. serrata stand and 7.5 and 0.5 for the Q. variabilis stand, respectively. Snags covered 72% of total CWD mass for the Q. variabilis stand and 42% for the Q. serrata stand. Most of CWD was classified into decay class 1 for both stands. CWD N and P concentrations for the Q. variabilis stand significantly increased along decay class and sampling time, except for P concentration in 2002. There were no differences in CWD N concentration for the Q. serrata stand along decay class and sampling time. However, CWD P concentration decreased along sampling time. CWD N and P contents (kg/ha) ranged from 3.5∼4.7 and 0.8∼1.3 for the Q. serrata stand to 22.8∼23.6 and 3.7∼4.7 for the Q. variabilis stand. Nitrogen and P inputs (kg/ha/yr) into mineral soil through the CWD decomposition were 0.7 and 0.3 for the Q. serrata stand and 1.6 and 0.3 for the Q. variabilis stand, respectively. The number of CWD and decay rate were main factors influencing the difference in CWD mass and nutrient dynamics between both stands.

• Journal of applied mathematics & informatics
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• 제7권3호
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• pp.1017-1027
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• 2000

On the positive real number, we obtain the Hyers-Ulam stability and a stability in the sense of R. Ger for the generalized beta function g(x+p,y+q) = ${\varphi}(x,y)g(x,y)$ in the following settings: $$\mid$g(x+p,y+q)-{\varphi}(x,y)g(x,y)$\mid${\leq}{\delta}$ and $$\mid$\frac{g(x+p,y+q)}{\varphi(x,y)g(x,y)}-1$\mid${\leq}{\psi}(x,y). As a consequence we obtain stability theorems for the gamma functional equation and the beta functional equation.