• 제목/요약/키워드: operation chain detection

검색결과 10건 처리시간 0.037초

Detection for Operation Chain: Histogram Equalization and Dither-like Operation

  • Chen, Zhipeng;Zhao, Yao;Ni, Rongrong
    • KSII Transactions on Internet and Information Systems (TIIS)
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    • 제9권9호
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    • pp.3751-3770
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    • 2015
  • Many sorts of image processing software facilitate image editing and also generate a great number of doctored images. Forensic technology emerges to detect the unintentional or malicious image operations. Most of forensic methods focus on the detection of single operations. However, a series of operations may be used to sequentially manipulate an image, which makes the operation detection problem complex. Forensic investigators always want to know as much exhaustive information about a suspicious image's entire processing history as possible. The detection of the operation chain, consisting of a series of operations, is a significant and challenging problem in the research field of forensics. In this paper, based on the histogram distribution uniformity of a manipulated image, we propose an operation chain detection scheme to identify histogram equalization (HE) followed by the dither-like operation (DLO). Two histogram features and a local spatial feature are utilized to further determine which DLO may have been applied. Both theoretical analysis and experimental results verify the effectiveness of our proposed scheme for both global and local scenarios.

CPU 환경에서의 실시간 동작을 위한 딥러닝 기반 다중 객체 추적 시스템 (Towards Real-time Multi-object Tracking in CPU Environment)

  • 김경훈;허준호;강석주
    • 방송공학회논문지
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    • 제25권2호
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    • pp.192-199
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    • 2020
  • 최근 딥러닝 모델을 기반으로 한 객체 추적 알고리즘의 활용도가 증가하고 있다. 영상에서의 다중 객체의 추적을 위한 시스템은 대표적으로 객체 검출 알고리즘과 객체 추적 알고리즘의 연쇄된 형태로 구성되어있다. 하지만 여러 모듈로 구성된 연쇄 형태의 시스템은 고성능 컴퓨팅 환경을 요구하며 실제 어플리케이션으로의 적용에 제한사항으로 존재한다. 본 논문에서는 위와 같은 객체 검출-추적의 연쇄 형태의 시스템에서 객체 검출 모듈의 연산 관련 프로세스를 조정하여 저성능 컴퓨팅 환경에서도 실시간 동작을 가능하게 하는 방법을 제안한다.

연속시간 흡수 마코프체인을 활용한 신뢰도 중복 최적화 문제 (A Reliability Redundancy Optimization Problem with Continuous Time Absorbing Markov Chain)

  • 김각규;백승원;윤봉규
    • 대한산업공학회지
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    • 제39권4호
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    • pp.290-297
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    • 2013
  • The increasing level of operation in high-tech industry is likely to require ever more complex structure in reliability problem. Furthermore, system failures are more significant on society as a whole than ever before. Reliability redundancy optimization problem (RROP) plays a important role in the designing and analyzing the complex system. RROP involves selection of components with multiple choices and redundancy levels for maximizing system reliability with constraints such as cost, weight, etc. Meanwhile, previous works on RROP dealt with system with perfect failure detection, which gave at most a good solution. However, we studied RROP with imperfect failure detection and switching. Using absorbing Markov Chain, we present not a good solution but the optimal one. In this study, the optimal system configuration is designed with warm and cold-standby redundancy for k-out-of-n system in terms of MTTF that is one of the performance measures of reliability.

Development of a ladder-shape melting temperature isothermal amplification (LMTIA) assay for detection of African swine fever virus (ASFV)

  • Wang, Yongzhen;Wang, Borui;Xu, Dandan;Zhang, Meng;Zhang, Xiaohua;Wang, Deguo
    • Journal of Veterinary Science
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    • 제23권4호
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    • pp.51.1-51.10
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    • 2022
  • Background: Due to the unavailability of an effective vaccine or antiviral drug against the African swine fever virus (ASFV), rapid diagnosis methods are needed to prevent highly contagious African swine fever. Objectives: The objective of this study was to establish the ladder-shape melting temperature isothermal amplification (LMTIA) assay for the detection of ASFV. Methods: LMTIA primers were designed with the p72 gene of ASFV as the target, and plasmid pUC57 was used to clone the gene. The LMTIA reaction system was optimized with the plasmid as the positive control, and the performance of the LMTIA assay was compared with that of the commercial real-time polymerase chain reaction (PCR) kit in terms of sensitivity and detection rate using 200 serum samples. Results: Our results showed that the LMTIA assay could detect the 104 dilution of DNA extracted from the positive reference serum sample, which was the same as that of the commercial real-time PCR kit. The coincidence rate between the two assays was 100%. Conclusions: The LMTIA assay had high sensitivity, good detection, and simple operation. Thus, it is suitable for facilitating preliminary and cost-effective surveillance for the prevention and control of ASFV.

