Segmentation of chromosome image is an important aspect in chromosome analysis and recognition.
染色体图像分割是染色体图像分析与识别的重要内容之一。
Chromosome analysis is an important and difficult task in clinical diagnosis, mutagen dosimetry and biological research.
引言染色体分析是临床诊断、诱变因素剂量学和生物学研究的一个重要而困难的任务。
Conclusion Chromosome analysis and detection of fusion genes are helpful in the diagnosis of AML and the differentiation diagnosis of AML subtype.
结论儿童aml进行染色体分析及融合基因的检测，有助于AML诊断及亚型之间的鉴别诊断。
Methods Routine G banding chromosome analysis and fluorescent in situ hybridization(FISH)were performed on lymph node specimens from 155 NHL patients.
方法采用常规染色体G 带分析和荧光原位杂交（FISH）方法对155例NHL患者的淋巴结组织进行细胞和分子遗传学研究。
In this paper, chromosomal karyotype of Wushen horse in Inner Mongolia was studied by using the peripheral blood lymphocytes culture method and conventional chromosome analysis techniques.
采用外周血淋巴细胞培养方法和常规染色体制备技术，对内蒙古乌审马染色体核型进行了分析研究。
The mechanism of carcinogenesis induced by CdCl 2 was studied through experiments of the malignant transformation of human embryo lung fibroblast in vitro, chromosome analysis and flow cytometry.
应用氯化镉致人胚肺成纤维细胞恶性转化实验、染色体分析、流式细胞术对氯化镉的致癌机理进行研究。
Acoording the ploidy analysis of chromosome, sequences and the survey of cultivation in field, Opisthopappus is primarily divided into two species.
结合这两个种的染色体倍性鉴定、序列分析和栽培观察实验，初步确定划分为两个种。
Genetic analysis of linkage used recombination to analyze the structure of chromosomes, to determine the locations of genes and their linear order along a chromosome.
遗传学的连锁分析是指通过遗传重组来研究染色体的结构，定位基因的位置，并确定基因在染色体上的排列顺序。
The methods of analysis of the chromosome aberrations mainly include routine staining method, G-banding method and FISH technique.
目前染色体畸变分析方法主要包括常规染色法、G显带法和FISH技术等。
Yeast Artificial Chromosome (YAC) techniques play an important role in the analysis of human genome and the isolation and cloning of disease related genes.
人工酵母染色体（YAC）技术是人类基因组分析及疾病相关基因的分离、克隆中的关键技术。
During the clinical and scientific research of cell genetics, the analysis of chromosome is an important task.
在细胞遗传学的临床与科学研究中，染色体分析是一项很重要的任务。
This paper mainly studies image preprocessing, feature extraction and classification analysis, accordingly realizes the chromosome recognition.
本文对染色体图像进行预处理、特征提取和分类分析，实现对染色体的识别。
Conclusion FISH is a more rapid, accurate and sensitive technique in analysis of chromosome aberrations in CLL. FISH may provide accurate information of molecular cytogenetics for CLL.
结论FISH是一种在分析CLL染色体数目和结构异常方面较为快速、准确和敏感的方法，可为CLL的研究提供较为准确的分子遗传学信息。
Objective:To analysis the aberration of chromosome 9 heterochromatin for persons suspected to have chromosome abnormalities.
目的分析疑有染色体异常个体的9号染色体异染色质区的变异。
Conclusion MN assay is simple, quick and accurate. It is a reliable biodosimetry in addition to chromosome aberration analysis.
结论MN法简便快速，结果准确，是除染色体畸变分析之外又一种可靠的生物剂量计。
Chromosome preparation and karyological analysis of Pleurobrachia globasa , a kind of Ctenophore, inhabiting in Xiamen Waters were studied and reported.
报道厦门港球型侧腕水母的染色体制备方法及核型分析结果。
Chromosome image analysis is one of the essential tasks in cytogenetics, especially in genetic syndrome diagnosis.
染色体图像分析是细胞遗传学研究的重要课题之一，它对人类疾病的诊断具有重要意义。
Conclusion: chromosome abnormality is one of the main causes of amenorrhea. Karyotype analysis of chromosome is absolutely necessary for the diagnosis and treatment of patient with amenorrhea.
结论染色体异常是闭经的主要原因之一，染色体核型分析对闭经患者的诊断和治疗是必要的。
Methods: The incidence rates of early reproduction inability of chromosome heteromorphism group and normal karyotype group were compared by using G, C-banded chromosome karyotype analysis.
方法：采用G、C显带染色体核型分析等方法，比较染色体异态核型人群和正常核型人群的早期生殖障碍的发生率。
Linkage map — a chromosome map showing the relative positions of genes and other DNA markers on the chromosomes, as determined by linkage analysis.
连锁基因或遗传标记在染色体上的相对位置的线性图。
Objective to search the forming cause and the correlation between the clinical phenotype and chromosome band by the cytogenetic analysis on a case of ring chromosome 21 syndrome.
目的通过对1例21号环状染色体综合征患者的细胞遗传学分析，探讨21号环状染色体的形成原因，临床表型与染色体区带的关系。
Methods Karyotypes of 2477 infertile men were analyzed by chromosome G banding and C banding analysis.
方法采取2477例不育男性的外周血进行染色体核型分析。
To analyze deletion of chromosome 16 by microsatellite analysis.
应用微卫星序列分析16号染色体缺失情况。
Conclusion Our data indicate that DXS10011 and DXS8377 are highly informative X chromosome markers for complicated kinship analysis.
结论本数据表明DXS10011和DXS8377在复杂的亲权鉴定中可提供高的遗传多态性信息。
The incidence rates of reproduction abnormality of chromosome polymorphism group and normal karyotype group have been compared by G-banded chromosome karyotype analysis.
本研究将染色体多态核型人群和正常核型人群分组，进行G显带染色体核型分析，以比较两组人群的生殖异常的发生率。
The result shows that the chromosome banding technique is more sensitive than the common chromosome aberration analysis for detecting complicated chromosome aberration, increasing the positive rate.
结果表明，染色体分带技术比一般分析方法更为敏感，并且能提高阳性检出率。
This method is applicable to the mulberry tree karyotype analysis as well as to the mulberry tree chromosome banding pattern study.
该方法适用于桑树核型分析，进一步可用于桑染色体分带。
The disease gene is exactly located on the chromosome 5 and chromosome 12 through parameter and non-parameter linkage analysis.
综合运用参数和非参数连锁分析，将致病基因定位到5号染色体和12号染色体上。
The disease gene is exactly located on the chromosome 5 and chromosome 12 through parameter and non-parameter linkage analysis.
综合运用参数和非参数连锁分析，将致病基因定位到5号染色体和12号染色体上。
应用推荐