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“二元法”在混合基因型数据库比对应用中的效能估计
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作者 冯冬亮 刘长晖 +1 位作者 韩晓龙 余政梁 《生命科学仪器》 2021年第5期21-25,共5页
目的以随机模拟法进行"二元法"混合基因型数据库比对应用效能分析。方法利用随机模拟法产生1000万个无关个体样本,从中随机选取个体分别组合成10000个两人、三人和四人样本混合基因型。分别在13,15,17,19,20,21,22,23个常染色... 目的以随机模拟法进行"二元法"混合基因型数据库比对应用效能分析。方法利用随机模拟法产生1000万个无关个体样本,从中随机选取个体分别组合成10000个两人、三人和四人样本混合基因型。分别在13,15,17,19,20,21,22,23个常染色体STR检测系统上进行"二元法"混合基因型数据库比对应用效能比较分析。结果利用随机模拟算法构建的模拟随机个体数据库接近真实无关个体数据库。在最大23个STR基因座检测体系下,二、三和四样本混合DNA分型的数据库比中个体中位数分别为2、3和68,最大值为2、100和11323;在15个STR基因座时,中位数分别为2、336和12826,最大值为136、40100和517283。结论"二元法"在混合基因型的数据库搜索应用中具有一定的实践价值。 展开更多
关键词 随机模拟 二元法 数据库搜索 常染色体STR 混合基因型
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乙型肝炎病毒基因型与混合基因型对越南肝脏疾病进程的影响 被引量:1
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作者 Toan N.L. Kremsner P.G. +1 位作者 C.-T.Bock 王顺涛 《世界核心医学期刊文摘(胃肠病学分册)》 2006年第12期47-47,共1页
Eight genotypes(A-H) of hepatitis B virus(HBV) have been identified.However,the impact of different genotypes on the clinical course of hepatitis B infection remains controversial.We investigated the frequency and cli... Eight genotypes(A-H) of hepatitis B virus(HBV) have been identified.However,the impact of different genotypes on the clinical course of hepatitis B infection remains controversial.We investigated the frequency and clinical outcome of HBV genotypes and genotype mixtures in HBV-infected patients from Vietnam,Europe,and Africa.In addition,we analyzed the effects of genotype mixtures on alterations in in vitro viral replication.In Asian patients,seven genotypes(A-G) were detected,with A,C,and D predominating.In European and African patients,only genotypes A,C,D,and G were identified.Genotype mixtures were more frequently encountered in African than in Asian(P =.01) and European patients(P =.06) .In Asian patients,the predominant genotype mixtures included A/C and C/D,compared to C/D in European and A/D in African patients.Genotype A was more frequent in asymptomatic compared with symptomatic patients(P <.0001) .Genotype C was more frequent in patients with hepatocellular carcinoma(HCC;P =.02) .Genotype mixtures were more frequently encountered in patients with chronic hepatitis in comparison to patients with acute hepatitis B(P =.015) ,liver cirrhosis(P =.013) ,and HCC(P =.002) .Viral loads in patients infected with genotype mixtures were significantly higher in comparison to patients with a single genotype(P =.019) .Genotype mixtures were also associated with increased in vitro HBV replication.In conclusion,infection with mixtures of HBV genotypes is frequent in Asia,Africa,and Europe.Differences in the replication-phenotype of single genotypes compared to genotype-mixtures suggest that co-infection with different HBV-genotypes is associated with altered pathogenesis and clinical outcome. 展开更多
关键词 混合基因型 肝脏疾病 乙型肝炎病毒 病毒复制 急性乙型肝炎 肝细胞性肝癌 分布频率 病毒载量 慢性肝
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混合基因型拆分分析1例 被引量:3
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作者 李旭鹏 张玉红 +5 位作者 贾东涛 林子清 韩海军 姚建 杨敏 伊海 《中国法医学杂志》 CSCD 北大核心 2011年第3期246-246,共1页
1案例资料 1.1简要案情 2009年12月24.日,某车库内发生1起抢劫案,一男子用砖头打击受害人(女性)头部,并实施抢劫。类似案例在当地连续发生4起,提取受害人所穿外套进行DNA检验。
关键词 法医物证学 STR基因座 混合基因型 Y-STR
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混合基因型拆分确定单亲遗传关系鉴定
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作者 拜永强 周栋 +1 位作者 张颖 王瑞瑞 《中国法医学杂志》 CSCD 2016年第3期293-294,共2页
1案例资料1.1简要案情2015年2月3日,我市某公路旁发现一棉被包裹的男性尸体,四肢被绳索捆绑。1.2法医学检验死者颈部有勒痕,体内检出药物"氯氮平"但未达致死量,分析为死者生前患有精神类疾病。推断死因为机械性窒息,认为系他杀。根据... 1案例资料1.1简要案情2015年2月3日,我市某公路旁发现一棉被包裹的男性尸体,四肢被绳索捆绑。1.2法医学检验死者颈部有勒痕,体内检出药物"氯氮平"但未达致死量,分析为死者生前患有精神类疾病。推断死因为机械性窒息,认为系他杀。根据死者被包裹、捆绑及抛尸等特点,考虑与其共宿者作案可能性大。遂提取包裹所用的棉被、床单、绳索及受害人血样送检。 展开更多
