They identified 5,351 non-synonymous SNPs per individual.
他们在每个个体中鉴定出5,351个非同义snp。
They identified 5, 351 non-synonymous SNPs per individual.
他们在每个个体中鉴定出5,351个非同义SNP。
Analysing SNPs is not the same as analysing a full genetic sequence.
分析SNPs和分析整个遗传序列是不一样的。
Some SNPs occur in genes themselves. Others are found in the DNA between genes.
有些单核苷酸多态性会出现于基因体本身，而其它一些则出现于基因体之间的脱氧核糖核酸之中。
All four SNPs demonstrated significant gender-by-gene interaction effects on blood pressure.
四个基因变异均表明性别在基因对血压的影响环节中起很大的作用。
Altogether she found 11 genes, in four neurotransmitter systems, where SNPs made a difference.
她总计发现了11个这样的基因，分布于四个神经递质系统，都与SNPs有关系。
People with a common ancestry, however, tend to have similar collections of SNPs (pronounced "snips").
但是，有相同祖先的人倾向于拥有相似的SNPs。
They found that the average person carries at least 2, 000 SNPs that change the meaning of a genetic "word."
他们发现平均每人携带有至少2000种基因“单词”已经改变的SNPs。
So far, the mapping work has nearly ended, however, the effort to explore new SNPs locus still continues.
目前，除了单核苷酸多态性位点的开发仍在进行之外，遗传图的绘制工作可以说已经完成。
Conclusion There are great differences in the SNPs of ATM gene between Chinese of Han ethnicity and Caucasian.
结论中国汉族人atm基因的单核苷酸多态与白人存在较大差异。
We studied SNPs at nine loci in 5414 subjects from the cardiovascular cohort of the malmo Diet and Cancer Study.
我们把马尔默饮食和癌研究的心血管组的5414位受试者中分成九个亚组来研究单核苷酸多态性。
Many SNPs are associated with disease-causing forms of genes, and more associations are being discovered every month.
许多SNPs都是与致病型基因有关的，并每个月都有新的关联被发现。
Scientists later refined the map by looking for single variations called SNPs or single nucleotide polymorphisms.
科学家们稍后通过利用称为SNP的单核苷酸多态性使遗传图谱更加精细。
They found three SNPs strongly associated with delusions, and all three SNPs are located in the neuregulin 3 gene.
他们发现三个单核苷酸多态性和妄想症有很大的关联，而且这三个单核苷酸多态性都位于Neuregulin3基因上。
The importance of developing rice SNPs for the rice breeding and functional genomics research was also elucidated.
最后阐述了SNP的开发对于水稻育种和功能基因组学研究的重要作用。
Current genetic tests analyze about 600,000 SNPs (single nucleotide polymorphisms) or 0.1 percent of the entire genome.
当前的基因检测分析了大约600,000个SNP(单核苷酸多态性)，只是整个基因组的千分之一。
It may be that in the rebound after the bottleneck, the slight hazardousness of these SNPs did not make much difference.
可能是在瓶颈期过后，群体数量回升时，数量很少的危险SNPs并没有多少作用。
Research on correlation between SNPs and efficacy may provide substantial rationale for tailored therapy of breast cancer.
研究不同基因的SNP与乳腺癌治疗反应的相关性可以为实现乳腺癌个体化治疗提供坚实的理论基础。
Now, tens of thousands SNPs have been discovered among the human genome and are introduced by many biological medicine networks.
目前已发现数万个SNP标记，且有多个生物医学网站开辟了专页对其加以介绍。
With time, natural selection will tend to flush the deleterious SNPs out, as it has done — relatively speaking — in African populations.
假以时日，自然选择会逐渐清除有害的SNPs，就像它曾经对非洲群体——相对而言——所作的那样。
Using about 50 different variations - single-nucleotide polymorphisms (otherwise known as SNPs) - researchers created a risk score.
研究者使用了约50种不同的变异——单核苷酸多态性(亦称SNPs)——创建了风险评分系统。
Each person's collection of these changes (called "single nucleotide polymorphisms, or SNPs) contributes to his or her individuality.
每个人带有的这些差异的集合（称作单核苷酸多态性，简称SNPs）造成了他/她的独特性。
Indeed, this year has seen a bumper harvest of strong, well-replicated associations between SNPs and diseases such as cancer and diabetes.
事实上，对于对那些与如癌症和糖尿病的疾病有密切并被完备复制的关联的SNPs研究，今年是一个丰收年。
Special attention has been drawn on the deleterious non-synonymous SNPs prediction based on sequence features and structure features.
其中重点介绍了基于序列特征和基于结构特征的有害错义snp预测方法。
Two other SNPs also showed significant gene-by-gender interactions, but their effects were not significant in either men or women alone.
另有两个基因变异表明，同性中，基因的变异对血压也会产生影响，但无论在男性还是女性中，这种影响和前者相比要小很多。
First, we carried out Electrophoretic Mobility Shift Assay (EMSA) to investigate the binding difference of SNPs and transcription factors.
首先使用凝胶迁移检测和疾病关联的SNP是否会影响某些转录因子的结合。
Using just one SNP, it got the origins of sole correct 96 per cent of the time, and with hake it was almost perfectly accurate with 10 SNPs.
仅用一个SNP，识别鲽鱼来源准确率为96%。用10个SNP识别鳕鱼类准确率几乎达到百分之百。
Dr Quintana-Murci's data were drawn from a project called HapMap, which catalogues what are known as single-nucleotide polymorphisms, or SNPs.
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.
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。
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