Integrated RT-PCR Microdevice with an Immunochromatographic Strip for Colorimetric Influenza H1N1 virus detection

  • Heo, Hyun Young;Kim, Yong Tae;Chen, Yuchao;Choi, Jong Young;Seo, Tae Seok
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2013년도 제45회 하계 정기학술대회 초록집
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    • pp.273-273
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    • 2013
  • Recently, Point-of-care (POC) testing microdevices enable to do the patient monitoring, drug screening, pathogen detection in the outside of hospital. Immunochromatographic strip (ICS) is one of the diagnostic technologies which are widely applied to POC detection. Relatively low cost, simplicity to use, easy interpretations of the diagnostic results and high stability under any circumstances are representative advantages of POC diagnosis. It would provide colorimetric results more conveniently, if the genetic analysis microsystem incorporates the ICS as a detector part. In this work, we develop a reverse transcriptase-polymerase chain reaction (RT-PCR) microfluidic device integrated with a ROSGENE strip for colorimetric influenza H1N1 virus detection. The integrated RT-PCR- ROSGENE device is consist of four functional units which are a pneumatic micropump for sample loading, 2 ${\mu}L$ volume RT-PCR chamber for target gene amplification, a resistance temperature detector (RTD) electrode for temperature control, and a ROSGENE strip for target gene detection. The device was fabricated by combining four layers: First wafer is for RTD microfabrication, the second wafer is for PCR chamber at the bottom and micropump channel on the top, the third is the monolithic PDMS, and the fourth is the manifold for micropump operation. The RT-PCR was performed with subtype specific forward and reverse primers which were labeled with Texas-red, serving as a fluorescent hapten. A biotin-dUTP was used to insert biotin moieties in the PCR amplicons, during the RT-PCR. The RT-PCR amplicons were loaded in the sample application area, and they were conjugated with Au NP-labeled hapten-antibody. The test band embedded with streptavidins captures the biotin labeled amplicons and we can see violet colorimetric signals if the target gene was amplified with the control line. The off-chip RT-PCR amplicons of the influenza H1N1 virus were analyzed with a ROSGENE strip in comparison with an agarose gel electrophoresis. The intensities of test line was proportional to the template quantity and the detection sensitivity of the strip was better than that of the agarose gel. The test band of the ROSGENE strip could be observed with only 10 copies of a RNA template by the naked eyes. For the on-chip RT-PCR-ROSGENE experiments, a RT-PCR cocktail was injected into the chamber from the inlet reservoir to the waste outlet by the micro-pump actuation. After filling without bubbles inside the chamber, a RT-PCR thermal cycling was executed for 2 hours with all the microvalves closed to isolate the PCR chamber. After thermal cycling, the RT-PCR product was delivered to the attached ROSGENE strip through the outlet reservoir. After dropping 40 ${\mu}L$ of an eluant buffer at the end of the strip, the violet test line was detected as a H1N1 virus indicator, while the negative experiment only revealed a control line and while the positive experiment a control and a test line was appeared.

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Combined Detection of Serum MiR-221-3p and MiR-122-5p Expression in Diagnosis and Prognosis of Gastric Cancer