关键词 法医物证学 混合基因型 拆分 单亲遗传关系
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基于变长基因型遗传算法的多供应点应急物资调度优化 被引量:7
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作者 吴凡 杨冰 洪思 《计算机应用研究》 CSCD 北大核心 2022年第4期1148-1154,共7页
如何及时、高效地调度应急物资以减小突发事件带来的伤害成为社会关注的焦点问题。在综合考虑新冠肺炎疫情这类特殊突发事件特点的前提下,构建了一类多供应点多式联运应急物资调度网络,并以运输成本最低、时间惩罚最少、配送员被感染风... 如何及时、高效地调度应急物资以减小突发事件带来的伤害成为社会关注的焦点问题。在综合考虑新冠肺炎疫情这类特殊突发事件特点的前提下,构建了一类多供应点多式联运应急物资调度网络,并以运输成本最低、时间惩罚最少、配送员被感染风险最小为优化目标建立了一类多目标调度优化模型。考虑到基于聚类思想的优化算法在解决多供应点,尤其是多目标调度优化问题中缩减可行域方法科学性存疑的局限性,提出了一类考虑完全可行域思想的变长基因型混合小生境遗传算法,并借助23个基准测试实例验证了这一算法的有效性,更新了部分实例的现有最优解。在此基础上,通过比较多供应点应急物资多式联运算例中四类遗传算法的仿真结果进一步验证了混合小生境等改进策略的优越性。 展开更多
关键词 变长基因型混合小生境遗传算法 应急物资调度 多供应点 多式联运 完全可行域
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Genetic Analysis on Plant Height in Rice in Different Growing Seasons
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作者 陈小荣 陈志彬 +5 位作者 贺浩华 朱昌兰 彭小松 贺晓鹏 傅军如 欧阳林娟 《Agricultural Science & Technology》 CAS 2010年第11期114-118,共5页
[Objective] The aim was to carry out the genetic analysis on plant height of rice(Oryza sativa L.)cultivated in different seasons.[Method] Three rice parents with great difference in plant height including CB1(83.1... [Objective] The aim was to carry out the genetic analysis on plant height of rice(Oryza sativa L.)cultivated in different seasons.[Method] Three rice parents with great difference in plant height including CB1(83.1 cm),CB4(105.5 cm)and CB7(115.6 cm)were chosen to construct two parental combinations:CB1×CB4 and CB7×CB4,and the corresponding filial generations P1,F1,P2,B1,B2 and F2 were obtained.The 6 populations were planted in middle and late seasons respectively to measure their height traits.The Akaike's information criterion(AIC)of the mixed major gene and polygene model was used to indentify the existence of major genes affecting quantitative traits in B1,B2,F2 populations.When the major genes existed,the genetic effects of the major genes and polygenes and their genetic variance were estimated through segregation analysis.[Result] One additive major gene plus additive-dominance polygenes was the most fitted genetic model for the trait in all B1,B2,F2 populations in two planting seasons.The heritability values of the major genes varied from 38.63% to 78.53% and those of polygenes varied from 1.72% to 36.04%,and the total heritability values were 45.52-92.93%.The additive effect d value of the two genetic populations under two planting seasons was-4.56,-9.16,-7.19,and-9.38,respectively,as suggested that additive effect of the major genes would decrease the express of the plant height trait.[Conclusion] The heritability of plant height trait was affected by planting seasons and the combinations clearly as a whole. 展开更多
关键词 RICE Plant height Different planting seasons Major genes plus polygenes mixed inheritance model Genetic effect
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Genetic Analysis of Embryo Production Frequency in Wheat × Maize Cross
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作者 刘琨 宁波 +4 位作者 李宏生 李绍祥 顾坚 赵红 杨木军 《Agricultural Science & Technology》 CAS 2015年第9期1869-1872,共4页
A DH population derived from C49S-87/01Y1-1069 was used to study the inheritance of wheat haploid embryo production frequency(EPF) in wheat × maize cross with the mixed major gene and polygene inheritance model... A DH population derived from C49S-87/01Y1-1069 was used to study the inheritance of wheat haploid embryo production frequency(EPF) in wheat × maize cross with the mixed major gene and polygene inheritance model of quantitative traits. The results showed that the EPF of wheat × maize cross was controlled by two dominant epistatic genes and polygene with gene effects of 1.95 for the first major gene, 6.69 for the second one and 2.80 for the polygene. The inheritability of major genes was as high as 72.09%, suggesting that the differences in EPF among wheat materials were mainly influenced by genotype. However, non-genetic factors were still important, especially for wheat materials with low EPF. 展开更多
