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Simple sequence repeats,alternatively called microsatellites,are regarded as useful and efficient markers for map construction of cotton,which are abundant,locus-specific,often codominant and multiallelic.

在众多的分子标记中,SSR标记具有分布广泛、位点特异性、共显性、信息量高等优点,是构建棉花遗传连锁图谱最有优势的标记

A 1172 bp fragment was detected for Wx-7A gene using dominant marker primer from the Wx-A1 normal wheat, a 593 bp and a 574 bp fragment were detected using codominant marker primer from the Wx-A1α normal and Wx-A1 null wheat, respectively.

STS标记结果中,Wx-7A位点的显性标记引物在野生型中扩增出一条1172bp的特异带,即Wx-A1α基因出现;Wx-7A位点的共显性标记引物在野生型中扩增出一条593bp的特异带,在缺失类型中扩增出一条574bp的特异带。

The original data used were 5 in 12 RFLPs of a mouse F2 population including333 individuals presented in the software MAPMAKER.Classical and successive x2 testswere used to check segregation distortions of the codominant markers. And the resultexhibited that successive x2 tests was more efficient.

以MAPMAKER中提供的老鼠F2群体中333个体12个RFLP标记中的5个连锁标记为原始数据,用传统x2检测和连续x2检测两种方法处理共显性分子标记数据,比较它们对偏分离情况分析的能力,发现连续x2检测比传统的x2检测更加准确有效。

After analyzing glutinous rice waxy gene sequence reported by previous studies, two pairs of dominant and codominant STS molecular markers based PCR were designed for distinguishing glutinous rice, according to the distinctions between glutinous rice wx gene and nonglutinous rice Wx gene. Moreover, the whole sequences of the two Wx genes of nonglutinous rice reported by others were also aligned, and another two pairs of dominant STS molecular markers were designed to discriminate Wxa from Wxb based on the special site between the two genotypes. Then, corresponding rice genotypes were identified by the established new markers.

通过对前人公布的糯性水稻蜡质基因全序列测定结果的分析,根据糯性水稻与非糯性水稻蜡质基因序列位点的差异,设计了两个基于PCR扩增反应的可特异识别糯性水稻的显性和共显性STS分子标记;同时在前人公布的非糯性水稻蜡质基因的不同类型的全序列比对分析的基础上,选取了两种基因型特定的差异位点,设计了两个基于PCR扩增反应用于特异识别这两种Wx基因的显性STS分子标记,并用新建立的标记对相应的水稻基因型进行了检测。

Finally, the rules for ellipsis of conjunctional marks in C.A.S are concluded by studying whether these conjunctional marks can be omitted in sentences.

通过分析有这些关联标记的紧缩句,考察它们能否省略关联标记的情况,最后总结出紧缩句关联标记的省略规律。

The patterns are unlabeled and, therefore, there is no explicit correspondence between cluster labels in different partitions of an ensemble. An extra complexity arises when different partitions contain different numbers of clusters, often resulting in a label correspondence problem.

一方面,聚类的模式是未标记的,由不同聚类算法得到的标记之间无明显的联系;另一方面,各种划分可能含有不同的聚类个数,这就涉及到标记对应问题。

One hundred and eighty three pairs of SSR markers were selected to construct a genetic linkage map, covering 1 762.2 cM and on the average distance of 9.63 cM between the markers.

在两种环境条件下种植以普通玉米自交系丹232和爆裂玉米自交系N04为亲本构建的259个F2:3家系群体,采用SSR标记构建了包含183个标记的玉米遗传连锁图谱,覆盖玉米基因组1 762.2 cM,标记间平均距离为9.6 cM。

A linkage map was constructed using 151 polymorphismic markers.The map spans1841.9 cM covering 12 rice chromosomes with an average interval of 12.1 cM,which wellintegrated the markers from the high density linkage maps of rice.

以151个多型性标记位点构建了12条染色体的遗传连锁图谱,该图谱以标记间平均间距为12.1cM覆盖了水稻基因组的1841.9cM,该图谱较好地整合了目前已发表的水稻遗传图谱上的分子标记

A method is provided for encoding and decoding a sequence of digital data, according to which a portion of the sequence of digital data corresponds to a data block that includes several data packets, at least two data packets per data block containing an identifier. The position of the data packet within the corresponding data block can be determined based on the identifier, and the data is encoded or decoded by taking into account the identifier.

本发明给出了一种用于对数字数据序列进行编码和解码的方法,其中该数字数据序列的一部分相当于一个数据块,其中该数据块包含多个数据包,其中每个数据块的至少两个数据包分别包含一个特征标记,其中根据该特征标记确定数据包在所属的数据块中的位置,以及其中在考虑该特征标记的情况下对数据进行编码或解码。

Two hundred fifty-nine F2:3 families, developed from the cross between a dent corn inbred Dan232 and a popcorn inbred N04 were evaluated for its starch content in a replicated experiments under two environments. 183 pairs SSR were selected to construct a genetic linkage map with the genetic distance of 1 762.2 cM and on average 9.6 cM every marker.

在两种环境条件下种植以普通玉米自交系丹232和爆裂玉米自交系N04为亲本构建的259个F2∶3家系群体,采用SSR标记构建了包含183个标记的爆裂玉米遗传连锁图谱,覆盖玉米基因组1 762.2 cM,标记间平均距离为9.6 cM。

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