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최소거리탐지 알고리즘(MDSA)을 이용한 ML 탐지 MIMO 시스템 연구
권오주,Kwon, Oh-Ju 한국통신학회 2007 韓國通信學會論文誌 Vol.32 No.4C
This paper proposes Minimum Distance Searching Algorithm (MDSA) which reduces the computational complexity (CC) of the ML, the kind of Spatial Multiplexing (SM) MIMO system. The MDSA searchs candidate symbols with a starting symbol, which is called reference bits. We used the linear receiver of MIMO techniques to find a starting symbol. The MDSA searchs the shortest path to a transmitted symbol using reference bits and Minimum Distance(MD) concept. The CC of MDSA is reduced to the 0.21% to the ML as the transmit antennas is 4 in 16QAM. The simulation result shows the BER of MDSA is nearly same to the BER of ML as the transmit antennas is 2 and the receive antennas is 3 in 16QAM and slightly degraded to the BER of ML as the transmit antennas is 4 and the receive antennas is 6 in QPSK. 본 논문은 공간다중화 MIMO 시스템인 ML 수신기법의 연산량을 감소시키는 최소거리탐지 알고리즘 (MDSA: Minimum Distance Searching Algorithm)을 제안한다. 선형수신기의 출력값을 기준비트로 설정하여 탐색공간을 줄이고 기준비트와 수신심벌과의 최소거리를 이용하여 최종송신심벌로의 최적경로를 구함으로써 ML의 연산량을 효율적으로 감소시킨다. 제안한 기법의 연산 반복수는 송신안테나 4개, 성상차수 16일 때, ML 방식에 비해 0.21%로 감소되었다. 성능분석 시뮬레이션 결과는 16QAM에서 송신 안테나 2개, 수신안테나 3개 이상일 때 MDS 는 ML과 성능이 거의 동일하였고, QPSK에서 송신 안테나 4개, 수신안테나 6개 이상일 때 MDS의 성능은 ML에 비해 약간 열화됨을 확인 할 수 있었다.
다중반송파 PAPR 감소를 위한 임계치 적용 적응 부최적 PTS 기법 연구
권오주,하영호 한국통신학회 2001 韓國通信學會論文誌 Vol.26 No.12
본 논문은 다중반송파로 인한 높은 최대 전력 대 평균 전력 비 감소를 위한 PTS 방식에서 시스템의 복잡도를 줄이기 위해 임계간을 활용하여 부 블록 계수를 최적화시키는 적응 부 최적 PTS 알고리즘을 제안한다. 제안 방법의 성능은 부 블록수가 4인 경우, $10^{-3}$에서 PAPR은 Cimini방법보다 0.4dB 향상된 8.1dB로 PTS성능과 거의 동일하였고, 평균 계산은 임계값 8dB를 적용할 경우, PTS방법에 비해 대략 22%로 감소하였으며, Cimini 방법에 비해서는 44%정도로 감소하였다. 부 블록수가 8인 경우, 10-3에서 제안방법의 PAPR은 PTS방법에 비해 0.7dB성능이 열화 되었으나, Cimini방법에 비해서는 0.4dB 성능이 향상되었다. 평균 계산은 임계값 7.5dB를 적용할 경우. PTS방법에 비해 대략 2.4%로 감소하였으며, Cimini방법에 비해서는 39%정도로 감소하였다. This paper proposes the adaptive suboptimal iterative algorithm using threshold to reduce system complexity in the PTS\`s. Performance of the proposed adaptive suboptimal iteration algorithm is represented in terms of iteration number and CDF. In the case of the number of sub-block is 4, the 10-3 PAPR of the proposed method and P S improved this by 0.4dB compared to Cimini\`s. And the complexity of the proposed method was reduced to nearly 22% for the PTS\`s and 44% for the Cimini\`s for 8dB threshold. For the 8 sub-blocks, the 10$\^$-3/ PAPR of the proposed method reduced by 0.7dB compared to PTS\`s, but improved by 0.4dB compared to Cimini\`s. And the complexity of the proposed method was reduced to nearly 2.4% for the PTS\`s and 39% for the Cimini\`s.
권오주,임용관,김보현,이미경,김혜련 대한진단검사의학회 2019 Annals of Laboratory Medicine Vol.39 No.1
Background: High on-treatment platelet reactivity (HTPR) is the phenomenon wherein patients exhibit normal platelet activity in laboratory testing despite adequate adherence to anti-platelet treatment. We investigated the detection rates of Platelet Function Analyzer (PFA)-100 (Dade Behring AG, Düdingen, Switzerland) for drug-induced platelet dysfunction and analyzed potential contributors to HTPR with practical PFA-100 data over six years. Methods: We used data from 6,957 patients who underwent PFA-100 testing after receiving aspirin, clopidogrel, or non-steroidal anti-inflammatory drugs (NSAIDs). Of these, 6,163 patients were tested with only the collagen/epinephrine cartridge (Col/EPI) of PFA-100; 794 were tested with both Col/EPI and the collagen/ADP cartridge (Col/ADP). We calculated PFA-100 closure time (CT) for each drug and compared the clinical and laboratory characteristics of the patients with prolonged CTs and normal CTs (i.e., HTPR). Results: In Col/EPI, 73.2% (365/499), 72.6% (390/537), and 55.3% (3,442/6,228) patients showed prolonged CTs for aspirin, clopidogrel, and NSAIDs, respectively. In Col/ADP, prolonged CTs were observed in 37.4% (34/91), 43.2% (35/81), and 29.6% (200/676) of patients receiving aspirin, clopidogrel, and NSAIDs, respectively. Of the patients tested with both cartridges, 88.9% (48/54), 95.3% (41/43), and 89.0% (577/648) of the patients receiving aspirin, clopidogrel, and NSAIDs had prolonged CTs, and 10.0% (79/794) showed normal CTs regardless of drugs. For clopidogrel users (both cartridges), there were more patients with malignancies in the normal CT than prolonged CT group. Conclusions: PFA-100 is not sufficiently effective for laboratory screening of drug-induced platelet dysfunction. Malignancy may contribute to clopidogrel-related HTPR in PFA-100.