关键词 Wheat × maize cross Haploid embryo production frequency Double Haploid population Mixed major gene and polygene inheritance model
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混合分型拆分结合DNA亲缘比对查找弃婴身源1例
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作者 张浩 陈洋洋 +1 位作者 伊海 韩海军 《中国法医学杂志》 CSCD 2023年第2期215-217,共3页
1案例简介2022年2月,某区一高架立交桥附近的绿化带内发现一名被毛毯包裹的男婴,“120”到现场确认已死亡,为消除社会影响,尽快查清男婴身源,确定遗弃男婴尸体人员身份,技术人员提取包裹男婴尸体的毛毯与男婴肋软骨至本实验室。经综合... 1案例简介2022年2月,某区一高架立交桥附近的绿化带内发现一名被毛毯包裹的男婴,“120”到现场确认已死亡,为消除社会影响,尽快查清男婴身源,确定遗弃男婴尸体人员身份,技术人员提取包裹男婴尸体的毛毯与男婴肋软骨至本实验室。经综合运用多波段光源搜索取材、混合基因型拆分、亲缘关系比对等多种手段,为查明案件事实提供精确线索。2检验和分析过程2.1DNA初检取材观察送检的毛毯,毛毯呈灰褐色,大小为210cm×250 cm的双人毛毯,用柯莱ML2生物发现仪蓝光照射搜索毛毯表面,多处呈现荧光反应,剪取荧光反应部位做好标记。 展开更多
关键词 法医物证学 混合基因型 Y-STR
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A robust statistical procedure to discover expression biomarkers using microarray genomic expression data
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作者 ZOU Yang-yun YANG Jian ZHU Jun 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2006年第8期603-607,共5页
Microarray has become increasingly popular biotechnology in biological and medical researches, and has been widely applied in classification of treatment subtypes using expression patterns of biomarkers. We developed ... Microarray has become increasingly popular biotechnology in biological and medical researches, and has been widely applied in classification of treatment subtypes using expression patterns of biomarkers. We developed a statistical procedure to identify expression biomarkers for treatment subtype classification by constructing an F-statistic based on Henderson method Ⅲ. Monte Carlo simulations were conducted to examine the robustness and efficiency of the proposed method. Simulation results showed that our method could provide satisfying power of identifying differentially expressed genes (DEGs) with false discovery rate (FDR) lower than the given type I error rate. In addition, we analyzed a leukemia dataset collected from 38 leukemia patients with 27 samples diagnosed as acute lymphoblastic leukemia (ALL) and 11 samples as acute myeloid leukemia (AML). We compared our results with those from the methods of significance analysis of microarray (SAM) and microarray analysis of variance (MAANOVA). Among these three methods, only expression biomarkers identified by our method can precisely identify the three human acute leukemia subtypes. 展开更多
关键词 MICROARRAY BIOMARKER Henderson method Gene expression pattern Mixed linear model
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基因组疾病风险单倍型段的置换筛选检验(英文)
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作者 ALI Fadhaa 张健 《系统科学与数学》 CSCD 北大核心 2015年第12期1402-1417,共16页
通过测试的一群而不是单个的变异与疾病的关联捕获变异的集体行为,文章提出了单倍型关联分析.这种分析通常涉及未知相位多位置基因型在病例和对照组中稀疏频率.它从推断单倍型基因型,共同分类和边际筛查疾病相关的基因单倍型开始.不幸的... 通过测试的一群而不是单个的变异与疾病的关联捕获变异的集体行为,文章提出了单倍型关联分析.这种分析通常涉及未知相位多位置基因型在病例和对照组中稀疏频率.它从推断单倍型基因型,共同分类和边际筛查疾病相关的基因单倍型开始.不幸的是,解未知相位的不确定性可能对单倍型共同分类(因此对预测风险单倍型的精度)产生强烈影响.在这里,为了解决这一问题,文章提出一个替代办法:在阶段一中,选择风险基因型而不是共同分类推断单倍型.在阶段二中,从前一阶段选择风险基因型推断出风险单体型.采用仿真研究和实际数据分析评定提议的程序性能.相比现有的多个Z-检验程序,通过使用建议的程序可增加全基因组关联研究的功效. 展开更多
关键词 基于区域的关联分析 基因型混合模型 胜算比 基因组关联研究 期望及最大化算法
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