splice site

Splice Site Identification Based on Improved Winnow Algorithm

基于改进的Winnow算法的剪接位点识别

In this paper , grouped weight matrix ( GWM ) method is proposed for splice site recognition.

摘要提出识别剪切位点的分组权重 矩阵 方法.

There was a wide spectrum of mutation type including frame shift, nonsense, splice site mutation, in frame insertion or deletion and missense mutations.

突变类型包括移码突变、无义突变、剪接异常、框架内插入或缺失以及错义突变。

An acceptor splice site mutation responsible for complete androgen insensitivity syndrome

雄激素受体基因剪接受点突变G~（3346）→T引起一例完全型雄激素不敏感综合征

Prediction of Alternative Splice Site and Analysis of Sequence Characteristic in Model Organism Genome

模式生物基因组中可变剪接位点的预测及序列特征分析

About 129 different HHT-related mutations have been reported so far, 79 in ENG and 50 in ALK-1, including missense, nonsense, frameshift, splice-site.

目前发现与HHT有关的不同的突变有129个，其中有79个与ENG基因突变有关，50个与ALK-1基因突变有关。ENG基因或ALK-1基因的突变有错义突变、无义突变、剪接点突变。

Two kinds of band type appeared in exon 8. A g/ t polymorphism was found 32 bp from the splice donor site of intron 8 in six tumors.

但外显子8表现出两种不同带型，该基因存在多态性，6例肿瘤在内含子8距拼接部32bp处存在两种不同碱基，基因型为g/t。

Hyperinsulinism of infancy associated with a novel splice site mutation in the SCHAD gene

婴儿高胰岛素血症可能与SCHAD基因的一处新的剪切位点突变有关

The cDNA sequencing was performed to analyze the change of FV coding sequence by splice site mutation.

通过cDNA测序分析剪切位点突变引起编码序列的变化。