这是比较基因组杂交的网页。
该程序为比较基因组序列分析产生印刷质量的图像。
The program serves to generate print-quality images for comparative genome sequence analysis.
此网站是有关河豚比较基因组图谱和基因组测序的资源数据库。
The site is the resource database concerning the comparative mapping and genome sequencing of fugu.
就像一个好的校对，它比较基因组复制一个新的原始和纠正错误。
Like a good proofreader, it compares a newly copied genome to the original and corrects mistakes.
比较基因组学的创立、内容及应用都充分体现着辩证思维的哲学观点。
There shows dialectic thinking in the foundation, content and application of comparative genome.
目的：评价比较基因组杂交(CGH)技术在白血病研究中应用的价值。
Objective: To evaluate the implication of comparative genomic hybridization (CGH) in leukemia study.
本文结果可用于禾谷类植物比较基因组学分析和植物功能基因组学的研究。
The data described in this paper shows a great potential in the comparative genomics of cereal crops and plant function genomics.
借助比较基因组学、模拟分析和具体试验，快速获取直向同源序列结构和功能信息。
The objective of this study is to efficiently obtain the structural and functional information of orthologs .
斑马鱼基因组测序计划在突变图谱与克隆，及比较基因组研究计划中扮演着重要的角色。
The zebrafish genome sequencing project has played important roles in mutant mapping and cloning, and comparative genomic research projects.
简介了关联分析和功能分子标记的概念，基于比较基因组学和生物信息开发分子标记的策略。
The concepts of association analysis and functional markers, and strategies of developing functional markers based on comparative genetics and bio-information were also introduced.
方法用比较基因组杂交技术(CGH)检测17例原发性NPC遗传物质的增多和丢失情况。
Methods Comparative genomic hybridization (CGH) was performed on 17 primary NPC biopsy specimens to find out any gain or loss of genetic material.
目的：鉴定用于肿瘤比较基因组杂交(CGH)微阵列细菌人工染色体(BAC)克隆的质量。
Objective To evaluate the quality of BAC clones for CGH microarrays in the detection of tumors.
猫和狗的基因组计划的长足进步，使猫和狗的基因组成为食肉目动物比较基因组研究理想的参照物。
The rapid progress in the canine and feline genome projects has made both genomes the ideal references for comparative genomic studies of carnivores.
用比较基因组杂交分析皮肤肿瘤高频率的染色体变异，将为相应肿瘤易感基因的筛选提供定位资料。
By analyzing altofrequent chromosome mutations, CGH can provide locating information for screening susceptibility genes of cutaneous tumors.
该数据库的目的就是加速从不同的观察点例如基因序列比较，主旨分析，聚类等进行比较基因组的研究。
The aim of MBGD is to facilitate comparative genomics from various points of view such as ortholog identification, paralog clustering, motif analysis and gene order comparison.
遗传图谱是数量性状基因定位(QTL)、基因图位克隆、比较基因组学研究以及分子标记辅助育种等的基础。
Genetic linkage map is a QTL mapping, the genetic map Spaces cloning, comparative genomics research and and molecular marker-assisted breeding the foundation.
比较基因组杂交技术用于分析染色体dna水平的改变，能获得良好结果并具有可重复性，从而提供了一条肿瘤细胞遗传学研究的可行路径。
CGH are applied to analyze DNA level changes of chromosome, can get good results and can be repeated well, it is an advisable way of tumor cellular genetic research.
他们确定了从线粒体基因组提取的一个368碱基对片段的化学结构序列，并且把它与古代犬以及现代犬、狼和郊狼的序列进行了比较。
They sequenced a 368 base pair fragment from the mitochrondrial genome and then compared it to sequences from ancient dogs, as well as to sequences from modern dogs, wolves, and coyotes.
狗的基因组序列能帮助研究人员更快的找到引起人类疾病的基因，因而这种动物是比较有用的疾病模型。
And a dog genome sequence has made the animals an even more useful model by quickening the search for disease-causing genes.
现在最重要的是，其他研究小组绘制出癌细胞的表观基因组图谱，然后与我们的图谱相比较。
What is important now is for other groups to map the epigenomes of cancer cells and compare those to ours.
在第一次全面比较了人类和尼安德特人的基因组以后，科学家们发现，人类有4%的DNA来自于这些遭到恣意诽谤的远亲们。
Scientists revealed that up to 4% of our DNA is Neanderthal after the first comparison of the complete genomes of humans and our much maligned Cousins.
为了将所得的结果片段重新整合到一张图谱上，paabo博士及其同事将他们的片段与已经完整测出的人类基因组进行了比较。
To reassemble the resulting pieces of information into a coherent picture, Dr Paabo and his colleagues compared their pieces with the human genome, which has been fully sequenced.
通过与现代同种族同文化的人群的基因组比较，该团队发现东西伯利亚的楚克族与Saqqa q族有最近的亲缘关系。
By comparing the genome with sequences from modern ethnic groups, the team found the Saqqaq's closest relatives to be the Chukchis of eastern Siberia.
这时需要引入计算机，对个人基因组序列中的30亿组碱基对进行比较。
This is where the computing comes in. Computers allow individual genomes-all 3 billion base pairs of them-to be compared.
马萨诸塞剑桥Broad研究所正在对美国真菌的基因组进行测序，待测序完成后，将该基因组与欧洲真菌的相比较，试图查明美国真菌对蝙蝠如此致命的原因所在。
The genome of the suspect American fungus is currently being sequenced at the Broad Institute in Cambridge, Massachusetts.
通过比较该图谱与病变细胞的表观基因组，科学家将能够弄清表观基因组的变异如何引起癌症及其他疾病的问题。
By comparing this with the epigenomes of diseased cells, scientists will be able to work out how glitches in the epigenome lead to cancers and other diseases.
研究人员发现，在个子比较矮的人身上，会出现低发生率拷贝数变异过剩——部分基因组缺失。
And the researchers found an excess of low frequency CNV deletions - where part of the genome is missing - in shorter people.
研究人员发现，在个子比较矮的人身上，会出现低发生率拷贝数变异过剩——部分基因组缺失。
And the researchers found an excess of low frequency CNV deletions - where part of the genome is missing - in shorter people.
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