1,748 research outputs found

    State Complexity of Regular Tree Languages for Tree Matching

    Get PDF
    We study the state complexity of regular tree languages for tree matching problem. Given a tree t and a set of pattern trees L, we can decide whether or not there exists a subtree occurrence of trees in L from the tree t by considering the new language L′ which accepts all trees containing trees in L as subtrees. We consider the case when we are given a set of pattern trees as a regular tree language and investigate the state complexity. Based on the sequential and parallel tree concatenation, we define three types of tree languages for deciding the existence of different types of subtree occurrences. We also study the deterministic top-down state complexity of path-closed languages for the same problem.</jats:p

    Third-order exceptional point in an ion-cavity system

    Full text link
    We investigate a scheme for observing the third-order exceptional point (EP3) in an ion-cavity setting. In the lambda-type level configuration, the ion is driven by a pump field, and the resonator is probed with another weak laser field. We exploit the highly asymmetric branching ratio of an ion's excited state to satisfy the weak-excitation limit, which allows us to construct the non-Hermitian Hamiltonian (HnH)(H_{\textrm{nH}}). Via fitting the cavity-transmission spectrum, the eigenvalues of HnHH_{\textrm{nH}} are obtained. The EP3 appears at a point where the Rabi frequency of the pump laser and the atom-cavity coupling constant balance the loss rates of the system. Feasible experimental parameters are provided.Comment: 9 pages, 6 figure

    Diagnostic Performance of Core Needle Biopsy and Fine Needle Aspiration Separately or Together in the Diagnosis of Intrathoracic Lesions Under C-arm Guidance

    Get PDF
    Purpose: To evaluate and compare the diagnostic accuracy of fine needle aspiration (FNA) and core needle biopsy (CNB) of intrathoracic lesions using the same coaxial guide-needle under a C-arm Cone-Beam computed tomography system. Materials and Methods: Two hundred and eighty-eight patients (181 male, 107 female; 65.8 ± 13.3 years) with 293 lesions underwent 300 procedures, in which both FNA and CNB were performed. After inserting the coaxial guide-needle into the target lesion, we performed 18-gauge CNB, followed by 20-gauge FNA through the same coaxial guide-needle. The comparison of the procedures in which both showed adequate sample was performed with McNemar’s test (n = 229). Results: Of 300 procedures, 293 were technically successful. Adequate samples were obtained in 248/300 FNA and 288/300 CNB cases. The sensitivity and specificity for diagnosis of malignancy were respectively 84.7% (133/157), 100% (72/72) for FNA, when atypical cells included benign entity; 97.5% (153/157), 100% (72/72) for FNA, when atypical cells included malignancy; 97.6% (162/166), 100% (102/102) for CNB; and 100% (166/166), 100% (102/102) for combined FNA and CNB. Diagnosis of malignancy was significantly higher for CNB than for FNA ('p' < 0.001); however, it was not significantly higher when atypical cells included malignancy for FNA. Pneumothorax occurred in 50 (16.7%) and hemoptysis in 18 (6.0%) procedures. Conclusions: Combined use of CNB and FNA using the same coaxial guide-needle showed better diagnostic performance than using one alone. When comparing CNB and FNA, CNB showed significantly better performance, when atypical cells included a benign entity in FNA

    Avoid Contamination in Soybean (Glycine Max, L. [Merrill]) Microspores Culture

    Full text link
    Microspore culture is done to obtain pure strains. The purpose of soybean microspore culture to obtainquality seeds. Two important step that must be done is isolation of microspores in starvation medium andsubculture into embryogenesis medium. Many factors contributing to the contamination of soybeanmicrospore culture. Contamination in the B medium temperature 34 0C is more common than 4 0C. Vulnerableto contamination because of embryogenesis medium rich in nutrients. Bacterial contaminationcan be caused by internal contaminants such as shape of the anther. Other internal contaminants thatcause diseases such as fungi Colletotrichum truncatum and Phakopsora pachyrhizi. Antagonistic fungiwhich contaminate cultures that Trichoderma spp., Alternaria spp., Fusarium spp. Handling of contaminationis done by selecting the appropriate methods in order to remain viable microspores. Sterilization soybeanflower buds with 20% Tween for 10 minutes and then rinsed with distilled water. Moreover sterilizationwith 4% Hg Cl2 and 10% NaOCl for 10 minutes, rinsed with distilled water times, followed by 96%alcohol for 1 minute, can press up to 70% contamination
    • …
    corecore