他还要求结果要按单体型基因来标出。
单体型是一组这样的基因，它们在遗传过程中能够以一个整体得到遗传。
A haplotype is a group of genes that tend to travel through the generations as a block.
Kedes博士要求测序的结果能够清晰地表明每一个单体型来自母本或是父本。
Dr Kedes wants it to be clear which haplotypes came from which parent.
异常核型涉及到三体型、单体型、罗伯逊易位、相互易位、不平衡重排等。
The abnormal is concerned in trisomy, monosomy, Robertsonian translocation, reciprocal translocation and rearrange.
本文还对祖传单体型研究的意义及随机个体单体型分型的可能性进行了探讨。
Moreover, the importance and the possibility of AH haplotyping of random individuals were discussed.
这些研究结果为水稻产量和品质育种中充分利用基因GW8的优异等位基因或单体型奠定了基础。
The results paved a way to apply the useful allelic variations or haplotypes of gene GW8 in rice yield and quality breeding programs.
这些等位基因的一个显著特点是：相同的AH具有相同的Y、X、V等位基因型（即呈单体型性质）。
A striking feature of the allelic patterns detected by these probes was that cells with the same AH had identical Y, X and V alleles(i. e, the alleles were haplotypic).
方法以脐带血库单体型频率和脐带血库容量为基础计算出某一具体表型的理论值与实际查询结果相比较。
Methods the theoretical value calculated on the basis of haplotype frequencies and actual finding result from cord blood bank were compared.
研究了在门德尔遗传定理和哈代-维恩伯格平衡假设下，三元家庭基因型数据的单体分型和单体型频率估计问题。
The problems of haplotyping and haplotype frequency estimation on trio genotype data under the Mendelian law of inheritance and the assumption of Hardy-Weinberg equilibrium are studied in this paper.
在结构上，染色体型断裂、染色单体型断裂、双着丝粒、双微小体这些畸变，差异也非常显著（P<0.01）。
Structurally, the aberrations of the chromosome-type break, chromatid break, double minute chromosome were also remarkably different (P<0.01).
由于基因组作图信息显示DXS713 2和DXS680 4之间存在紧密连锁，故用家系分析法确定女性的单体型。
On the genomic mapping information linkage disequilibrium between DXS7132 and DXS6804 was shown. Female haplotypes were determined by analyzing family trios.
并且发现，在相同的辐照剂量下，添加聚合物型HALS的PE的黄度比添加相应的单体型HALS的PE的黄度低一些。
It is also found that polymeric HALS is more effective in preventing PE from radiation-induced discoloration than corresponding monomeric HALS when radiation dose is higher than 200kGy.
Quintana - Murci博士的数据来自人类基因组单体型计划图，旨在对单核苷酸多态性，即SNPs进行归类。
Dr Quintana-Murci's data were drawn from a project called HapMap, which catalogues what are known as single-nucleotide polymorphisms, or SNPs.
人类基因组单体型图在检测在许多疾病涉及的基因变异方面的作用不言而喻并且这些结论也表明变异基因拷贝数指数也有类似的作用。
The HapMap has been invaluable in detecting variants involved in many diseases and these results suggest that the CNV index will prove similarly useful.
目的探讨云南汉族系统性红斑狼疮（SLE）患者抗U 1RNP抗体与HLADRB1、DQA1、DQB1等位基因及单体型的相关性。
Objective To investigate the association of HLA DRB1, DQA1, DQB1 alleles and haplotypes with Anti U1RNP of SLE in Yunnan Han Nationality.
本研究的另一目的就是应用病例对照单体型分析的方法研究在不同性别中，CYP4F 2基因单体型与心肌梗死的关系以及与高血压的关系。
Another aim of the present study was to assess the association between the human CYP4F2 gene and MI and EH, using a haplotype-based case-control study with a separate analysis of the gender groups.
单体型作图将精确定位区域确定于D1S1653和D1S2675之间7厘摩的范围。这些结果将为进一步克隆寻常型鱼鳞病致病基因提供帮助。
Haplotype analysis placed the critical region to a 7cM interval defined by D1S1653 and D1S2675. These results provide the basis for further identifying the gene responsible for IV disorder.
单体型作图将精确定位区域确定于D1S1653和D1S2675之间7厘摩的范围。这些结果将为进一步克隆寻常型鱼鳞病致病基因提供帮助。
Haplotype analysis placed the critical region to a 7cM interval defined by D1S1653 and D1S2675. These results provide the basis for further identifying the gene responsible for IV disorder.
应用推荐