  • Zhang, Yan;Huang, Huifeng;Zhang, Yun;Liao, Nansheng
    • Journal of Gastric Cancer
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    • 제19권3호
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    • pp.315-328
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    • 2019
  • Purpose: To investigate the clinical value of serum miR-221-3p and miR-122-5p expression levels in the diagnosis and prognosis of gastric cancer. Materials and Methods: Serum samples from 141 gastric cancer cases (gastric cancer group), 110 gastric polyps (gastric polyp group), and 75 healthy people (healthy control) were used to detect miR-221-3p and miR-122-5p expression using real-time reverse transcription polymerase chain reaction. Results: Serum miR-221-3p expression was significantly higher in the gastric cancer group than in the gastric polyp group, and it was significantly lower than that before operation. The miR-221-3p expression was significantly higher in the death group than in the survival group. The proliferation and migration ability significantly increased and the apoptosis rate significantly decreased by miR-221-3p transfection in gastric cancer cells. In contrast, the function of miR-122-5p in gastric cancer cells was opposite of miR-221-3p. Serum miR-221-3p expression was negatively correlated with that of miR-122-5p in gastric cancer. Serum miR-221-3p and miR-122-5p expressions were significantly correlated with the degree of differentiation, tumor, node, metastasis stage, lymph node metastasis, and invasion depth. miR-221-3p and miR-122-5p expression levels were independent prognostic factors for postoperative gastric cancer. In the diagnosis and predicting prognosis of gastric cancer, receiver operating characteristic analysis revealed that the area under curve of combined detection of serum miR-221-3p and miR-122-5p expression had a greater diagnostic effect than either single maker. Conclusions: The miR-221-3p and miR-122-5p are involved in the development of gastric cancer, and they have important clinical values in gastric cancer diagnosis and prognosis.

중합효소 연쇄반응에 의한 식중독성 황색포도상구균의 신속한 검출 (Rapid Detection of Enterotoxigenic Staphylococcus aureus by Polymerase Chain Reaction)

  • 김은선;전덕영
    • 한국식품과학회지
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    • 제28권6호
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    • pp.1001-1008
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    • 1996
  • 우리나라의 세균성 식중독의 주된 원인은 식중독성 황색포도상구균에 의한다. 따라서 식품공전에는 도시락, 빵, 떡으로부터는 이 미생물이 검출되지 않도록 규정되어있다. 현행의 황백포도상구균의 검사 방법은 적어도 5일 이상을 요하므로 이 식중독에 대한 대처가 미흡한 설정이다. 이 연구에서는 식중독성 황색포도상구균의 검출법을 중합효소 연쇄반응을 이용하여 개선하였다. 이 반응을 위해 황색포도상구균의 장도속도를 암호하는 유전자를 유형별로 증폭할 수 있는 시발물질들을 고안하였다. 한 황색포도상구균으로부터 중합효소 연쇄반응에 적합한 DNA를 신속하게 추출하는 방법을 개발하였다. 중합효소 반응조건은 다음과 같다. 반응액의 총부피, $(50\;{\mu}l)$; 표적 DNA, $2\;{\mu}l$ (약 20ng); 10배 진한 반응완충액, $5\;{\mu}l$; 시발물질, 100pmole; dNTP (10 mM), $4\;{\mu}l$; Taq DNA 중합효소, 205단위, 작동조건은 변성전, $94^{\circ}C$-5분; 변성, $94^{\circ}C$ 15초; 냉각, $50^{\circ}C$15초; 연장, $72^{\circ}C$ 20초; 연장후, $72^{\circ}C$-5분이었으며 변성-냉각-연장을 30회 되풀이하였다. dlj한 검출조건으로 황색포도상구균을 5시간 이내에 독소 유형별로 확인할 수 있었으며 이를 시판되는 떡과 빵에 적용하여 이 미생물의 존재를 확인하였다.

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Comparative Assessment of Diagnostic Performances of Two Commercial Rapid Diagnostic Test Kits for Detection of Plasmodium spp. in Ugandan Patients with Malaria

  • Bahk, Young Yil;Park, Seo Hye;Lee, Woojoo;Jin, Kyoung;Ahn, Seong Kyu;Na, Byoung-Kuk;Kim, Tong-Soo
    • Parasites, Hosts and Diseases
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    • 제56권5호
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    • pp.447-452
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    • 2018
  • Prompt diagnosis of malaria cases with rapid diagnostic tests (RDTs) has been widely adopted as an effective malaria diagnostic tool in many malaria endemic countries, primarily due to their easy operation, fast result output, and straightforward interpretation. However, there has been controversy about the diagnostic accuracy of RDTs. This study was conducted to evaluate the diagnostic performances of the 2 commercially available malaria RDT kits, RapiGEN Malaria Ag Pf/Pv (pLDH/pLDH) and Asan $EasyTest^{TM}$ Malaria Ag Pf/Pv (HRP-2/pLDH) for their abilities to detect Plasmodium species in blood samples collected from Ugandan patients with malaria. To evaluate the diagnostic performances of these 2 RDT kits, 229 blood samples were tested for malaria infection by microscopic examination and a species-specific nested polymerase chain reaction. The detection sensitivities for P. falciparum of Malaria Ag Pf/Pv (pLDH/pLDH) and Asan $EasyTest^{TM}$ Malaria Ag Pf/Pv (HRP-2/pLDH) were 87.83% and 89.57%, respectively. The specificities of the 2 RDTs were 100% for P. falciparum and mixed P. falciparum/P. vivax infections. These results suggest that the 2 RDT kits showed reasonable levels of diagnostic performances for detection of the malaria parasites from Ugandan patients. However, neither kit could effectively detect P. falciparum infections with low parasitaemia (<$500parasites/{\mu}l$).

