A lot of work has been focused on desig-ning and analyzing various cooperative diversity pro-tocols for wireless relay networks. To provide a uni-fied queuing analytic framework, we fonmlate an em-bedded Markov chain,...A lot of work has been focused on desig-ning and analyzing various cooperative diversity pro-tocols for wireless relay networks. To provide a uni-fied queuing analytic framework, we fonmlate an em-bedded Markov chain, which rams out to be a Quasi-Birth-and-Death （QBD） process. Using the Matrix-Ce-ometric method, we can analyze the average delay in a unified way. Theoretical analysis is validated by simu-lation results. We show that the delay performances of Amplify-and-Forward or Decode-and-Forwaxd （AF/ DF） and incremental AF/DF schemes can be analyzed in the unified way. Thus, we can always choose the best cooperative diversity scheme in different scenari-os for delay minimization.展开更多
Let S\-n be the symmetric group, g\++\-i=(123i),g\+-\-i=(1i32) and M\++\-n={g\++\-i∶4≤i≤n}, then M\++\-n is a minimal generating set of S\-n ,where n ≥5.It is proved that Cayley graph Cay( S\-...Let S\-n be the symmetric group, g\++\-i=(123i),g\+-\-i=(1i32) and M\++\-n={g\++\-i∶4≤i≤n}, then M\++\-n is a minimal generating set of S\-n ,where n ≥5.It is proved that Cayley graph Cay( S\-n,M\++\-n∪M\+-\-n) is Hamiltonian and edge symmetric.展开更多
In this paper,a sem iparam etric regression m odel in w hich errors are i.i.d random variables from an unknow n density f(·) is considered.Based on Hallet al.(1995),a nonlinear w avelet estim ation of f(·)...In this paper,a sem iparam etric regression m odel in w hich errors are i.i.d random variables from an unknow n density f(·) is considered.Based on Hallet al.(1995),a nonlinear w avelet estim ation of f(·) withoutrestrictions ofcontinuity everyw here on f(·) is given,and the convergence rate ofthe estim ators in L2 is obtained.展开更多
The DNA content of tumor all was analyzed by flow cytometry on parafflnembedded specimens in 73 patients with epithelial ovarian tumor, and its clinical significance was evaluated. One of the 5 benign (20%), 2 of the ...The DNA content of tumor all was analyzed by flow cytometry on parafflnembedded specimens in 73 patients with epithelial ovarian tumor, and its clinical significance was evaluated. One of the 5 benign (20%), 2 of the 11 borderline (18.18%), and 30 of the 57 malignant (52. 63%) tumors were aneuplold. The occurrence rate of aneuploidy In malignant tumors was higher than In benign and borderline tumors ( P < 0. 05 ). Furthermore, aneuploidy was more frequently In the advanced stages (Ⅲ -Ⅳ ) (77. 7%) than in the early stages (Ⅰ - Ⅱ ) (9. 5%) (P<0. 005). The occurrence rate of DNA aneuploidy was higher in patients associated with ascites and the residual tumor≥.2 cm. Patients with aneuploid tumors had more of ten ascites (P<0. 005) and residual tumor size≥2cm (P< 0.005). There was no apparent correlation between the DNA ptoidy and the histologic grade, histologic type of the tumors. G0/G1 cell proportion of DNA diplold tumors in advanced carcinoma (64. 6%) was less than those of early stage carcinoma (75. 9% ) (P<0. 05). The survival rate of diplold tumor patients was higher than that of aneuploid tumor patients in the different time after operation, and the median survival time was 30. 2 months and 10. 3 months, respectively. Multivariate analysis revealed that cellular DNA ploidy was the most Important predictive factor (P = 0. 007) of prognosis, followed by residual tumor size (P= 0. 05). Different tumor specimen of the same patient can exhibit variation sometime (38. 9%).The results revealed that the DNA ploidy may reflect tumor biological characteristics, I. e. , Its proliferative ability. Analysis of cellular DNA content of epithelial ovarian tumors would help us to predict the prognosis of the patients better.展开更多
基金This work was supported by the National Basic Research Program of China under Crant No. 2012CB316001 the National Science Foundation of China under Crants No. （：13832008, No. 03902001.
文摘A lot of work has been focused on desig-ning and analyzing various cooperative diversity pro-tocols for wireless relay networks. To provide a uni-fied queuing analytic framework, we fonmlate an em-bedded Markov chain, which rams out to be a Quasi-Birth-and-Death （QBD） process. Using the Matrix-Ce-ometric method, we can analyze the average delay in a unified way. Theoretical analysis is validated by simu-lation results. We show that the delay performances of Amplify-and-Forward or Decode-and-Forwaxd （AF/ DF） and incremental AF/DF schemes can be analyzed in the unified way. Thus, we can always choose the best cooperative diversity scheme in different scenari-os for delay minimization.
文摘Let S\-n be the symmetric group, g\++\-i=(123i),g\+-\-i=(1i32) and M\++\-n={g\++\-i∶4≤i≤n}, then M\++\-n is a minimal generating set of S\-n ,where n ≥5.It is proved that Cayley graph Cay( S\-n,M\++\-n∪M\+-\-n) is Hamiltonian and edge symmetric.
文摘In this paper,a sem iparam etric regression m odel in w hich errors are i.i.d random variables from an unknow n density f(·) is considered.Based on Hallet al.(1995),a nonlinear w avelet estim ation of f(·) withoutrestrictions ofcontinuity everyw here on f(·) is given,and the convergence rate ofthe estim ators in L2 is obtained.
文摘The DNA content of tumor all was analyzed by flow cytometry on parafflnembedded specimens in 73 patients with epithelial ovarian tumor, and its clinical significance was evaluated. One of the 5 benign (20%), 2 of the 11 borderline (18.18%), and 30 of the 57 malignant (52. 63%) tumors were aneuplold. The occurrence rate of aneuploidy In malignant tumors was higher than In benign and borderline tumors ( P < 0. 05 ). Furthermore, aneuploidy was more frequently In the advanced stages (Ⅲ -Ⅳ ) (77. 7%) than in the early stages (Ⅰ - Ⅱ ) (9. 5%) (P<0. 005). The occurrence rate of DNA aneuploidy was higher in patients associated with ascites and the residual tumor≥.2 cm. Patients with aneuploid tumors had more of ten ascites (P<0. 005) and residual tumor size≥2cm (P< 0.005). There was no apparent correlation between the DNA ptoidy and the histologic grade, histologic type of the tumors. G0/G1 cell proportion of DNA diplold tumors in advanced carcinoma (64. 6%) was less than those of early stage carcinoma (75. 9% ) (P<0. 05). The survival rate of diplold tumor patients was higher than that of aneuploid tumor patients in the different time after operation, and the median survival time was 30. 2 months and 10. 3 months, respectively. Multivariate analysis revealed that cellular DNA ploidy was the most Important predictive factor (P = 0. 007) of prognosis, followed by residual tumor size (P= 0. 05). Different tumor specimen of the same patient can exhibit variation sometime (38. 9%).The results revealed that the DNA ploidy may reflect tumor biological characteristics, I. e. , Its proliferative ability. Analysis of cellular DNA content of epithelial ovarian tumors would help us to predict the prognosis of the patients better.