Enhancing Internet of Things Security with Random Forest-Based Anomaly Detection

  • Ahmed Al Shihimi;Muhammad R Ahmed;Thirein Myo;Badar Al Baroomi
    • International Journal of Computer Science & Network Security
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    • 제24권6호
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    • pp.67-76
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    • 2024
  • The Internet of Things (IoT) has revolutionized communication and device operation, but it has also brought significant security challenges. IoT networks are structured into four levels: devices, networks, applications, and services, each with specific security considerations. Personal Area Networks (PANs), Local Area Networks (LANs), and Wide Area Networks (WANs) are the three types of IoT networks, each with unique security requirements. Communication protocols such as Wi-Fi and Bluetooth, commonly used in IoT networks, are susceptible to vulnerabilities and require additional security measures. Apart from physical security, authentication, encryption, software vulnerabilities, DoS attacks, data privacy, and supply chain security pose significant challenges. Ensuring the security of IoT devices and the data they exchange is crucial. This paper utilizes the Random Forest Algorithm from machine learning to detect anomalous data in IoT devices. The dataset consists of environmental data (temperature and humidity) collected from IoT sensors in Oman. The Random Forest Algorithm is implemented and trained using Python, and the accuracy and results of the model are discussed, demonstrating the effectiveness of Random Forest for detecting IoT device data anomalies.

안전하지 않은 I/O핀 노이즈 환경에서 MCU 클럭 보호를 위한 자동 온칩 글리치 프리 백업 클럭 변환 기법 (Automatic On-Chip Glitch-Free Backup Clock Changing Method for MCU Clock Failure Protection in Unsafe I/O Pin Noisy Environment)

  • 안중현;윤지애;조정훈;박대진
    • 전자공학회논문지
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    • 제52권12호
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    • pp.99-108
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    • 2015
  • 클럭 펄스에 동기 되어 동작하는 임베디드 마이크로컨트롤러는 미션 크리티컬한 응용환경에서 입력 클럭에 가해지는 급격한 전기적 왜란의 영향에 의해 오동작이 발생되기 쉽다. 다양한 외부 전기적 노이즈에 대한 내성 있는 시스템 동작이 요구되며 시스템 클럭 관점에서 견고한 회로 디자인 기술이 점차 중요한 이슈가 되고 있다. 본 논문에서는 이러한 시스템의 비이상적인 상황을 방지하기 위해 자동 클럭 에러 검출을 위한 온 칩클럭 컨트롤러 구조를 제안한다. 이를 위해 에지 검출기, 노이즈 제거기와 글리치 프리 클럭 스위칭 회로를 적용하였고, 에지 검출기는 입력 클럭의 비이상적인 저주파수 상태를 검출하는데 사용 되었으며, 딜레이 체인 회로를 이용한 클럭 펄스의 노이즈 제거기는 글리치 성분을 검출 할 수 있도록 하였다. 이렇게 검출된 입력 클럭의 비이상적인 상황은 글리치 프리 클럭 변환기에 의해 백업 클럭으로 스위칭하게 된다. 회로 시뮬레이션을 통해 제안된 백업 클럭 변환기의 동작을 검증하였고 테스트환경에서 방사노이즈를 인가하였을 때 시스템 클럭의 내성에 대한 주파수 특성을 평가하였다. 본 기법을 범용 MCMCU 구조에 추가적으로 적용하여 작은 하드웨어의 추가만으로도 시스템 클럭의 안전성을 확보하는 하나의 방법을 제시한다.